The DOI matches its Crossref record; 109 of the 110 references it cites were found in a registry or an index; 62 of the 157 sources its claims cite were checked for support.
Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function
Open accessAbstract
Neural circuits must maintain stable function in the face of many plastic challenges, including changes in synapse number and strength, during learning and development. Recent work has shown that these destabilizing influences are counterbalanced by homeostatic plasticity mechanisms that act to stabilize neuronal and circuit activity. One such mechanism is synaptic scaling, which allows neurons to detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites. Additional homeostatic mechanisms may allow local changes in synaptic activation to generate local synaptic adaptations, and network-wide changes in activity to generate network-wide adjustments in the balance between excitation and inhibition. The signaling pathways underlying these various forms of homeostatic plasticity are currently under intense scrutiny, and although dozens of molecular pathways have now been implicated in homeostatic plasticity, a clear picture of how homeostatic feedback is structured at the molecular level has not yet emerged. On a functional level, neuronal networks likely use this complex set of regulatory mechanisms to achieve homeostasis over a wide range of temporal and spatial scales.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
Homeostatic synaptic plasticity stabilizes neuronal firing through mechanisms such as synaptic scaling, which uses calcium-dependent sensors to bidirectionally regulate glutamate receptor accumulation at synapses. The review distinguishes global, cell-autonomous scaling from local/quasi-local and network-level mechanisms, and highlights that the molecular logic of homeostatic feedback remains incompletely understood.
Key findings
- Synaptic scaling is a cell-autonomous, global form of homeostatic plasticity: perturbing activity bidirectionally scales quantal amplitude (mEPSC/mini amplitude) up or down, regulating both AMPA and NMDA currents proportionally, and requires the GluA2 subunit of AMPARs.
- Scaling up and scaling down share some calcium/CaMKK/CaMKIV signaling but diverge in other molecular requirements; for example, scaling up depends completely on PSD-95, whereas scaling down can be supported by either PSD-95 or PSD-93.
- Local or quasi-local homeostatic mechanisms also exist: combined TTX and glutamate receptor block locally enhances GluA1-containing/GluA2-lacking AMPAR insertion via retinoic acid/RARα, and presynaptic release probability can be regulated quasi-locally by dendritic depolarization.
- Network-level and secreted-factor mechanisms contribute to excitation/inhibition balance: BDNF and glial TNFα are implicated, with TNFα suggested to be permissive/maintenance rather than instructive for scaling; in vivo visual deprivation can scale mEPSC amplitude and insert GluA2-containing AMPARs.
Methods
- This is a review article, not a primary experimental study; it synthesizes findings from in vitro and in vivo work on homeostatic synaptic plasticity at the neuromuscular junction and central mammalian synapses.
- The paper reviews signaling pathways, expression mechanisms, and functional roles of synaptic scaling, local/quasi-local plasticity, secreted factors, and synapse-type-specific rules.
- No new experimental sample, dataset, or statistical analysis is reported.
Limitations
- Stated: the signaling pathways underlying homeostatic plasticity are under intense scrutiny, but “a clear picture of how homeostatic feedback is structured at the molecular level has not yet emerged.”
- Stated: whether mechanisms underlying synaptic scaling in vivo and in other brain regions are similar to or distinct from those in cultured cortical neurons remains an open question.
- Stated: local homeostatic regulation remains controversial, and the physiological significance of some presynaptic changes, such as VGlut changes, remains to be determined. Evident: as a narrative review, it does not systematically quantify evidence or resolve conflicting findings across studies.
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Claims the paper makes
38 No full text of the sources · 25 Partly supported · 24 Own interpretation · 18 Supported · 10 Supported so far · 3 Not checked yet · 2 Not supported · 2 Sources not found · 2 No basis given · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“However, scaling up can also be induced by chronic changes in the level of depolarization in a BDNF-independent manner (Leslie et al. 2001), and the relationship between BDNF-mediated synaptic scaling and cell-autonomous synaptic scaling of excitatory inputs (Ibata et al. 2008) remains unclear.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Disputedcites Leslie et al. 2001 sourceExperimental — accuracy not yet measured
The Abstract (page unavailable) says chronic depolarization reduced excitatory quantal amplitude in a BDNF-independent manner—the opposite of scaling up. It attributes scaling up to low levels of BDNF, and the Discussion likewise distinguishes the BDNF-dependent increase from the depolarization-induced decrease. (LLM, conf=0.94)
Checked by a reasoning model — may be wrong.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Disputed
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Central neurons are embedded in complex networks composed of many cell types, including both excitatory and inhibitory neurons, and small changes in the balance between excitation and inhibition can have major effects on ongoing activity (Nelson and Turrigiano 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT CENTRAL MAMMALIAN SYNAPSES
What the sources say
- Partly supportedcites Nelson and Turrigiano 2008 sourceExperimental — accuracy not yet measured
The Inhibitory Plasticity section discusses balancing excitation and inhibition, and the Homeostatic Plasticity section says changes in synaptic strength can alter neuronal activity. The copy does not establish the more specific claim that small shifts in excitation–inhibition balance have major effects on ongoing activity. Page numbers are unavailable in our copy. (LLM, conf=0.78)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“where it was observed that loss of synaptic innervation initiated an increase in muscle excitability through changes in postsynaptic receptor number and localization.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT THE NEUROMUSCULAR JUNCTION
What the sources say
- Partly supportedcites Berg and Hall, 1975 sourceExperimental — accuracy not yet measured
The Abstract reports that chronic neuromuscular blockade increased extrajunctional acetylcholine-receptor binding and sensitivity in rat muscle, with changes similar to those after denervation. But the nerve remained active during blockade, so the paper does not establish that loss of synaptic innervation initiated the change or that receptor changes caused increased muscle excitability. (LLM, conf=0.84)
- Not checked — no full text of the sourcecites Sharpless 1975
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“One such mechanism is synaptic scaling, which allows neurons to detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
What the sources say
- Not checked — no full text of the sourcecites Turrigiano et al. 1998 source
- Partly supportedcites Gainey et al. 2009 sourceExperimental — accuracy not yet measured
The Introduction says that a drop in postsynaptic firing leads to AMPA-receptor accumulation at synapses, and the Discussion describes synaptic strengths scaling up or down in response to chronic changes in activity. The paper also links scaling to receptor trafficking, but the passages do not identify calcium-dependent sensors that detect firing-rate changes or regulate that trafficking. Page numbers are unavailable in our copy. (LLM, conf=0.86)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“One interesting implication of this model is that the firing rate set point is an emergent property that represents the stable point of all the opposing signaling pathways that operate on synaptic strength (Turrigiano 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Partly supportedcites Turrigiano 2008 sourceExperimental — accuracy not yet measured
In Concluding Remarks, the paper proposes that the activity set point could arise where opposing forces regulating receptor accumulation equalize. The citing sentence presents this proposed model as fact and extends it to all opposing signaling pathways that affect synaptic strength, which the passage does not establish. (LLM, conf=0.87)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“This global enhancement of AMPAR abundance in response to activity blockade requires sequences on the carboxyl terminus of the GluA2 subunit of the AMPAR (Gainey et al. 2009)”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Gainey et al. 2009 source
The Results section, “The GluR2 C-Tail is required for the expression of synaptic scaling” (page unavailable), reports that replacing the GluR2 C-tail with the GluR1 C-tail blocks synaptic scaling. The Discussion explicitly concludes that regulatory sequences on the GluR2 (GluA2) C-tail are required for TTX-induced AMPAR accumulation. (LLM, conf=0.94)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“the majority of studies that have blocked activity with tetrodotoxin (TTX) or AMPAR antagonists have observed a coordinated increase in GluA1 and GluA2 (O'Brien et al. 1998;Wierenga et al. 2005;Cingolani et al. 2008;Sun and Wolf 2009;Anggono et al. 2011; but see Thiagarajan et al. 2005).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites O'Brien et al. 1998 source
- Supportedcites Wierenga et al. 2005 source
The Results section, “Effect of activity blockade on cell-surface GluR1 and GluR2,” reports that TTX treatment increased synaptic GluR1 and GluR2 accumulation proportionally in cultured neocortical neurons. This supports citing the study as an example of a coordinated increase; it does not need to establish the collective claim about the majority of studies on its own. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites Cingolani et al. 2008 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“by measuring minis arising from many synapses onto the same neuron, it was observed that modulating network activity induced uniform increases or decreases in the entire mini amplitude distribution, in effect scaling postsynaptic strength up or down (Turrigiano et al. 1998;Desai et al. 2002;Gainey et al. 2009).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Turrigiano et al. 1998 source
- Not checked — no full text of the sourcecites Desai et al. 2002 source
- Partly supportedcites Gainey et al. 2009 sourceExperimental — accuracy not yet measured
The Results section ('GluR2 knockdown blocks synaptic scaling, but does not block LTP'; page not provided) reports that activity blockade proportionally scaled up the mEPSC amplitude distribution. The copy does not report a corresponding activity-induced decrease across that distribution. Its reference to scaling a distribution down describes a mathematical comparison with controls, not a physiological decrease in postsynaptic strength. (LLM, conf=0.86)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Every source the paper cites for this claim was checked and supports it.
In the paper
“On the presynaptic side, there is compelling evidence that homeostatic modulation of neurotransmitter release probability (P r ) can happen at the level of individual dendritic branches.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Branco et al. 2008 source
The Introduction reports that release probability homeostatically adapts to the number of synapses on a dendritic branch and to selective increases in postsynaptic activity. The Discussion adds that selectively stimulating a small group of synapses caused a compensatory decrease confined to the stimulated area, supporting local modulation at or below the branch level. (LLM, conf=0.93)
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“It is widely agreed that synaptic scaling involves postsynaptic changes in receptor accumulation (Turrigiano 2008), but under some circumstances additional presynaptic changes can also be recruited (Davis and Bezprozvanny 2001;Rich and Wenner 2007;Thiagarajan et al. 2007).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Turrigiano 2008 source
In “Homeostatic Regulation of AMPA Receptor Trafficking,” the review states that there is consensus that changes in postsynaptic receptor accumulation are a major expression mechanism of synaptic scaling. This directly supports the claim attributed to Turrigiano (2008). (LLM, conf=0.95)
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Supported
- It may state two separate claims as one. 41
- Probably not a substantial claim. 8
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Further, whereas scaling up is completely dependent on the scaffold protein PSD-95, scaling down can be supported by either PSD-95 or PSD-93 (Sun and Turrigiano 2011).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Disputedcites Sun and Turrigiano 2011 sourceExperimental — accuracy not yet measured
The Discussion states the reverse: scaling down is critically dependent on PSD-95, while scaling up can be supported by either PSD-95 or PSD-93 in young neurons. The Results section ‘PSD-95 is necessary for scaling down’ likewise says PSD-93 cannot compensate for loss of PSD-95 during scaling down. The paper adds that scaling up becomes dependent on PSD-95 in older neurons. (LLM, conf=0.90)
Checked by a reasoning model — may be wrong.
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Disputed
Every source the paper cites for this claim was checked and supports it.
In the paper
“It is worth noting, however, that postsynaptic knockdown of GluA2 is able to completely block synaptic scaling (Gainey et al. 2009), suggesting that if there is a presynaptic change in transmitter packaging it is not sufficient to enhance mini amplitude on its own.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Gainey et al. 2009 source
The Results section (‘GluR2 knockdown blocks synaptic scaling, but does not block LTP’) reports that TTX increased mEPSC amplitude in control neurons but not in GluR2-knockdown neurons. The Discussion explicitly says the knockdown completely blocked synaptic scaling. The statement about presynaptic transmitter packaging is the citing authors’ inference, not a separate finding attributed to this source. (LLM, conf=0.94)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Given that the postsynaptic and presynaptic responses to activity deprivation can occur independently (Wierenga et al. 2005(Wierenga et al. , 2006)), it is likely that they represent distinct forms of plasticity induced by distinct signaling pathways.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Wierenga et al. 2005 source
The Discussion states that increased postsynaptic receptor accumulation can occur without measurable changes in presynaptic function and describes the changes as separable, independent homeostatic mechanisms. The statement about distinct signaling pathways is the citing authors’ inference, not the part directly attributed to this source. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites Wierenga et al. 2006 source
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Like scaling up, scaling down in response to elevated network activity is a cell-autonomous function of postsynaptic firing, and involves enhanced calcium influx (Fig. 2), gene transcription, the CaMKK/CaMKIV signaling pathway, and targets the GluA2 subunit (Goold and Nicoll 2010).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Partly supportedcites Goold and Nicoll 2010 sourceExperimental — accuracy not yet measured
The Discussion reports that cell-autonomous excitation drives calcium-dependent synaptic depression through CaMKK/CaMK4. It also limits the transcription and GluA2 requirements to AMPAR depression: NMDAR depression does not require them. The citing sentence omits that distinction when describing scaling down generally. (LLM, conf=0.85)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Lowering presynaptic firing with an inwardly rectifying K ir channel was observed to selectively enhance the accumulation of GluA1 at postsynaptic sites, suggesting the existence of a synapse-specific form of homeostatic compensation to reduced receptor activation (Hou et al. 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Hou et al. 2008 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Interestingly, synaptic scaling protocols homeostatically regulate both the NMDA and the AMPA component of glutamatergic synaptic currents, and the change in AMPA and NMDA currents are proportional at individual synapses (Watt et al. 2000;Perez-Otano and Ehlers 2005).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Supportedcites Watt et al. 2000 source
The Abstract reports that long-lasting changes in activity scaled AMPA and NMDA currents up and down proportionally. It also says their ratio at different synapses onto the same neuron was preserved after scaling. The findings concern neocortical synapses expressing both receptor types. (LLM, conf=0.93)
- Not checked — no full text of the sourcecites Perez-Otano and Ehlers 2005 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Interestingly, the same manipulation (activity blockade using TTX or AMPAR antagonists) that only affects mini amplitude in young cultures (Turrigiano et al. 1998;Wierenga et al. 2005) can also induce changes in mini frequency and in presynaptic release probability in older neuronal cultures (Wierenga et al. 2006), through a process that involves postsynaptic hyperpolarization and a drop in”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Turrigiano et al. 1998 source
- Supportedcites Wierenga et al. 2005 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Not checked — no full text of the sourcecites Wierenga et al. 2006 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Additionally, there is evidence that the neurotrophin brain-derived neurotrophic factor (BDNF) (Rutherford et al. 1998), the immediate early gene Arc (Shepherd et al. 2006), the cytokine TNFa (Stellwagen and Malenka 2006;Steinmetz and Turrigiano, 2010), the immune molecule MHC1 (Goddard et al. 2007), b3 integrins (Cingolani et al. 2008), the AMPAR binding protein PICK1 (Anggono et al. 2011), and”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
- Supportedcites Shepherd et al. 2006 source
The cited paper supports the Arc portion of the multi-citation claim. In “Arc/Arg3.1 Regulates Homeostatic Synaptic Scaling of AMPARs” (page unavailable), cultured wild-type hippocampal neurons showed activity-dependent changes in surface AMPA receptors, while Arc/Arg3.1 knockout neurons lacked those changes. The other molecules are attributed to other citations, not to this paper. (LLM, conf=0.94)
- Not matchedcites Stellwagen and Malenka 2006;Steinmetz and Turrigiano, 2010
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
plainconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Interestingly, chronic hyperpolarization of an entire neuron by expression of an inwardly rectifying K channel (K ir ) does not induce postsynaptic scaling (Burrone et al. 2002;Hou et al. 2008), suggesting that chronic global hyperpolarization of neuronal dendrites and somata overrides the signals that induce scaling up in response to a drop in firing.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Burrone et al. 2002 source
- Partly supportedcites Hou et al. 2008 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“A number of reports have suggested that activity-dependent BDNF release is critical for scaling of inhibitory synapses onto pyramidal neurons as well as the homeostatic regulation of excitatory synapses onto inhibitory neurons (Rutherford et al. 1997(Rutherford et al. , 1998;;Copi et al. 2005;Swanwick et al. 2006).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Partly supportedcites Rutherford et al. 1997 sourceExperimental — accuracy not yet measured
The Discussion reports that activity blockade reduces inhibition onto cortical pyramidal neurons and that exogenous BDNF prevents this reduction, supporting the inhibitory part of the claim. It infers reduced endogenous BDNF production rather than directly demonstrating activity-dependent release, and it does not establish homeostatic regulation of excitatory synapses onto inhibitory neurons; the excitatory currents it mentions are onto pyramidal neurons. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
- Not checked — no full text of the sourcecites Copi et al. 2005 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“TNFa signaling was not necessary for the induction of early (6 h) scaling, but became essential for maintenance of scaling during prolonged (.24 h) activity blockade.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Supportedcites Steinmetz and Turrigiano 2010 source
The Results section reports that blocking TNFα signaling for 6 hours did not prevent early scaling, whereas 24 hours of blockade prevented scaling and reversed scaling that had already been induced. The Discussion interprets this as a requirement for TNFα signaling to maintain synapses’ ability to express or maintain scaling during prolonged activity blockade. (LLM, conf=0.92)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“This model is based on the observations that TNFa levels are elevated by prolonged (48 h) activity blockade, acute application of TNFa (or conditioned media from activity-blocked cultures) increases mEPSC amplitude, and scaling up in response to prolonged activity blockade is prevented by blocking TNFa signaling (Beattie et al. 2002;Stellwagen et al. 2005;Stellwagen and Malenka 2006).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not checked — no full text of the sourcecites Beattie et al. 2002 source
- Partly supportedcites Stellwagen et al. 2005 sourceExperimental — accuracy not yet measured
The culture electrophysiology methods (page not provided) say TNFα was applied 15–25 minutes before recording, and the Figure 5 caption reports a significant increase in mEPSC amplitude in TNFα-treated cultures. The passages do not support the separate claim about conditioned media from activity-blocked cultures. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites Stellwagen and Malenka 2006 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Synapses onto the same dendrite tended to have similar P r , and there was an inverse relationship between synapse number and P r onto individual dendrites, suggesting that this regulation happens in a”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Partly supportedcites Branco et al. 2008 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In apparent conflict with this model, a positive correlation between P r and synaptic strength at cortical synapses has been reported (Hardingham et al. 2010;Kay et al. 2011), but because in these studies synaptic strength was measured at unitary connections, it remains an open possibility that such an inverse correlation exists at the level of summed dendritic input.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Hardingham et al. 2010 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Could not verifycites Kay et al. 2011 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 0 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 2 unverifiable. Expand the claim to see per-atom verdicts.
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“This quasi-local (dendrite-wide) form of presynaptic homeostasis has been suggested to prevent synaptic saturation owing to strong depolarization from summed inputs onto a dendrite, by reducing P r when postsynaptic activation rises too high (Branco et al. 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Supportedcites Branco et al. 2008 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“BDNF was the first such secreted factor suggested to play a role in homeostatic plasticity (Rutherford et al. 1997(Rutherford et al. , 1998)).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Partly supportedcites Rutherford et al. 1997 sourceExperimental — accuracy not yet measured
The Discussion (page not specified in our copy) says BDNF regulates inhibition in cortical cultures and may help reduce inhibition when activity falls too low, supporting a role in homeostatic plasticity. The paper does not establish the historical claim that BDNF was the first secreted factor suggested to have that role. (LLM, conf=0.84)
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Unlike TTX treatment, acute TNFa application does not scale up mini amplitude and adding TNFa to prescaled synapses actually reduces synaptic strength, indicating that scaling and TNFa are neither additive nor simply occlusive (Steinmetz and Turrigiano 2010).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Supportedcites Steinmetz and Turrigiano 2010 source
The Results section, “Synaptic scaling modulates but does not occlude the effect of TNFα application,” reports that TNFα increased mEPSC amplitude at control synapses but did not produce the multiplicative change characteristic of TTX-induced scaling. Applied after 24 hours of TTX, it reduced mEPSC amplitude rather than adding to or merely occluding the increase. The supplied copy gives no page number for these passages. (LLM, conf=0.91)
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In contrast, dark rearing increases the abundance of GluA2-lacking receptors and requires GluA1 phosphorylation, suggesting that these two modes of deprivation may induce different forms of compensatory synaptic plasticity (Goel and Lee 2007;Goel et al. 2011).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Partly supportedcites Goel and Lee 2007 sourceExperimental — accuracy not yet measured
The Results section (page unavailable) reports that two days of dark rearing increased AMPA receptor-mediated mEPSC amplitude in mouse visual cortex. The Discussion (page unavailable) says dark rearing increased GluR1 (GluA1) phosphorylation, but our copy does not establish that phosphorylation is required or that GluA2-lacking receptors become more abundant. (LLM, conf=0.83)
- Partly supportedcites Goel et al. 2011 sourceExperimental — accuracy not yet measured
The Results report that two days of dark exposure increased functional calcium-permeable AMPA receptors, consistent with more GluA2-lacking receptors; the Discussion says deprivation-induced synaptic changes require GluA1 phosphorylation. But the Methods specify that mice were raised under normal lighting until postnatal day 21, then exposed to darkness for two days. The paper does not establish these effects for dark rearing from birth. (LLM, conf=0.83)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Interestingly, binocularly driven neurons maintained a similar average level of combined responsiveness to the two eyes, suggesting that the drop in deprived eye responsiveness was compensated by an increase in nondeprived eye responsiveness (Mrsic-Flogel et al. 2007); a very similar response homeostasis following visual deprivation has been reported at retinotectal synapses (Chandrasekaran et al.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Supportedcites Mrsic-Flogel et al. 2007 source
The paper states that neurons with binocular input adjusted their eye-specific responses so the summed visual response remained roughly preserved. It also reports that after monocular deprivation, deprived-eye responses fell while nondeprived-eye responses rose (Results, page unavailable). (LLM, conf=0.93)
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“When one eye is deprived of patterned vision during the classical critical period (using lid suture) there is a change in the ability of the two eyes to drive neurons within the binocular portion of visual cortex: cortical neurons rapidly (within 2 or 3 days) lose responsiveness to the deprived eye, and then more slowly (over 4 -6 days) gain responsiveness to the nondeprived eye (Frenkel and Bear”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Not checked — no full text of the sourcecites Frenkel and Bear 2004 source
- Partly supportedcites Mrsic-Flogel et al. 2007 sourceExperimental — accuracy not yet measured
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Not checked — no full text of the sourcecites Kaneko et al. 2008 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“This possibility is raised by the finding that the same visual deprivation paradigm that scales minis up in younger mice produces nonmultiplicative changes in minis in older mice, suggesting that not all synapses are affected equally (Goel and Lee 2007); however, this could also reflect the simultaneous activation of synaptic scaling and Hebbian, synapse-specific mechanisms (see Turrigiano 2011”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Supportedcites Goel and Lee 2007 source
The “Loss of multiplicative synaptic scaling in adult mice” section reports that two days of dark rearing increased mEPSC amplitude multiplicatively in P23 mice (Fig. 4a). The same section reports that the increase in P97 mice did not follow a global multiplicative mechanism (Fig. 4e). (LLM, conf=0.94)
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Visual deprivation induced by optic nerve block scale ups mEPSC amplitude in vivo as in vitro, and results in insertion of GluA2-containing AMPAR (Desai et al. 2002;Maffei and Turrigiano 2008;Gainey et al. 2009).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Not checked — no full text of the sourcecites Desai et al. 2002 source
- Partly supportedcites Maffei and Turrigiano 2008 sourceExperimental — accuracy not yet measured
The Results section on experience-dependent plasticity at excitatory layer 2/3 synapses reports that visual deprivation by intraocular TTX injection increased AMPA mEPSC amplitude in rats. The paper does not establish an in vitro comparison or report insertion of GluA2-containing AMPARs, so those parts of the sentence are unsupported by this source. (LLM, conf=0.88)
- Supportedcites Gainey et al. 2009 source
The Results section reports that visual deprivation by intraocular TTX significantly increased mEPSC amplitude in visual cortical neurons. The Discussion states that scaling in vivo after monocular TTX injection increased accumulation of GluR2-containing AMPARs (now called GluA2-containing AMPARs), consistent with the claim. (LLM, conf=0.92)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In visual cortex the expression of synaptic scaling is developmentally regulated (Desai et al. 2002;Maffei et al. 2004Maffei et al. , 2006;;Maffei and Turrigiano 2008); synaptic scaling is expressed by pyramidal neurons in layer 4 early in postnatal development, but then turns off in layer 4 and begins to be expressed in layer 2/3 pyramidal neurons around the opening of the classical visual system”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Desai et al. 2002 source
- Supportedcites Maffei and Turrigiano 2008 source
Split into 2 atoms — 2 confirmed, 0 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
- Partly supportedcites Goel and Lee 2007 sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) reports scaling in layer 4 at P14–P16 but not P21–P23, with the opposite pattern in layer 2/3; it also says the authors’ data extend layer 2/3 plasticity through adulthood. Our copy does not establish that the switch coincides with the opening of the classical visual critical period, or identify the early layer 4 cells specifically as pyramidal neurons. (LLM, conf=0.82)
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“For example, reductions in glutamate receptor function, or chronic hyper-polarization of the muscle, lead to compensatory increases in transmitter release that restore evoked transmission to control levels (Paradis et al. 2001).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT THE NEUROMUSCULAR JUNCTION
What the sources say
- Not checked — no full text of the sourcecites Paradis et al. 2001 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“When cortical or hippocampal neurons are induced to fire more than normal, over many hours firing returns to baseline levels, and similarly, if neuronal firing is reduced over time, neurons compensate and again firing is restored (Fig. 1A) (Turrigiano et al. 1998;Burrone et al. 2002).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT CENTRAL MAMMALIAN SYNAPSES
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, without forces that prevent the excitability of the postsynaptic neuron from changing in response to correlation-based plasticity mechanisms, their specificity breaks down and information can no longer be effectively stored through differences in synaptic strengths.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“On a functional level, neuronal networks likely use this complex set of regulatory mechanisms to achieve homeostasis over a wide range of temporal and spatial scales.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: fails — It may be too vague to check against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. It may be too vague to check against evidence.
In the paper
“More recently work at the mammalian and invertebrate NMJ has shown that perturbations in postsynaptic function can lead to compensatory changes in presynaptic release, and vice versa (Davis and Bezprozvanny 2001).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > HOMEOSTATIC PLASTICITY AT THE NEUROMUSCULAR JUNCTION
What the sources say
- Not checked — no full text of the sourcecites Davis and Bezprozvanny 2001 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper states this without a source or data behind it here, so there is nothing to check it against. The quote shows it is in the paper.
In the paper
“Although all of these phenomena are theoretically capable of serving a homeostatic function, for many of them such a function has not been directly shown.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > Abstract
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: fails — The paper may give no reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. The paper may give no reason why it holds.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Thus, cell-autonomously induced synaptic scaling is fundamentally different from LTP and LTD: it operates over a longer temporal scale (hours), a wider spatial scale (global), and utilizes distinct trafficking steps and molecular machinery to enhance or reduce the synaptic accumulation of GluA2-containing AMPAR at most if not all synapses onto a neuron.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“The ability of synapses to undergo postsynaptic homeostatic regulation as a function of purely local changes in transmitter release and receptor activation thus remains controversial and may require either extreme presynaptic hyperpolarization (such as would be obtained with presynaptic expression of K ir ) or a situation in which spiking and transmitter release are both severely impaired (see”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“On the other hand, theoretical work has suggested that quasi-local forms of homeostasis that act on groups of nearby synapses can serve a useful normalization function without severely disrupting Hebbian plasticity (Rabinowitch and Segev 2006a,b).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Not matchedcites Rabinowitch and Segev 2006a,b
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgedconditional- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
- Not matched
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“This suggests that a drop in somatic calcium influx will simultaneously enhance signaling in the pathways that scale synapses up and reduce signaling in the pathways that scale synapses down, and vice versa when firing rises.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Such a postsynaptic scaling process has the attractive property of allowing neurons to stabilize activity without changing the relative strength of synaptic inputs, thus avoiding disrupting information storage or processing mechanisms that rely on differences in synaptic weights (Fig. 1B).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“The locus of change during homeostatic plasticity has important consequences for circuit function, because (for example) presynaptic changes in release probability will strongly affect short-term plasticity and thus the dynamics of information transfer across synapses, whereas a postsynaptic change in receptor accumulation can scale postsynaptic responsiveness without affecting the short-term”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Abbott and Nelson 2000 source
boosteddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Selectively blocking firing by microperfusion of TTX to the soma of individual neurons scales up synaptic strengths to the same degree as blockade of network activity, whereas local block of synaptic transmission does not induce a local enhancement of receptor accumulation (Ibata et al. 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
What the sources say
- Not checked — no full text of the sourcecites Ibata et al. 2008 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“In dissociated cortical cultures it has been shown that excitatory synapses onto excitatory pyramidal neurons are scaled up by activity blockade, whereas excitatory synapses onto GA-BAergic interneurons are not (Rutherford et al. 1998).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“If this mechanism operates in vivo, it predicts an inverse relationship between P r and the summed synaptic strength onto a dendritic branch.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
hedgedcorrelational- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
In the paper
“This is consistent with evidence that chronic hyperpolarization of entire neurons (including dendrites) results in enhanced P r (Burrone et al. 2002), suggesting that P r can be bidirectionally regulated by changes in the amount of dendritic depolarization.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > LOCAL AND QUASI-LOCAL FORMS OF HOMEOSTATIC SYNAPTIC PLASTICITY IN CENTRAL NEURONS
What the sources say
- Not checked — no full text of the sourcecites Burrone et al. 2002 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“Blocking BDNF signaling mimics, and exogenous BDNF application prevents, the effects of activity blockade on excitatory minis, suggesting that in neocortical neurons activitydependent BDNF release could mediate synaptic scaling (Rutherford et al. 1998).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not checked — no full text of the sourcecites Rutherford et al. 1998 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“BDNF is thought to be released as a function of pyramidal neuron activity, and activates Trk receptors on both pyramidal and interneurons (Lu 2003).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not matchedcites Lu 2003
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Not matched
In the paper
“It was recently proposed that prolonged activity blockade (with TTX) increases glial release of TNFa, which then acts on neurons to enhance AMPAR insertion and scale up mEPSC amplitude (Stellwagen and Malenka 2006).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > ROLE OF NETWORK ACTIVITY AND SECRETED FACTORS IN THE INDUCTION OF HOMEOSTATIC PLASTICITY
What the sources say
- Not checked — no full text of the sourcecites Stellwagen and Malenka 2006 source
hedgeddirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
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In the paper
“These distinct plasticity rules at different classes of excitatory and inhibitory synapse are consistent with an overall homeostatic shift in the balance between excitation and inhibition, as the net effect of the changes induced by activity blockade are to enhance excitation and reduce inhibition, which will act to restore network excitability.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Interestingly, not all excitatory neurons in cortical networks express synaptic scaling.In hippocampal networks CA1 neurons scale synapses up in response to activity blockade, whereas CA3 neurons do not (Kim and Tsien 2008).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Kim and Tsien 2008 source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Interestingly, in visual cortical microcircuits the locus of homeostatic plasticity changes as the circuit matures.Early in postnatal development layer 4 (the first input layer to cortex, and the first layer to mature) responds homeostatically to brief (2 days) inactivation of the optic nerve with TTX (Desai et al. 2002;Maffei et al. 2004), whereas later (at the opening of the classical visual”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“When sensory drive to primary visual cortex is lowered in vivo, connections from fast-spiking basket cells onto layer 4 pyramidal neurons are reduced in amplitude, whereas connections from another class of interneuron become sparser but stronger (Maffei et al. 2004).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > SPECIFICITY OF SYNAPTIC SCALING RULES FOR SYNAPSE TYPE
What the sources say
- Not checked — no full text of the sourcecites Maffei et al. 2004 source
plaindirect- Asserted: passes — The authors put it forward as true.
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In the paper
“Similarly, in visual cortex during the second and third postnatal weeks when synaptogenesis is high, there is an inverse relationship between the frequency and amplitude of mEPSCs onto pyramidal neurons, and this can be prevented by raising animals in the dark (Desai et al. 2002).”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > FUNCTIONS OF HOMEOSTATIC PLASTICITY IN VIVO
What the sources say
- Not checked — no full text of the sourcecites Desai et al. 2002 source
plaincorrelational- Asserted: passes — The authors put it forward as true.
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In the paper
“Neurons and networks use a family of homeostatic synaptic plasticity mechanisms to stabilize firing rates in the face of developmental or learning-induced changes in drive, and this contributes to the ability of central neuronal networks to maintain stable function and enables networks to maintain the specificity of synaptic changes that encode information.”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CONCLUDING REMARKS
plaindirect- Asserted: passes — The authors put it forward as true.
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The paper relies on this without support.
Neural circuits must maintain stable function in the face of plastic challenges including changes in synapse number and strength during learning and development.
“Neural circuits must maintain stable function in the face of many plastic challenges, including changes in synapse number and strength, during learning and development.”
The paper relies on this without support.
At the neuromuscular junction, as muscle fibers grow, motor neurons must remain capable of bringing them over threshold for contraction.
“The stability problem at the neuromuscular junction (NMJ) is fairly simple: As muscle fibers grow, motor neurons must remain capable of bringing them over threshold for contraction.”
The paper relies on this without support.
The forces that generate flexibility and those that generate stability are able to coexist without interfering with each other.
“Somehow the forces that generate flexi-bility and those that generate stability are able to coexist without interfering with each other, and together enable the remarkable ability of organisms to generate behaviors that are both coherent and adaptable.”
Claims other papers make about this one
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In the citing paper
“normalizing by the total number of incoming synapses provides a form of homeostatic synaptic scaling46.”
From Predicting modular functions and neural coding of behavior from a synaptic wiring diagram (2024) · cites this paper as [46]
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In the paper
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > CELL-AUTONOMOUS, GLOBAL SYNAPTIC SCALING OF EXCITATORY SYNAPSES
“(Evers et al. 2011)”
§ Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function > References
“29. Evers DM, Matta JA, Hoe HS, Zarkowsky D, Lee SH, Isaac JT, Pak DT. 2010. Plk2 attachment to NSF induces homeo- static removal of GluA2 during chronic overexcitation.”
Citations
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“The online first http://cshperspectives.cshlp.org/site/misc/subscribe.xhtml go to: Cold Spring Harbor Perspectives in BiologyTo subscribe to Copyright © 2011 Cold Spring Harbor Laboratory Press; all rights reserved”
MethodActivity-dependent scaling of quantal amplitude in neocortical neurons
Turrigiano, G. G., Leslie, K. R., Desai, N. S., Rutherford, L. C., & Nelson, S. B. (1998) · Nature · doi:10.1038/36103 · Cited by 2,226
Self-citationSynaptic scaling mediated by glial TNF-α
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The self-tuning neuron: synaptic scaling of excitatory synapses
Turrigiano, G. G. (2008) · Cell · doi:10.1016/j.cell.2008.10.008 · Cited by 1,533
Self-citationControl of Synaptic Strength by Glial TNFα
Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344
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Variability, compensation and homeostasis in neuron and network function
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Cited by
Sorted by citations
Items 501–600 of 1,136
Modeling Resilience to Damage in Multiple Sclerosis: Plasticity Meets Connectivity
Bassi, M. S., Iezzi, E., Pavone, L., Mandolesi, G., Musella, A., Gentile, A., Gilio, L., Centonze, D., & Buttari, F. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms21010143 · Cited by 20
“Anti-homeostatic and homeostatic plasticity cooperate to promote optimal brain network topology and are involved in symptom compensation and remodeling after brain damage [35,36].”
BackgroundBasic mechanism of neuroplasticity
Kossut, M. M. (2019) · Neuropsychiatria i Neuropsychologia · doi:10.5114/nan.2019.87727 · Cited by 20
“Daje to efekt regulacji progu dla wywoływania LTP i LTD zależny od doświadczenia i stanu neuronu (Turrigiano 2012).”
BackgroundEffects of prenatal opioid exposure on synaptic adaptations and behaviors across development
Simmons, S. C., Grecco, G. G., Atwood, B. K., & Nugent, F. S. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109312 · Cited by 18
Astrocyte strategies in the energy-efficient brain
Fernández-González, I., & Galea, E. (2022) · Essays in Biochemistry · doi:10.1042/ebc20220077 · Cited by 16
The endoplasmic reticulum puts a new spin on synaptic tagging
Konietzny, A., Wegmann, S., & Mikhaylova, M. (2022) · Trends in Neurosciences · doi:10.1016/j.tins.2022.10.012 · Cited by 18
Acoustic deprivation modulates central gain in human auditory brainstem and cortex
Hutchison, P., Maeda, H., Formby, C., et al. (2022) · Hearing Research · doi:10.1016/j.heares.2022.108683 · Cited by 16
Fukata, Y., Fukata, M., MacGillavry, H. D., Nair, D. K., & Hosy, E. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.2104-23.2024 · Cited by 18
Werner, C. T., Murray, C. H., Reimers, J. M., Chauhan, N. M., Woo, K., Molla, H. M., Loweth, J. A., & Wolf, M. E. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.12.014 · Cited by 15
“…after scaling up Synaptic scaling is a form of homeostatic plasticity used by neuronal circuits to maintain stable function in response to destabilizing influences (Fernandes and Carvalho, 2016; Lee, 2012; Lee et al., 2014; Turrigiano, 2012; Turrigiano and Nelson, 2004; Vitureira et al., 2012).”
InfluentialTinnitus: Prospects for Pharmacological Interventions With a Seesaw Model
Tetteh, H., Lee, M.-S., Lau, C. G., Yang, S., & Yang, S. (2017) · The Neuroscientist · doi:10.1177/1073858417733415 · Cited by 16
“These receptors contribute to neuronal excitability, plasticity and modulating homeostatic E/I balance (Asztély and Gustafsson 1996; Lau and Zukin 2007; Malenka and Nicoll 1993; Plested and others 2004; Turrigiano 2012; Yang and others 2016).”
Developmental plasticity of GABAergic neurotransmission to brainstem motoneurons
Wollman, L., Levine, R. B., & Fregosi, R. F. (2018) · The Journal of Physiology · doi:10.1113/jp274923 · Cited by 16
“This is broadly consistent with the concept of homeostatic plasticity whereby presynaptic firing rate is altered based on the activity of the postsynaptic neuron (Kirov et al. 1999; Turrigiano, 2012; Davis & Muller, 2015).”
ResultClosed-Loop Systems and In Vitro Neuronal Cultures: Overview and Applications
Bisio, M., Pimashkin, A. S., Buccelli, S., Tessadori, J., Semprini, M., Levi, T., Colombi, I., Gladkov, A., Mukhina, I. V., Averna, A., et al. (2019) · Advances in neurobiology · doi:10.1007/978-3-030-11135-9_15 · Cited by 19
Falck, J. E., Bruns, C., Hoffmann-Conaway, S., Straub, I., Plautz, E. J., Orlando, M., Munawar, H., Rivalan, M., Winter, Y., Izsvák, Z., et al. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2316-19.2020 · Cited by 16
“8) indicate that the network has triggered compensatory changes to overcome a smaller size or impaired strength of MFs reaching the GC layer, for instance, by increasing both input resistance and release probability (Turrigiano, 2012).”
BackgroundTrafficking and Activity of Glutamate and GABA Receptors: Regulation by Cell Adhesion Molecules
Keable, R., Leshchyns’ka, I., & Sytnyk, V. (2020) · The Neuroscientist · doi:10.1177/1073858420921117 · Cited by 16
“surface and at synapses, as well as the conductance of individual receptors and their subunit composition, dictates synaptic strength, is key to both Hebbian and homeostatic synaptic plasticity, and plays a significant role in learning and memory (Malinow and Malenka 2002; Turrigiano 2012).”
BackgroundDendritic spine density changes and homeostatic synaptic scaling: a meta-analysis of animal studies
Moulin, T. C., Rayêe, D., & Schiöth, H. (2021) · Neural Regeneration Research · doi:10.4103/1673-5374.314283 · Cited by 16
“One of the most intensively studied forms of homeostatic plasticity is synaptic scaling, in which the synaptic strengths of a neuron are adjusted in a compensatory manner following a global multiplicative scaling factor (Abbott and Nelson, 2000; Turrigiano, 2012).”
BackgroundInfluentialTest-Retest Reliability of Homeostatic Plasticity in the Human Primary Motor Cortex
Thapa, T., & Schabrun, S. M. (2018) · Neural Plasticity · doi:10.1155/2018/6207508 · Cited by 16
Loweth, J. A., Reimers, J. M., Caccamise, A. J., Stefanik, M. T., Woo, K., Chauhan, N. M., Werner, C. T., & Wolf, M. E. (2018) · European Journal of Neuroscience · doi:10.1111/ejn.14151 · Cited by 19
“For example, prolonged inactivity leads to the strengthening of synapses (scaling up) via mechanisms including postsynaptic AMPAR insertion (Turrigiano, 2012).”
BackgroundInsulin-Dependent Maturation of Newly Generated Olfactory Sensory Neurons after Injury
Kuboki, A., Kikuta, S., Otori, N., Kojima, H., Matsumoto, I., Reisert, J., & Yamasoba, T. (2021) · eNeuro · doi:10.1523/eneuro.0168-21.2021 · Cited by 16
“…OSNs in the STZ mice Insulin in the brain acts as a neuromodulator influencing synaptic plasticity, dendritic outgrowth, and neurotransmitter release, while also promoting neuronal survival and proliferation (Bruning et al., 2000; Plum et al., 2005; Mielke et al., 2006; Valenciano et al., 2006).”
BackgroundRue, M. C. P., Alonso, L. M., & Marder, E. (2022) · iScience · doi:10.1016/j.isci.2022.104919 · Cited by 15
“…the face of extended physiological perturbation (Brickley et al., 2001; Desai, 2003; Golowasch et al., 1999; Hengen et al., 2013; Marder and Goaillard, 2006; Mease et al., 2013; O’Leary and Marder, 2014; Temporal et al., 2014; Turrigiano, 2012; Turrigiano et al., 1998; Turrigiano and Nelson, 2004).”
Teichner, E. M., You, J. C., Hriso, C., Wintering, N., Zabrecky, G. P., Alavi, A. A., Bazzan, A. J., Monti, D., & Newberg, A. B. (2021) · Nuclear Medicine Communications · doi:10.1097/mnm.0000000000001397 · Cited by 16
Liu, B., Seay, M. J., & Buonomano, D. V. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1104-22.2022 · Cited by 18
Homeostatic Plasticity in the Nervous System
Maffei, A., Bucher, D. M., & Fontanini, A. (2012) · Neural Plasticity · doi:10.1155/2012/913472 · Cited by 18
Cross‐Modal Plasticity Results in Increased Inhibition in Primary Auditory Cortical Areas
Mao, Y., & Pallas, S. L. (2013) · Neural Plasticity · doi:10.1155/2013/530651 · Cited by 16
“For example, a homeostatic downregulation of inhibition makes cortical neurons more sensitive to any remaining inputs (see [1], for review).”
Ephrin-B3 controls excitatory synapse density through cell-cell competition for EphBs
Henderson, N. T., Le Marchand, S. J., Hruska, M., Hippenmeyer, S., Luo, L., & Dalva, M. B. (2019) · eLife · doi:10.7554/elife.41563 · Cited by 15
“Our findings suggest that while neurons possess activity-dependent mechanisms that regulate the input-output relationship of neurons (Turrigiano, 2012), molecular cues can also set the density of excitatory inputs.”
BackgroundValderhaug, V. D., Heiney, K., Ramstad, O. H., Bråthen, G., Kuan, W., Nichele, S., Sandvig, A., & Sandvig, I. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00413.2020 · Cited by 13
Friend or Foe? The Varied Faces of Homeostatic Synaptic Plasticity in Neurodegenerative Disease
Taylor, H. B. C., & Jeans, A. F. (2021) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2021.782768 · Cited by 18
“HSP is therefore a critical check that is required to maintain both neuronal health and the fidelity of information transfer (Turrigiano, 2012).”
BackgroundA Simplified Plasticity Model Based on Synaptic Tagging and Capture Theory: Simplified STC
Ding, Y., Wang, Y., & Cao, L. (2022) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2021.798418 · Cited by 14
“From the viewpoint of spatial scale, the plasticity rule includes local plasticity depending only on the activity of the presynaptic and postsynaptic neuron and global plasticity modulated by global factors, such as neuromodulator (Turrigiano, 2012).”
BackgroundMusazzi, L., Tornese, P., Sala, N., Lee, F. S., Popoli, M., & Ieraci, A. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30833 · Cited by 14
Blurring the boundaries: developmental and activity-dependent determinants of neural circuits
Wolfram, V., & Baines, R. (2013) · Trends in Neurosciences · doi:10.1016/j.tins.2013.06.006 · Cited by 15
Bachatene, L., Bharmauria, V., Cattan, S., Chanauria, N., Rouat, J., & Molotchnikoff, S. (2015) · BMC Neuroscience · doi:10.1186/s12868-015-0203-1 · Cited by 16
“Maintaining stable excitation-inhibition ratio could thus prevent an exceeding augmentation or diminution of global strengths within networks allowing sensory processing to remain stable [18].”
BackgroundControl of lung ventilation following overwintering conditions in bullfrogs,Lithobates catesbeianus
Santin, J. M., & Hartzler, L. K. (2016) · Journal of Experimental Biology · doi:10.1242/jeb.136259 · Cited by 15
“However, models to study these processes use pharmacological or pathological paradigms to manipulate neuronal activity in vivo and in vitro primarily at early developmental stages (Hengen et al., 2013; Knogler et al., 2010; Ngodup et al., 2015; Schacher and Hu, 2014; Turrigiano, 2012; Wilhelm and Wenner, 2008).”
BackgroundDo group I metabotropic glutamate receptors mediate LTD?
Jones, O. D. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.08.010 · Cited by 16
Gabrieli, D. J., Schumm, S. N., Vigilante, N. F., & Meaney, D. F. (2020) · Neural Computation · doi:10.1162/neco_a_01343 · Cited by 15
“Specifically, one recovery mechanism (HSP) might lead to a risk of developing pathology, and a second mechanism (STDP) quickly adjusts the network to avoid such uncontrollable bursting.”
BackgroundInfluentialA human in vitro neuronal model for studying homeostatic plasticity at the network level
Yuan, X., Puvogel, S., van Rhijn, J.-R., Ciptasari, U., Esteve‐Codina, A., Meijer, M., Rouschop, S., van Hugte, E., Oudakker, A. R., Schoenmaker, C., et al. (2023) · Stem Cell Reports · doi:10.1016/j.stemcr.2023.09.011 · Cited by 16
“Eventually, the homeostatic changes that occur through these mechanisms prevent the neuronal networks from becoming hypo- or hyper-active (Tien and Kerschensteiner, 2018; Wefelmeyer et al., 2016; Turrigiano, 2012; Watt and Desai, 2010).”
Building and modifying diverse synaptic properties: Insights from Drosophila
He, K., & Dickman, D. K. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.102995 · Cited by 14
Visual Plasticity in Adulthood: Perspectives from Hebbian and Homeostatic Plasticity
Bang, J. W., Hamilton-Fletcher, G., & Chan, K. C. (2021) · The Neuroscientist · doi:10.1177/10738584211037619 · Cited by 17
“1B) refers to the global readjustment of all synapses toward baseline (Turrigiano 2011; Turrigiano 1999).”
BackgroundLu, H., Gallinaro, J. V., Normann, C., Rotter, S., & Yalçın, İ. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab281 · Cited by 13
Chancey, J. H., & Howard, M. A. (2022) · eNeuro · doi:10.1523/eneuro.0080-22.2022 · Cited by 14
“Pyramidal neurons are well-known to have the capacity to change synaptic strength (Turrigiano, 2012) and intrinsic excitability (Remy et al., 2010) in response to long-term changes in activity.”
BackgroundBreakdown of the central synapses in C9orf72-linked ALS/FTD
Ghaffari, L., Trotti, D., Haeusler, A. R., & Jensen, B. K. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.1005112 · Cited by 16
“Furthermore, neuronal activity controls proper neuronal development, synaptic function, and ultimately health and survival of the individuals and organisms (Flavell and Greenberg, 2008; Turrigiano, 2012; Yap and Greenberg, 2018).”
BackgroundBaertsch, N. A., & Baker‐Herman, T. L. (2015) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00359.2014 · Cited by 14
Lindsly, C., Gonzalez-Islas, C. E., & Wenner, P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0094559 · Cited by 14
“Further, following activity blockade there was no change in the conductance of GABAergic mPSCs suggesting there were not alterations in the number or conductance of postsynaptic receptors; this is distinct from previous work demonstrating changes in postsynaptic receptors mediating AMPAergic and GABAergic scaling in c…”
ResultCompensatory plasticity restores locomotion after chronic removal of descending projections
Harley, C. M., Reilly, M. G., Stewart, C., Schlegel, C., Morley, E., Puhl, J. G., Nagel, C., Crisp, K. M., & Mesce, K. A. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00135.2015 · Cited by 14
Santin, J. M., & Hartzler, L. K. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.153544 · Cited by 14
“First, compensatory mechanisms at the cellular level could offset typical degradative processes caused by reduced activity in muscles and neurons as occurs in heterothermic hibernators and silent neural networks (Lee et al., 2008; Lin et al., 2012; Tessier and Storey, 2014; Turrigiano, 2012; Young et al., 2013).”
Developmental nicotine exposure alters potassium currents in hypoglossal motoneurons of neonatal rat
Cholanian, M., Wealing, J., Levine, R. B., & Fregosi, R. F. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00774.2016 · Cited by 14
“Considerable work on homeostatic synaptic plasticity in a range of neuron types shows that it can occur by balancing inhibitory and excitatory synaptic inputs and/or by changing intrinsic neuron properties (Hengen et al. 2013; Turrigiano 2008, 2012).”
BackgroundNaro, A., Bramanti, A., Leo, A., Bramanti, P., & Calabrò, R. S. (2017) · International Journal of Neural Systems · doi:10.1142/s0129065717500599 · Cited by 14
Seung, H. S., & Zung, J. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1704.00646 · Cited by 14
“Such homeostatic synaptic scaling has been extensively studied for biological synapses [Turrigiano, 2012].”
BackgroundPredicting modular functions and neural coding of behavior from a synaptic wiring diagramPreprint
Vishwanathan, A., Ramirez, A. D., Wu, J., Sood, A., Yang, R., Kemnitz, N., Ih, D., Turner, N. L., Lee, K., Tartavull, I., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.28.359620 · Cited by 14
“Scaling the strength of an individual synapse by the total number of synapses incoming to a neuron is similar in concept to homeostatic synaptic scaling as observed experimentally (Turrigiano, 2012).”
BackgroundRaab‐Graham, K. F., Workman, E. R., Namjoshi, S. V., & Niere, F. (2016) · Brain Research · doi:10.1016/j.brainres.2016.04.020 · Cited by 13
“For example, in seminal studies that deprive rodents of light during a critical period of visual developmental, the absence of visual input alters the threshold for synaptic plasticity in the forms of long-term potentiation (LTP) and long-term depression (LTD) (Kirkwood et al., 1996; Philpot et al., 2003).”
BackgroundInfluentialMolecular mechanisms of homeostatic plasticity in central pattern generator networks
Northcutt, A. J., & Schulz, D. J. (2019) · Developmental Neurobiology · doi:10.1002/dneu.22727 · Cited by 15
NGPF2 Triggers Synaptic Scaling Up Through ALK-LIMK-Cofilin Mediated Mechanisms
Zhou, Z., He, G., Zhang, X., Lv, X., Zhang, X., Liu, A., Xia, S., Xie, H., Dang, R., Han, L., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2021.109515 · Cited by 13
ACh Transfers: Homeostatic Plasticity of Cholinergic Synapses
Djemil, S., Sames, A. M., & Pak, D. T. S. (2022) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-022-01227-2 · Cited by 13
Ma, Y., Bendl, J. M., Hartley, B. J., Fullard, J. F., Abdelaal, R., Ho, S., Kosoy, R., Gochman, P., Rapoport, J. L., Hoffman, G. E., et al. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.07.003 · Cited by 13
Synaptic remodeling follows upper motor neuron hyperexcitability in a rodent model of TDP-43
Dyer, M. S., Odierna, G. L., Clark, R. M., et al. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1274979 · Cited by 13
“Also, since changes in synapses follow the induction of intrinsic hyperexcitability they may represent a protective adaptation that normalizes neuronal output via a process such as synaptic scaling (Turrigiano, 2012).”
BackgroundMulti-layer network utilizing rewarded spike time dependent plasticity to learn a foraging task
Šanda, P., Skorheim, S. W., & Bazhenov, M. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005705 · Cited by 11
Zhang, X., Jiang, H., Xu, L., Yang, S., Wang, G.-Z., Jiang, H.-D., Wu, T., Du, H., Yu, Z.-P., Zhao, Q.-Q., et al. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108231 · Cited by 13
Neural Functional Connectivity Reconstruction with Second‐Order Memristor Network
Wu, Y., Moon, J., Zhu, X., & Lu, W. D. (2021) · Advanced Intelligent Systems · doi:10.1002/aisy.202000276 · Cited by 13
Inouye, M. O., Colameo, D., Ammann, I., Winterer, J., & Schratt, G. M. (2022) · Life Science Alliance · doi:10.26508/lsa.202201520 · Cited by 15
“Homeostatic synaptic depression (HSD) is a type of homeostatic plasticity by which excitatory neurons compensate for increased network activity to maintain a physiological range of excitatory transmission (reviewed in Turrigiano [2008], Yu and Goda [2009], and Turrigiano [2012]).”
Rethinking the network determinants of motor disability in Parkinson’s disease
Surmeier, D. J., Zhai, S., Cui, Q., & Simmons, D. V. (2023) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2023.1186484 · Cited by 17
“In other cell types it is clear that sustained deviations in spiking rate from a certain set-point are capable of inducing alterations in intrinsic excitability and synaptic strength that normalize activity (Marder and Goaillard, 2006; Turrigiano, 2012).”
BackgroundAdaptive Rewiring in Weighted Networks Shows Specificity, Robustness, and Flexibility
Rentzeperis, I., & van Leeuwen, C. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.580569 · Cited by 14
“Homeostatic mechanisms are crucial in maintaining the functionality of the brain in the face of constant changes (Turrigiano and Nelson, 2004; Turrigiano, 2012).”
BackgroundCytokines as Neuromodulators: Insights From Experimental Studies With Humans and Nonhuman Primates
Martins, D., & Harrison, N. A. (2025) · Biological Psychiatry · doi:10.1016/j.biopsych.2025.06.037 · Cited by 16
Intrinsic plasticity of Purkinje cell serves homeostatic regulation of fear memory
Lee, J., Kim, S. H., Jang, M., Jang, M., Bak, M. S., Shim, H. G., Lee, Y., & Kim, S. J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02320-8 · Cited by 13
“This homeostatic regulation maintains a stable neural network [20, 21]; otherwise, dysregulation of homeostatic plasticity causes neuropsychiatric diseases, such as schizophrenia and autism [22, 23].”
Distinct input-specific mechanisms enable presynaptic homeostatic plasticity
Chien, C., He, K., Perry, S., Tchitchkan, E., Han, Y., Li, X., & Dickman, D. K. (2025) · Science Advances · doi:10.1126/sciadv.adr0262 · Cited by 14
Papatheodoropoulos, C. (2025) · Biology · doi:10.3390/biology14040363 · Cited by 15
“One example is the homeostatic control of synaptic strengths that helps restore initial firing rates [24,27,77–79].”
Aberrant plasticity in musculoskeletal pain: a failure of homeostatic control?
Thapa, T., Graven‐Nielsen, T., & Schabrun, S. M. (2021) · Experimental Brain Research · doi:10.1007/s00221-021-06062-3 · Cited by 13
“However, in addition to plasticity mechanisms that promote neural ‘changeability’, the human brain is governed by plasticity mechanisms that promote stability (Turrigiano 2012; Turrigiano 1999; Turrigiano 2006; Turrigiano and Nelson 2000).”
BackgroundDai, W., Geng, Y., Liu, H., Guo, C., Chen, W., Ma, J., Chen, J., Jia, Y., Shen, Y., & Wang, T. (2021) · Neural Plasticity · doi:10.1155/2021/8966584 · Cited by 13
“With changes in neural activity and intracellular Ca 2+ level, the fi ring rate of neurons is stabilized through an increase or decrease in synaptic strength, thus ensuring normal information processing and storage [29, 31].”
Mizumori, S. J. Y., & Tryon, V. L. (2015) · Progress in brain research · doi:10.1016/bs.pbr.2015.03.010 · Cited by 15
A blueprint for research on Shankopathies: A view from research on autism spectrum disorder
Carbonetto, S. (2013) · Developmental Neurobiology · doi:10.1002/dneu.22150 · Cited by 13
“Such homeostatic plasticity occurs (Ting et al., 2012) when reduced excitatory inputs trigger a reduction in inhibitory synaptic efficacy, making the cell better able to respond to reduced levels of excitation (Turrigiano, 2012).”
BackgroundProteomic analysis of PSD-93 knockout mice following the induction of ischemic cerebral injury
Rong, R., Yang, H., Rong, L., Wei, X., Li, Q., Liu, X., Gao, H., Xu, Y., & Zhang, Q. C. (2015) · NeuroToxicology · doi:10.1016/j.neuro.2015.12.005 · Cited by 12
Sakurai, A., Tamvacakis, A. N., & Katz, P. S. (2016) · eNeuro · doi:10.1523/eneuro.0056-16.2016 · Cited by 11
Pingel, J., Hultborn, H., Näslund-Koch, L., et al. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00276.2017 · Cited by 12
“A central feature of neural plasticity is that it is maintained within relatively narrow limits by homeoplastic mechanisms (Giachello and Baines 2017; Pozo and Goda 2010; Turrigiano 2012).”
BackgroundCheng, J., Huang, X., Yue, L., Xue, T., Wang, L., & Bao, J. (2018) · Journal of Biological Rhythms · doi:10.1177/0748730417754162 · Cited by 13
“, 2000), their spike output (Carter and Regehr, 2002; Sharma and Vijayaraghvan, 2003), and their synaptic efficacy in the absence of presynaptic action potentials (McKinney et al., 1999; Sutton and Schuman, 2006; Turrigiano, 2012).”
BackgroundActivity-Dependent Mitochondrial Plasticity and Mitoproteome are Dysregulated in Fragile X Syndrome
Bülow, P., Zlatic, S. A., Wenner, P., Bassell, G. J., & Faúndez, V. (2020) · Molecular Brain · doi:10.1186/s13041-021-00783-w · Cited by 13
“Alterations in cytoplasmic calcium and modifications of protein synthesis are two components of the signaling cascades that underlie these homeostatic mechanisms [4, 7, 8].”
BackgroundSelf-organization of a doubly asynchronous irregular network state for spikes and bursts
Vercruysse, F., Naud, R., & Sprekeler, H. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009478 · Cited by 13
Paredes, C. C., Herrero-Turrión, M. J., & Merchán, M. Á. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00086 · Cited by 12
“It is known that changes in the balance of excitation and inhibition trigger synaptic plasticity, adapting biophysical membrane properties (synaptic strength and axon conductance properties) or modifying the synthesis and trafficking of receptors (Perez-Otano and Ehlers, 2005; Turrigiano, 2012).”
BackgroundDevelopment of the central nervous system
Cabej, N. R. (2021) · Elsevier eBooks · doi:10.1016/b978-0-323-85154-1.00003-5 · Cited by 12
Sanderson, J. L., Freund, R. K., Castano, A. M., Benke, T. A., & Dell’Acqua, M. L. (2022) · Neuropharmacology · doi:10.1016/j.neuropharm.2022.109271 · Cited by 11
“E) to maintain some basal target level of neuronal firing (Turrigiano, 2012).”
Huang, Z. (2023) · Journal of Alzheimer s Disease · doi:10.3233/jad-221042 · Cited by 12
“Homeostatic synaptic plasticity protects synapses from destabilizing forces and is essential for maintaining lifelong normal brain function [170].”
Gross, J., Knipper, M., & Mazurek, B. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01405-w · Cited by 11
“The causes of tinnitus induce changes in activity-dependent synaptic plasticity of the neural network due to homeostatic regulation (Turrigiano 2012).”
BackgroundO’Neill, K. M., Anderson, E. D., Mukherjee, S., Gandu, S. R., McEwan, S. A., Omelchenko, A., Rodriguez, A. R., Losert, W., Meaney, D. F., Babadi, B., et al. (2023) · Communications Biology · doi:10.1038/s42003-023-05638-9 · Cited by 9
“5 ).”
Contribution of membrane-associated oscillators to biological timing at different timescales
Stengl, M., & Schneider, A. C. (2024) · Frontiers in Physiology · doi:10.3389/fphys.2023.1243455 · Cited by 15
“…concepts of neuronal homeostasis and plasticity, referring to more extensive reviews (Marder et al., 1996; Turrigiano, 1999; Turrigiano, 2008; Turrigiano, 2012; Turrigiano and Nelson, 2000; Caporale and Dan, 2008; Masquelier et al., 2009; Schulz and Lane, 2017; Lee and Kirkwood, 2019;…”
BackgroundInfluentialSun, S. D., Levenstein, D., Li, B., Mandelberg, N. J., Chenouard, N., Suutari, B. S., Sanchez, S., Tian, G., Rinzel, J., Buzsáki, G., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.113839 · Cited by 16
“Using experimental and computational approaches, they describe how synapses use Hebbian and homeostatic elements to adapt to changing activity levels while retaining the capacity for plasticity.”
Hwang, E.-K., Wunsch, A. M., & Wolf, M. E. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03026-9 · Cited by 10
“For example, prolonged inactivity can lead to strengthening of synapses [15].”
Early Phase of Plasticity-Related Gene Regulation and SRF Dependent Transcription in the Hippocampus
Iacono, G., Altafini, C., & Torre, V. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068078 · Cited by 11
“In the past decade the mechanisms involved in the homeostatic regulation of synaptic strength have emerged as a fundamental complement to Hebbian plasticity [172][173][174].”
BackgroundBariatric surgery restores visual cortical plasticity in nondiabetic subjects with obesity
Daniele, G., Lunghi, C., Dardano, A., Binda, P., Ceccarini, G., Santini, F., Giusti, L., Ciccarone, A., Bellini, R., Moretto, C., et al. (2021) · International Journal of Obesity · doi:10.1038/s41366-021-00851-0 · Cited by 12
“In normal-weight adult subjects, a short period of monocular deprivation (MD) transiently shifts ocular dominance in favor of the deprived eye both at the perceptual [19–22] and at the neural level [23, 24] reflecting a compensatory regulation of ocular dominance in response to deprivation consistent with homeostatic…”
BackgroundFalkenburger, B. H., Καλλιακούδας, Θ., & Reichmann, H. (2022) · Journal of Neural Transmission · doi:10.1007/s00702-022-02510-8 · Cited by 10
“These processes are summarized as homeostatic plasticity (Turrigiano 2012).”
BackgroundPorciatti, V., & Chou, T.-H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105751 · Cited by 12
“While the tipping point is a well-established intuitive concept (Figure 1), its identification is challenging as phenotypic expression and molecular changes occurring during the critical period overlap with those of the normal condition, and homeostatic neuroplasticity mechanisms to maintain normal vision offset patho…”
BackgroundHuman iPSC-Derived Cortical Neurons Display Homeostatic Plasticity
Cordella, F., Ferrucci, L., D’Antoni, C., Ghirga, S., Brighi, C., Soloperto, A., Gigante, Y., Ragozzino, D., Bezzi, P., & Angelantonio, S. D. (2022) · Life · doi:10.3390/life12111884 · Cited by 11
Acute ampakines increase voiding function and coordination in a rat model of SCI
Rana, S. D., Alom, F., Martinez, R. C., et al. (2024) · eLife · doi:10.7554/elife.89767.3 · Cited by 11
Siddoway, B. A., Hou, H., Yang, J., Sun, L., Yang, H. S., Wang, G.-Y., & Xia, H. (2014) · Neuroscience Letters · doi:10.1016/j.neulet.2014.08.051 · Cited by 10
HIV-1 Tat-Induced Changes in Synaptically-Driven Network Activity Adapt During Prolonged Exposure
Krogh, K. A., Green, M., & Thayer, S. A. (2015) · Current HIV Research · doi:10.2174/1570162x13666150121110402 · Cited by 11
“The synaptic changes produced by Tat appear to be a coping mechanism, somewhat analogous to homeostatic plasticity [18].”
BackgroundMalerba, P., Straudi, S., Fregni, F., Bazhenov, M., & Basaglia, N. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00058 · Cited by 10
“Other plasticity mechanisms that could prove relevant in neurorehabilitation after stroke include heterosynaptic plasticity (120, 121), in which a synapse is strengthened/depressed depending on spillage of neurotransmitter from nearby synaptic clefts, and homeostatic plasticity (122, 123), in which the overall network…”
BackgroundBabiec, W. E., & O’Dell, T. J. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00628.2017 · Cited by 11
Goel, P., Nishimura, S., Chetlapalli, K., Li, X., Chen, C., & Dickman, D. K. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00196 · Cited by 10
“Both Hebbian and homeostatic plasticity mechanisms can work locally and globally at specific synapses to tune synapse function, enabling stable yet flexible ranges of synaptic strength (Turrigiano, 2012; Vitureira and Goda, 2013; Diering and Huganir, 2018).”
BackgroundFunctional strengthening through synaptic scaling upon connectivity disruption in neuronal cultures
Estévez-Priego, E., Teller, S., Granell, C., Arenas, À., & Soriano, J. (2020) · Network Neuroscience · doi:10.1162/netn_a_00156 · Cited by 13
Bülow, P., Wenner, P., Faúndez, V., & Bassell, G. J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.702020 · Cited by 12
“While HIP can regulate intrinsic excitability by altering ion channel expression/function at the axon initial segment (AIS), synaptic scaling regulates the expression of neurotransmitter receptors in dendrites (Turrigiano, 2012).”
BackgroundAnthelmintic resistance and homeostatic plasticity (Brugia malayi)
Kashyap, S. S., Verma, S., McHugh, M. A., Wolday, M., Williams, P., Robertson, A. P., & Martin, R. J. (2021) · Scientific Reports · doi:10.1038/s41598-021-93911-4 · Cited by 12
A data-informed mean-field approach to mapping of cortical parameter landscapes
Xiao, Z.-C., Lin, K. K., & Young, L.-S. (2021) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1009718 · Cited by 11
“, synaptic depression of I-neurons [57, 58]; increased thresholds for potential generation of E-spikes due to Kv currents [59]; and a host of other homeostatic mechanisms [60].”
BackgroundLenz, M., Eichler, A., Kruse, P., Stöhr, P., Kleidonas, D., Galanis, C., Lu, H., & Vlachos, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1148219 · Cited by 13
“Based on negative feedback mechanisms, homeostatic synaptic plasticity adjusts synaptic weights to maintain neuronal activity within a dynamic range (Davis and Bezprozvanny, 2001; Marder and Prinz, 2003; Pozo and Goda, 2010; Turrigiano, 2012; Keck et al., 2013; Bissen et al., 2021; Cao et al., 2022).”
BackgroundBains, A., & Schweighofer, N. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00433.2013 · Cited by 12
“However, homeoplasticity in vivo is controlled through a variety of signaling pathways, some of which overlap with LTP pathways (Guzman-Karlsson et al. 2014; Turrigiano 2012; Turrigiano 2011).”
BackgroundPerissinotti, P. P., Ethington, E., Almazan, E., Martínez‐Hernández, E., Kalil, J. A., Koob, M. D., & Piedras-Renterı́a, E. S. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00444 · Cited by 11
“Synaptic homeostasis mechanisms have been thoroughly demonstrated to maintain neuronal excitability (Davis and Bezprozvanny, 2001; Turrigiano, 2012) and GAD67 is a target for activity-dependent regulation (Lau and Murthy, 2012); however changes in expression of gephyrin has not been ruled out.”
BackgroundSzücs-Bencze, L., Vékony, T., Pesthy, O., Szabó, N., Kincses, Z. T., Turi, Z., & Németh, D. (2023) · Journal of Intelligence · doi:10.3390/jintelligence11100201 · Cited by 10
“Third, these issues may be also explained by homeostatic plastic effects, which are a form of plasticity that is thought to balance the effects of Hebbian (synapse-specific) plasticity to maintain the stability of neuronal networks (Turrigiano 2012).”
Background
Metadata
- Authors
- Turrigiano, G.
- Affiliations
- Brandeis University (US)
- Corresponding author
- Turrigiano, G.
- ORCID
- Turrigiano, G.
- Venue
- Cold Spring Harbor Perspectives in Biology
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2011-11-15
- Volume
- 4
- Issue
- 1
- Pages
- a005736-a005736
- ISSN
- 1943-0264 (ISSN-L)
- PMC
- PMC3249629
- OpenAlex
- W2115900486
- Semantic Scholar
- a5724cd9f8c115624f0538915997ae22b3136e77
- Cited by
- 1,139
- References
- 110
- Citations by year
- 2026: 95 · 2025: 98 · 2024: 82 · 2023: 92 · 2022: 91 · 2021: 107 · 2020: 92 · 2019: 80 · 2018: 77 · 2017: 89 · 2016: 59 · 2015: 69 · 2014: 41 · 2013: 51 · 2012: 15
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cold Spring Harbor Perspectives in Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (submittedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- homeostatic plasticity, synaptic scaling, glutamate receptor trafficking, excitation-inhibition balance, neuronal firing rate
- MeSH terms
- Animals, Homeostasis, Humans, Nerve Net, Neuromuscular Junction, Neuronal Plasticity, Neurons, Synapses
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