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.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
62 of 157 cited sources checked · 34 supported · 2 flagged · 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.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- 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
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe 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)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- 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
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesEvery 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passes- 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)
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- 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.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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.
Strength:plain· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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.
Strength:hedged· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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.
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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)
Load-bearingStrength:hedged· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✗ Checkable: fails✓ Load-bearing: passes✓ Based: passesProbably 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✗ Based: failsProbably 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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.
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
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
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt 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
“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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt 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
“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
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
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
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The check wasn’t confident either way, so it gives no verdict — never disputed.
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]
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Evers study has conflicting publication years
MinorThe text cites the Evers study as published in 2011, but the corresponding reference lists it as published in 2010.
“(Evers et al. 2011)”
“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
Cites
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Self-citationSynaptic plasticity: taming the beast
Abbott, L. F., & Nelson, S. B. (2000) · Nature Neuroscience · doi:10.1038/81453 · Cited by 2,263 · cited 1×
“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
Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715
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
Cannon, W. B. (1932) · The American Journal of the Medical Sciences · doi:10.1097/00000441-193212000-00028 · Cited by 1,259
Variability, compensation and homeostasis in neuron and network function
Marder, E., & Goaillard, J.-M. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1949 · Cited by 1,212
Flagged first, then by citations
1 of the 110 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 201–300 of 1,136
Zhong, L. R., Chen, X., Park, E., Südhof, T. C., & Chen, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1133-18.2018 · Cited by 53
“…et al., 1994, 1998; O’Brien et al., 1998), homeostatic plasticity is now well accepted as an essential mechanism through which neural circuits maintain their stability in response to chronic changes in neuronal firing activity and/or synaptic excitation and inhibition (Turrigiano, 2012).”
BackgroundThe Role of Kv7 Channels in Neural Plasticity and Behavior
Baculis, B. C., Zhang, J., & Chung, H. J. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.568667 · Cited by 55
“While activity-dependent modulation of glutamate release and glutamate receptors serves as key mechanisms for LTP expression (Turrigiano, 2012; Humeau and Choquet, 2019), Kv7 channels and upstream muscarinic acetylcholine receptors have emerged as important regulators of excitatory synaptic…”
BackgroundDendritic mechanisms of hippocampal place field formation
Sheffield, M. E. J., & Dombeck, D. A. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.07.004 · Cited by 61
“An increased prevalence of branch spiking during subsequent place field firing could therefore lead to more precise place fields due to dendritic spike amplification of inputs [54 ,55] or through a potentiation and renormalization process [25 ,56,57].”
Growing Critical: Self-Organized Criticality in a Developing Neural System
Kossio, Y. F. K., Goedeke, S., van den Akker, B., Ibarz, B., & Memmesheimer, R.-M. (2018) · Physical Review Letters · doi:10.1103/physrevlett.121.058301 · Cited by 51
Kikuma, K., Li, X., Perry, S., Li, Q., Goel, P., Chen, C., Kim, D., Stavropoulos, N., & Dickman, D. K. (2019) · Nature Communications · doi:10.1038/s41467-019-10992-6 · Cited by 53
Tantillo, E., Vannini, E., Cerri, C., Spalletti, C., Colistra, A., Mazzanti, C. M., Costa, M., & Caleo, M. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104942 · Cited by 60
Progesterone modulates neuronal excitability bidirectionally
Kapur, J., & Joshi, S. (2021) · Neuroscience Letters · doi:10.1016/j.neulet.2020.135619 · Cited by 56
“Prolonged blockade or potentiation of neuronal activity triggers homeostatic plasticity, which restores the neuron’s target firing rate [44, 109, 153, 160].”
BackgroundHale, C. R., Sawicka, K., Mora, K., Fak, J. J., Kang, J. J., Cutrim, P., Cialowicz, K. I., Carroll, T. S., & Darnell, R. B. (2021) · eLife · doi:10.7554/elife.71892 · Cited by 51
Reconsolidation and the regulation of plasticity: moving beyond memory
Bonin, R. P., & Koninck, Y. D. (2015) · Trends in Neurosciences · doi:10.1016/j.tins.2015.04.007 · Cited by 55
Developmental neuroplasticity and the origin of neurodegenerative diseases
Schaefers, A. T. U., & Teuchert, G. (2013) · The World Journal of Biological Psychiatry · doi:10.3109/15622975.2013.797104 · Cited by 57
“destabilizing plasticity is, hence, counterbalanced by homeostatic plasticity mechanisms (Turrigiano and nelson 2000; Turrigiano 2012).”
BackgroundNeural ECM molecules in axonal and synaptic homeostatic plasticity
Frischknecht, R., Chang, K.-J., Rasband, M. N., & Seidenbecher, C. I. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00004-9 · Cited by 56
Persistent memories of long-term potentiation and the N -methyl-d-aspartate receptor
Bliss, T. V. P., & Collingridge, G. L. (2019) · Brain and Neuroscience Advances · doi:10.1177/2398212819848213 · Cited by 58
“There is also a homeostatic mechanism that prevents LTP from increasing synaptic strength without bound (Turrigiano, 2012).”
BackgroundKennedy, B. E., Leblanc, V., Mailman, T. M., Fice, D., Burton, I. W., Karakach, T. K., & Karten, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082685 · Cited by 54
Temporal dynamics of a homeostatic pathway controlling neural network activity
Bateup, H. S., Denefrio, C. L., Johnson, C. A., Saulnier, J. L., & Sabatini, B. L. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00028 · Cited by 52
“Importantly, mechanisms that regulate the strength of synapses as a means to normalize excitatory drive must still preserve differences in the weight of individual synapses to allow specific connections to be strengthened or weakened (Turrigiano, 2012).”
BackgroundInfluentialMapping pathologic circuitry in schizophrenia
Glausier, J. R., & Lewis, D. A. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63639-3.00025-6 · Cited by 53
Skosnik, P. D., Sloshower, J., Safi-Aghdam, H., Pathania, S., Syed, S., Pittman, B., & D’Souza, D. C. (2023) · Journal of Psychopharmacology · doi:10.1177/02698811231179800 · Cited by 51
“One form of synaptic plasticity is the ability of synapses to strengthen over time, in response to increases or decreases in their activity (Turrigiano, 2012).”
BackgroundPlasticity in the Hippocampus, Neurogenesis and Drugs of Abuse
Avchalumov, Y., & Mandyam, C. D. (2021) · Brain Sciences · doi:10.3390/brainsci11030404 · Cited by 49
“This homeostatic plasticity regulates synaptic scaling and is thought to stabilize synaptic strength at the level of a single neuron [46,47].”
BackgroundIt is time for a moonshot to find “Cures” for diabetic retinal disease
Levine, S. R., Sapieha, P. S., Dutta, S., Sun, J. K., & Gardner, T. W. (2022) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2022.101051 · Cited by 53
“Homeostatic neuroplasticity refers to the ability of neural tissue to adapt to physiologic and pathologic alterations during development, and particularly involves dendrites and synapses (Turrigiano, 2012); (Leinonen et al., 2020; Shen et al., 2020).”
Spinal cord retinoic acid receptor signaling gates mechanical hypersensitivity in neuropathic pain
Cao, B., Scherrer, G., & Chen, L. (2022) · Neuron · doi:10.1016/j.neuron.2022.09.027 · Cited by 60
Degoulet, M., Stelly, C. E., Ahn, K.-C., & Morikawa, H. (2015) · Molecular Psychiatry · doi:10.1038/mp.2015.84 · Cited by 50
“Alternatively, although speculative, this might represent a form of homeostatic synaptic plasticity 62 , in which NMDAR transmission at inputs not activated by cocaine-associated cues (e.g., interoceptive cocaine cues or the experimenter performing injection 40 ) are scaled down in response to LTP…”
Selective molecular impairment of spontaneous neurotransmission modulates synaptic efficacy
Crawford, D. C., Ramirez, D. M. O., Trauterman, B., Monteggia, L. M., & Kavalali, E. T. (2017) · Nature Communications · doi:10.1038/ncomms14436 · Cited by 51
The CNS theory of osteoarthritis: Opportunities beyond the joint
Morris, J. L., Letson, H. L., Gillman, R., Hazratwala, K., Wilkinson, M., McEwen, P. J. C., & Dobson, G. P. (2019) · Seminars in Arthritis and Rheumatism · doi:10.1016/j.semarthrit.2019.03.008 · Cited by 50
Synaptic Properties and Plasticity Mechanisms of Invertebrate Tonic and Phasic Neurons
Aponte-Santiago, N. A., & Littleton, J. T. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.611982 · Cited by 46
“In this form of plasticity, synaptic activity is maintained within specific ranges through homeostatic mechanisms that set a desired baseline level of output in a variety of neuronal types from invertebrates to humans (Pozo and Goda, 2010; Turrigiano, 2012; Davis and Müller, 2015).”
BackgroundLinking α-synuclein-induced synaptopathy and neural network dysfunction in early Parkinson’s disease
Kulkarni, A. S., Burns, M. R., Brundin, P., & Wesson, D. W. (2022) · Brain Communications · doi:10.1093/braincomms/fcac165 · Cited by 48
“Conversely, if one raises firing rates, synaptic strengthwill decline.(223) In the early stages of Parkinson’s disease, before significant neuronal death, it is possible that the”
BackgroundHearing loss differentially affects thalamic drive to two cortical interneuron subtypes
Takesian, A. E., Kotak, V. C., Sharma, N., & Sanes, D. H. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00182.2013 · Cited by 49
“Sensory deprivation, such as developmental hearing loss, can lead to an imbalance of cortical excitation and inhibition (Turrigiano 2012).”
BackgroundEvans, A. J., Gurung, S., Wilkinson, K. A., Stephens, D. J., & Henley, J. M. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.06.001 · Cited by 47
“KARs Is Controlled by Chronic Changes in Synaptic Activity and Mediated by Changes in the RNA Editing of GluK2 NMDAR and AMPAR surface expression scales in response to chronic down- or upregulation of synaptic activity (Rao and Craig, 1997; Shepherd et al., 2006; Turrigiano, 2012).”
BackgroundInfluentialNovel Players in the Aging Synapse: Impact on Cognition
Temido‐Ferreira, M., Coelho, J. E., Pousinha, P. A., & Lopes, L. V. (2019) · Journal of Caffeine and Adenosine Research · doi:10.1089/caff.2019.0013 · Cited by 57
“Conversely, excessive LTD would also proliferate, resulting in a silent state with inputs fully depressed.(38) Homeostatic plasticity acts as a compensatory stabilizing mechanism that, using a negative feedback system, keeps the activity of the network within a dynamic range.”
BackgroundHow to scale down postsynaptic strength
Tatavarty, V., Sun, Q., & Turrigiano, G. G. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1676-13.2013 · Cited by 50
“Together with a number of studies showing that the molecular underpinnings of scaling up and down are also distinct (Turrigiano, 2012), these data strongly suggest that scaling up and scaling down represent two distinct molecular processes that act in a “push–pull” manner to regulate postsynaptic…”
BackgroundSelf-citationAn Age-Dependent Change in the Set Point of Synaptic Homeostasis
Mahoney, R. E., Rawson, J. M., & Eaton, B. A. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3556-13.2014 · Cited by 49
“…data is that synaptic homeostatic set points at individual synapses are adjustable, so that the homeostatic regulation of synapse strength can support a long-term change in synaptic strength, such as LTP or the agedependent potentiation observed here (Thiagarajan et al., 2007; Turrigiano, 2012).”
BackgroundMy Neighbour Hetero — deconstructing the mechanisms underlying heterosynaptic plasticity
Chater, T. E., & Goda, Y. (2020) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2020.10.007 · Cited by 48
A Glutamate Homeostat Controls the Presynaptic Inhibition of Neurotransmitter Release
Li, X., Goel, P., Wondolowski, J., Paluch, J., & Dickman, D. K. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.03.130 · Cited by 44
“In these physiological systems, destabilizing perturbations to neurotransmission are offset by compensatory adaptations to postsynaptic neurotransmitter receptors (synaptic scaling) and/or presynaptic efficacy that maintains normal levels of functionality (Davis and Müller, 2015; Turrigiano, 2012).”
BackgroundA Friend or Foe: Calcineurin across the Gamut of Neurological Disorders
Saraf, J., Bhattacharya, P., Kalia, K., Borah, A., Sarmah, D., Kaur, H., Dave, K. R., & Yavagal, D. R. (2018) · ACS Central Science · doi:10.1021/acscentsci.8b00230 · Cited by 46
Sabitha, K. R., Shetty, A. K., & Upadhya, D. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.12.025 · Cited by 50
“These features contribute to a significant synaptic dysfunction because RA signaling plays a critical role in homeostatic synaptic plasticity, stabilizing firing rates required for network activity during developmental changes and learning (Turrigiano, 2012).”
BackgroundTuning into diversity of homeostatic synaptic plasticity
Lee, K. F. H., Soares, C., & Béïque, J.-C. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.03.016 · Cited by 45
LRRK2 regulates retrograde synaptic compensation at the Drosophila neuromuscular junction
Penney, J., Tsurudome, K., Liao, E. H., Kauwe, G., Gray, L. A., Yanagiya, A., Calderon, M. R., Sonenberg, N., & Haghighi, A. P. (2016) · Nature Communications · doi:10.1038/ncomms12188 · Cited by 48
“omeostatic mechanisms ensure stability in neural circuits by adjusting synaptic strength within an optimal range in response to perturbations in synaptic activity 1,2 .”
Santin, J. M., & Schulz, D. J. (2019) · Current Biology · doi:10.1016/j.cub.2019.04.008 · Cited by 44
“Thus, a fundamental question is how do neurons coordinate channel expression to uphold their firing patterns over long time scales [1, 5]? One major hypothesis purports that neurons homeostatically regulate their ongoing activity through mechanisms that link membrane voltage to expression relationships among ion chann…”
BackgroundSteffens, H., Mott, A. C., Li, S., Wegner, W., Švehla, P., Kan, V. W. Y., Wolf, F., Liebscher, S., & Willig, K. I. (2021) · Science Advances · doi:10.1126/sciadv.abf2806 · Cited by 45
Regulation of postsynaptic signaling in structural synaptic plasticity
Fu, A. K., & Ip, N. Y. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.05.016 · Cited by 43
“To maintain the stability of neuronal network activity, neurons adopt a compensatory mechanism, termed homeostatic synaptic plasticity, in order to prevent runaway excitation [42].”
Jang, S.-S., Royston, S. E., Xu, J., Cavaretta, J. P., Vest, M. O., Lee, K. Y., Lee, S., Jeong, H. G., Lombroso, P. J., & Chung, H. J. (2015) · Molecular Brain · doi:10.1186/s13041-015-0148-4 · Cited by 45
“org/publicdomain/ze synaptic transmission [1].”
Becker, D., Zahn, N., Deller, T., & Vlachos, A. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00257 · Cited by 48
“Hence, in response to a prolonged reduction in network activity neurons increase ( " scale up " ) the strength of their excitatory synapses (Turrigiano, 2012; Vitureira et al., 2012; Wang et al., 2012; Davis, 2013).”
BackgroundCochlear Injury and Adaptive Plasticity of the Auditory Cortex
Fetoni, A. R., Troiani, D., Petrosini, L., & Paludetti, G. (2015) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00008 · Cited by 46
“The cellular compensatory mechanisms involve the regulation of inhibitory and excitatory neurotransmission, since changes in one system produce reactive changes in the other one (Turrigiano, 2012).”
BackgroundZhai, S., Cui, Q., Simmons, D. V., & Surmeier, D. J. (2023) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2023.102798 · Cited by 47
“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 [109,110].”
Kim, S., Violette, C. J., & Ziff, E. B. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.09.007 · Cited by 46
“Homeostatic synaptic plasticity (HSP) also known as synaptic scaling is an important regulatory mechanism that compensates for altered neuronal activity (Turrigiano, 2012) and that recently has drawn attention as a means for counterbalancing synaptic alterations Neurobiol Aging.”
BackgroundLong-term optical stimulation of channelrhodopsin-expressing neurons to study network plasticity
Lignani, G., Ferrea, E., Difato, F., Amarù, J., Ferroni, E., Lugarà, E., Espinoza, S., Gainetdinov, R. R., Baldelli, P., & Benfenati, F. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00022 · Cited by 43
“…48–60 h after the onset of the light Frontiers in Molecular Neuroscience www.frontiersin.org August 2013 | Volume 6 | Article 22 | 7 stimulation and that are likely to reflect adaptive modifications of intrinsic excitability and synaptic strength at single neuronal units (Turrigiano, 2012).”
BackgroundInfluentialOkuno, H., Minatohara, K., & Bito, H. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.025 · Cited by 45
Parvalbumin fast‐spiking interneurons are selectively altered by paediatric traumatic brain injury
Nichols, J., Bjorklund, G. R., Newbern, J. M., & Anderson, T. R. (2018) · The Journal of Physiology · doi:10.1113/jp275393 · Cited by 40
“The strengthening of excitatory events may also be a result of post-synaptic receptor changes, potentially driven by homeostatic mechanisms (Pozo & Goda, 2010; Turrigiano, 2012).”
BackgroundSynapse-specific and compartmentalized expression of presynaptic homeostatic potentiation
Li, X., Goel, P., Chen, C., Angajala, V. T., Chen, X., & Dickman, D. K. (2018) · eLife · doi:10.7554/elife.34338 · Cited by 41
“However, these processes of Hebbian plasticity are inherently destabiliz- ing, and homeostatic mechanisms have been proposed to adaptively counteract such forces to maintain synaptic strength within physiologically stable levels (Davis, 2013; Pozo and Goda, 2010; Turrigiano, 2012).”
BackgroundCarlson, K. D., Richert, M., Dutt, N. D., & Krichmar, J. L. (2013) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2013.6706961 · Cited by 51
“runaway increases or decreases in synaptic strength [7], [9],”
BackgroundWei, H., Ma, Y., Liu, J., Ding, C., Hu, F., & Li, Y. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.11.003 · Cited by 47
“Homeostatic regulation of the nervous system could maintain the restructuring and refinement of neural circuits that occur during postembryonic development (Davis and Bezprozvanny, 2001; Turrigiano, 2012).”
BackgroundIlluminating the Multifaceted Roles of Neurotransmission in Shaping Neuronal Circuitry
Okawa, H., Hoon, M., Yoshimatsu, T., Santina, L. D., & Wong, R. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.029 · Cited by 46
The Yin and Yang of Memory Consolidation: Hippocampal and Neocortical
Genzel, L., Rossato, J. I., Jacobse, J., Grieves, R. M., Spooner, P. A., Battaglia, F. P., Fernández, G., & Morris, R. (2017) · PLoS Biology · doi:10.1371/journal.pbio.2000531 · Cited by 52
Chen, Y., Cai, L., Wang, R., Song, Z., Deng, B., Wang, J., & Yu, H. (2017) · Physica A Statistical Mechanics and its Applications · doi:10.1016/j.physa.2017.08.009 · Cited by 44
Remembering to Forget: A Dual Role for Sleep Oscillations in Memory Consolidation and Forgetting
Langille, J. J. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00071 · Cited by 50
“For more Frontiers in Cellular Neuroscience | www.frontiersin.org 3 March 2019 | Volume 13 | Article 71 information, readers should consider the following detailed reviews (Turrigiano, 2012; Piochon et al., 2013).”
BackgroundGalliano, E., Hahn, C., Browne, L., Villamayor, P. R., Tufo, C., Crespo, A., & Grubb, M. S. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1606-20.2020 · Cited by 46
“…need to activate homeostatic plasticity mechanisms and inhibitory neurons to downscale their own fast-acting plastic response, to reach a new network set point while maintaining an appropriate dynamic range (Gainey and Feldman, 2017; Keck et al., 2017; Turrigiano, 2012; Wefelmeyer et al., 2016).”
BackgroundGao, C., Liu, D., Xu, C., Bai, J., Li, E., Zhang, X., Zhu, X., Hu, Y., Lin, Z., Guo, T., et al. (2024) · Advanced Functional Materials · doi:10.1002/adfm.202313217 · Cited by 44
Engaging homeostatic plasticity to treat depression
Workman, E. R., Niere, F., & Raab‐Graham, K. F. (2017) · Molecular Psychiatry · doi:10.1038/mp.2017.225 · Cited by 43
Synaptic plasticity mechanisms common to learning and alcohol use disorderPreprint
Lovinger, D. M., & Abrahao, K. P. (2018) · Learning & Memory · doi:10.1101/lm.046722.117 · Cited by 47
Compensating for synaptic loss in Alzheimer’s disease
Abuhassan, K., Coyle, D., Belatreche, A., & Maguire, L. (2013) · Journal of Computational Neuroscience · doi:10.1007/s10827-013-0462-8 · Cited by 43
Wentzel, C., Delvendahl, I., Sydlik, S., Georgiev, O., & Müller, M. (2018) · Nature Communications · doi:10.1038/s41467-017-02494-0 · Cited by 40
Lee, K. Y., Jewett, K. A., Chung, H. J., & Tsai, N. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddy189 · Cited by 41
Mohan, V., Wade, S. D., Sullivan, C. S., Kasten, M. R., Sweetman, C., Stewart, R. K., Truong, Y. K.-N., Schachner, M., Manis, P. B., & Maness, P. F. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.2984-18.2019 · Cited by 43
“Spine formation and retraction contribute to remodeling and fine tuning of cortical networks in the developing and mature brain (Turrigiano, 2012; Stein and Zito, 2019).”
BackgroundNMDA-receptor agonist reveals LTP-like properties of 10-Hz rTMS in the human motor cortex
Brown, J. C., Yuan, S., DeVries, W. H., Armstrong, N. M., Korte, J. E., Sahlem, G. L., Carpenter, L. L., & George, M. S. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.03.016 · Cited by 41
“We speculate that this effect may be the result of concurrent homeostatic depression superimposed on a short-term plasticity ICI protocol [10].”
How Is Homeostatic Plasticity Important in Epilepsy?
Swann, J. W., & Rho, J. M. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-94-017-8914-1_10 · Cited by 44
Neural signatures of auditory hypersensitivity following acoustic trauma
McGill, M., Hight, A. E., Watanabe, Y. L., Parthasarathy, A., Cai, D., Clayton, K. K., Hancock, K. E., Takesian, A. E., Kujawa, S. G., & Polley, D. B. (2022) · eLife · doi:10.7554/elife.80015 · Cited by 36
“…calcium levels, which triggers a cascade of genetic, epigenetic, post-transcriptional, and post-translational processes that collectively adjust the electrical excitability of neurons to restore activity back to the baseline set point (for review see Harris and Rubel, 2006; Turrigiano, 2012).”
BackgroundInfluentialIsler, B., von Burg, N., Kleinjung, T., Meyer, M. E., Stämpfli, P., Zoelch, N., & Neff, P. K. A. (2022) · Scientific Reports · doi:10.1038/s41598-022-07835-8 · Cited by 42
Triiodothyronine modulates neuronal plasticity mechanisms to enhance functional outcome after stroke
Talhada, D., Feiteiro, J., Costa, A. R., Talhada, T., Cairrão, E., Wieloch, T. W., Englund, E. M., Santos, C. R. A., Gonçalves, I., & Ruscher, K. (2019) · Acta Neuropathologica Communications · doi:10.1186/s40478-019-0866-4 · Cited by 41
Asl, M. M., Vahabie, A., Valizadeh, A., & Tass, P. A. (2022) · Frontiers in Network Physiology · doi:10.3389/fnetp.2022.817524 · Cited by 39
“It has been suggested that homeostatic plasticity may function on a slower time-scale than that of Hebbian plasticity so that they may not interfere with each other (Kirov and Harris, 1999; Turrigiano, 2012).”
BackgroundShao, H., Mi, Z., Ji, W.-G., Zhang, C.-H., Zhang, T., Ren, S., & Zhu, Z.-R. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1730-y · Cited by 41
“Calcium (Ca) is a highly versatile intracellular second messenger in the central nervous system, and regulates neural excitation [32].”
BackgroundCaspase-3 Deficiency Results in Disrupted Synaptic Homeostasis and Impaired Attention Control
Lo, S., Wang, Y. Y., Weber, M., Larson, J. L., Scearce-Levie, K. A., & Sheng, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3280-14.2015 · Cited by 44
“Homeostatic synaptic plasticity, such as synaptic scaling, can be evoked to keep neuronal firing rates within a suitable range for optimal information processing (Turrigiano, 2012).”
BackgroundHomeostatic regulation of memory systems and adaptive decisions
Mizumori, S. J. Y., & Jo, Y. S. (2013) · Hippocampus · doi:10.1002/hipo.22176 · Cited by 43
Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders
Kim, K. C., Gonzales, E. L., Lázaro, M. T., Choi, C. S., Bahn, G. H., Yoo, H. J., & Shin, C. Y. (2016) · Biomolecules & Therapeutics · doi:10.4062/biomolther.2016.061 · Cited by 44
“One important aspect of this model is the role that synaptic activity modulators have in the overall E/I state, as they become key determinants of whether or not autistic behaviors arise, in a way that might involve the metaplastic regulation of LTP and LTD (Abraham, 2008; Turrigiano, 2012).”
BackgroundInfluentialGoel, P., & Dickman, D. K. (2018) · Nature Communications · doi:10.1038/s41467-018-04270-0 · Cited by 46
Hebbian and Homeostatic Synaptic Plasticity—Do Alterations of One Reflect Enhancement of the Other?
Galanis, C., & Vlachos, A. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00050 · Cited by 43
“It has been proposed, for example, that homeostatic plasticity operates on a longer time scale (Turrigiano, 2012; Tononi and Cirelli, 2014; Hengen et al., 2016)—thus not interfering with synaptic changes induced by Hebbian plasticity—and that all synapses of a neuron are adjusted by the same factor…”
BackgroundVlachos, A., Helias, M., Becker, D., Diesmann, M., & Deller, T. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.07.018 · Cited by 38
“Homeostatic synaptic plasticity maintains stability in neuronal networks As has been pointed out in several recent reviews (Turrigiano, 2012; Vitureira et al., 2012; Wang et al., 2012), the brain has to allow plastic changes to occur without compromising the stability and integrity of the…”
InfluentialAn Improved Test for Detecting Multiplicative Homeostatic Synaptic Scaling
Kim, J., Tsien, R. W., & Alger, B. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037364 · Cited by 37
“This model contains two slightly different concepts: first, ‘‘global’’ scaling means that neurons can sense their own firing rate and adjust the strengths of all synapse onto them in a cell-autonomous manner [4,15].”
BackgroundMethodSynaptic Dysfunction and Plasticity in Amyotrophic Lateral Sclerosis
Gulino, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054613 · Cited by 38
Homeostatic regulation of neuronal function: importance of degeneracy and pleiotropy
Yang, J., & Prescott, S. A. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1184563 · Cited by 40
“…(O’Brien et al., 1998; Turrigiano et al., 1998) as well as the thresholds for inducing synaptic plasticity (Kirkwood et al., 1996) (for reviews, see Davis and Bezprozvanny, 2001; Turrigiano, 2008, 2011, 2012; Davis, 2013; Gainey and Feldman, 2017; Keck et al., 2017; Lee and Kirkwood, 2019).”
BackgroundAnil, S., Lu, H., Rotter, S., & Vlachos, A. (2023) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011027 · Cited by 42
Wang, X., McIntosh, J. M., & Rich, M. M. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1789-17.2018 · Cited by 38
“Block of synaptic transmission at the NMJ triggers rapid up-regulation of presynaptic transmitter release that serves to counteract the block of transmission and is thus termed homeostatic synaptic plasticity (Rich and Wenner, 2007; Turrigiano, 2012; Davis and Mu¨ller, 2015).”
BackgroundRegulation of Ion Channels by MicroRNAs and the Implication for Epilepsy
Groß, C., & Tiwari, D. (2018) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-018-0870-2 · Cited by 36
Hanes, A. L., Koesters, A. G., Fong, M., Altimimi, H. F., Stellwagen, D., Wenner, P., & Engisch, K. L. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1393-19.2020 · Cited by 37
“…strengths, established by other forms of activity-dependent plasticity, will be exactly as they were before (Turrigiano et al., 1998; Turrigiano and Nelson, 2004; Pozo and Goda, 2010; Watt and Desai, 2010; Turrigiano, 2012, 2017; Vitureira and Goda, 2013; Keck et al., 2017a,b; Yee et al., 2017).”
BackgroundInfluentialDesch, K., Langer, J. D., & Schuman, E. M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109583 · Cited by 34
Adaptive control of synaptic plasticity integrates micro- and macroscopic network function
Scott, D. N., & Frank, M. J. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01374-6 · Cited by 40
“Rough conservation in aggregate has largely been born out in the form of "synaptic scaling" [201, 202], and remarkably there is also evidence that local excitatoryinhibitory balance and synaptic strength are conserved on dendritic sub-domains as well [5, 11].”
BackgroundHarnessing brain plasticity to improve binocular vision in amblyopia: An evidence-based update
Thompson, B. S., Morrone, M. C., Bex, P. J., Lozama, A., & Sabel, B. A. (2023) · European Journal of Ophthalmology · doi:10.1177/11206721231187426 · Cited by 42
“20 The Bienenstock – Cooper – Munro model is a modi fi ed version of the Hebbian model in which synaptic strength can be modi fi ed bidirectionally to promote synaptic weakening as well as strengthening with the threshold change in synaptic input, depending on the history of postsynaptic activity.”
Method(Re)building the nervous system: A review of neuron–glia interactions from development to disease
Demmings, M. D., Chagas, L. D. S., Traetta, M. E., Rodrigues, R. S., Acutain, M. F., Barykin, E. P., Datusalia, A. K., German‐Castelan, L., Mattera, V. S., Mazengenya, P., et al. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16258 · Cited by 44
“Indeed, a form of homeostatic plasticity seems to be relevant in mature circuits as prolonged changes in activity result in synaptic adaptations (reviewed by (Turrigiano, 2012 )).”
Memory labilization in reconsolidation and extinction – Evidence for a common plasticity system?
Almeida-Corrêa, S., & Amaral, O. B. (2014) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2014.08.006 · Cited by 37
Regulation of synaptic scaling by action potential–independent miniature neurotransmission
Gonzalez-Islas, C. E., Bülow, P., & Wenner, P. (2017) · Journal of Neuroscience Research · doi:10.1002/jnr.24138 · Cited by 36
“…networks, neurons responded in what appeared to be a compensatory direction by increasing the strength of all their excitatory synaptic inputs, as measured by miniature excitatory postsynaptic current (mEPSC) amplitude (Turrigiano, 2012; Turrigiano, Leslie, Desai, Rutherford, & Nelson, 1998).”
BackgroundGallinaro, J. V., & Rotter, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-22077-3 · Cited by 39
“There is growing evidence for homeostatic regulation of cortical connectivity (for a review, see Turrigiano [55]).”
InfluentialHuang, Y.-C., Pirri, J. K., Rayes, D., Gao, S., Mulcahy, B., Grant, J., Saheki, Y., Francis, M. M., Zhen, M., & Alkema, M. J. (2019) · eLife · doi:10.7554/elife.45905 · Cited by 37
“unc-2(zf35gf) differentially affects excitatory and inhibitory synapses How does an increase of UNC-2/CaV2a activity lead to an E/I imbalance? Since changes in neuronal activity can modulate synaptic protein distribution (Frank, 2014; Turrigiano, 2012), we examined the morphology of pre- and post-synaptic markers at c…”
BackgroundMitochondria: new players in homeostatic regulation of firing rate set points
Ruggiero, A., Katsenelson, M., & Slutsky, I. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.03.002 · Cited by 37
“How does the network’s behavior relate to properties of its single components? Multiple spatial set points may exist, and the specific set point may undergo regulation by homeostatic mechanisms implemented at these various spatial scales [18,19].”
Lane, B. J., Samarth, P. S., Ransdell, J. L., Nair, S. S., & Schulz, D. J. (2016) · eLife · doi:10.7554/elife.16879 · Cited by 40
“…the nervous system has been the subject of intense interrogation, with studies focusing on both homeostatic synaptic scaling (Turrigiano, 2012; Lee et al., 2014) and tuning of ionic conductance relationships to maintain a target level of excitability (Turrigiano et al., 1994; Desai et al., 1999).”
BackgroundInfluentialIbrahim, B. A., & Llano, D. A. (2019) · Brain Sciences · doi:10.3390/brainsci9120351 · Cited by 34
“This view comports with a growing body of literature demonstrating that neural networks homeostatically adjust their overall magnitude of excitation and inhibition to maintain a balance between the two (reviewed in [14]).”
BackgroundChen, X., & Yan, C. (2021) · NeuroImage · doi:10.1016/j.neuroimage.2021.118427 · Cited by 36
“…2017 ). ecent studies have highlighted one key dynamic physiological feaure of neural activities, which is a state that can generate flexibilty to envision the full range of behavior while maintaining stability ver extended spans of time ( Gonzalez-Castillo and Bandettini, 2018 ; urrigiano, 2012 ).”
Single-dose ethanol intoxication causes acute and lasting neuronal changes in the brain
Knabbe, J., Protzmann, J., Schneider, N., Berger, M., Dannehl, D., Wei, S., Strahle, C., Tegtmeier, M., Jaiswal, A., Zheng, H., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2122477119 · Cited by 37
NR2B subunit of the NMDA glutamate receptor regulates appetite in the parabrachial nucleus
Wu, Q., Zheng, R., Srisai, D., McKnight, G. S., & Palmiter, R. D. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1314137110 · Cited by 38
A molecular mechanism underlying gustatory memory trace for an association in the insular cortex
Adaikkan, C., & Rosenblum, K. (2015) · eLife · doi:10.7554/elife.07582 · Cited by 34
“…interval as discussed above, homeostatic plasticity may play a crucial role to encode multiple memory traces via coordinating several brain structures such as the IC, amygdala, hippocampus, prefrontal cortices in the long-trace CTA (Vitureira et al., 2012; Turrigiano, 2012; Pozo and Goda, 2010).”
BackgroundBannon, N. M., Chistiakova, M., & Volgushev, M. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00204 · Cited by 38
“…synaptic scaling’’, which induce plastic changes after many hours or days of dramatic alterations of activity level (Watt and Desai, 2010; Wenner, 2011; Turrigiano, 2012; Keck et al., 2017) and play a role during development or recovery after injury and deafferentation, cannot serve the…”
BackgroundMartinsson, I., Quintino, L., Garcia, M. G., Konings, S. C., Torres-Garcia, L., Svanbergsson, A., Stange, O., England, R., Deierborg, T., Li, J., et al. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.946297 · Cited by 35
“These modulatory processes enable neuronal communication to be maintained within an appropriate window, allowing meaningful information transfer (Turrigiano, 2012).”
BackgroundWang, Y., Wu, Y., Luo, L., & Li, F. Y. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.371349 · Cited by 35
“This increase may imply the functional plasticity of neurons and a compensatory increase for the deficit of visual input from the amblyopic eye (Turrigiano, 2012).”
BackgroundMo, J., Kim, C., Lee, D., Sun, W., Lee, H. W., & Kim, H. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13077 · Cited by 34
“Neuronal activity regulated by excitatory and inhibitory receptors induces the structural and functional synaptic plasticity that accompanies the alteration of the E/I balance (Turrigiano 2012; Vitureira et al. 2012; Wang et al. 2012; Davis 2013).”
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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
A language model drew the claims from the paper on 2026-10-12, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-12 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
Cited sources are checked with a language model’s help (gpt-6-sol).
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review