The DOI matches its Crossref record; 35 of the 36 references it cites were found in a registry or an index; none of the 6 sources its claims cite is checked for support yet.
Dynamic actin filaments are required for stable long-term potentiation (LTP) in area CA1 of the hippocampus
Open accessAbstract
The hypothesis that dynamic actin filaments participate in specific aspects of synaptic plasticity was investigated at the Schaffer-collateral-CA1 pyramidal cell synapse of mouse hippocampus. Low concentrations (0.01–1 μM) of compounds that inhibit actin filament assembly were bath applied to hippocampal slices during extracellular recording of field excitatory postsynaptic potentials. Cytochalasin D, cytochalasin B, and latrunculin A all impaired the maintenance of LTP induced by brief high-frequency stimulation. This effect on LTP maintenance was specific, because none of the compounds affected basal synaptic transmission, paired-pulse facilitation, LTP induction, or post-tetanic potentiation. The effect of cytochalasin B was reversible. The results are consistent with a model in which dynamic actin filaments play an essential role in the molecular mechanisms underlying the early maintenance phase of LTP, such as growth of new synaptic connections or conversion of silent synapses.
Overview
AI snapshot
Written from the paper’s full text.
TL;DR
Low concentrations of actin filament assembly inhibitors selectively impaired maintenance of LTP at Schaffer-collateral–CA1 synapses without affecting basal synaptic transmission, paired-pulse facilitation, LTP induction, or post-tetanic potentiation. The results suggest dynamic actin filaments are required during the early maintenance phase of LTP, possibly for structural remodeling or receptor trafficking.
Key findings
- Cytochalasin D, cytochalasin B, and latrunculin A (0.01–1 μM) did not significantly alter basal pEPSPs, pharmacologically isolated NMDA-pEPSPs, presynaptic fiber volleys, or paired-pulse facilitation over 90 min.
- In untreated slices, LTP was stable at 214 ± 17% of baseline at 100 min and 211 ± 20% at 130 min after tetanus. Pretreatment with actin assembly inhibitors reduced maintained LTP: cytochalasin D reached about 140% of baseline after 60 min, cytochalasin B about 148% at 130 min, and latrunculin A about 139% at 130 min.
- When superfused after LTP induction, cytochalasin D reduced LTP to 165 ± 17% at 100 min and 121 ± 12% at 180 min; cytochalasin B to 182 ± 12% at 100 min and 146 ± 15% at 180 min; latrunculin A to 165 ± 3% at 100 min and 140 ± 12% at 180 min.
- Cytochalasin B effects were at least partially reversible: after washout and a second tetanus, LTP was stable, and 0.01 μM cytochalasin B for 5 min reduced first LTP but allowed robust, nondecremental LTP of about 200% after the second tetanus.
Methods
- Hippocampal slices (400 μm) from normal C57BL/6 male mice (32 ± 0.8 days old) were maintained in oxygenated ACSF at 32 ± 0.2°C.
- Extracellular recordings of presynaptic fiber volleys and population EPSPs were made in stratum radiatum of CA1 with Schaffer-collateral stimulation; input–output curves and paired-pulse facilitation at 20, 50, 100, and 200 ms were tested.
- LTP was induced by two tetani of 100 Hz, 20 sec apart, with responses followed up to 180 min; drugs were bath-applied before or immediately after LTP induction. pEPSP slope, amplitude, and area were analyzed, with Mann–Whitney U tests and P ≤ 0.05 considered significant.
Limitations
- The paper states that the precise time window when dynamic actin filaments participate in LTP maintenance remains to be determined, and the precise nature and location of the essential actin filaments are not identified.
- The authors state their studies do not rule out a role for dynamic actin in other regions of the neuron or in glial cells.
- Evident from the text: experiments used only male C57BL/6 mice at one developmental age, in vitro slices, extracellular field recordings, and small group sizes (e.g., n = 3–7 per condition), which limits generalization and statistical power.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
21 Own result · 8 Own interpretation · 3 Not checked yet · 3 No basis given · 2 Own method
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“none of the compounds affected basal synaptic transmission, paired-pulse facilitation, LTP induction, or post-tetanic potentiation.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — 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 presynaptic volley amplitude did not change during the entire recording time, suggesting that there were no modifications of the fiber input (data not shown).”
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- Rests on an assumption: The presynaptic volley amplitude is proportional to the number of presynaptic neurons recruited by stimulation.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“none of the compounds affected basal synaptic transmission, paired-pulse facilitation, LTP induction, or post-tetanic potentiation.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“none of the compounds affected basal synaptic transmission, paired-pulse facilitation, LTP induction, or post-tetanic potentiation.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Indeed, a lower concentration of cytochalasin B (0.01 μM, n = 5) superfused for 5 min also reduced the magnitude of LTP in a manner indistinguishable from the effect of higher concentrations.”
plaindirectn = 5- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“none of the compounds affected basal synaptic transmission, paired-pulse facilitation, LTP induction, or post-tetanic potentiation.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Control (untreated) slices exhibited stable LTP of 214 ± 17% of baseline at 100 min and 211 ± 20% at 130 min after tetanus.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, all LTP magnitudes at 100 and 130 min were significantly reduced relative to control (P < 0.012).”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
The 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
“Pretreatment with Actin Assembly Inhibitors Impairs LTP.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“slices incubated with cytochalasin D (1 μM, n = 4; 0.1 μM, n = 3; data pooled) showed reduced PTP but were subsequently potentiated to about 200% of baseline after 10 min, then declined steadily to reach a plateau of about 140% of baseline after 60 min of LTP induction.”
plaindirectn = 4- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
- It may state two separate claims as one. 13
- Probably not a substantial claim. 6
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“At 100 min after LTP induction, LTP magnitude was 165 ± 17% of baseline (significantly different from untreated slices, P < 0.015) and further declined to 121 ± 12% of baseline after 180 min.”
plainn = 7 ·- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Like the cytochalasin D effect, after 100 min of LTP induction, cytochalasin B (0.1 μM, n = 3) and latrunculin A (0.1 μM, n = 5) reduced the average pEPSP slope to 182 ± 12% and 165 ± 3% of baseline, respectively. After 180 min, both drugs reduced LTP magnitude significantly (P < 0.02) to 146 ± 15% and 140 ± 12% of baseline, respectively.”
plaindirectn = 5 ·- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Slices incubated with cytochalasin B (0.1 μM, n = 5) also showed reduced PTP, although this was not significant. Responses were potentiated after 10 min to values similar to those in control slices but then declined steadily afterward and reached about 148% of baseline 130 min after tetanus.”
plaindirectn = 5- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“slices incubated with latrunculin A (0.1 μM, n = 5) showed nonsignificantly reduced PTP, were potentiated for 10 min, and declined to about 139% of baseline 130 min after tetanus.”
plainn = 5- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Cytochalasin D, cytochalasin B, and latrunculin A all impaired the maintenance of LTP induced by brief high-frequency stimulation.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“In addition, the presynaptic fiber volley and PPF remain unchanged.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Rests on an assumption: The presynaptic volley amplitude is proportional to the number of presynaptic neurons recruited by stimulation.
A result the paper reports from its own data — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“However, we observed robust LTP after the second set of tetani. This enhancement declined only slightly and reached a plateau of about 200% of control after 30 min.”
plainn = 5- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“our results also suggest that dynamic actin filaments in the presynaptic compartment do not take part in basal synaptic transmission or in short-term plasticity.”
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The final concentration of DMSO in the slice chamber never exceeded 0.1%, a concentration found in control experiments to have no detectable effects on the slices.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
In the paper
“Latrunculins bind to G-actin in a 1:1 molar complex, thereby limiting the availability of actin monomers for polymerizing at either barbed or pointed ends of actin filaments (4).”
What the sources say
- Not checked yetcites [4] Spector I, Shochet N R, Blasberger D, Kashman Y. Cell Motil Cytoskeleton. 1989;13:127–144. doi: 10.1002/cm.970130302. [DOI] [PubMed] [Google Scholar] source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it. It may state two separate claims as one.
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
“These actin inhibitors selectively disrupt filaments undergoing rapid length excursions, leaving intact the more stable and slowly-turning-over actin filaments.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
What the paper did — it cites no source for this, so there is none to check. The quote shows it is in the paper.
In the paper
“The use of low but effective concentrations of actin inhibitors was designed to avoid nonspecific effects.”
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim.
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
“Indeed, whereas dynamic filaments in dendrites and spines are logical candidates, our studies do not rule out a role for dynamic actin in other regions of the neuron or in glial cells.”
plain- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
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
“Because this LTP magnitude resembled normal levels and was nondecremental, this finding suggests that cytochalasin B effects are reversible.”
hedgedconditionaln = 5- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: unclear — It is unclear whether the paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
- Rests on an assumption: Cytochalasin D exhibits poor washout in intact preparations, whereas cytochalasin B effects are more readily reversible.
None of the sources cited for this claim have been checked yet.
In the paper
“The concentrations of latrunculin A and cytochalasins used here (0.01–1 μM) are similar to those that have been shown previously to alter actin filament organization in cultured cells, prevent lamellipodial ruffling in fibroblasts, inhibit motility and retrograde flow in neuronal growth cones, and arrest dendritic spine motility in hippocampal neurons (3, 4, 7, 10).”
What the sources say
- Not checked yetcites [3] Cooper J A. J Cell Biol. 1987;105:1473–1478. doi: 10.1083/jcb.105.4.1473. [DOI] [PMC free article] [PubMed] [Google Scholar] source
- Not checked yetcites [4] Spector I, Shochet N R, Blasberger D, Kashman Y. Cell Motil Cytoskeleton. 1989;13:127–144. doi: 10.1002/cm.970130302. [DOI] [PubMed] [Google Scholar] source
- Not checked yetcites [7] Forscher P, Smith S J. J Cell Biol. 1988;107:1505–1516. doi: 10.1083/jcb.107.4.1505. [DOI] [PMC free article] [PubMed] [Google Scholar] source
- Not checked yetcites [10] Fischer M, Kaech S, Knutti D, Matus A. Neuron. 1998;20:847–854. doi: 10.1016/s0896-6273(00)80467-5. [DOI] [PubMed] [Google Scholar] source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
In the paper
“at low concentrations, their primary effect in cells is to cap the barbed ends of actin filaments (3).”
What the sources say
- Not checked yetcites [3] Cooper J A. J Cell Biol. 1987;105:1473–1478. doi: 10.1083/jcb.105.4.1473. [DOI] [PMC free article] [PubMed] [Google Scholar] source
plaindirect- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: fails — The paper’s conclusions may not depend on it.
- Based: passes — The paper gives a reason why it holds.
Probably not a substantial claim. The paper’s conclusions may not depend on it.
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
“Under the conditions used here, the application of actin perturbing agents is not expected to disrupt stable actin filaments or induce collapse of dendritic spines.”
hedged- Asserted: passes — The authors put it forward as true.
- Checkable: passes — It can be checked against evidence.
- Load-bearing: passes — The paper’s conclusions depend on it.
- Based: passes — The paper gives a reason why it holds.
It may state two separate claims as one.
The paper relies on this without support.
Cytochalasin D exhibits poor washout in intact preparations, whereas cytochalasin B effects are more readily reversible.
“It has been reported that cytochalasin D exhibits poor washout in intact preparations, but that effects of cytochalasin B are more readily reversible.”
The paper relies on this without support.
The presynaptic volley amplitude is proportional to the number of presynaptic neurons recruited by stimulation.
“the amplitude of the presynaptic volley, which is proportional to the number of presynaptic neurons recruited by stimulation”
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The expression of AMPA receptors in spines is dependent on F-actin11,17 and scaffolding proteins18,19.”
From Structural basis of long-term potentiation in single dendritic spines (2004) · cites this paper as [11]
Experimental — accuracy not yet measuredIn the citing paper
“Actin polymerization is an essential step of this kind (9, 15–17)”
From Synaptic evidence for the efficacy of spaced learning (2012) · cites this paper as [17]
In the citing paper
“consistent with the previous observation that a low concentration of this agent blocked long-term but not early potentiation11”
From Structural basis of long-term potentiation in single dendritic spines (2004) · cites this paper as [11]
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.
Rated major: it would touch a result — a value a result rests on, reported and recomputed p-values on opposite sides of the significance level, two passages that conflict with no sign which is right, or a cited work retracted before this paper was published.
In the paper
§ Methods
“To assess drug effects on synaptic efficacy, we generated additional I-O curves at 20 and 40 min after the start of drug superfusion with the same stimulation intensities as those under control conditions.”
§ Results
“After 40 and 80 min of cytochalasin D superfusion, additional I-O curves performed at the same stimulation intensities as under control conditions also showed no detectable changes (Fig. 2A).”
Rated minor: it would not touch a result — a value no result rests on, a p-value that stays on the same side of the significance level, or a conflict that is clerical, resolved elsewhere in the paper, or outside its own findings.
In the paper
§ Discussion
“In addition, drug wash-out experiments show that the inhibition of LTP by AAIs is reversible.”
§ Results
“Similarly, we observed that, in contrast to the effects of cytochalasin D and latrunculin A, the effects of cytochalasin B on LTP appeared to be at least partially reversible (Fig. 4C).”
Citations
Cites
Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729
Effects of cytochalasin and phalloidin on actin.
Cooper, J. A. (1987) · The Journal of cell biology · doi:10.1083/jcb.105.4.1473 · Cited by 2,009
Actin-Based Cell Motility and Cell Locomotion
Mitchison, T. J., & Cramer, L. P. (1996) · Cell · doi:10.1016/s0092-8674(00)81281-7 · Cited by 1,538
Dendritic spine changes associated with hippocampal long-term synaptic plasticity
Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412
Rapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation
Shi, S.-H., Hayashi, Y., Petralia, R. S., Zaman, S. H., Wenthold, R. J., Svoboda, K., & Malinow, R. (1999) · Science · doi:10.1126/science.284.5421.1811 · Cited by 1,276
Rapid Dendritic Morphogenesis in CA1 Hippocampal Dendrites Induced by Synaptic Activity
Maletic-Savatic, M., Malinow, R., & Svoboda, K. (1999) · Science · doi:10.1126/science.283.5409.1923 · Cited by 1,009
Rapid Actin-Based Plasticity in Dendritic Spines
Fischer, M., Kaech, S., Knutti, D., & Matus, A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80467-5 · Cited by 905
Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation
Ziv, N. E., & Smith, S. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80283-4 · Cited by 882
Forscher, P., & Smith, S. J. (1988) · The Journal of cell biology · doi:10.1083/jcb.107.4.1505 · Cited by 854
Synaptogenesis Via Dendritic Filopodia in Developing Hippocampal Area CA1
Fiala, J. C., Feinberg, M., Popov, V., & Harris, K. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08900.1998 · Cited by 758
Research works printed but not linked: 1
- H Wigstrom, B Gustafsson J Physiol 81, 228–236 (1986).
Cited by
Sorted by citations
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
AMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588
Structural basis of long-term potentiation in single dendritic spines
Matsuzaki, M., Honkura, N., Ellis-Davies, G. C. R., & Kasai, H. (2004) · Nature · doi:10.1038/nature02617 · Cited by 2,483
Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity
Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269
TrkB signalling pathways in LTP and learning
Minichiello, L. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2738 · Cited by 1,055
Balancing Structure and Function at Hippocampal Dendritic Spines
Bourne, J. N., & Harris, K. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125646 · Cited by 916
Structural plasticity and memory
Lamprecht, R., & LeDoux, J. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1301 · Cited by 1,010
Okamoto, K.-I., Nagai, T., Miyawaki, A., & Hayashi, Y. (2004) · Nature Neuroscience · doi:10.1038/nn1311 · Cited by 854
Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy.
Cingolani, L. A., & Goda, Y. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2373 · Cited by 831
Actin in dendritic spines: connecting dynamics to function
Hotulainen, P., & Hoogenraad, C. C. (2010) · Journal of Cell Biology · doi:10.1083/jcb.201003008 · Cited by 815
Actin-based plasticity in dendritic spines
Matus, A. (2000) · Science · doi:10.1126/science.290.5492.754 · Cited by 815
Structure-stability-function relationships of dendritic spines
Kasai, H., Matsuzaki, M., Noguchi, J., Yasumatsu, N., & Nakahara, H. (2003) · Trends in Neurosciences · doi:10.1016/s0166-2236(03)00162-0 · Cited by 847
Fukazawa, Y., Saitoh, Y., Ozawa, F., Ohta, Y., Mizuno, K., & Inokuchi, K. (2003) · Neuron · doi:10.1016/s0896-6273(03)00206-x · Cited by 695
Abnormal Spine Morphology and Enhanced LTP in LIMK-1 Knockout Mice
Meng, Y., Zhang, Y., Tregoubov, V., Janus, C., Cruz, L., Jackson, M., Lu, W.-Y., MacDonald, J. F., Wang, J. Y., Falls, D. L., et al. (2002) · Neuron · doi:10.1016/s0896-6273(02)00758-4 · Cited by 688
The Subspine Organization of Actin Fibers Regulates the Structure and Plasticity of Dendritic Spines
Honkura, N., Matsuzaki, M., Noguchi, J., Ellis-Davies, G. C. R., & Kasai, H. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.013 · Cited by 490
Lisman (2001) · doi:10.1016/s0896-6273(01)00364-6 · Cited by 480
Rapid turnover of actin in dendritic spines and its regulation by activity
Star, E. N., Kwiatkowski, D. J., & Murthy, V. N. (2002) · Nature Neuroscience · doi:10.1038/nn811 · Cited by 481
The actin cytoskeleton: integrating form and function at the synapse
Dillon, C., & Goda, Y. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135757 · Cited by 447
The role of calmodulin as a signal integrator for synaptic plasticity
Xia, Z., & Storm, D. R. (2005) · Nature reviews. Neuroscience · doi:10.1038/nrn1647 · Cited by 454
BDNF and Hippocampal Synaptic Plasticity
Leal, G., Bramham, C. R., & Duarte, C. B. (2017) · Vitamins and Hormones · doi:10.1016/bs.vh.2016.10.004 · Cited by 425
Spine-Neck Geometry Determines NMDA Receptor-Dependent Ca2+ Signaling in Dendrites
Noguchi, J., Matsuzaki, M., Ellis-Davies, G. C. R., & Kasai, H. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.015 · Cited by 419
Structural plasticity of dendritic spines
Bosch, M., & Hayashi, Y. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.09.002 · Cited by 415
Balance and Stability of Synaptic Structures during Synaptic Plasticity
Meyer, D., Bonhoeffer, T., & Scheuss, V. (2014) · Neuron · doi:10.1016/j.neuron.2014.02.031 · Cited by 395
Increasing Numbers of Synaptic Puncta during Late-Phase LTP
Bozdagi, O., Shan, W., Tanaka, H., Benson, D. L., & Huntley, G. W. (2000) · Neuron · doi:10.1016/s0896-6273(00)00100-8 · Cited by 384
Molecular mechanisms of dendritic spine development and remodeling
Ethell, I. M., & Pasquale, E. B. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.02.003 · Cited by 367
Regulation of AMPA receptor extrasynaptic insertion by 4.1N, phosphorylation and palmitoylation
Lin, D.-T., Makino, Y., Sharma, K., Hayashi, T., Neve, R., Takamiya, K., & Huganir, R. L. (2009) · Nature Neuroscience · doi:10.1038/nn.2351 · Cited by 347
Rex, C. S., Lin, C.-Y., Kramár, E. A., Chen, L. Y., Gall, C. M., & Lynch, G. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.4037-06.2007 · Cited by 324
Roles of serine/threonine phosphatases in hippocampel synaptic plasticity
Winder, D. G., & Sweatt, J. D. (2001) · Nature reviews. Neuroscience · doi:10.1038/35081514 · Cited by 320
Wang, X.-B., Bozdagi, O., Nikitczuk, J. S., Zhai, Z. W., Zhou, Q., & Huntley, G. W. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807248105 · Cited by 316
mTORC2 controls actin polymerization required for consolidation of long-term memory
Huang, W., Zhu, P. J., Zhang, S., Zhou, H., Stoica, L., Galiano, M., Krnjević, K., Roman, G., & Costa-Mattioli, M. (2013) · Nature Neuroscience · doi:10.1038/nn.3351 · Cited by 307
Kinase-Independent Requirement of EphB2 Receptors in Hippocampal Synaptic Plasticity
Kadow, I. C. G., Körte, M., Wolfer, D. P., Wilkinson, G. A., Unsicker, K., Lipp, H., Bonhoeffer, T., & Klein, R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00550-5 · Cited by 311
Rapid formation and remodeling of postsynaptic densities in developing dendrites
Marrs, G. S., Green, S. H., & Dailey, M. E. (2001) · Nature Neuroscience · doi:10.1038/nn717 · Cited by 311
Local protein synthesis, actin dynamics, and LTP consolidation
Bramham, C. R. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.09.013 · Cited by 301
Shen, L., Liang, F., Walensky, L. D., & Huganir, R. L. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-21-07932.2000 · Cited by 305
Rex, C. S., Chen, L. Y., Sharma, A., Liu, J., Babayan, A. H., Gall, C. M., & Lynch, G. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200901084 · Cited by 293
Hayashi, M. L., Choi, S.-Y., Rao, B. S. S., Jung, H.-Y., Lee, H.-K., Zhang, D., Chattarji, S., Kirkwood, A., & Tonegawa, S. (2004) · Neuron · doi:10.1016/j.neuron.2004.05.003 · Cited by 280
Tracy, T. E., Sohn, P. D., Minami, S. S., Wang, C., Min, S.-W., Li, Y., Zhou, Y., Le, D., Lo, I., Ponnusamy, R., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.03.005 · Cited by 277
The Persistence of Long-Term Memory
Bailey, C. H., Kandel, E. R., & Si, K. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.017 · Cited by 282
Actin-Dependent Regulation of Neurotransmitter Release at Central Synapses
Morales, M., Colicos, M. A., & Goda, Y. (2000) · Neuron · doi:10.1016/s0896-6273(00)00064-7 · Cited by 300
Activity-induced targeting of profilin and stabilization of dendritic spine morphology
Ackermann, M., & Matus, A. I. (2003) · Nature Neuroscience · doi:10.1038/nn1135 · Cited by 289
Essential role for cholesterol in synaptic plasticity and neuronal degeneration
Koudinov, A. R., & Koudinova, N. V. (2001) · The FASEB Journal · doi:10.1096/fj.00-0815fje · Cited by 281
Cytoskeletal changes underlie estrogen’s acute effects on synaptic transmission and plasticity.
Kramár, E. A., Chen, L. Y., Brandon, N. J., Rex, C. S., Liu, F., Gall, C. M., & Lynch, G. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3059-09.2009 · Cited by 264
Frost, N. A., Shroff, H., Kong, H., Betzig, E., & Blanpied, T. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.026 · Cited by 275
Stages of Synapse Development Defined by Dependence on F-Actin
Zhang, W., & Benson, D. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05169.2001 · Cited by 262
Altered morphology and 3D architecture of brain vasculature in a mouse model for Alzheimer's disease
Meyer, E. P., Ulmann-Schuler, A., Staufenbiel, M., & Krucker, T. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0709788105 · Cited by 260
Self-citationOn the Role of Nitric Oxide in Hippocampal Long-Term Potentiation
Bon, C. L. M., & Garthwaite, J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01941.2003 · Cited by 259
TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines
Fujii, R., & Takumi, T. (2005) · Journal of Cell Science · doi:10.1242/jcs.02692 · Cited by 253
Form follows function: BDNF and its involvement in sculpting the function and structure of synapses
Zagrebelsky, M., & Korte, M. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.029 · Cited by 241
Guidance Molecules in Synapse Formation and PlasticityPreprint
Shen, K., & Cowan, C. W. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a001842 · Cited by 233
Integrin-driven actin polymerization consolidates long-term potentiation
Kramár, E. A., Lin, B., Rex, C. S., Gall, C. M., & Lynch, G. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0601354103 · Cited by 221
GluR1 Links Structural and Functional Plasticity at Excitatory Synapses
Kopec, C. D., Réal, É., Kessels, H. W. H. G., & Malinow, R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3503-07.2007 · Cited by 226
Fischer, A., Sananbenesi, F., Schrick, C., Spiess, J., & Radulović, J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5112-03.2004 · Cited by 222
A quantitative overview of biophysical forces impinging on neural function
Mueller, J. K., & Tyler, W. J. (2014) · Physical Biology · doi:10.1088/1478-3975/11/5/051001 · Cited by 225
Wang, H., Lu, F.-M., Jin, I., Udo, H., Kandel, E. R., de Vente, J., Walter, U., Lohmann, S. M., Hawkins, R. D., & Antonova, I. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.011 · Cited by 216
Relapse Induced by Cues Predicting Cocaine Depends on Rapid, Transient Synaptic Potentiation
Gipson, C. D., Kupchik, Y. M., Shen, H., Reissner, K. J., Thomas, C. A., & Kalivas, P. W. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.005 · Cited by 226
LTP consolidation: Substrates, explanatory power, and functional significance
Lynch, G., Rex, C. S., & Gall, C. M. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.027 · Cited by 214
Myosin IIb regulates actin dynamics during synaptic plasticity and memory formation
Rex, C. S., Gavin, C. F., Rubio, M. D., Kramar, E. A., Chen, L. Y., Jia, Y., Huganir, R. L., Muzyczka, N., Gall, C. M., Miller, C. A., et al. (2010) · Neuron · doi:10.1016/j.neuron.2010.07.016 · Cited by 213
Excitation control: balancing PSD-95 function at the synapse
Keith, D. J. (2008) · Frontiers in Molecular Neuroscience · doi:10.3389/neuro.02.004.2008 · Cited by 223
Frick, K. M., Kim, J., Tuscher, J. J., & Fortress, A. M. (2015) · Learning & Memory · doi:10.1101/lm.037267.114 · Cited by 219
Biochemical Computation for Spine Structural Plasticity
Nishiyama, J., & Yasuda, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.043 · Cited by 199
Okamoto, K., Bosch, M., & Hayashi, Y. (2009) · Physiology · doi:10.1152/physiol.00029.2009 · Cited by 213
Synaptic evidence for the efficacy of spaced learning
Kramár, E. A., Babayan, A. H., Gavin, C. F., Cox, C. D., Jafari, M., Gall, C. M., Rumbaugh, G., & Lynch, G. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120700109 · Cited by 192
Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 189
Sabo, S. L., Ikin, A. F., Buxbaum, J. D., & Greengard, P. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05407.2003 · Cited by 187
Bozdagi, O., Nagy, V., Kwei, K. T., & Huntley, G. W. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00202.2007 · Cited by 182
Theta Stimulation Polymerizes Actin in Dendritic Spines of Hippocampus
Lin, B., Kramár, E. A., Bi, X., Brücher, F., Gall, C. M., & LYNCH, G. S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4283-04.2005 · Cited by 187
Spine dynamics in the brain, mental disorders and artificial neural networks
Kasai, H., Ziv, N. E., Okazaki, H., Yagishita, S., & Toyoizumi, T. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00467-3 · Cited by 184
Park, E., Na, M., Choi, J., Kim, S., Lee, J.-R., Yoon, J., Park, D., Sheng, M., & Kim, E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m301052200 · Cited by 175
The BDNF effects on dendritic spines of mature hippocampal neurons depend on neuronal activity
Kellner, Y., Gödecke, N., Dierkes, T., Thieme, N., Zagrebelsky, M., & Körte, M. (2014) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2014.00005 · Cited by 184
Regulation of neuronal PKA signaling through AKAP targeting dynamics
Dell’Acqua, M. L., Smith, K. E., Gorski, J. A., Horne, E. A., Gibson, E. S., & Gomez, L. L. (2006) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2006.01.010 · Cited by 176
Gomez, L. L., Alam, S., Smith, K. E., Horne, E., & Dell'Acqua, M. L. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-16-07027.2002 · Cited by 170
Chan, C.-S., Weeber, E. J., Zong, L., Fuchs, E., Sweatt, J. D., & Davis, R. L. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4110-05.2006 · Cited by 165
Rapid Increase in Clusters of Presynaptic Proteins at Onset of Long-Lasting Potentiation
Antonova, I., Arancio, O., Trillat, A., Wang, H., Zablow, L., Udo, H., Kandel, E. R., & Hawkins, R. D. (2001) · Science · doi:10.1126/science.1066273 · Cited by 163
Karpova, A., Mikhaylova, M., Thomas, U., Knöpfel, T., & Behnisch, T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.4573-05.2006 · Cited by 162
Calcium regulation of actin dynamics in dendritic spines
Oertner, T. G., & Matus, A. I. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.01.016 · Cited by 164
Kainate Seizures Cause Acute Dendritic Injury and Actin Depolymerization In Vivo
Zeng, L.-H., Xu, L., Rensing, N. R., Sinatra, P. M., Rothman, S. M., & Wong, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0983-07.2007 · Cited by 158
Remodeling of axo-spinous synapses in the pathophysiology and treatment of depression
Licznerski, P., & Duman, R. S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2012.09.057 · Cited by 157
Postsynaptic signaling during plasticity of dendritic spines
Murakoshi, H., & Yasuda, R. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.12.002 · Cited by 158
Yang, Y., Wang, X.-B., Frerking, M. E., & Zhou, Q. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802978105 · Cited by 156
Mice lacking 5‐HT7 receptors show specific impairments in contextual learning
Roberts, A. J., Krucker, T., Levy, C. L., Slanina, K. A., Sutcliffe, J. G., & Hedlund, P. B. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03288.x · Cited by 151
Self-citationKasri, N. N., Nakano-Kobayashi, A., Malinow, R., Li, B., & Aelst, L. V. (2009) · Genes & Development · doi:10.1101/gad.1783809 · Cited by 153
Murakoshi, H., Lee, S.-J., & Yasuda, R. (2008) · Journal of Neurocytology · doi:10.1007/s11068-008-9024-9 · Cited by 145
Schell, M. J., Erneux, C., & Irvine, R. F. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104101200 · Cited by 142
Identification and engineering of the cytochalasin gene cluster from Aspergillus clavatus NRRL 1
Qiao, K., Chooi, Y., & Tang, Y. (2011) · Metabolic Engineering · doi:10.1016/j.ymben.2011.09.008 · Cited by 141
Chen, L. Y., Rex, C. S., Babayan, A. H., Kramár, E. A., LYNCH, G. S., Gall, C. M., & Lauterborn, J. C. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1077-10.2010 · Cited by 142
Kim, J., Udo, H., Li, H.-L., Youn, T. Y., Chen, M., Kandel, E. R., & Bailey, C. H. (2003) · Neuron · doi:10.1016/s0896-6273(03)00595-6 · Cited by 134
Temporally distinct demands for classic cadherins in synapse formation and maturation
Bozdagi, O., Valcin, M., Poskanzer, K. E., Tanaka, H., & Benson, D. L. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.08.008 · Cited by 135
Ramachandran, B., & Frey, J. U. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2045-09.2009 · Cited by 133
Chapter 10 Synaptic remodeling, synaptic growth and the storage of long-term memory in Aplysia
Bailey, C. H., & Kandel, E. R. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00010-6 · Cited by 134
Regulation of hippocampal long-term potentiation by p21-activated protein kinase 1 (PAK1)
Asrar, S., Meng, Y., Zhou, Z., Todorovski, Z., Huang, W., & Jia, Z. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.06.055 · Cited by 137
Regulation of ADF/cofilin phosphorylation and synaptic function by LIM-kinase
Meng, Y., Takahashi, H., Meng, J., Zhang, Y., Lu, G., Asrar, S., Nakamura, T., & Jia, Z. (2004) · Neuropharmacology · doi:10.1016/j.neuropharm.2004.06.030 · Cited by 129
Cellular and System Biology of Memory: Timing, Molecules, and Beyond
Körte, M., & Schmitz, D. (2016) · Physiological Reviews · doi:10.1152/physrev.00010.2015 · Cited by 132
Offenhäuser, N., Castelletti, D., Mapelli, L., Soppo, B. E., Regondi, M. C., Rossi, P., D'Angelo, E. U., Frassoni, C., Amadeo, A., Tocchetti, A., et al. (2006) · Cell · doi:10.1016/j.cell.2006.09.011 · Cited by 124
Enhancement of learning and memory after activation of cerebral Rho GTPases
Diana, G., Valentini, G., Travaglione, S., Falzano, L., Pieri, M., Zona, C., Meschini, S., Fabbri, A., & Fiorentini, C. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610059104 · Cited by 125
Dendritic spine morphogenesis and plasticity
Lippman, J., & Dunaevsky, A. (2005) · Journal of Neurobiology · doi:10.1002/neu.20149 · Cited by 142
Learning rules and persistence of dendritic spines
Kasai, H., Hayama, T., Ishikawa, M., Watanabe, S., Yagishita, S., & Noguchi, J. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07344.x · Cited by 123
Loss of Cdc42 leads to defects in synaptic plasticity and remote memory recall
Kim, I. H., Wang, H., Soderling, S. H., & Yasuda, R. (2014) · eLife · doi:10.7554/elife.02839 · Cited by 119
Structural Modulation of Dendritic Spines during Synaptic Plasticity
Fortin, D. A., Srivastava, T., & Soderling, T. R. (2011) · The Neuroscientist · doi:10.1177/1073858411407206 · Cited by 118
CaMKIIβ Association with the Actin Cytoskeleton Is Regulated by Alternative Splicing
O'Leary, H., Lasda, E., & Bayer, K. U. (2006) · Molecular Biology of the Cell · doi:10.1091/mbc.e06-03-0252 · Cited by 113
Fear Memory Formation Involves p190 RhoGAP and ROCK Proteins through a GRB2-Mediated Complex
Lamprecht, R., Farb, C. R., & LeDoux, J. E. (2002) · Neuron · doi:10.1016/s0896-6273(02)01047-4 · Cited by 111
Metadata
- Authors
- Krucker, T., Siggins, G. R., & Halpain, S.
- Affiliations
- Scripps Research Institute (US)
- ORCID
- Halpain, Shelley
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2000-05-23
- Volume
- 97
- Issue
- 12
- Pages
- 6856-6861
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC18765
- OpenAlex
- W2041963785
- Semantic Scholar
- 879b8456d922579733d332c78244f89936f74a66
- Cited by
- 374
- References
- 36
- Citations by year
- 2026: 6 · 2025: 4 · 2024: 7 · 2023: 8 · 2022: 1 · 2021: 11 · 2020: 7 · 2019: 5 · 2018: 10 · 2017: 8 · 2016: 10 · 2015: 10 · 2014: 17 · 2013: 23 · 2012: 23
- FWCI
- 6.96
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (R01MH050861, MH47680, P50MH047680)
- National Institute of Neurological Disorders and Stroke (R01NS037311, NS37311)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- F-actin, long-term potentiation, hippocampus, CA1 pyramidal neurons, Schaffer collateral synapses, synaptic plasticity, cytochalasin B, cytochalasin D, latrunculin A, actin filament assembly, silent synapses, field excitatory postsynaptic potentials
- MeSH terms
- Actins, Animals, Cytochalasin B, Hippocampus, Male, Mice, Inbred C57BL, Synaptic Transmission, Neuronal Plasticity, Long-Term Potentiation, Mice
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 2026-10-10, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).
A second model labelled each claim on 2026-10-10 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).
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