Cited by 111Memory and Neural MechanismsStress Responses and CortisolNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 71 of the 71 references it cites were found in a registry or an index.

Long-Term Effects of Brief Acute Stress on Cellular Signaling and Hippocampal LTP

Open access

Ahmed, Tariq, Frey, Julietta U., Korz, Volker·2006·The Journal of Neuroscience

DOI 10.1523/jneurosci.4901-05.2006PMC PMC6673904

Open this paper in CoChat — free account Open PDF

Abstract

In a previous study, we reported that a brief exposure to swim stress transforms an electrically induced, protein synthesis-independent early long-term potentiation (early LTP) into a protein synthesis-dependent late LTP [“reinforcement of LTP” in the hippocampal dentate gyrus (DG)] (Korz and Frey, 2003). This transformation depends on activation of mineralocorticoid receptors (MRs) by corticosterone, and on intact basolateral amygdala (BLA) function. Here, we demonstrate that a brief swim experience results in lasting changes in levels of hippocampal cellular signaling molecules that are known to be involved in the induction of late LTP. Within the DG, MRs were rapidly upregulated, whereas glucocorticoid receptor (GR) levels were elevated with a 3 h delay. Levels of phosphorylated mitogen-activated protein kinase 2 (pMAPK2) and p38 MAPK, as well as phosphorylated calcium/calmodulin-dependent protein kinase II (pCaMKII) were enhanced shortly after swim stress and remained elevated until 24 h, whereas levels of phosphorylated cAMP response element-binding protein (pCREB) remained unchanged. MR and GR were upregulated with a longer delay within the CA1 region, whereas levels of pMAPK2 and p38MAPK were rapidly increased, but the former returned to basal levels after 3 h. Levels of pCREB and pCaMKII were maintained in an enhanced state after swim stress. DG-LTP reinforcement requires a serotonergic but not dopaminergic heterosynaptic receptor activation that probably mediates the BLA-dependent modulation of LTP under stress. Thus, molecular alterations induced by specific stress resemble late LTP-related molecular changes. These changes, in interaction with stress-specific heterosynaptic processes, may support the transformation of early LTP into late LTP. The results contribute to the understanding of the rapid consolidation of cellular and possibly systemic memories triggered by stress.

Integrity signals

Registry

Crossref · 10.1523/jneurosci.4901-05.2006

Cites

71 of 71 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302
Stress and the brain: from adaptation to disease
de Kloet, E. R., Joëls, M., & Holsboer, F. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1683 · Cited by 4,621
The molecular basis of CaMKII function in synaptic and behavioural memory
Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860
Synaptic tagging and long-term potentiation
Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736
The neuronal MAP kinase cascade: a biochemical signal integration system subserving synaptic plasticity and memory
Sweatt, J. D. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00054.x · Cited by 1,131
Translational Control by MAPK Signaling in Long-Term Synaptic Plasticity and Memory
Kelleher, R. J., Govindarajan, A., Jung, H.-Y., Kang, H., & Tonegawa, S. (2004) · Cell · doi:10.1016/s0092-8674(04)00115-1 · Cited by 845
Brain corticosteroid receptor balance and homeostatic control
de Kloet, E. R. (1991) · Frontiers in Neuroendocrinology · Cited by 842
Translational Regulatory Mechanisms in Persistent Forms of Synaptic Plasticity
Kelleher, R. J., Govindarajan, A., & Tonegawa, S. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.013 · Cited by 592
The neuronal mineralocorticoid eeceptor as a mediator of glucocorticoid response
Arriza, J. L., Simerly, R. B., Swanson, L. W., & Evans, R. M. (1988) · Neuron · doi:10.1016/0896-6273(88)90136-5 · Cited by 591
Persistent protein kinase activity underlying long-term potentiation
Malinow, R., Madison, D. V., & Tsien, R. W. (1988) · Nature · doi:10.1038/335820a0 · Cited by 552

Flagged first, then by citations

Show all 71 references

Research works printed but not linked: 3

(1995), Pol J Pharmacol, 47, 299
(1991), Front Neuroendocrinol, 12, 95
(1995), Mol Pharmacol, 48, 623

Sorted by citations

Stress, Depression, and Neuroplasticity: A Convergence of Mechanisms
Pittenger, C., & Duman, R. S. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301574 · Cited by 1,795
The Temporal Dynamics Model of Emotional Memory Processing: A Synthesis on the Neurobiological Basis of Stress-Induced Amnesia, Flashbulb and Traumatic Memories, and the Yerkes-Dodson Law
Diamond, D. M., Campbell, A. M., Park, C. R., Halonen, J., & Zoladz, P. R. (2007) · Neural Plasticity · doi:10.1155/2007/60803 · Cited by 762
“[209]; Lemon and Manahan-Vaughan [249]), and norepinephrine (Gray and Johnston [250]; Hopkins and Johnston [251]; Katsuki et al.”
Background
Dynorphin, stress, and depression
Knoll, A. T., & Carlezon, W. A. (2010) · Brain Research · doi:10.1016/j.brainres.2009.09.074 · Cited by 465
Unraveling the Time Domains of Corticosteroid Hormone Influences on Brain Activity: Rapid, Slow, and Chronic Modes
Joëls, M., Sarabdjitsingh, R. A., & Karst, H. (2012) · Pharmacological Reviews · doi:10.1124/pr.112.005892 · Cited by 445
Chronic stress: Implications for neuronal morphology, function and neurogenesis
Joëls, M., Karst, H., Krugers, H. J., & Lucassen, P. J. (2007) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2007.04.001 · Cited by 381
Calcium homeostasis and modulation of synaptic plasticity in the aged brain
Foster, T. C. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00283.x · Cited by 303
Stress-Induced p38 Mitogen-Activated Protein Kinase Activation Mediates κ-Opioid-Dependent Dysphoria
Bruchas, M. R., Land, B. B., Aita, M., Xu, M., Barot, S. K., Li, S., & Chavkin, C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3769-07.2007 · Cited by 282
Dopaminergic modulation of the persistence of one-trial hippocampus-dependent memoryPreprint
O’Carroll, C., Martin, S. J., Sandin, J., Frenguelli, B. G., & Morris, R. G. M. (2006) · Learning & Memory · doi:10.1101/lm.321006 · Cited by 243
Neuroactive steroids: State of the art and new perspectives
Melcangi, R. C., García‐Segura, L. M., & Mensah‐Nyagan, A. G. (2007) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-007-7403-5 · Cited by 249
Striking Variations in Corticosteroid Modulation of Long-Term Potentiation along the Septotemporal Axis of the Hippocampus
Maggio, N., & Segal, M. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0155-07.2007 · Cited by 230
Stress, the hippocampus, and epilepsy
Joëls, M. (2008) · Epilepsia · doi:10.1111/j.1528-1167.2008.01902.x · Cited by 224
The forced swimming‐induced behavioural immobility response involves histone H3 phospho‐acetylation and c‐Fos induction in dentate gyrus granule neurons via activation of the N‐methyl‐ d ‐aspartate/extracellular signal‐regulated kinase/mitogen‐ and stress‐activated kinase signalling pathway
Chandramohan, Y., Droste, S. K., Arthur, J. S. C., & Reul, J. M. H. M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06230.x · Cited by 182
Glucocorticoids act on glutamatergic pathways to affect memory processes
Sandi, C. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.01.006 · Cited by 167
Antistress Effect of TRPV1 Channel on Synaptic Plasticity and Spatial Memory
Li, H.-B., Mao, R., Zhang, J., Yang, Y., Cao, J., & Xu, L. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.02.020 · Cited by 165
β-Adrenergic Control of Hippocampal Function: Subserving the Choreography of Synaptic Information Storage and Memory
Hagena, H., Hansen, N., & Manahan‐Vaughan, D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv330 · Cited by 174
Synaptic Plasticity, Metaplasticity and Depression
Vose, L. R., & Stanton, P. K. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160202121111 · Cited by 131
Stress exacerbates neuropathic pain via glucocorticoid and NMDA receptor activation
Alexander, J., DeVries, A. C., Kigerl, K. A., Dahlman, J. M., & Popovich, P. G. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.04.001 · Cited by 135
New aspects of rapid aldosterone signaling
Großmann, C., & Gekle, M. (2009) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2009.02.005 · Cited by 129
Involvement of noradrenergic and corticoid receptors in the consolidation of the lasting anxiogenic effects of predator stress
Adamec, R. E., Muir, C. A., Grimes, M. T., & Pearcey, K. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.02.001 · Cited by 114
The genetics of insomnia – Evidence for epigenetic mechanisms?
Palagini, L., Biber, K. P. H., & Riemann, D. W. (2013) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2013.05.002 · Cited by 122
Stress-induced changes in hippocampal function
Joëls, M., Krugers, H. J., & Karst, H. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)67001-0 · Cited by 111
Pre-learning stress differentially affects long-term memory for emotional words, depending on temporal proximity to the learning experience
Zoladz, P. R., Clark, B., Warnecke, A., Smith, L., Tabar, J., & Talbot, J. N. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.01.016 · Cited by 102
Repeated swim stress induces kappa opioid-mediated activation of extracellular signal-regulated kinase 1/2
Bruchas, M. R., Xu, M., & Chavkin, C. (2008) · Neuroreport · doi:10.1097/wnr.0b013e32830dd655 · Cited by 82
Acute Stress Alters Amygdala microRNA miR-135a and miR-124 Expression: Inferences for Corticosteroid Dependent Stress Response
Mannironi, C., Camon, J., Vito, F. D., Biundo, A., Stefano, M. E. D., Persiconi, I., Bozzoni, I., Fragapane, P., Mele, A., & Presutti, C. (2013) · PLoS ONE · doi:10.1371/journal.pone.0073385 · Cited by 81
Synapse-specific stabilization of plasticity processes: The synaptic tagging and capture hypothesis revisited 10 years later
Barco, Á., de Armentia, M. L., & Alarcón, J. M. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.01.002 · Cited by 81
Impact of glucocorticoids on brain function: Relevance for mood disorders
Joëls, M. (2010) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2010.03.004 · Cited by 83
Neural ageing and synaptic plasticity: prioritizing brain health in healthy longevity
Navakkode, S., & Kennedy, B. K. (2024) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2024.1428244 · Cited by 75
Individual variability in the stress response of C57BL/6J male mice correlates with trait anxiety
Jakovcevski, M., Schachner, M., & Morellini, F. (2007) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2007.00345.x · Cited by 74
cGMP Signaling, Phosphodiesterases and Major Depressive Disorder
Reierson, G. W., Guo, S., Mastronardi, C. A., Licinio, J., & Wong, M. (2011) · Current Neuropharmacology · doi:10.2174/157015911798376271 · Cited by 72
Multiomic profiling of the acute stress response in the mouse hippocampus
von Ziegler, L., Floriou‐Servou, A., Waag, R., Gupta, R. R. D., Sturman, O., Gapp, K., Maat, C. A., Kockmann, T., Lin, H.-Y., Duss, S. N., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-29367-5 · Cited by 68
Post-training administration of corticosterone enhances consolidation of contextual fear memory and hippocampal long-term potentiation in rats
Abrari, K., Rashidy‐Pour, A., Semnanian, S., & Fathollahi, Y. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.10.008 · Cited by 68
Role of corticosteroid hormones in the dentate gyrus
Joëls, M. (2007) · Progress in brain research · doi:10.1016/s0079-6123(07)63021-0 · Cited by 67
Hypothesized mechanisms through which acute exercise influences episodic memory
Loprinzi, P. D., Ponce, P., & Frith, E. (2018) · Physiology International · doi:10.1556/2060.105.2018.4.28 · Cited by 67
Maternal separation during a specific postnatal time window prevents reinforcement of hippocampal long-term potentiation in adolescent rats
Gruss, M., Braun, K., Frey, J. U., & Korz, V. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2007.12.033 · Cited by 64
Self-citation
Corticosteroids: way upstream
Riedemann, T., Patchev, A. V., Cho, K., & Almeida, O. F. X. (2010) · Molecular Brain · doi:10.1186/1756-6606-3-2 · Cited by 65
Modulation of presynaptic glucocorticoid receptors on glutamate release from rat hippocampal nerve terminals
Wang, C., & Wang, S. (2009) · Synapse · doi:10.1002/syn.20654 · Cited by 61
Modulation of Synaptic Plasticity by Stress Hormone Associates with Plastic Alteration of Synaptic NMDA Receptor in the Adult Hippocampus
Tse, Y. C., Bagot, R. C., Hutter, J. A., Wong, A. S., & Wong, T. P. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027215 · Cited by 59
Interplay of hippocampal long-term potentiation and long-term depression in enabling memory representations
Hagena, H., & Manahan‐Vaughan, D. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0229 · Cited by 54
Chewing ameliorates stress-induced suppression of hippocampal long-term potentiation
Ono, Y., Kataoka, T., Miyake, S., Cheng, S., Tachibana, A., Sasaguri, K., & Onozuka, M. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.057 · Cited by 53
Overexpression of mineralocorticoid and transdominant glucocorticoid receptor blocks the impairing effects of glucocorticoids on memory
Ferguson, D., & Sapolsky, R. M. (2008) · Hippocampus · doi:10.1002/hipo.20467 · Cited by 49
The dose makes the poison: From glutamate-mediated neurogenesis to neuronal atrophy and depression
Rubio-Casillas, A., & Fernández-Guasti, A. (2016) · Reviews in the Neurosciences · doi:10.1515/revneuro-2015-0066 · Cited by 49
Stress Increases Peripheral Axon Growth and Regeneration through Glucocorticoid Receptor-Dependent Transcriptional Programs
Lerch, J. K., Alexander, J., Madalena, K. M., Motti, D., Quach, T., Dhamija, A., Zha, A. M., Gensel, J. C., Marketon, J. I. W., Lemmon, V., et al. (2017) · eNeuro · doi:10.1523/eneuro.0246-17.2017 · Cited by 50
Modulating role of serotonergic signaling in sleep and memory
Vaseghi, S., Arjmandi-Rad, S., Eskandari, M., Ebrahimnejad, M., Kholghi, G., & Zarrindast, M. (2021) · Pharmacological Reports · doi:10.1007/s43440-021-00339-8 · Cited by 52
Acute Stress Impairs Hippocampal Mossy Fiber-CA3 Long-Term Potentiation by Enhancing cAMP-Specific Phosphodiesterase 4 Activity
Chen, C., Yang, C., Huang, C., & Hsu, K. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.33 · Cited by 49
Enhancing Cognition after Stress with Gene Therapy
Nicholas, A. C., Munhoz, C. D., Ferguson, D., Chappell-Campbell, L., & Sapolsky, R. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3122-06.2006 · Cited by 45
Dynamic interplays between memory systems depend on practice: The hippocampus is not always the first to provide solution
Martel, G., Blanchard, J., Mons, N. E., Gastambide, F., Micheau, J., & Guillou, J.-L. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.10.004 · Cited by 44
Role of Stress, Depression, and Aging in Cognitive Decline and Alzheimer’s Disease
Daulatzai, M. A. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_350 · Cited by 42
Stress-Induced Enhancement of Mouse Amygdalar Synaptic Plasticity Depends on Glucocorticoid and ß-Adrenergic Activity
Sarabdjitsingh, R. A., Kofink, D., Karst, H., de Kloet, E. R., & Joëls, M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042143 · Cited by 41
Active place avoidance is no more stressful than unreinforced exploration of a familiar environment
Lesburguères, E., Sparks, F. T., O’Reilly, K. C., & Fenton, A. A. (2016) · Hippocampus · doi:10.1002/hipo.22666 · Cited by 38
Linear and Non-Linear Dose-Response Functions Reveal a Hormetic Relationship between Stress and Learning
Zoladz, P. R., & Diamond, D. M. (2008) · Dose-Response · doi:10.2203/dose-response.08-015.zoladz · Cited by 37
Hormonal and monoamine signaling during reinforcement of hippocampal long-term potentiation and memory retrievalPreprint
Korz, V., & Frey, J. U. (2007) · Learning & Memory · doi:10.1101/lm.459807 · Cited by 37
Self-citation
Mifepristone Prevents Stress-Induced Apoptosis in Newborn Neurons and Increases AMPA Receptor Expression in the Dentate Gyrus of C57/BL6 Mice
Llorens-Martı́n, M., & Trejo, J. L. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028376 · Cited by 38
Fasting induces a form of autonomic synaptic plasticity that prevents hypoglycemia
Wang, M., Wang, Q., & Whim, M. D. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517275113 · Cited by 38
Temporal modulation of hippocampal excitatory transmission by corticosteroids and stress
Chaouloff, F., & Groc, L. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.07.004 · Cited by 50
Stimulus intensity-dependent modulations of hippocampal long-term potentiation by basolateral amygdala priming
Li, Z., & Richter‐Levin, G. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00021 · Cited by 35
Cellular mechanisms of long-term depression induced by noradrenaline in rat prefrontal neurons
Marzo, A., Bai, J., Caboche, J., Vanhoutte, P., & Otani, S. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.046 · Cited by 34
Unpredictable chronic mild stress differentially impairs social and contextual discrimination learning in two inbred mouse strains
Boxelaere, M. V., Clements, J., Callaerts, P., D’Hooge, R., & Callaerts‐Vegh, Z. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188537 · Cited by 34
Stress induced hippocampal mineralocorticoid and estrogen receptor β gene expression and long-term potentiation in male adult rats is sensitive to early-life stress experience
Wang, H., Meyer, K., & Korz, V. (2012) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2012.06.004 · Cited by 29
Self-citation
The Effects of Exercise on Long-Term Potentiation: A Candidate Mechanism of the Exercise-Memory Relationship
Loprinzi, P. D. (2019) · OBM Neurobiology · doi:10.21926/obm.neurobiol.1902026 · Cited by 26
Effects of single swim stress on changes in TRPV1-mediated plasticity in the amygdala
Kulisch, C., & Albrecht, D. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.09.003 · Cited by 24
Epinephrine converts long‐term potentiation from transient to durable form in awake rats
Korol, D. L., & Gold, P. E. (2007) · Hippocampus · doi:10.1002/hipo.20372 · Cited by 23
Low-dose neonatal domoic acid causes persistent changes in behavioural and molecular indicators of stress response in rats
Gill, D. A., Perry, M. A., McGuire, E. P., Pérez‐Gómez, A., & Tasker, R. A. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.02.036 · Cited by 23
Acute restraint stress reverses impaired LTP in the hippocampal CA1 region in mouse models of Alzheimer’s disease
Wang, M., Ramasamy, V. S., Samidurai, M., & Jo, J. (2019) · Scientific Reports · doi:10.1038/s41598-019-47452-6 · Cited by 22
Memory-Enhancing Drugs
Gold, P. E. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00162-5 · Cited by 21
Learning-Related Hippocampal Long-Term Potentiation and Long-Term Depression
Manahan‐Vaughan, D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21104-8 · Cited by 22
Basolateral amygdala GABA-A receptors mediate stress-induced memory retrieval impairment in rats
Sardari, M., Rezayof, A., Khodagholi, F., & Zarrindast, M. (2013) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713001363 · Cited by 20
5-HT1A receptor blockade targeting the basolateral amygdala improved stress-induced impairment of memory consolidation and retrieval in rats
Sardari, M., Rezayof, A., & Zarrindast, M. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.05.031 · Cited by 20
Acute stress increases neuropsin mRNA expression in the mouse hippocampus through the glucocorticoid pathway
Harada, A., Shiosaka, S., Ishikawa, Y., & Komai, S. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2008.03.042 · Cited by 16
Dopamine type 1- and 2-like signaling in the modulation of spatial reference learning and memory
Feyissa, D. D., Sialana, F. J., Keimpema, E., Kalaba, P., Paunkov, A., Engidawork, E., Höger, H., Lübec, G., & Korz, V. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.01.028 · Cited by 17
Self-citation
Glucocorticoid Receptor and Myocyte Enhancer Factor 2 Cooperate to Regulate the Expression of c-JUN in a Neuronal Context
Speksnijder, N., Christensen, K. V., Didriksen, M., de Kloet, E. R., & Datson, N. A. (2012) · Journal of Molecular Neuroscience · doi:10.1007/s12031-012-9809-2 · Cited by 17
Cocaine decreases the expression of PSA‐NCAM protein and attenuates long‐term potentiation via glucocorticoid receptors in the rat dentate gyrus
Maćkowiak, M., Grzegorzewska, M., Budziszewska, B., Chocyk, A., Hess, G., & Wędzony, K. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06255.x · Cited by 16
The effects of prenatal stress on expression of p38 MAPK in offspring hippocampus
Cai, Q., Huang, S., Zhu, Z., Li, H., Li, Q., Jia, N., & Liu, J. (2008) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2008.06.001 · Cited by 16
Neurobiological Basis of the Complex Effects of Stress on Memory and Synaptic Plasticity
Zoladz, P. R., Park, C. R., & Diamond, D. M. (2011) · Wiley eBooks · doi:10.1002/9781118083222.ch8 · Cited by 16
Sucrose-induced plasticity in the basolateral amygdala in a ‘comfort’ feeding paradigm
Packard, A. E. B., Di, S., Egan, A. E., Fourman, S. M., Tasker, J. G., & Ulrich‐Lai, Y. M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1454-7 · Cited by 17
Effects of Acute Exercise and Learning Strategy Implementation on Memory Function
Loprinzi, P. D., Harris, F., McRaney, K., Chism, M., Deming, R., Jones, T. W., Zou, L., & Tan, M. (2019) · Medicina · doi:10.3390/medicina55090568 · Cited by 16
Priming stimulation of basal but not lateral amygdala affects long-term potentiation in the rat dentate gyrus in vivo
Li, Z., & Richter‐Levin, G. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.059 · Cited by 15
The effect of acute swim stress and training in the water maze on hippocampal synaptic activity as well as plasticity in the dentate gyrus of freely moving rats: Revisiting swim-induced LTP reinforcement
Tabassum, H., & Frey, J. U. (2013) · Hippocampus · doi:10.1002/hipo.22166 · Cited by 13
Self-citation
Antidepressant behavior in thyroidectomized Wistar rats is induced by hippocampal hypothyroidism
da Conceição, R. R., Laureano‐Melo, R., Oliveira, K. C., Melo, M. C. D. C., Kasamatsu, T. S., Maciel, R. M. B., de Souza, J. S., & Giannocco, G. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.02.005 · Cited by 12
Synaptic plasticity and the analysis of the field-EPSP as well as the population spike using separate recording electrodes in the dentate gyrus in freely moving rats
Frey, S., & Frey, J. U. (2009) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2009.07.024 · Cited by 12
Self-citation
Emotional and cognitive information processing: Relations to behavioral performance and hippocampal long-term potentiation in vivo during a spatial water maze training in ratsPreprint
Schulz, K., & Korz, V. (2010) · Learning & Memory · doi:10.1101/lm.1855610 · Cited by 11
Self-citation
A brief, but repeated, swimming protocol is sufficient to overcome amyloid β‐protein inhibition of hippocampal long‐term potentiation
Li, S., Feig, L. A., & Hartley, D. M. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05760.x · Cited by 9
The combined effects of corticosterone and brain-derived neurotrophic factor on plasticity-related receptor phosphorylation and expression at the synaptic surface in male Sprague-Dawley rats
Thacker, J. S., & Mielke, J. G. (2022) · Hormones and Behavior · doi:10.1016/j.yhbeh.2022.105233 · Cited by 10
NAN-190 potentiates the impairment of retention produced by swim stress
Schneider, A. M., & Simson, P. E. (2007) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2007.04.002 · Cited by 8
Methylprednisolone as a memory enhancer in rats: Effects on aversive memory, long-term potentiation and calcium influx
de Vargas, L. D. S., Gonçalves, R., de Lara, M. V. S., Costa‐Ferro, Z. S. M., Salamoni, S. D., Domingues, M. F., Piovesan, A. R., de Assis, D. R., Vinadé, L., Corrado, A. P., et al. (2017) · Brain Research · doi:10.1016/j.brainres.2017.06.007 · Cited by 8
Enhanced brain performance in mice following postnatal stress.
Loizzo, A., Spampinato, S., Campana, G., Vella, S., Fortuna, A., Costa, L., Capasso, A., Monteleone, P., Renzi, P., & Loizzo, S. (2012) · Journal of Endocrinology · doi:10.1530/joe-12-0369 · Cited by 7
Effects of individual stressors used in a battery of “chronic unpredictable stress” on long-term plasticity in the hippocampus of juvenile rats
Gorbunova, A. A., Kudryashova, I. V., Манолова, А. О., Novikova, M. R., Stepanichev, M. Y., & Gulyaeva, N. V. (2017) · Acta Neurobiologiae Experimentalis · doi:10.21307/ane-2017-058 · Cited by 7
“Unpredictable Stress”: Ambiguity of Stress Reactivity in Studies of Long-Term Plasticity
Kudryashova, I. V., & Gulyaeva, N. V. (2017) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-017-0496-x · Cited by 5
The Post-conditioning Acute Strength Exercise Facilitates Contextual Fear Memory Consolidation Via Hippocampal N-methyl-D-aspartate-receptors
Leite, A. K. O., Farias, C. P., Schmidt, B. E., Teixeira, L., Rieder, A. S., Furini, C. R. G., & Wyse, Â. T. D. S. (2023) · Neuroscience · doi:10.1016/j.neuroscience.2023.10.016 · Cited by 6
“Information”—from an Evolutionary Point of View
Kofler, W. W. (2014) · Information · doi:10.3390/info5020272 · Cited by 5
Effects of Exercise on Long-Term Potentiation in Neuropsychiatric Disorders
Loprinzi, P. D. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-1792-1_30 · Cited by 4
The effects of prenatal stress on expression of CaMK-II and L-Ca2+ channel in offspring hippocampus
Cai, Q., Zhang, B., Huang, S., Wang, T., & Zhou, T. (2011) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmr057 · Cited by 5
11ß hydroxysteroid dehydrogenases regulate circulating glucocorticoids but not central gene expression
Rensel, M. A., & Schlinger, B. A. (2021) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2021.113734 · Cited by 4
Hormetic and Non-Hormetic Dose-Response Functions in Stress Effects on Memory and Synaptic Plasticity: Issues and Mechanisms
Zoladz, P. R., & Diamond, D. M. (2008) · American Journal of Pharmacology and Toxicology · doi:10.3844/ajptsp.2008.111.124 · Cited by 4
Effects of the suppression of 5-HT1A receptors in the left, right, or bilateral basolateral amygdala on memory consolidation in chronic stress in male rats
Valipour, H., Jahromi, G. P., Mohammadi, A., & Meftahi, G. H. (2023) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-023-02790-1 · Cited by 3
Ameliorative Effect of Moringa oleifera Against CUMS-Induced Anxiety in Rats: β-Catenin and 5-HT1 A Crosstalk
El‐Kadi, R. A., Sedeek, M. S., Abdelkader, N. F., Zaki, H. F., & Kamel, A. S. E. D. (2025) · Molecular Neurobiology · doi:10.1007/s12035-025-04911-8 · Cited by 4
Early- and late-phase changes of brain activity and early-phase neuromodulation in the posttraumatic stress disorder rat model
Chang, S., Chen, H., Shaw, F.-Z., & Shyu, B. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100554 · Cited by 4
Molecular roadmap of the healthy stress response in the mouse hippocampusPreprint
von Ziegler, L., Floriou‐Servou, A., Waag, R., Gupta, R. R. D., Sturman, O., Gapp, K., Maat, C. A., Kockmann, T., Lin, H.-Y., Duss, S. N., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.26.436970 · Cited by 3
Developing a functional non-animal CNS stress model utilizing long-term potentiation with human iPSC-cortical neurons to evaluate therapeutics
Autar, K., Guo, X., Powell, H., Patel, A., Malik, M., Grillo, M., Akanda, N., Narasimhan, N. S., Bogen, W., Long, C. J., et al. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.118556 · Cited by 2
Evolutionary, Historical and Mechanistic Perspectives on How Stress Affects Memory and Hippocampal Synaptic Plasticity
Farmer, G. E., Park, C. R., Bullard, L. A., & Diamond, D. M. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1056-4_10 · Cited by 2
Analysis of conditions that are important for the beginning of consolidation in a model of long-term synaptic potentiation
Kudryashova, I. V. (2013) · Neurochemical Journal · doi:10.1134/s1819712413030070 · Cited by 2

Authors: Ahmed, T., Frey, J. U., & Korz, V.
Affiliations: Leibniz Institute for Neurobiology (DE)
University of Bayreuth (DE)
ORCID: Ahmed, Tariq
Korz, Volker
Venue: The Journal of Neuroscience
Publisher: Society for Neuroscience
Published: 2006-04-12
Volume: 26
Issue: 15
Pages: 3951-3958
ISSN: 0270-6474 (ISSN-L)
1529-2401
DOI: 10.1523/jneurosci.4901-05.2006
PMC: PMC6673904
OpenAlex: W2013192604
Cited by: 111
References: 71
Citations by year: 2026: 1 · 2025: 2 · 2024: 2 · 2023: 3 · 2022: 2 · 2021: 3 · 2020: 1 · 2019: 5 · 2018: 2 · 2017: 8 · 2016: 7 · 2015: 1 · 2014: 4 · 2013: 6 · 2012: 8
FWCI: 6.64
Type: journal article
Language: en
Open access: hybrid
doi.org
Licence: public-domain
creativecommons.org/licenses/by-nc-sa/4.0/ (vor, 183 d)
Locations: Journal of Neuroscience (publishedVersion, public-domain)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: acute stress, swim stress, long-term potentiation, dentate gyrus, hippocampus, mineralocorticoid receptor, glucocorticoid receptor, p38 MAPK, CaMKII, CREB, basolateral amygdala, memory consolidation, corticosterone
MeSH terms: Animals, Benzazepines, Disease Models, Animal, Electrophysiology, Hippocampus, Male, Stress, Psychological, Swimming, Time Factors, Signal Transduction, Rats, Wistar, Dopamine Antagonists, Rats

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.

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

Long-Term Effects of Brief Acute Stress on Cellular Signaling and Hippocampal LTP

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks