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Effects of glucocorticoids on hippocampal long‐term potentiation
Abstract
The effects of chronic and acute corticosterone (CORT) administration were investigated on hippocampal long‐term potentiation (LTP) in the dentate gyrus granule cell layer of the rat. Electrophysiological experiments were performed in vivo under urethane anesthesia. Chronic CORT treatment (40 mg/kg/day) over 21 days decreased LTP compared to vehicle controls, even when LTP was measured 48 hours after cessation of CORT treatment, when serum CORT levels had returned to baseline. A single injection of CORT also decreased LTP compared to vehicle controls, but only when CORT levels were high, since at 48 hours after a single acute CORT injection LTP was not depressed. The decrements in LTP were seen both for the slope of the excitatory postsynaptic potential and for the population spike. Yet CORT had no effects on posttetanic potentiation or neuronal excitability. These findings are consistent with previous reports showing a reduction in LTP in the CAI field of animals exposed to stress or acute CORT administration.
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“Conversely, stress levels of corticosterone applied for a longer period of time (>20 minutes) increased the magnitude of inhibitory components of electrophysiological activity, such as the afterhyperpolarization (Joëls and de Kloet [233]; Kerr et al. [234]; Joëls and de Kloet [235]; Karst and Joëls [236]), and suppressed the induction of LTP (Pavlides et al. [237]; Rey et al. [238]; Kerr et al. [”
From 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 (2007) · cites this paper as Pavlides et al. [237]
Citations
Cites
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Two receptor systems for corticosterone in rat brain: Microdistribution and differential occupation
REUL, J. M. H. M., & KLOET, E. R. D. (1985) · Endocrinology · doi:10.1210/endo-117-6-2505 · Cited by 2,580
Adrenal steroid receptors and actions in the nervous system
McEwen, B. S., de Kloet, E. R., & Rostène, W. H. (1986) · Physiological Reviews · doi:10.1152/physrev.1986.66.4.1121 · Cited by 1,238
Self-citationStress induces atrophy of apical dendrites of hippocampal CA3 pyramidal neurons
Watanabe, Y., Gould, E., & McEwen, B. S. (1992) · Brain Research · doi:10.1016/0006-8993(92)91597-8 · Cited by 1,212
Self-citationProlonged glucocorticoid exposure reduces hippocampal neuron number: implications for aging
Sapolsky, R., Krey, L., & McEwen, B. (1985) · The Journal of Neuroscience · doi:10.1523/jneurosci.05-05-01222.1985 · Cited by 1,129
Self-citationHippocampal damage associated with prolonged glucocorticoid exposure in primates
Sapolsky, R., Uno, H., Rebert, C., & Finch, C. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-09-02897.1990 · Cited by 1,103
Woolley, C. S., Gould, E., & McEwen, B. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)90778-a · Cited by 1,020
Self-citationPurdy, R. H., Morrow, A. L., Moore, P. H., & Paul, S. M. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.10.4553 · Cited by 951
Selective Loss of Hippocampal Granule Cells in the Mature Rat Brain After Adrenalectomy
Sloviter, R. S., Valiquette, G., Abrams, G., Ronk, E. C., Sollas, A. L., Paul, L. A., & Neubort, S. (1989) · Science · doi:10.1126/science.2911756 · Cited by 522
Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus
Shors, T. J., Seib, T. B., Levine, S., & Thompson, R. F. (1989) · Science · doi:10.1126/science.2704997 · Cited by 458
Research works printed but not linked: 1
- Cotman CW, 1989, The role of the NMDA receptor in central nervous system plasticity and pathology, J NIH Res, 1, 65
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Sapolsky, R. M., Romero, L. M., & Munck, A. U. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.1.0389 · Cited by 7,541
Brain corticosteroid receptor balance in health and disease
de Kloet, E. R., Vreugdenhil, E., Oitzl, M. S., & Joëls, M. (1998) · Endocrine Reviews · doi:10.1210/edrv.19.3.0331 · Cited by 2,614
Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,074
McEwen, B. S., & Sapolsky, R. M. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80028-x · Cited by 1,889
Self-citationLupien, S. J., Maheu, F., Tu, M., Fiocco, A., & Schramek, T. E. (2007) · Brain and Cognition · doi:10.1016/j.bandc.2007.02.007 · Cited by 1,474
The acute effects of corticosteroids on cognition: integration of animal and human model studies
LUPIEN, S., & MCEWEN, B. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00004-0 · Cited by 1,024
Self-citationA Comprehensive Overview on Stress Neurobiology: Basic Concepts and Clinical Implications
Godoy, L. D., Rossignoli, M. T., Delfino-Pereira, P., Garcia‐Cairasco, N., & Umeoka, E. H. D. L. (2018) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00127 · Cited by 991
Kirschbaum, C., Wolf, O. T., May, M., Wippich, W., & Hellhammer, D. H. (1996) · Life Sciences · doi:10.1016/0024-3205(96)00118-x · Cited by 815
Stress and hippocampal neurogenesis
Gould, E., & Tanapat, P. (1999) · Biological Psychiatry · doi:10.1016/s0006-3223(99)00247-4 · Cited by 818
Conrad, C. D., Galea, L. A. M., Kuroda, Y., & McEwen, B. S. (1996) · Behavioral Neuroscience · doi:10.1037/0735-7044.110.6.1321 · Cited by 805
Self-citationDiamond, D. M., Campbell, A. M., Park, C. R., Halonen, J., & Zoladz, P. R. (2007) · Neural Plasticity · doi:10.1155/2007/60803 · Cited by 762
Neuropathogenesis of Delirium: Review of Current Etiologic Theories and Common Pathways
Maldonado, J. R. (2013) · The American Journal of Geriatric Psychiatry · doi:10.1016/j.jagp.2013.09.005 · Cited by 745
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Tottenham, N. (2009) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.068.2009 · Cited by 651
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Maldonado, J. R. (2018) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.4823 · Cited by 617
Stranahan, A. M., Arumugam, T. V., Cutler, R. G., Lee, K. M., Egan, J. M., & Mattson, M. P. (2008) · Nature Neuroscience · doi:10.1038/nn2055 · Cited by 626
Stress hormones and human memory function across the lifespan
Lupien, S. J., Fiocco, A., Wan, N., Maheu, F., Lord, C., Schramek, T., & Tu, M. T. (2005) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2004.08.003 · Cited by 562
Millan, M. J. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2005.11.006 · Cited by 569
Bodnoff, S., Humphreys, A., Lehman, J., Diamond, D. M., Rose, G., & Meaney, M. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00061.1995 · Cited by 529
Stress, memory, and the hippocampus: can't live with it, can't live without it
LUPIEN, S. J., & Lepage, M. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00361-8 · Cited by 522
Stress and Plasticity in the Limbic System
Sapolsky, R. M. (2003) · Neurochemical Research · doi:10.1023/a:1026021307833 · Cited by 503
Stress and memory in humans: twelve years of progress?
Wolf, O. T. (2009) · Brain Research · doi:10.1016/j.brainres.2009.04.013 · Cited by 456
Sandi, C., Loscertales, M., & Guaza, C. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01412.x · Cited by 447
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Leal, G., Bramham, C. R., & Duarte, C. B. (2017) · Vitamins and Hormones · doi:10.1016/bs.vh.2016.10.004 · Cited by 425
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Conrad, C. D. (2008) · Reviews in the Neurosciences · doi:10.1515/revneuro.2008.19.6.395 · Cited by 425
Joëls, M., Sarabdjitsingh, R. A., & Karst, H. (2012) · Pharmacological Reviews · doi:10.1124/pr.112.005892 · Cited by 445
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Groeneweg, F. L., Karst, H., de Kloet, E. R., & Joëls, M. (2011) · Journal of Endocrinology · doi:10.1530/joe-10-0472 · Cited by 414
McDermott, C. M., LaHoste, G. J., Chen, C., Musto, A., Bazan, N. G., & Magee, J. C. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-29-09687.2003 · Cited by 407
Joëls, M., & de Kloet, E. R. (1994) · Progress in Neurobiology · doi:10.1016/0301-0082(94)90014-0 · Cited by 394
Do Corticosteroids Damage the Brain?
Herbert, J., Goodyer, I. M., Grossman, A. B., Hastings, M. H., de Kloet, E. R., Lightman, S. L., LUPIEN, S. J., Roozendaal, B., & Seckl, J. R. (2006) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2006.01429.x · Cited by 398
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
Roozendaal, B., Okuda, S., de Quervain, D. J.-F., & McGaugh, J. L. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.049 · Cited by 382
Stress, cognitive impairment and cell adhesion molecules
Sandi, C. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1555 · Cited by 374
Downregulation of BDNF mRNA and protein in the rat hippocampus by corticosterone
Schaaf, M. J. M., de Jong, J., de Kloet, E. R., & Vreugdenhil, E. (1998) · Brain Research · doi:10.1016/s0006-8993(98)01010-5 · Cited by 360
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Lupien, S. J., Wilkinson, C. W., Brière, S., Ménard, C., Ng Ying Kin, N. M. K., & Nair, N. P. V. (2002) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(01)00061-0 · Cited by 353
Duffy, S. N., Craddock, K. J., Abel, T. G., & Nguyen, P. (2001) · Learning & Memory · doi:10.1101/lm.36301 · Cited by 349
Diamond, D. M., Fleshner, M., Ingersoll, N., & Rose, G. M. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.4.661 · Cited by 340
Murray, F., Smith, D., & Hutson, P. H. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.01.014 · Cited by 334
Li, S., Wang, C., Wang, M., Murakami, Y., & Matsumoto, K. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.01.004 · Cited by 346
Effects of chronic stress on hippocampal long‐term potentiation
Pavlides, C., Nivón, L. G., & McEwen, B. S. (2002) · Hippocampus · doi:10.1002/hipo.1116 · Cited by 316
Self-citationBelanoff, J. K., Gross, K., Yager, A., & Schatzberg, A. F. (2001) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(01)00018-8 · Cited by 314
Roozendaal, B., & McGaugh, J. L. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01355.x · Cited by 307
Long-term effects of social stress on brain and behavior: a focus on hippocampal functioning
Buwalda, B., Kole, M. H. P., Veenema, A. H., Huininga, M., de Boer, S. F., Korte, S. M., & Koolhaas, J. M. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.05.005 · Cited by 310
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Wang, Z., Neylan, T. C., Mueller, S. G., Lenoci, M., Truran, D., Marmar, C. R., Weiner, M. W., & Schuff, N. W. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2009.205 · Cited by 307
Venero, C., & Borrell, J. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00668.x · Cited by 277
Lathe, R. (2001) · Journal of Endocrinology · doi:10.1677/joe.0.1690205 · Cited by 278
Exposing Rats to a Predator Blocks Primed Burst Potentiation in the Hippocampus In Vitro
Mesches, M. H., Fleshner, M., Heman, K. L., Rose, G. M., & Diamond, D. M. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-14-j0004.1999 · Cited by 276
Molecular Mechanisms of Glucocorticoid-Induced Insulin Resistance
Beaupere, C., Liboz, A., Fève, B., Blondeau, B., & Guillemain, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22020623 · Cited by 271
Zheng, P. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.07.001 · Cited by 268
Effects of cognitive-behavioral therapy on brain activation in specific phobia
Straube, T., Glauer, M., Dilger, S., Mentzel, H.-J., & Miltner, W. H. R. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.07.007 · Cited by 264
Opposing roles of type I and type II adrenal steroid receptors in hippocampal long-term potentiation
Pavlides, C., Watanabe, Y., Magarin˜os, A. M., & McEwen, B. S. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00151-8 · Cited by 261
Self-citationSuri, D., & Vaidya, V. A. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.08.065 · Cited by 269
Akirav, I., & Richter-Levin, G. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10530.1999 · Cited by 250
Restraint stress reversibly enhances spatial memory performance
Luine, V. N., Martinez, C., Villegas, M., Magariños, A. M., & McEwen, B. S. (1996) · Physiology & Behavior · doi:10.1016/0031-9384(95)02016-0 · Cited by 249
Self-citationGupta, R., Sen, S., Diepenhorst, L. L., Rudick, C., & Maren, S. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03116-4 · Cited by 263
Pavlides, C., Ogawa, S., Kimura, A., & McEwen, B. S. (1996) · Brain Research · doi:10.1016/s0006-8993(96)00776-7 · Cited by 240
Self-citationXu, L., Hölscher, C., Anwyl, R., & Rowan, M. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3204 · Cited by 234
Mechanisms of Amygdala Modulation of Hippocampal Plasticity
Akirav, I., & Richter‐Levin, G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-22-09912.2002 · Cited by 225
Roozendaal, B., Nguyen, B. T., Power, A. E., & McGaugh, J. L. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.20.11642 · Cited by 293
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Joëls, M. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.11.064 · Cited by 220
BDNF protects against stress‐induced impairments in spatial learning and memory and LTP
Radecki, D. T., Brown, L. M., Martinez, J., & Teyler, T. J. (2004) · Hippocampus · doi:10.1002/hipo.20048 · Cited by 215
The effect on memory of chronic prednisone treatment in patients with systemic disease
Keenan, P. A., Jacobson, M. W., Soleymani, R., Mayes, M. D., Stress, M., & Yaldoo, D. T. (1996) · Neurology · doi:10.1212/wnl.47.6.1396 · Cited by 208
Joo, E. Y., Kim, H., Suh, S. A., & Hong, S. B. (2014) · SLEEP · doi:10.5665/sleep.3836 · Cited by 201
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Joëls, M. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00688.x · Cited by 196
Short-term reverberant memory model of hippocampal field CA3
Wiebe, S. P., St�ubli, U. V., & Ambros-Ingerson, J. (1997) · Hippocampus · doi:10.1002/(sici)1098-1063(1997)7:6 · Cited by 33
Insight into zinc signaling from dietary zinc deficiency
Takeda, A., & Tamano, H. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.09.003 · Cited by 197
Amygdala-Hippocampus Dynamic Interaction in Relation to Memory
Richter‐Levin, G., & Akirav, I. (2000) · Molecular Neurobiology · doi:10.1385/mn:22:1-3:011 · Cited by 204
Chen, C., Nakagawa, S., An, Y., Ito, K., Kitaichi, Y., & Kusumi, I. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.12.001 · Cited by 209
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Atrooz, F., Alkadhi, K. A., & Salim, S. (2021) · Current Research in Neurobiology · doi:10.1016/j.crneur.2021.100013 · Cited by 213
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Bains, J. S., Cusulin, J. I. W., & Inoue, W. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3881 · Cited by 200
Systems mediating acute glucocorticoid effects on memory consolidation and retrieval
Roozendaal, B. (2003) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2003.09.015 · Cited by 191
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Richter‐Levin, G. (2004) · The Neuroscientist · doi:10.1177/1073858403259955 · Cited by 182
Takahashi, T., Kimoto, T., Tanabe, N., Hattori, T., Yasumatsu, N., & Kawato, S. (2002) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2002.01251.x · Cited by 176
Tartar, J. L., Ward, C. P., McKenna, J. T., Thakkar, M., Arrigoni, E., McCarley, R. W., Brown, R. E., & Strecker, R. E. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04808.x · Cited by 206
Hui, G. K. (2003) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2003.09.002 · Cited by 168
Park, C. R., Campbell, A. M., & Diamond, D. M. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01255-0 · Cited by 170
Kumar, A. (2011) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2011.00007 · Cited by 175
Hippocampal vulnerability to stress and aging: possible role of neurotrophic factors
Smith, M. A. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00220-0 · Cited by 162
Korz, V., & Frey, J. U. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-19-07281.2003 · Cited by 155
Gerges, N. Z., Stringer, J. L., & Alkadhi, K. A. (2001) · Brain Research · doi:10.1016/s0006-8993(01)03181-x · Cited by 155
Human amygdala development in the absence of species‐expected caregiving
Tottenham, N. (2012) · Developmental Psychobiology · doi:10.1002/dev.20531 · Cited by 149
Psychosocial stress, glucocorticoids, and structural alterations in the tree shrew hippocampus
Fuchs, E., Flügge, G., Ohl, F., Lucassen, P. J., Vollmann-Honsdorf, G. K., & Michaelis, T. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(01)00497-8 · Cited by 150
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Piroli, G. G., Grillo, C. A., Reznikov, L. R., Adams, S., McEwen, B. S., Charron, M. J., & Reagan, L. P. (2007) · Neuroendocrinology · doi:10.1159/000101694 · Cited by 152
Self-citationKrystal, J. H., Abdallah, C. G., Averill, L. A., Kelmendi, B., Harpaz-Rotem, I., Sanacora, G., Southwick, S. M., & Duman, R. S. (2017) · Current Psychiatry Reports · doi:10.1007/s11920-017-0829-z · Cited by 145
Alfarez, D. N., Wiegert, O., Joëls, M., & Krugers, H. J. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00483-9 · Cited by 145
Joëls, M., & Krugers, H. J. (2007) · Neural Plasticity · doi:10.1155/2007/93202 · Cited by 141
Joca, S. R. L., Ferreira, F. R., & Guimarães, F. S. (2007) · Stress · doi:10.1080/10253890701223130 · Cited by 139
Prevention of stress-induced morphological and cognitive consequences
McEwen, B. S., Conrad, C. D., Kuroda, Y., Frankfurt, M., Magariños, A. M., & McKittrick, C. R. (1997) · European Neuropsychopharmacology · doi:10.1016/s0924-977x(97)00064-3 · Cited by 137
Self-citationStress-induced metaplasticity: From synapses to behavior
Schmidt, M. V., Abraham, W. C., Maroun, M., Stork, O., & Richter‐Levin, G. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.06.059 · Cited by 137
Rao, R. P., Anilkumar, S., McEwen, B. S., & Chattarji, S. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.04.008 · Cited by 131
Self-citationMechanism of altered synaptic strength due to experience: relation to long-term potentiation
Foster, T. C., Gagné, J., & Massicotte, G. (1996) · Brain Research · doi:10.1016/0006-8993(96)00707-x · Cited by 131
Hippocampal homosynaptic long-term depression/depotentiation induced by adrenal steroids
Pavlides, C., Kimura, A., Magarin˜os, A. M., & Mcewen, B. S. (1995) · Neuroscience · doi:10.1016/0306-4522(95)94332-s · Cited by 126
Self-citationGlucocorticoids, epigenetic control and stress resilience
Reul, J. M. H. M., Collins, A., Saliba, R. S., Mifsud, K. R., Carter, S. D., Gutièrrez‐Mecinas, M., Qian, X., & Linthorst, A. C. E. (2014) · Neurobiology of Stress · doi:10.1016/j.ynstr.2014.10.001 · Cited by 124
Neurocognitive effects of stress: a metaparadigm perspective
Kim, E. J., & Kim, J. J. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-01986-4 · Cited by 154
ffrench-Mullen, J. M. H. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-01-00903.1995 · Cited by 118
Cellular and Molecular Differences Between Area CA1 and the Dentate Gyrus of the Hippocampus
Alkadhi, K. A. (2019) · Molecular Neurobiology · doi:10.1007/s12035-019-1541-2 · Cited by 113
Weina, H., Yuhu, N., Christian, H., Birong, L., Feiyu, S., & Le, W. (2018) · Brain Research · doi:10.1016/j.brainres.2018.04.031 · Cited by 115
Metcalfe, J., & Jake Jacobs, W. (1998) · Psychology of Learning and Motivation · doi:10.1016/s0079-7421(08)60187-5 · Cited by 115
REM sleep deprivation inhibits LTP in vivo in area CA1 of rat hippocampus
Kim, E. Y., Mahmoud, G. S., & Grover, L. M. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.06.057 · Cited by 114
Vouimba, R., Yaniv, D., Diamond, D., & Richter‐Levin, G. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03294.x · Cited by 114
Stress-induced alterations in large-scale functional networks of the rodent brain
Henckens, M. J. A. G., van der Marel, K., van der Toorn, A., Pillai, A. G., Fernández, G., Dijkhuizen, R. M., & Joëls, M. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.10.037 · Cited by 119
Metadata
- Authors
- Pavlides, C., Watanabe, Y., & McEwen, B. S.
- Affiliations
- Rockefeller University (US)
- Corresponding author
- Pavlides, Constantine
- Venue
- Hippocampus
- Publisher
- Wiley
- Published
- 1993-04
- Volume
- 3
- Issue
- 2
- Pages
- 183-192
- ISSN
- 1050-9631 (ISSN-L)
- 1098-1063
- OpenAlex
- W2046273515
- Cited by
- 323
- References
- 61
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 5 · 2023: 2 · 2022: 6 · 2021: 12 · 2020: 7 · 2019: 7 · 2018: 12 · 2017: 7 · 2016: 4 · 2015: 7 · 2014: 13 · 2013: 8 · 2012: 13
- FWCI
- 3.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Hippocampus (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Whitehall Foundation
- National Institute of Mental Health (MH-41256)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- glucocorticoids, corticosterone, hippocampal long-term potentiation, dentate gyrus granule cells, excitatory postsynaptic potentials, population spike, post-tetanic potentiation, neuronal excitability, stress, CA1 field
- MeSH terms
- Animals, Corticosterone, Electric Stimulation, Electrophysiology, Hippocampus, Male, Reaction Time, Rats, Sprague-Dawley, 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 ›
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