The DOI matches its Crossref record; 26 of the 26 references it cites were found in a registry or an index.
Hippocampal pathway to the amygdala and stress ulcer development.
Abstract
The objective of the first study was to localize the reported aggravation of stress ulcers found after large bilateral hippocampal lesions in rats. Lesions in the ventral hippocampus produced a similar increase in the severity of gastric erosions after cold-restraint, as was seen after large bilateral lesions. Dorsal hippocampal damage produced no differential effects. In the second experiment, high-frequency electrical stimulation of the ventral CA1 region of the hippocampus, a procedure known to induce long-term potentiation, increased the evoked potentials in the lateral central nucleus of the amygdala, and in adjacent parts of the lateral and basolateral nuclei. The increase in the efficacy of synaptic transmission in this pathway attenuated stress ulcer development. It was concluded that the ventral hippocampus is part of a coping system, and a strengthening of synaptic connections with the central amygdala increases the coping ability of rats under stress conditions.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“Enhanced associative learning of tone-dependent fear through hippocampal CRFR1 could result from activation of hippocampal pathways to the amygdala (Henke, 1990), a brain region identified as being crucial for acquisition of fear responses.”
From Modulation of learning and anxiety by corticotropin-releasing factor (CRF) and stress: differential roles of CRF receptors 1 and 2 (1999) · cites this paper as Henke, 1990
Citations
Cites
The Psychology of Learning and Motivation: Advances in Research and Theory
(2010) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/c2009-0-62209-1 · Cited by 6,035
Long-term potentiation phenomena in the rat limbic forebrain
Racine, R. J., Milgram, N. W., & Hafner, S. (1983) · Brain Research · doi:10.1016/0006-8993(83)90676-5 · Cited by 556
"Psychic blindness" and other symptoms following bilateral temporal lobectomy in Rhesus monkeys.
Klüver, H., & Bucy, P. C. (1937) · American Journal of Physiology-Legacy Content · Cited by 545
Psychopathology : experimental models
Maser, J. D., & Seligman, M. E. P. (1977) · W.H. Freeman eBooks · Cited by 487
Behavioral stress impairs long-term potentiation in rodent hippocampus
Foy, M. R., Stanton, M. E., Levine, S., & Thompson, R. F. (1987) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(87)90664-9 · Cited by 436
Long-Term Potentiation of Hippocampal Synaptic Transmission Affects Rate of Behavioral Learning
Berger, T. W. (1984) · Science · doi:10.1126/science.6324350 · Cited by 259
Stress ulcer susceptibility and depression in Wistar Kyoto (WKY) rats
Paré, W. P. (1989) · Physiology & Behavior · doi:10.1016/0031-9384(89)90203-5 · Cited by 162
Davis, M. E., Hitchcock, J. M., & Rosen, J. B. (1988) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/s0079-7421(08)60031-6 · Cited by 139
Siegel, A., & Flynn, J. P. (1968) · Brain Research · doi:10.1016/0006-8993(68)90102-9 · Cited by 113
Paxinos, G. (1985) · Academic Press eBooks · Cited by 110
Research works printed but not linked: 1
- de Olmos, 1985, Amygdala, vol. 1
Cited by
Sorted by citations
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
Fanselow, M. S., & Dong, H.-W. (2010) · Neuron · doi:10.1016/j.neuron.2009.11.031 · Cited by 3,358
Functional organization of the hippocampal longitudinal axis
Strange, B. A., Witter, M. P., Lein, E. S., & Moser, E. I. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3785 · Cited by 1,738
Regional dissociations within the hippocampus-memory and anxiety
Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462
Adult hippocampal neurogenesis and cognitive flexibility — linking memory and mood
Anacker, C., & Hen, R. (2017) · Nature Reviews Neuroscience · doi:10.1038/nrn.2017.45 · Cited by 1,014
Human Hippocampal Neurogenesis Persists in Aged Adults and Alzheimer’s Disease Patients
Tobin, M. K., Musaraca, K., Disouky, A., Shetti, A., Bheri, A., Honer, W. G., Kim, N., Dawe, R. J., Bennett, D. A., Arfanakis, K., et al. (2019) · Cell Stem Cell · doi:10.1016/j.stem.2019.05.003 · Cited by 603
Ventral hippocampal lesions affect anxiety but not spatial learning
Bannerman, D. M., Grubb, M., Deacon, R. M. J., Yee, B. K., Feldon, J., & Rawlins, J. N. P. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00268-1 · Cited by 530
Radulovic, J., Rühmann, A., Liepold, T., & Spiess, J. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05016.1999 · Cited by 402
Amygdala and Ventral Hippocampus Contribute Differentially to Mechanisms of Fear and Anxiety.
McHugh, S. B., Deacon, R. M. J., Rawlins, J. N. P., & Bannerman, D. M. (2004) · Behavioral Neuroscience · doi:10.1037/0735-7044.118.1.63 · Cited by 384
Control of Stress-Induced Persistent Anxiety by an Extra-Amygdala Septohypothalamic Circuit
Anthony, T. E., Dee, N., Bernard, A., Lerchner, W., Heintz, N., & Anderson, D. J. (2014) · Cell · doi:10.1016/j.cell.2013.12.040 · Cited by 310
Ayhan, F., Kulkarni, A., Berto, S., Sivaprakasam, K., Douglas, C., Lega, B. C., & Konopka, G. (2021) · Neuron · doi:10.1016/j.neuron.2021.05.003 · Cited by 207
Lü, L., Uejima, J. L., Gray, S. M., Bossert, J. M., & Shaham, Y. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.04.011 · Cited by 192
A short review on emotion processing: a lateralized network of neuronal networks
Palomero‐Gallagher, N., & Amunts, K. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02331-7 · Cited by 201
On the Run for Hippocampal PlasticityPreprint
Cooper, C. P., Moon, H. Y., & van Praag, H. (2017) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029736 · Cited by 168
Acute Minocycline Treatment Mitigates the Symptoms of Mild Blast-Induced Traumatic Brain Injury
Kövesdi, E., Kamnaksh, A., Wingo, D., Ahmed, F. A. K. M., Grunberg, N. E., Long, J. B., Kasper, C. E., & Agoston, D. V. (2012) · Frontiers in Neurology · doi:10.3389/fneur.2012.00111 · Cited by 162
Rogers, J. L., & See, R. E. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.01.003 · Cited by 153
Lee, S. W., Clemenson, G. D., & Gage, F. H. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.009 · Cited by 164
Floriou‐Servou, A., von Ziegler, L., Stalder, L., Sturman, O., Privitera, M., Rassi, A., Cremonesi, A., Thöny, B., & Bohacek, J. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.02.003 · Cited by 129
Stress and Traumatic Brain Injury: A Behavioral, Proteomics, and Histological Study
Kwon, S.-K. C., Kövesdi, E., Gyorgy, A. B., Wingo, D., Kamnaksh, A., Walker, J., Long, J. B., & Agoston, D. V. (2011) · Frontiers in Neurology · doi:10.3389/fneur.2011.00012 · Cited by 134
Neurobiology of stress ulcers.
Glavin, G. B., Murison, R. C. C., Overmier, J. B., Paré, W. P., Bakke, H.-K., Henke, P. G., & Hernández, D. E. (1990) · PubMed · Cited by 120
Self-citationKövesdi, E., Gyorgy, A. B., Kwon, S.-K. C., Wingo, D., Kamnaksh, A., Long, J. B., Kasper, C. E., & Agoston, D. V. (2011) · Frontiers in Neuroscience · doi:10.3389/fnins.2011.00042 · Cited by 117
The neurobiology of stress ulcers
Glavin, G. B., Murison, R. C. C., Overmier, J. B., Paré, W. P., Bakke, H.-K., Henke, R. G., & Hernández, D. E. (1991) · Brain Research Reviews · doi:10.1016/0165-0173(91)90012-w · Cited by 113
Przeździk, I., Faber, M., Fernández, G., Beckmann, C. F., & Haak, K. V. (2019) · Cortex · doi:10.1016/j.cortex.2019.04.015 · Cited by 103
Whole-brain spatial organization of hippocampal single-neuron projectomes
Qiu, S., Hu, Y., Huang, Y., Gao, T., Wang, X., Wang, D., Ren, B., Shi, X., Chen, Y., Wang, X., et al. (2024) · Science · doi:10.1126/science.adj9198 · Cited by 116
Tanti, A., Westphal, W.-P., Girault, V., Brizard, B., Devers, S., Leguisquet, A.-M., Surget, A., & Belzung, C. (2013) · Hippocampus · doi:10.1002/hipo.22134 · Cited by 109
Effects of ventral and dorsal CA1 subregional lesions on trace fear conditioning
Rogers, J. L., Hunsaker, M. R., & Kesner, R. P. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.01.002 · Cited by 95
Revisiting the hippocampal–amygdala pathway in primates: Association with immature-appearing neurons
Fudge, J. L., deCampo, D. M., & Becoats, K. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.03.040 · Cited by 96
Dorsal and ventral hippocampal adult-born neurons contribute to context fear memory
Huckleberry, K. A., Shue, F., Copeland, T., Chitwood, R. A., Yin, W., & Drew, M. R. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0109-6 · Cited by 97
Neuronal Responses to Conspecifics in the Ventral CA1
Rao, R. P., von Heimendahl, M., Bahr, V., & Brecht, M. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.081 · Cited by 85
Neuron loss and shrinkage in the amygdala in Alzheimer's disease
Vereecken, T. H. L. G., Vogels, O. J. M., & Nieuwenhuys, R. (1994) · Neurobiology of Aging · doi:10.1016/0197-4580(94)90143-0 · Cited by 85
Katzman, M., & Sternat, T. (2016) · Neuropsychiatric Disease and Treatment · doi:10.2147/ndt.s111818 · Cited by 83
CA2: A Highly Connected Intrahippocampal Relay
Middleton, S. J., & McHugh, T. J. (2019) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-080719-100343 · Cited by 80
Major Depression: A Role for Hippocampal Neurogenesis?
Lee, M. M., Reif, A., & Schmitt, A. G. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_226 · Cited by 77
Wang, M. E., Fraize, N., Yin, L. X., Yuan, R. K., Petsagourakis, D., Wann, E. G., & Muzzio, I. A. (2013) · Hippocampus · doi:10.1002/hipo.22105 · Cited by 83
Early life stress accelerates age-induced effects on neurogenesis, depression, and metabolic risk
Ruiz, R., Roque, A., Pineda, E., Licona-Limón, P., Valdez-Alarcón, J. J., & Lajud, N. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.07.012 · Cited by 74
Huff, M. L., Emmons, E. B., Narayanan, N. S., & LaLumiere, R. (2016) · Learning & memory (Cold Spring Harbor, N.Y.) · doi:10.1101/lm.039909.115 · Cited by 73
Serotonergic dysfunction in the A53T alpha‐synuclein mouse model of Parkinson's disease
Deusser, J., Schmidt, S., Ettle, B., Plötz, S., Huber, S. E., Müller, C. P., Masliah, E., Winkler, J., & Kohl, Z. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13253 · Cited by 66
Anacker, C. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_275 · Cited by 63
What Is the Functional Significance of Hippocampal Pathology in Schizophrenia?
Goldman, M. B., & Mitchell, C. P. (2004) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a007086 · Cited by 60
Karabeg, M. M., Grauthoff, S., Kollert, S. Y., Weidner, M., Heiming, R. S., Jansen, F., Popp, S., Kaiser, S., Lesch, K.-P., Sachser, N., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078238 · Cited by 56
Decker, A. L., Duncan, K. D., Finn, A. S., & Mabbott, D. (2020) · Nature Communications · doi:10.1038/s41467-020-17854-6 · Cited by 61
Zhang, L., Hernández, V. S., Gerfen, C. R., Jiang, S. Z., Zavala, L., Barrio, R. A., & Eiden, L. E. (2021) · eLife · doi:10.7554/elife.61718 · Cited by 54
The role of hippocampal mossy cells in novelty detection
Fredes, F., & Shigemoto, R. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107486 · Cited by 52
Galinato, M. H., Orío, L., & Mandyam, C. D. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.11.042 · Cited by 54
Wahlstrom, K. L., Huff, M. L., Emmons, E. B., Freeman, J. H., Narayanan, N. S., McIntyre, C. K., & LaLumiere, R. T. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2848-17.2018 · Cited by 54
Grigoryan, G., & Segal, M. (2016) · Neural Plasticity · doi:10.1155/2016/2540462 · Cited by 54
Centrifugal Inputs to the Main Olfactory Bulb Revealed Through Whole Brain Circuit-Mapping
Padmanabhan, K., Osakada, F., Anna, T., Erin, K., Callaway, E. M., Gage, F. H., & B, T. J. S. A. (2019) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2018.00115 · Cited by 56
Ewin, S. E., Morgan, J. W., Niere, F., McMullen, N. P., Barth, S. H., Almonte, A. G., Raab‐Graham, K. F., & Weiner, J. L. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.11.028 · Cited by 45
Henke, P. G., Ray, A., & Sullivan, R. M. (1991) · Digestive Diseases and Sciences · doi:10.1007/bf01296409 · Cited by 48
Self-citationRiaz, S., Schumacher, A., Sivagurunathan, S., van der Meer, M. A. A., & Ito, R. (2017) · Hippocampus · doi:10.1002/hipo.22734 · Cited by 53
Beeman, C. L., Bauer, P. S., Pierson, J. L., & Quinn, J. J. (2013) · Learning & Memory · doi:10.1101/lm.031161.113 · Cited by 46
Ventral hippocampus-lateral septum circuitry promotes foraging-related memory
Décarie-Spain, L., Liu, C. M., Lauer, L. T., Subramanian, K. S., Bashaw, A. G., Klug, M. E., Gianatiempo, I. H., Suarez, A. N., Noble, E. E., Donohue, K. N., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111402 · Cited by 44
Divergence in Population Coding for Space between Dorsal and Ventral CA1
Chockanathan, U., & Padmanabhan, K. (2021) · eNeuro · doi:10.1523/eneuro.0211-21.2021 · Cited by 45
Micro-, Meso- and Macro-Dynamics of the Brain
Buzsáki, G., Christen, Y., & Publishing, S. I. (2016) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-28802-4 · Cited by 44
Neural Activity Patterns Underlying Spatial Coding in the Hippocampus
Sosa, M., Gillespie, A. K., & Frank, L. M. (2016) · Current topics in behavioral neurosciences · doi:10.1007/7854_2016_462 · Cited by 43
Sadighi, M., Bourmpoula, M. T., Homberg, J. R., & Fathollahi, Y. (2017) · Addiction Biology · doi:10.1111/adb.12547 · Cited by 39
Lopes, M. W., Lopes, S. C., Costa, A. P., Gonçalves, F. M., Rieger, D. K., Peres, T. V., Eyng, H., Prediger, R. D., Díaz, A. P., Nunes, J. C., et al. (2015) · Neurochemistry International · doi:10.1016/j.neuint.2015.05.003 · Cited by 39
Understanding the neural code of stress to control anhedonia
Xia, F., Fascianelli, V., Vishwakarma, N., Ghinger, F. G., Kwon, A., Gergues, M. M., Lalani, L. K., Fusi, S., & Kheirbek, M. A. (2024) · Nature · doi:10.1038/s41586-024-08241-y · Cited by 38
Zhou, Q.-G., Lee, D., Ro, E. J., & Suh, H. (2016) · Scientific Reports · doi:10.1038/srep35572 · Cited by 36
Brivio, P., Corsini, G., Riva, M. A., & Calabrese, F. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.02.006 · Cited by 35
Guercio, L. A., Wimmer, M. E., Schmidt, H. D., Swinford-Jackson, S. E., Pierce, R. C., & Vassoler, F. M. (2020) · Brain Research · doi:10.1016/j.brainres.2020.147011 · Cited by 31
Rudobeck, E., Nelson, G. A., Sokolova, I. V., & Vlkolinský, R. (2014) · Radiation Research · doi:10.1667/rr13484.1 · Cited by 32
van Doeselaar, L., Stark, T., Mitra, S., Yang, H., Bordes, J., Stolwijk, L., Engelhardt, C., Kovarova, V., Narayan, S., Brix, L. M., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2300722120 · Cited by 30
Hypothalamic melanin-concentrating hormone projections to the septo-hippocampal complex in the rat
de Lima, F. F. B., Sita, L. V., de Oliveira, A. R., Costa, H. C., da Silva, J. M., Mortara, R. A., Haemmerle, C. A. D. S., Xavier, G. F., Canteras, N. S., & Bittencourt, J. C. (2012) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2012.10.003 · Cited by 30
Stress Gastric Ulcers and Cytoprotective Strategies: Perspectives and Trends
Ray, A., Gulati, K., & Henke, P. G. (2020) · Current Pharmaceutical Design · doi:10.2174/1381612826666200521143203 · Cited by 27
Self-citationJung, H. Y., Yoo, D. Y., Nam, S. M., Kim, J. W., Choi, J. H., Yoo, M., Lee, S., Yoon, Y. S., & Hwang, I. K. (2015) · Journal of Medicinal Food · doi:10.1089/jmf.2014.3412 · Cited by 26
Ordemann, G. J., Apgar, C. J., & Brager, D. H. (2019) · Journal of Neurophysiology · doi:10.1152/jn.00737.2018 · Cited by 25
Donohue, J. D., Amidon, R. F., Murphy, T. R., Wong, A. J., Liu, E. D., Saab, L., King, A. J., Pae, H., Ajayi, M. T., & Anderson, G. R. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110031 · Cited by 25
Kassab, R., & Alexandre, F. (2015) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2015.00087 · Cited by 25
Grid Cells and Spatial Maps in Entorhinal Cortex and Hippocampus
Stensola, T., & Moser, E. I. (2016) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-28802-4_5 · Cited by 27
Gould, T. J., Wilkinson, D. S., Yildirim, E., Poole, R. L., Leach, P. T., & Simmons, S. J. (2014) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2014.01.009 · Cited by 25
Yagi, S., Lee, A. J., Truter, N., & Galea, L. A. M. (2022) · Biology of Sex Differences · doi:10.1186/s13293-022-00450-2 · Cited by 24
Farahimanesh, S., Karimi, S., & Haghparast, A. (2017) · Peptides · doi:10.1016/j.peptides.2017.12.017 · Cited by 23
Dopaminergic system in CA1 modulates MK-801 induced anxiolytic-like responses
Zarrindast, M., Nasehi, M., Pournaghshband, M., & Yekta, B. G. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2012.07.016 · Cited by 23
Neuronal loss and β-amyloid removal in the amygdala of people with Down syndrome☆
Węgiel, J., Wı́sniewski, H. M., Moryś, J., Tarnawski, M. J., Kuchna, I., Dziewíatkowski, J., Pirttilä, T., Krivimäki, T., Lehtimäki, T. J., & Lach, B. (1999) · Neurobiology of Aging · doi:10.1016/s0197-4580(99)00060-3 · Cited by 23
Hippocampus long‐axis specialization throughout development: A meta‐analysis
Nichols, E. S., Blumenthal, A., Kuenzel, E., Skinner, J. K., & Duerden, E. G. (2023) · Human Brain Mapping · doi:10.1002/hbm.26340 · Cited by 24
da Costa, V. F., Ramírez, J. C. C., Ramírez, S. V., Avalo-Zuluaga, J. H., Baptista‐de‐Souza, D., Canto‐de‐Souza, L., Planeta, C. S., Rico, J. L., & Nunes‐de‐Souza, R. L. (2023) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2023.1168640 · Cited by 24
Learning Promotes Subfield-Specific Synaptic Diversity in Hippocampal CA1 Neurons
Sakimoto, Y., Mizuno, J., Kida, H., Kamiya, Y., Ono, Y., & Mitsushima, D. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz022 · Cited by 23
Staples, M. C., Fannon, M. J., Mysore, K. K., Dutta, R. R., Ongjoco, A. T., Quach, L. W., Kharidia, K. M., Somkuwar, S. S., & Mandyam, C. D. (2017) · Brain Research · doi:10.1016/j.brainres.2017.02.028 · Cited by 18
Representations of stimulus features in the ventral hippocampus
Biane, J. S., Ladow, M. A., Fan, A., Choi, H. S., Zhou, L. Z., Hassan, S., Apodaca-Montano, D. L., Kwon, A. O., Bratsch-Prince, J. X., & Kheirbek, M. A. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.007 · Cited by 19
Bertagna, N. B., dos Santos, P. G. C., Queiroz, R. M., Fernandes, G. J. D., Cruz, F. C., & Miguel, T. T. (2020) · Pharmacological Reports · doi:10.1007/s43440-020-00182-3 · Cited by 19
Chen, Y., Akad, A., Aderogba, R., Chowdhury, T. G., & Aoki, C. J. (2018) · Synapse · doi:10.1002/syn.22034 · Cited by 17
Migratory Response of Cells in Neurogenic Niches to Neuronal Death: The Onset of Harmonic Repair?
Geribaldi‐Doldán, N., Carrascal, L., Pérez-García, P., Oliva, J. M., Pardillo-Díaz, R., Domínguez‐García, S., Utrera, C. B., Gómez‐Oliva, R., Martínez‐Ortega, S., Verástegui, C., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076587 · Cited by 16
Clemens, A. M., & Johnston, D. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00839.2013 · Cited by 15
Cyclin-Dependent Kinase Inhibitor 1a (p21) Modulates Response to Cocaine and Motivated Behaviors
Scholpa, N. E., Briggs, S. B., Wagner, J. J., & Cummings, B. S. (2016) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.115.230888 · Cited by 14
Liakath‐Ali, K., Refaee, R., & Südhof, T. C. (2024) · PLoS Biology · doi:10.1371/journal.pbio.3002599 · Cited by 13
Cole, S., Richardson, R., & McNally, G. P. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058701 · Cited by 12
Neuroimmunogastroenterology: At the Interface of Neuroimmunology and Gastroenterology
Sanchez, J. M. S., McNally, J. S., Cortez, M. M., Hemp, J., Pace, L., & Clardy, S. L. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00787 · Cited by 13
Chen, M.-X., Liu, Q., Chen, M.-X., Lei, L., Lin, A., Lei, L., Hui, T. C. K., Li, Q., Ao, L., & Sham, P. C. (2020) · Neural Regeneration Research · doi:10.4103/1673-5374.276358 · Cited by 11
Lodge, D. J., Reiley, H. B., Boley, A. M., & Donegan, J. J. (2023) · Nature Communications · doi:10.1038/s41467-023-42484-z · Cited by 11
Alijanpour, S., Jafaripour, S., Ghasemzadeh, Z., Khakpai, F., & Zarrindast, M. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173806 · Cited by 9
Systems genetic analysis of nicotine withdrawal deficits in hippocampus‐dependent learning
Goldberg, L. R., Kutlu, M. G., Zeid, D., Seemiller, L. R., & Gould, T. J. (2021) · Genes Brain & Behavior · doi:10.1111/gbb.12734 · Cited by 9
Socioeconomic status and subdivisions of the amygdala and hippocampus in children and adolescents
Hanson, J. L., Adkins, D. J., Nacewicz, B. M., & Barry, K. R. (2026) · Brain and Environment · doi:10.1016/j.braen.2026.100022 · Cited by 11
The role of hippocampal CaMKII in resilience to trauma-related psychopathology
Hazra, S., Hazra, J. D., Bar-On, R. A., Duan, Y., Edut, S., Cao, X., & Richter‐Levin, G. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100506 · Cited by 9
Topography of inputs into the hippocampal formation of a food‐caching bird
Applegate, M. C., Gutnichenko, K. S., & Aronov, D. (2023) · The Journal of Comparative Neurology · doi:10.1002/cne.25533 · Cited by 8
Magalhães, D. M., Stewart, N. A., Mampay, M., Rolle, S. O., Hall, C. M., Moeendarbary, E., Flint, M. S., Sebastião, A. M., Valente, C. A., Dymond, M. K., et al. (2024) · Journal of Neurochemistry · doi:10.1111/jnc.16073 · Cited by 6
Grant, C. V., Russart, K. L. G., & Pyter, L. M. (2021) · Endocrine · doi:10.1007/s12020-021-02931-7 · Cited by 7
Franco, N. D., Drutel, G., Roullot, V., Julio‐Kalajzić, F., Lalanne, V., Grel, A., Lesté-Lasserre, T., Matias, I., Cannich, A., Gonzales, D., et al. (2022) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2022.103705 · Cited by 9
Deutsch, M., Stegmayr, C., Balfanz, S., & Baumann, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22136699 · Cited by 6
Physical Activity Dynamically Regulates the Hippocampal Proteome along the Dorso-Ventral Axis
Frey, S., Schieweck, R., Forné, I., Imhof, A., Straub, T., Popper, B., & Kiebler, M. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21103501 · Cited by 7
Dickson, C. R., Holmes, G. L., & Barry, J. M. (2022) · eNeuro · doi:10.1523/eneuro.0414-21.2022 · Cited by 7
Metadata
- Authors
- Henke, P. G.
- Affiliations
- St. Francis Xavier University (CA)
- Corresponding author
- Henke, Peter G.
- Venue
- Brain Research Bulletin
- Publisher
- Elsevier BV
- Published
- 1990-11
- Volume
- 25
- Issue
- 5
- Pages
- 691-695
- ISSN
- 0361-9230 (ISSN-L)
- OpenAlex
- W2027122202
- Cited by
- 153
- References
- 26
- Citations by year
- 2026: 5 · 2025: 9 · 2024: 11 · 2023: 7 · 2022: 9 · 2021: 14 · 2020: 9 · 2019: 13 · 2018: 8 · 2017: 9 · 2016: 9 · 2015: 4 · 2014: 6 · 2013: 7 · 2012: 8
- FWCI
- 1.20
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Research Bulletin (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Natural Sciences and Engineering Research Council of Canada
- 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
- stress ulcer, gastric erosions, ventral hippocampus, central amygdala, dorsal hippocampus, hippocampal lesions, cold restraint stress, long-term potentiation, synaptic transmission, coping, stress response
- MeSH terms
- Amygdala, Animals, Electric Stimulation, Evoked Potentials, Hippocampus, Male, Neural Pathways, Rats, Inbred Strains, Stomach Ulcer, Stress, Physiological, 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