Differential Expression of c‐fos mRNA Within Neurocircuits of Male Hamsters Exposed to Acute or Chronic Defeat

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Stress and the Individual

McEwen, B. S. (1993) · Archives of Internal Medicine · doi:10.1001/archinte.153.18.2093 · Cited by 4,365 · see citing works

Neurocircuitry of stress: central control of the hypothalamo–pituitary–adrenocortical axis

Herman, J. P., & Cullinan, W. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10069-2 · Cited by 2,270 · see citing works

A Comparison of the Social Postures of Some Common Laboratory Rodents

Grant, E. C., & Mackintosh, J. H. (1963) · Behaviour · doi:10.1163/156853963x00185 · Cited by 1,167 · see citing works

Columnar organization in the midbrain periaqueductal gray: modules for emotional expression?

Bandler, R., & Shipley, M. T. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90047-7 · Cited by 1,051 · see citing works

Stimulus-transcription coupling in neurons: role of cellular immediate-early genes

Morgan, J. I., & Curran, T. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90096-9 · Cited by 969 · see citing works

Functional characteristics of the midbrain periaqueductal gray.

Behbehani, M. M. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(95)00009-k · Cited by 879 · see citing works

Transcriptional autoregulation of the proto-oncogene fos

Sassone‐Corsi, P., Sisson, J. C., & Verma, I. M. (1988) · Nature · doi:10.1038/334314a0 · Cited by 611 · see citing works

Noradrenergic mechanisms in stress and anxiety: I. preclinical studies

Bremner, J., Krystal, J., Southwick, S., & Charney, D. (1996) · Synapse · doi:10.1002/(sici)1098-2396(199605)23:1 · Cited by 571 · see citing works

Induction of a long-lasting AP-1 complex composed of altered Fos-like proteins in brain by chronic cocaine and other chronic treatments

Hope, B. T., Nye, H. E., Kelz, M. B., Self, D. W., Iadarola, M. J., Nakabeppu, Y., Duman, R. S., & Nestler, E. J. (1994) · Neuron · doi:10.1016/0896-6273(94)90061-2 · Cited by 563 · see citing works

Visible burrow system as a model of chronic social stress: behavioral and neuroendocrine correlates

Blanchard, D. C., Spencer, R. L., Weiss, S. M., Blanchard, R. J., McEwen, B., & Sakai, R. R. (1995) · Psychoneuroendocrinology · doi:10.1016/0306-4530(94)e0045-b · Cited by 475 · see citing works

Opioid-Like Analgesia in Defeated Mice

Miczek, K. A., Thompson, M. L., & Shuster, L. (1982) · Science · doi:10.1126/science.7199758 · Cited by 418 · see citing works

Social model of depression in mice of C57BL/6J strain

Kudryavtseva, N. N., Bakshtanovskaya, I. V., & Koryakina, L. A. (1991) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(91)90284-9 · Cited by 404 · see citing works

Induction and habituation of immediate early gene expression in rat brain by acute and repeated restraint stress

Melia, K. R., Ryabinin, A. E., Schroeder, R., Bloom, F. E., & Wilson, M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-10-05929.1994 · Cited by 359 · see citing works

Dynamic alterations occur in the levels and composition of transcription factor AP-1 complexes after seizure

Sonnenberg, J. L., Macgregor-Leon, P. F., Curran, T., & Morgant, J. I. (1989) · Neuron · doi:10.1016/0896-6273(89)90260-2 · Cited by 350 · see citing works

Corticotropin-releasing factor antagonist reduces emotionality in socially defeated rats via direct neurotropic action

Heinrichs, S. C., Pich, E. M., Miczek, K. A., Britton, K. T., & Koob, G. F. (1992) · Brain Research · doi:10.1016/0006-8993(92)90708-h · Cited by 329 · see citing works

Chronic Fos-Related Antigens: Stable Variants of ΔFosB Induced in Brain by Chronic Treatments

Chen, J., Kelz, M. B., Hope, B. T., Nakabeppu, Y., & Nestler, E. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-13-04933.1997 · Cited by 327 · see citing works

The neuroendocrinology of depression and chronic stress

Checkley, S. (1996) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a011570 · Cited by 323 · see citing works

Regional changes in c-fos expression in the basal forebrain and brainstem during adaptation to repeated stress: Correlations with cardiovascular, hypothermic and endocrine responses

Chen, X., & Herbert, J. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00532-a · Cited by 313 · see citing works

Long-term impairment of autonomic circadian rhythms after brief intermittent social stress

Tornatzky, W., & Miczek, K. A. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90278-n · Cited by 306 · see citing works

Connections of the posterior nucleus of the amygdala

Canteras, N. S., Simerly, R. B., & Swanson, L. W. (1992) · The Journal of Comparative Neurology · doi:10.1002/cne.903240203 · Cited by 273 · see citing works

Cardiovascular responses elicited by stimulation of neurons in the central amygdaloid nucleus in awake but not anesthetized rats resemble conditioned emotional responses

Iwata, J., Chida, K., & LeDoux, J. E. (1987) · Brain Research · doi:10.1016/0006-8993(87)90978-4 · Cited by 272 · see citing works

Social Stress in Hamsters: Defeat Activates Specific Neurocircuits within the Brain

Kollack‐Walker, S., Watson, S. J., & Akil, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-22-08842.1997 · Cited by 253 · see citing works

Adaptation in patterns of c‐fos expression in the brain associated with exposure to either single or repeated social stress in male rats

Martı́nez, M., Phillips, P. J., & Herbert, J. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00011.x · Cited by 253 · see citing works

Chronic infusion of a CRH1 receptor antisense oligodeoxynucleotide into the central nucleus of the amygdala reduced anxiety-related behavior in socially defeated rats

Liebsch, G., Landgraf, R., Gerstberger, R., Probst, J. C., Wotjak, C. T., Engelmann, M., Holsboer, F., & Montkowski, A. (1995) · Regulatory Peptides · doi:10.1016/0167-0115(95)00099-w · Cited by 220 · see citing works

Cardiovascular responses elicited by electrical stimulation of the amygdala central nucleus in the rabbit

Kapp, B. S., Gallagher, M., Underwood, M. D., McNall, C. L., & Whitehorn, D. (1982) · Brain Research · doi:10.1016/0006-8993(82)90866-6 · Cited by 208 · see citing works

Anxiety enhancement in the murine elevated plus maze by immediate prior exposure to social stressors

Rodgers, R. J., & Cole, J. C. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90222-2 · Cited by 200 · see citing works

Induction of c-fos mRNA in rat brain by conditioned and unconditioned stressors

Smith, M. A., Banerjee, S., Gold, P. W., & Glowa, J. R. (1992) · Brain Research · doi:10.1016/0006-8993(92)90240-a · Cited by 173 · see citing works

INTEGRATIVE ROLE OF THE LAMINA TERMINALIS IN THE REGULATION OF CARDIOVASCULAR AND BODY FLUID HOMEOSTASIS

Johnson, A. K., Cunningham, J. T., & Thunhorst, R. L. (1996) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.1996.tb02594.x · Cited by 166 · see citing works

Persistent c-fos expression in the brains of mice with chronic social stress

Matsuda, S., Peng, H., Yoshimura, H., Wen, T., Fukuda, T., & Sakanaka, M. (1996) · Neuroscience Research · doi:10.1016/s0168-0102(96)01088-7 · Cited by 157 · see citing works

Acute and repeated exposure to social conflict in male golden hamsters: Increases in plasma POMC-peptides and cortisol and decreases in plasma testosterone

Huhman, K. L., Moore, T. O., Ferris, C. F., Mougey, E. H., & Meyerhoff, J. L. (1991) · Hormones and Behavior · doi:10.1016/0018-506x(91)90051-i · Cited by 154 · see citing works

Development of olfactory glomeruli: Temporal and spatial interactions between olfactory receptor axons and mitral cells in opossums and rats

Malun, D., & Brunjes, P. C. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960422)368:1 · Cited by 133 · see citing works

Repeated Immobilization Stress Alters Tyrosine Hydroxylase, Corticotropin‐Releasing Hormone and Corticosteroid Receptor Messenger Ribonucleic Acid Levels in Rat Brain

Mamalaki, E., Kvetnan̆ský, R., Brady, L., Gold, P., & Herkenham, M. (1992) · Journal of neuroendocrinology · doi:10.1111/j.1365-2826.1992.tb00220.x · Cited by 131 · see citing works

Neural substrates of aggression and flight in the cat

Siegel, A., & Pott, C. B. (1988) · Progress in Neurobiology · doi:10.1016/0301-0082(88)90015-9 · Cited by 130 · see citing works

Restraint and stimulation of bed nucleus of the stria terminalis produce similar stress-like behaviors

Casada, J. H., & Dafny, N. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90069-v · Cited by 128 · see citing works

Social conflict activates status-dependent endogenous analgesic or hyperalgesic mechanisms in male mice: effects of naloxone on nociception and behaviour.

Rodgers, R., & Hendrie, C. (1983) · Physiology and Behavior · doi:10.1016/0031-9384(83)90177-4 · Cited by 126 · see citing works

Chronic Electroconvulsive Seizures Down–Regulate Expression of the Immediate‐Early Genes c‐fos and c‐jun in Rat Cerebral Cortex

Winston, S. M., Hayward, M. D., Nestler, E. J., & Duman, R. S. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb04892.x · Cited by 119 · see citing works

The agonistic behaviour of the golden hamster Mesocricetus auratus (waterhouse)

Lerwill, C. J., & Makings, P. (1971) · Animal Behaviour · doi:10.1016/s0003-3472(71)80175-6 · Cited by 117 · see citing works

Excitotoxic lesions of the septum produce anxiolytic effects in the elevated plus-maze and the shock-probe burying tests

Pesold, C., & Treit, D. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90431-z · Cited by 106 · see citing works

Implications of prolonged expression of Fos-related antigens

Pennypacker, K. R., Hong, J., & McMillian, M. (1995) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(00)89061-6 · Cited by 105 · see citing works

Mouse Brain c‐fos mRNA Distribution Following a Single Electroconvulsive Shock

Daval, J., Nakajima, T., Gleiter, C. H., Post, R. M., & Marangos, P. J. (1989) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1989.tb07285.x · Cited by 105 · see citing works

Induction and habituation of c-fos and zif/268 by acute and repeated stressors

Watanabe, Y., Stone, E. A., & McEwen, B. S. (1994) · Neuroreport · doi:10.1097/00001756-199406270-00006 · Cited by 103 · see citing works

Forebrain mechanisms in the relief of fear: The role of the lateral septum

Thomas, E. (1988) · Psychobiology · doi:10.3758/bf03327297 · Cited by 92 · see citing works

Opposed regulation by dorsal raphe nucleus 5-HT pathways of two types of fear in the elevated T-maze

Graeff, F. G. (1996) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(95)02012-8 · Cited by 87 · see citing works

Social stress by repeated defeat: effects on social behaviour and emotionality

Albonetti, M. E., & Farabollini, F. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90027-2 · Cited by 85 · see citing works

Blockade of pituitary-adrenal axis activation induced by peripheral immunoneutralization of corticotropin-releasing factor does not affect the behavioral response to social defeat stress in rats

Pich, E. M. (1993) · Psychoneuroendocrinology · doi:10.1016/0306-4530(93)90043-k · Cited by 82 · see citing works

Repeated stress reduces the subsequent stress-induced expression of Fos in rat brain

Umemoto, S., Noguchi, K., Kawai, Y., & Senba, E. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)91037-5 · Cited by 70 · see citing works

Lesions of the Medial Geniculate Nuclei Specifically Block Corticosterone Release and Induction of c- fos mRNA in the Forebrain Associated with Audiogenic Stress in Rats

Campeau, S., Akil, H., & Watson, S. J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-15-05979.1997 · Cited by 67 · see citing works

Effect of glutamate stimulation of bed nucleus of the stria terminalis on arterial pressure and heart rate

Ciriello, J., & Janßen, S. (1993) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1993.265.5.h1516 · Cited by 67 · see citing works

The bed nucleus of the stria terminalis and immobilization-stress

Henke, P. G. (1984) · Behavioural Brain Research · doi:10.1016/0166-4328(84)90006-8 · Cited by 66 · see citing works

Afferents and efferents of the rat cuneiformis nucleus: an anatomical study with reference to pain transmission

Bernard, J., Peschanski, M., & Besson, J. (1989) · Brain Research · doi:10.1016/0006-8993(89)90449-6 · Cited by 61 · see citing works

Electrophysiological activity in the central nucleus of the amygdala, emotionality and stress ulcers in rats.

Henke, P. G. (1988) · Behavioral Neuroscience · doi:10.1037//0735-7044.102.1.77 · Cited by 35 · see citing works

Behavioral effects after ibotenic acid, 6-OHDA and electrolytic lesions in the central amygdala nucleus of the rat

Jellestad, F. K., Markowska, A. L., Bakke, H. K., & Walther, B. T. (1986) · Physiology & Behavior · doi:10.1016/s0031-9384(86)80004-x · Cited by 34 · see citing works

Ethopharmacology of copulatory disorder induced by chronic social conflict in male mice

Yoshimura, H., & Kimura, N. (1991) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(05)80138-1 · Cited by 34 · see citing works

Differential regulation of IEGs in the rat PVH in single, and repeated stress models

Umemoto, S., Kawai, Y., & Senba, E. (1994) · Neuroreport · doi:10.1097/00001756-199412300-00051 · Cited by 32 · see citing works

FOREBRAIN PATHWAYS MEDIATING STRESS‐INDUCED RENIN SECRETION

de Kar, L. D. V. (1996) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.1996.tb02591.x · Cited by 15 · see citing works

Kainic acid stimulation of the lateral septum elicits tachycardia

Deutch, A. Y., Clark, L., & Peacock, L. J. (1984) · Brain Research Bulletin · doi:10.1016/0361-9230(84)90047-9 · Cited by 5 · see citing works

The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress

Smith, S. M., & Vale, W. W. (2006) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2006.8.4/ssmith · Cited by 1,948 · see citing works

Central mechanisms of stress integration: hierarchical circuitry controlling hypothalamo–pituitary–adrenocortical responsiveness

Herman, J. P., Figueiredo, H., Mueller, N. K., Ulrich-Lai, Y., Ostrander, M. M., Choi, D. C., & Cullinan, W. E. (2003) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2003.07.001 · Cited by 1,586 · see citing works

Stress and the social brain: behavioural effects and neurobiological mechanisms

Sandi, C., & Haller, J. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3918 · Cited by 614 · see citing works

The many paths to fear

Gross, C. T., & Canteras, N. S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3301 · Cited by 596 · see citing works

Limbic Regulation of Hypothalamo‐Pituitary‐Adrenocortical Function during Acute and Chronic Stress

Jankord, R., & Herman, J. P. (2008) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1410.012 · Cited by 578 · see citing works

ΔFosB in brain reward circuits mediates resilience to stress and antidepressant responses

Vialou, V., Robison, A. J., LaPlant, Q. C., Covington, H. E., Dietz, D. M., Ohnishi, Y. N., Mouzon, E., Rush, A. J., Watts, E. L., Wallace, D. L., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2551 · Cited by 479 · see citing works

Treatment resistant depression: A multi-scale, systems biology approach

Akil, H., Gordon, J. A., Hen, R., Javitch, J. A., Mayberg, H. S., McEwen, B. S., Meaney, M. J., & Nestler, E. J. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.08.019 · Cited by 443 · see citing works

Protein lactylation induced by neural excitation

Hagihara, H., Shoji, H., Otabi, H., Toyoda, A., Katoh, K., Namihira, M., & Miyakawa, T. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109820 · Cited by 349 · see citing works

Social stress, therapeutics and drug abuse: Preclinical models of escalated and depressed intake

MICZEK, K., YAP, J., & COVINGTONIII, H. (2008) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2008.07.006 · Cited by 338 · see citing works

Dissecting the brain's fear system reveals the hypothalamus is critical for responding in subordinate conspecific intruders

Motta, S. C., Goto, M., Gouveia, F. V., Baldo, M. V. C., Canteras, N. S., & Swanson, L. W. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0900939106 · Cited by 209 · see citing works

The neural circuits of innate fear: detection, integration, action, and memorization

Silva, B. A., Gross, C. T., & Gräff, J. (2016) · Learning & Memory · doi:10.1101/lm.042812.116 · Cited by 186 · see citing works

Wired for behaviors: from development to function of innate limbic system circuitry

Sokolowski, K., & Corbin, J. G. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00055 · Cited by 174 · see citing works

Fighting Females: Neural and Behavioral Consequences of Social Defeat Stress in Female Mice

Newman, E. L., Covington, H. E., Suh, J., Bicakci, M. B., Ressler, K. J., DeBold, J. F., & Miczek, K. A. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.05.005 · Cited by 167 · see citing works

Mapping Brain Response to Social Stress in Rodents With c-fos Expression: A Review

Martı́nez, M., Calvo-Torrent, A., & Herbert, J. (2002) · Stress · doi:10.1080/102538902900012369 · Cited by 167 · see citing works

The Fibroblast Growth Factor Family: Neuromodulation of Affective Behavior

Turner, C. A., Watson, S. J., & Akil, H. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.037 · Cited by 160 · see citing works

Long-term behavioral and neuronal cross-sensitization to amphetamine induced by repeated brief social defeat stress: Fos in the ventral tegmental area and amygdala

Nikulina, E. M., Covington, H. E., Ganschow, L., Hammer, R. P., & Miczek, K. A. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2003.10.029 · Cited by 158 · see citing works

Functional internal complexity of amygdala: focus on gene activity mapping after behavioral training and drugs of abuse.

Knapska, E., Radwańska, K., Werka, T., & Kaczmarek, L. (2007) · Physiological Reviews · doi:10.1152/physrev.00037.2006 · Cited by 152 · see citing works

Variations of maternal care differentially influence ‘fear’ reactivity and regional patterns of cFos immunoreactivity in response to the shock-probe burying test

Menard, J. L., Champagne, D. L., & Meaney, M. J. P. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.08.009 · Cited by 137 · see citing works

Cognitive and neural correlates of depression-like behaviour in socially defeated mice: an animal model of depression with cognitive dysfunction

Yu, T., Guo, M., Garza, J., Rendon, S., Sun, X.-L., Zhang, W., & Lu, X.-Y. (2011) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710000945 · Cited by 137 · see citing works

Aggression and defeat: persistent effects on cocaine self-administration and gene expression in peptidergic and aminergic mesocorticolimbic circuits

Miczek, K. A., Covington, H. E., Nikulina, E. M., & Hammer, R. P. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2003.11.005 · Cited by 136 · see citing works

Divergent medial amygdala projections regulate approach–avoidance conflict behavior

Miller, S. M., Marcotulli, D., Shen, A., & Zweifel, L. S. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0337-z · Cited by 112 · see citing works

Evidence for corticotropin-releasing factor regulation of serotonin in the lateral septum during acute swim stress: adaptation produced by repeated swimming

Price, M. L., Kirby, L. G., Valentino, R. J., & Lucki, I. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1114-2 · Cited by 115 · see citing works

The Effects of Social Defeat and Other Stressors on the Expression of Circadian Rhythms

Meerlo, P., Sgoifo, A., & Turek, F. W. (2002) · Stress · doi:10.1080/102538902900012323 · Cited by 111 · see citing works

Glucocorticoid interaction with aggression in non-mammalian vertebrates: Reciprocal action

Summers, C. H., Watt, M. J., Ling, T. J., Forster, G. L., Carpenter, R. E., Korzan, W. J., Lukkes, J. L., & Øverli, Ø. (2005) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2005.09.059 · Cited by 106 · see citing works

Neural background of glucocorticoid dysfunction‐induced abnormal aggression in rats: involvement of fear‐ and stress‐related structures

Halász, J., Liposits, Z., Kruk, M. R., & Haller, J. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01883.x · Cited by 105 · see citing works

Expression of c-fos gene activation during rough and tumble play in juvenile rats

Gordon, N. S., Kollack-Walker, S., Akil, H., & Panksepp, J. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(01)00762-6 · Cited by 103 · see citing works

c- fos mRNA Induction in Acute and Chronic Audiogenic Stress: Possible Role of the Orbitofrontal Cortex in Habituation

Campeau, S., Dolan, D. F., Akil, H., & Watson, S. J. (2002) · Stress · doi:10.1080/10253890290027895 · Cited by 99 · see citing works

Repeated social defeat increases reactive emotional coping behavior and alters functional responses in serotonergic neurons in the rat dorsal raphe nucleus

Paul, E. D., Hale, M. W., Lukkes, J. L., Valentine, M. J., Sarchet, D. M., & Lowry, C. A. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.01.006 · Cited by 84 · see citing works

Social descent with territory loss causes rapid behavioral, endocrine, and transcriptional changes in the brain

Maruska, K. P., Becker, L., Neboori, A., & Fernald, R. D. (2013) · Journal of Experimental Biology · doi:10.1242/jeb.088617 · Cited by 83 · see citing works

Stress, Synaptic Plasticity, and Psychopathology

Garcia, R. (2002) · Reviews in the Neurosciences · doi:10.1515/revneuro.2002.13.3.195 · Cited by 81 · see citing works

Social environment regulates corticotropin releasing factor, corticosterone and vasopressin in juvenile prairie voles

Ruscio, M. G., Sweeny, T., Hazelton, J., Suppatkul, P., & Sue Carter, C. (2007) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.08.004 · Cited by 81 · see citing works

The Retinohypothalamic tract: Comparison of axonal projection patterns from four major targets

Canteras, N. S., Ribeiro-Barbosa, É. R., Goto, M., Cipolla‐Neto, J., & Swanson, L. W. (2010) · Brain Research Reviews · doi:10.1016/j.brainresrev.2010.09.006 · Cited by 79 · see citing works

The distribution of fos immunoreactivity in rat brain following freezing and escape responses elicited by electrical stimulation of the inferior colliculus

Lamprea, M. R., Cárdenas, F. P., Vianna, D. M. L., Castilho, V. M., Cruz-Morales, S. E., & Brandão, M. L. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03036-6 · Cited by 78 · see citing works

Stress during adolescence alters behavioral sensitization to amphetamine

Kabbaj, M., Isgor, C., Watson, S. J., & Akil, H. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00188-4 · Cited by 76 · see citing works

Behavioural and Neuroendocrine Adaptations to Repeated Stress during Puberty in Male Golden Hamsters

Wommack, J. C., Salinas, A. G., Melloni, R. H., & Delville, Y. (2004) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2004.01233.x · Cited by 73 · see citing works

Differential expression of Fos protein in the rat brain induced by performance of avoidance or escape in the elevated T-maze

Silveira, M. C. L., Zangrossi, H., Viana, M. D. B., Silveira, R., & Graeff, F. G. (2001) · Behavioural Brain Research · doi:10.1016/s0166-4328(01)00233-9 · Cited by 71 · see citing works

Social defeat stress activates medial amygdala cells that express type 2 corticotropin-releasing factor receptor mRNA

Fekete, É. M., Zhao, Y., Li, C., Sabino, V., Vale, W. W., & Zorrilla, E. P. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.03.078 · Cited by 70 · see citing works

The fibroblast growth factor system is downregulated following social defeat

Turner, C. A., Calvo, N., Frost, D. O., Akil, H., & Watson, S. J. (2008) · Neuroscience Letters · doi:10.1016/j.neulet.2007.10.041 · Cited by 68 · see citing works

Brain responses to chronic social defeat stress: Effects on regional oxidative metabolism as a function of a hedonic trait, and gene expression in susceptible and resilient rats

Kanarik, M., O’Leary, A., Matrov, D., Kõiv, K., Sharp, T., Panksepp, J., & Harro, J. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.06.015 · Cited by 67 · see citing works

Coping with defeat: acute glucocorticoid and forebrain responses to social defeat vary with defeat episode behaviour

Walker, F. R., Masters, L. M., Dielenberg, R. A., & Day, T. A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.04.041 · Cited by 58 · see citing works

Repeated Social Defeat Selectively Increases FosB Expression and Histone H3 Acetylation in the Infralimbic Medial Prefrontal Cortex

Hinwood, M., Tynan, R. J., Day, T. A., & Walker, F. R. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq080 · Cited by 58 · see citing works

Brainstem origins of glutamatergic innervation of the rat hypothalamic paraventricular nucleus

Ziegler, D. R., Edwards, M., Ulrich‐Lai, Y. M., Herman, J. P., & Cullinan, W. E. (2012) · The Journal of Comparative Neurology · doi:10.1002/cne.23043 · Cited by 54 · see citing works

Immediate‐early gene response to repeated immobilization: Fos protein and arc mRNA levels appear to be less sensitive than c‐fos mRNA to adaptation

Ons, S., Rotllant, D., Marin‐Blasco, I., & Armario, A. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07242.x · Cited by 53 · see citing works

Activation of 5-HT1A autoreceptors in the dorsal raphe nucleus reduces the behavioral consequences of social defeat

Cooper, M. A., McIntyre, K. E., & Huhman, K. L. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.06.009 · Cited by 52 · see citing works

Corticotropin-Releasing Factor, Corticosteroids, Stress, and Sugar

Dallman, M. F., Viau, V., Bhatnagar, S., Gómez-Oliver, F., Laugero, K. D., & Bell, M. E. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50011-1 · Cited by 51 · see citing works

Agonistic encounters and brain activation in dominant and subordinate male greater long-tailed hamsters

Pan, Y., Xu, L., Young, K. A., Wang, Z., & Zhang, Z. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.05.001 · Cited by 49 · see citing works

Chronic stress produces enduring decreases in novel stress-evoked c-fosmRNA expression in discrete brain regions of the rat

Ostrander, M. M., Ulrich‐Lai, Y. M., Choi, D. C., Flak, J. N., Richtand, N. M., & Herman, J. P. (2009) · Stress · doi:10.3109/10253890802641966 · Cited by 45 · see citing works

Neural circuits for coping with social defeat

Diaz, V. E., & Lin, D. (2019) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2019.11.016 · Cited by 45 · see citing works

Repeated anabolic/androgenic steroid exposure during adolescence alters phosphate-activated glutaminase and glutamate receptor 1 (GluR1) subunit immunoreactivity in Hamster brain: correlation with offensive aggression

FISCHER, S., Ricci, L. A., & MELLONIJR, R. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.02.025 · Cited by 45 · see citing works

Mapping patterns of depression-related brain regions with cytochrome oxidase histochemistry: Relevance of animal affective systems to human disorders, with a focus on resilience to adverse events

Harro, J., Kanarik, M., Matrov, D., & Panksepp, J. (2011) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.02.016 · Cited by 44 · see citing works

Molecular Implications of Repeated Aggression: Th, Dat1, Snca and Bdnf Gene Expression in the VTA of Victorious Male Mice

Bondar, N. P., Boyarskikh, U. A., Kovalenko, I. L., Филипенко, М. Л., & Kudryavtseva, N. N. (2009) · PLoS ONE · doi:10.1371/journal.pone.0004190 · Cited by 44 · see citing works

Chronic social defeat downregulates the 5-HT1A receptor but not Freud-1 or NUDR in the rat prefrontal cortex

Kieran, N., Ou, X., & Iyo, A. H. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.12.032 · Cited by 43 · see citing works

Characterizing the behavioral and neuroendocrine features of susceptibility and resilience to social stress

Murra, D., Hilde, K. L., Fitzpatrick, A., Maras, P. M., Watson, S. J., & Akil, H. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100437 · Cited by 42 · see citing works

Maintenance of dominance status is necessary for resistance to social defeat stress in Syrian hamsters

Morrison, K. E., Bader, L. R., Clinard, C. T., Gerhard, D. M., Gross, S. E., & Cooper, M. A. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.05.041 · Cited by 41 · see citing works

Human Primary Olfactory Amygdala Subregions Form Distinct Functional Networks, Suggesting Distinct Olfactory Functions

Noto, T., Zhou, G., Yang, Q.-H., Lane, G., & Zelano, C. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.752320 · Cited by 38 · see citing works

Affective Neuronal Selection: The Nature of the Primordial Emotion Systems

Toronchuk, J. A., & Ellis, G. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00589 · Cited by 38 · see citing works

Lasting changes in neuronal activation patterns in select forebrain regions of aggressive, adolescent anabolic/androgenic steroid-treated hamsters

Ricci, L. A., Grimes, J. M., & MELLONIJR, R. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.10.025 · Cited by 38 · see citing works

Gene Expression in Aminergic and Peptidergic Cells During Aggression and Defeat: Relevance to Violence, Depression and Drug Abuse

Miczek, K. A., Nikulina, E. M., Takahashi, A., Covington, H. E., Yap, J. J., Boyson, C. O., Shimamoto, A., & de Almeida, R. M. M. (2011) · Behavior Genetics · doi:10.1007/s10519-011-9462-5 · Cited by 38 · see citing works

Sexual differentiation of neural mechanisms of stress sensitivity during puberty

Wright, E. C., Luo, P. X., Zakharenkov, H. C., Serna Godoy, A., Lake, A. A., Prince, Z. D., Sekar, S., Culkin, H. I., Ramirez, A. V., Dwyer, T., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2306475120 · Cited by 34 · see citing works

Effects of Social Stress on Hormones, Brain, and Behavior

Blanchard, D. C., McKittrick, C. R., Blanchard, R. J., & Hardy, M. P. (2002) · Elsevier eBooks · doi:10.1016/b978-012532104-4/50015-9 · Cited by 33 · see citing works

Social Defeat Stress, Sex, and Addiction-Like Behaviors

Shimamoto, A. (2018) · International review of neurobiology · doi:10.1016/bs.irn.2018.07.009 · Cited by 35 · see citing works

Long‐term effects of a single exposure to immobilization: A C‐fos mRNA study of the response to the homotypic stressor in the rat brain

Vallès, A., Martı́, O., & Armario, A. (2006) · Journal of Neurobiology · doi:10.1002/neu.20252 · Cited by 31 · see citing works

Brain circuits mediating baroreflex bradycardia inhibition in rats: an anatomical and functional link between the cuneiform nucleus and the periaqueductal grey

Netzer, F., Bernard, J., Verberne, A. J. M., Hamon, M., Camus, F., Benoliel, J. J., & Sévoz‐Couche, C. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2010.203737 · Cited by 30 · see citing works

Lack of elevations in glucocorticoids correlates with dysphoria-like behavior after repeated social defeat

Bowens, N. H., Heydendael, W., Bhatnagar, S., & Jacobson, L. (2011) · Physiology & Behavior · doi:10.1016/j.physbeh.2011.10.032 · Cited by 28 · see citing works

Persistent activation of select forebrain regions in aggressive, adolescent cocaine-treated hamsters

Knyshevski, I., Connor, D. F., Harrison, R. J., Ricci, L. A., & Melloni, R. H. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.11.027 · Cited by 27 · see citing works

Sexual experience modulates neuronal activity in male Japanese quail.

Can, A., Domjan, M., & Delville, Y. (2007) · Hormones and Behavior · doi:10.1016/j.yhbeh.2007.07.011 · Cited by 26 · see citing works

Changes in the Expression of Monoaminergic Genes under the Influence of Repeated Experience of Agonistic Interactions: From Behavior to Gene

Kudryavtseva, N. N., Филипенко, М. Л., Bakshtanovskaya, I. V., Avgustinovich, D. F., Алексеенко, О. В., & Beilina, A. G. (2004) · Russian Journal of Genetics · doi:10.1023/b:ruge.0000033307.59669.d6 · Cited by 24 · see citing works

Psychological and physiological stressors

(2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80041-0 · Cited by 24 · see citing works

Stimulatory and inhibitory regulators of the hypothalamo–pituitary–adrenocortical axis

Jessop, D. S. (1999) · Best Practice & Research Clinical Endocrinology & Metabolism · doi:10.1053/beem.1999.0039 · Cited by 24 · see citing works

Pubertal testosterone programs context-appropriate agonistic behavior and associated neural activation patterns in male Syrian hamsters

Lorme, K. C. D., & Sisk, C. L. (2013) · Physiology & Behavior · doi:10.1016/j.physbeh.2013.02.003 · Cited by 23 · see citing works

Forebrain glucocorticoid receptor gene deletion attenuates behavioral changes and antidepressant responsiveness during chronic stress

Jacobson, L. (2014) · Brain Research · doi:10.1016/j.brainres.2014.07.054 · Cited by 21 · see citing works

Chronic vortioxetine treatment in rodents modulates gene expression of neurodevelopmental and plasticity markers

Waller, J. A., Tamm, J. A., Abdourahman, A., Pehrson, A. L., Li, Y., Cajina, M., & Sánchez, C. (2017) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2016.11.014 · Cited by 20 · see citing works

Food competition and social experience effects on V1a receptor binding in the forebrain of male Long–Evans hooded rats

Askew, A., González, F., Stahl, J. M., & Karom, M. C. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.08.001 · Cited by 19 · see citing works

Genomic modules and intramodular network concordance in susceptible and resilient male mice across models of stress

Caradonna, S. G., Zhang, T., O’Toole, N., Shen, M., Khalil, H., Einhorn, N. R., Wen, X., Parent, C. I., Lee, F. S., Akil, H., et al. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01219-8 · Cited by 18 · see citing works

Distribution of methionine and leucine enkephalin neurons within the social behavior circuitry of the male Syrian hamster brain

Holt, A. G., & Newman, S. W. (2004) · Brain Research · doi:10.1016/j.brainres.2004.09.034 · Cited by 18 · see citing works

Short-Term Cold Exposure May Cause a Local Decrease of Neuropeptide Y in the Rat Hypothalamus

Park, J., Lee, H. K., Shin, M. W., Kim, S. J., Noh, S. Y., Shin, J. G., & Yu, W. S. (2007) · Molecules and Cells · doi:10.1016/s1016-8478(23)07393-4 · Cited by 18 · see citing works

The serotonin system in the hippocampus CA3 involves in effects of CSDS on social recognition in adult female mandarin voles (Microtus mandarinus)

Wang, L., He, Z., Zhu, Z., Yuan, W., Cai, W., Li, L., Zhang, J., Hou, W., Yang, Y., Zhang, X., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109704 · Cited by 16 · see citing works

The Contribution of Immediate Early Genes to the Understanding of Brain Processing of Stressors

Armario, A. (2006) · Springer eBooks · doi:10.1007/978-0-387-33604-6_11 · Cited by 16 · see citing works

Social Stress Effects on Hormones, Brain, and Behavior

McKittrick, C. R., Blanchard, D. C., Hardy, M. P., & Blanchard, R. J. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00009-7 · Cited by 14 · see citing works

Sensory Contact Model: Protocol, Control, ApplicationsPreprint

Kudryavtseva, N. N. (2009) · Nature Precedings · doi:10.1038/npre.2009.3299.1 · Cited by 14 · see citing works

Update on neurobiological mechanisms of fear: illuminating the direction of mechanism exploration and treatment development of trauma and fear-related disorders

Li, Y., Zhi, W.-J., Qi, B., Wang, L.-F., & Hu, X. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1216524 · Cited by 10 · see citing works

Hypothalamic Goal-directed Behavior – Ingestive, Reproductive and Defensive

Canteras, N. S. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10020-2 · Cited by 12 · see citing works

Dominance status alters restraint-induced neural activity in brain regions controlling stress vulnerability

Cooper, M. A., Seddighi, S., Barnes, A., Grizzell, J. A., Dulka, B. N., & Clinard, C. T. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.06.003 · Cited by 11 · see citing works

Chronic social stress in puberty alters appetitive male sexual behavior and neural metabolic activity

Bastida, C. C., Puga, F., Gonzalez-Lima, F., Jennings, K. J., Wommack, J. C., & Delville, Y. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.05.002 · Cited by 10 · see citing works

Stress-induced differences in the limbic system Fos expression are more pronounced in rats differing in responsiveness to novelty than social position

Majkutewicz, I., Myślińska, D., Jerzemowska, G., Plucińska, K., Listowska, M., Grembecka, B., Podlacha, M., & Wrona, D. (2012) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2012.06.011 · Cited by 9 · see citing works

The influence of acute and chronic open-field exposure on the hippocampal formation: an immunohistochemical study.

Badowska‐Szalewska, E., Klejbor, I., Dziwiatkowski, J., Spodnik, J. H., & Moryś, J. (2006) · PubMed · Cited by 9 · see citing works

Plasma Glucocorticoids and ACTH Levels During Different Periods of Activity in the European Beaver (Castor fiber L.)

Czerwińśka, J., Chojnowska, K., Kamiński, T., Bogacka, I., Panasiewicz, G., Smolińska, N., & Kamińska, B. (2015) · Folia Biologica · doi:10.3409/fb63_4.229 · Cited by 9 · see citing works

The immunoreactivity of c-Fos, NGF and its receptor TrkA after open-field exposure in the central and medial nuclei of the rat amygdala.

Badowska‐Szalewska, E., Ludkiewicz, B., Domaradzka-Pytel, B., Dziewíatkowski, J., Spodnik, J. H., & Moryś, J. (2006) · PubMed · Cited by 9 · see citing works

Human threat circuits: Threats of pain, aggressive conspecific, and predator elicit distinct BOLD activations in the amygdala and hypothalamus

Bertram, T., Ayala, D. H., Huber, M., Brandl, F., Starke, G., Sorg, C., & Bratec, S. M. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.1063238 · Cited by 8 · see citing works

Large-scale animal model study uncovers altered brain pH and lactate levels as a transdiagnostic endophenotype of neuropsychiatric disorders involving cognitive impairmentPreprint

Hagihara, H., Shoji, H., Hattori, S., Sala, G., Takamiya, Y., Tanaka, M., Ihara, M., Shibutani, M., Hatada, I., Hori, K., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.02.428362 · Cited by 8 · see citing works

Oxytocin treatment rescues irritability-like behavior in Cc2d1a conditional knockout mice

Cheng, K., Hung, Y.-C., Ling, P., & Hsu, K. (2024) · Neuropsychopharmacology · doi:10.1038/s41386-024-01920-4 · Cited by 5 · see citing works

The Fragrant Power of Collective Fear

Harb, R., & Taulor, J. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0123908 · Cited by 5 · see citing works

Chronic social defeat alters behaviors and neuronal activation in the brain of female Mongolian gerbils

Pan, Y., Mou, Q., Huang, Z., Chen, S., Shi, Y., Ye, M., Shao, M., & Wang, Z. (2023) · Behavioural Brain Research · doi:10.1016/j.bbr.2023.114456 · Cited by 3 · see citing works

Immunoreactivity of c-Fos, NGF and its receptor TrkA in the periventricular zone of the rat hypothalamus after open field exposure.

Badowska‐Szalewska, E., Klejbor, I., Ludkiewicz, B., Domaradzka-Pytel, B., Dziewíatkowski, J., Spodnik, J. H., & Moryś, J. (2006) · PubMed · Cited by 4 · see citing works

Aggression and Defense, Neurohormonal Mechanisms of

Blanchard, R. J., Markham, C. M., & Blanchard, D. C. (2005) · Wiley eBooks · doi:10.1002/0470018860.s00440 · Cited by 3 · see citing works

Glucocorticoids Regulate Kisspeptin Neurons during Stress and Contribute to Infertility and Obesity in Leptin-Deficient Mice

Wang, O. (2012) · Digital Access to Scholarship at Harvard (DASH) (Harvard University) · Cited by 2 · see citing works

Stress alters hypothalamic gene expression in adolescent male Golden hamsters

Moran, K. M., Milewski, T. M., Curley, J. P., & Delville, Y. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70067 · Cited by 1 · see citing works

Brain changes underlying the long-term effects of a single previous exposure to emotional or systemic stressors in rats a view from the hypothalamic-pituitary-adrenal axis

Vallès, A. (2003) · TDX (Tesis Doctorals en Xarxa) · Cited by 1 · see citing works

Genomic Modules and Intramodular Network Convergency of Susceptibility and Resilience in Multimodeled Stress in Male MicePreprint

Marrocco, J., Caradonna, S. G., Zhang, T., O’Toole, N., Shen, M., Khalil, H., Einhorn, N. R., Wen, X., Parent, C. I., Lee, F. S., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.06.30.450390 · Cited by 1 · see citing works

Análise de sistemas hipotalâmicos envolvidos na organização da defesa intraespecífica.

Motta, S. C. (2010) · doi:10.11606/t.42.2010.tde-27092010-120440

Persistent c-fos expression in the brains of mice with chronic social stress

Matsuda, S., Peng, H., Yoshimura, H., Wen, T., Fukuda, T., & Sakanaka, M. (1996) · Neuroscience Research · doi:10.1016/s0168-0102(96)01088-7 · Cited by 157 · see citing works

Mapping Brain Response to Social Stress in Rodents With c-fos Expression: A Review

Martı́nez, M., Calvo-Torrent, A., & Herbert, J. (2002) · Stress · doi:10.1080/102538902900012369 · Cited by 167 · see citing works

Adaptation in patterns of c‐fos expression in the brain associated with exposure to either single or repeated social stress in male rats

Martı́nez, M., Phillips, P. J., & Herbert, J. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00011.x · Cited by 253 · see citing works

Social Stress in Hamsters: Defeat Activates Specific Neurocircuits within the Brain

Kollack‐Walker, S., Watson, S. J., & Akil, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-22-08842.1997 · Cited by 253 · see citing works

Chronic stress produces enduring decreases in novel stress-evoked c-fosmRNA expression in discrete brain regions of the rat

Ostrander, M. M., Ulrich‐Lai, Y. M., Choi, D. C., Flak, J. N., Richtand, N. M., & Herman, J. P. (2009) · Stress · doi:10.3109/10253890802641966 · Cited by 45 · see citing works