Cited by 113Stress Responses and CortisolNeuroendocrine regulation and behaviorMemory and Neural Mechanisms

The DOI matches its Crossref record; 57 of the 59 references it cites were found in a registry or an index.

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

Kollack‐Walker, Don, Watson, Akil·1999·Journal of Neuroendocrinology

DOI 10.1046/j.1365-2826.1999.00354.x

Open this paper in CoChat — free account

Abstract

Chronic exposure to stress has been implicated in physical and mental illness, and such experiences can produce alterations in the connectivity and number of neurones within the brain to variations in the expression of specific genes. The purpose of this study was to determine how repeated exposure to social defeat affects neuronal activation patterns within the male Syrian hamster brain. Toward this end, the levels c-fos mRNA were compared among three groups: (1) handled controls (HC); (2) acutely defeated males (AD); and (3) chronically defeated males (15 min aggression daily, 7 days) exposed to an acute challenge (CD). Plasma glucocorticoids were also measured and compared among groups as an index of neuroendocrine activity. The results show a selective pattern of habituation of immediate early gene expression within the brains of chronically defeated males. In particular, c-fos mRNA levels were significantly decreased within the paraventricular nucleus of the hypothalamus (PVN), supraoptic nucleus of the hypothalamus, septohypothalamic nucleus, intermediate subdivision of the lateral septum, central amygdaloid nucleus, and the amygdalohippocampal area in the CD group exposed to an acute challenge when compared to males defeated only once. In contrast, c-fos expression within the anterior and ventromedial nuclei of the hypothalamus, dorsal periaqueductal grey, dorsal raphe, cuneiform nucleus, and locus coeruleus did not differ between AD and CD groups. Similarly, plasma le…

Integrity signals

Registry

Crossref · 10.1046/j.1365-2826.1999.00354.x

Cites

57 of 57 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

This paper’s full text isn’t openly available, 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?

The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
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
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
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
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
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
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
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 562
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
Opioid-Like Analgesia in Defeated Mice
Miczek, K. A., Thompson, M. L., & Shuster, L. (1982) · Science · doi:10.1126/science.7199758 · Cited by 418

Show all 59 references

Research works printed but not linked: 3

KupferDJBiological markers of depression. In: Feighner JPBoyer WF eds.The Diagnosis of Depression.New York: John Wiley & Sons 19917998
CullinanWE HermanJP HelmreichDL WatsonSJA neuroanatomy of stress. In: Friedman MJCharney DSDeutch AY eds.Neurobiological and Clinical Consequences of Stress: from Normal Adaptation to PTSD.New York: Raven Press Ltd 1995326
10.1037/0735-7044.102.1.77 · DOI

Sorted by citations

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
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
Stress and the social brain: behavioural effects and neurobiological mechanisms
Sandi, C., & Haller, J. (2015) · Nature reviews. Neuroscience · doi:10.1038/nrn3918 · Cited by 657
The many paths to fear
Gross, C. T., & Canteras, N. S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3301 · Cited by 596
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
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
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 463
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
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
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 222
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
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 181
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 177
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
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
Self-citation
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
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 161
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
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
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
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 119
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
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
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
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
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
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
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 90
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 90
Stress, Synaptic Plasticity, and Psychopathology
Garcia, R. (2002) · Reviews in the Neurosciences · doi:10.1515/revneuro.2002.13.3.195 · Cited by 81
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
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 82
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
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 77
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
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
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
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
Self-citation
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 71
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
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
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 53
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
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
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 52
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
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
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 48
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
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 45
Molecular Implications of Repeated Aggression: Th, Dat1, Snca and Bdnf Gene Expression in the VTA of Victorious Male MicePreprint
Bondar, N. P., Boyarskikh, U. A., Kovalenko, I. L., Филипенко, М. Л., & Kudryavtseva, N. N. (2008) · Nature Precedings · doi:10.1371/journal.pone.0004190 · Cited by 44
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
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 48
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
Human Primary Olfactory Amygdala Subregions Form Distinct Functional Networks, Suggesting Distinct Olfactory Functions
Noto, T., Zhou, G., Yang, Q., Lane, G., & Zelano, C. (2021) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2021.752320 · Cited by 44
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 39
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
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 40
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
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
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 36
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
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
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
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
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
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
Psychological and physiological stressors
(2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80041-0 · Cited by 24
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
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
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 23
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
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
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 21
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
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
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
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
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
Sensory Contact Model: Protocol, Control, ApplicationsPreprint
Kudryavtseva, N. N. (2009) · Nature Precedings · doi:10.1038/npre.2009.3299.1 · Cited by 14
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., Qi, B., Wang, L., & Hu, X. (2023) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2023.1216524 · Cited by 16
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
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 12
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
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
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
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
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
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 11
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
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
The Fragrant Power of Collective Fear
Harb, R., & Taulor, J. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0123908 · Cited by 5
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
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
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
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
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
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
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
Análise de sistemas hipotalâmicos envolvidos na organização da defesa intraespecífica.
Motta, S. C. (2010) · doi:10.11606/t.42.2010.tde-27092010-120440

Authors: Kollack‐Walker, Don, Watson, & Akil
Affiliations: University of Michigan (US)
Corresponding author: Kollack‐Walker
Venue: Journal of Neuroendocrinology
Publisher: Wiley
Published: 1999-07
Volume: 11
Issue: 7
Pages: 547-559
ISSN: 0953-8194 (ISSN-L)
1365-2826
DOI: 10.1046/j.1365-2826.1999.00354.x
OpenAlex: W1567486735
Cited by: 113
References: 59
Citations by year: 2025: 2 · 2024: 1 · 2023: 4 · 2022: 3 · 2021: 5 · 2019: 4 · 2018: 2 · 2017: 4 · 2016: 2 · 2015: 3 · 2014: 3 · 2013: 3 · 2012: 7
FWCI: 2.00
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 907 d)
Locations: Journal of Neuroendocrinology (publishedVersion)
PubMed (publishedVersion)
Deep Blue (University of Michigan) (submittedVersion)
Funders: National Institutes of Health (5p30hd018258-15)
National Institute of Mental Health (P01 MH 42251, P01MH042251)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (P-30 HD18258)
Topics: Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords: c-fos mRNA, social defeat, chronic stress, immediate early gene expression, hypothalamic paraventricular nucleus, supraoptic nucleus, central amygdala, plasma glucocorticoids, cortisol, corticosterone, hypothalamic-pituitary-adrenal axis, defensive behavior, neuroplasticity, golden hamster
MeSH terms: Aggression, Animals, Behavior, Animal, Brain, Corticosterone, Cricetinae, Hydrocortisone, Male, Mesocricetus, RNA, Messenger, Genes, fos, Genes, Immediate-Early

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

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

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