Time matters: pathological effects of repeated psychosocial stress during the active, but not inactive, phase of male mice.

Recent findings in rats indicated that the physiological consequences of repeated restraint stress are dependent on the time of day of stressor exposure. To investigate whether this is also true for clinically more relevant psychosocial stressors and whether repeated stressor exposure during the light phase or dark phase is more detrimental for an organism, we exposed male C57BL/6 mice to social defeat (SD) across 19 days either in the light phase between Zeitgeber time (ZT)1 and ZT3 (SDL mice) or in the dark phase between ZT13 and ZT15 (SDD mice). While SDL mice showed a prolonged increase in adrenal weight and an attenuated adrenal responsiveness to ACTH in vitro after stressor termination, SDD mice showed reduced dark phase home-cage activity on observation days 7, 14, and 20, flattening of the diurnal corticosterone rhythm, lack of social preference, and higher in vitro IFNγ secretion from mesenteric lymph node cells on day 20/21. Furthermore, the colitis-aggravating effect of SD was more pronounced in SDD than SDL mice following dextran sulfate sodium treatment. In conclusion, the present findings demonstrate that repeated SD effects on behavior, physiology, and immunology strongly depend on the time of day of stressor exposure. Whereas physiological parameters were more affected by SD during the light/inactive phase of mice, behavioral and immunological parameters were more affected by SD during the dark phase. Our results imply that repeated daily SD exposure has a more negative outcome when applied during the dark/active phase. By contrast, the minor physiological changes seen in SDL mice might represent beneficial adaptations preventing the formation of those maladaptive consequences.

[1]  S. Reber,et al.  Chronic psychosocial stress results in sensitization of the HPA axis to acute heterotypic stressors despite a reduction of adrenal in vitro ACTH responsiveness , 2012, Psychoneuroendocrinology.

[2]  D. Slattery,et al.  Behavioural consequences of two chronic psychosocial stress paradigms: Anxiety without depression , 2012, Psychoneuroendocrinology.

[3]  S. Reber Stress and animal models of inflammatory bowel disease—An update on the role of the hypothalamo–pituitary–adrenal axis , 2012, Psychoneuroendocrinology.

[4]  Jie Shi,et al.  Chronic unpredictable stress induces a reversible change of PER2 rhythm in the suprachiasmatic nucleus , 2011, Brain Research.

[5]  P. Konturek,et al.  Gut clock: implication of circadian rhythms in the gastrointestinal tract. , 2011, Journal of physiology and pharmacology : an official journal of the Polish Physiological Society.

[6]  R. Murison,et al.  Neuroscience and Biobehavioral Reviews Stress Revisited: a Critical Evaluation of the Stress Concept , 2022 .

[7]  T. Dinan,et al.  The effects of repeated social interaction stress on behavioural and physiological parameters in a stress-sensitive mouse strain , 2011, Behavioural Brain Research.

[8]  L. Carboni,et al.  Different susceptibility to social defeat stress of BalbC and C57BL6/J mice , 2011, Behavioural Brain Research.

[9]  M. Millan,et al.  Agomelatine, the first melatonergic antidepressant: discovery, characterization and development , 2010, Nature Reviews Drug Discovery.

[10]  G. Chrousos,et al.  Interactions of the circadian CLOCK system and the HPA axis , 2010, Trends in Endocrinology & Metabolism.

[11]  E. Nestler,et al.  Adult hippocampal neurogenesis is functionally important for stress-induced social avoidance , 2010, Proceedings of the National Academy of Sciences.

[12]  B. Czéh,et al.  Diurnal rhythm and stress regulate dendritic architecture and spine density of pyramidal neurons in the rat infralimbic cortex , 2009, Behavioural Brain Research.

[13]  A. Shalev,et al.  Posttraumatic stress disorder and stress-related disorders. , 2009, The Psychiatric clinics of North America.

[14]  Y. Sakaki,et al.  Ontogeny of Circadian Organization in the Rat , 2009, Journal of biological rhythms.

[15]  N. Singewald,et al.  Effect of chronic psychosocial stress-induced by subordinate colony (CSC) housing on brain neuronal activity patterns in mice , 2009, Stress.

[16]  F. Obermeier,et al.  Aggravation of DSS-induced colitis after chronic subordinate colony (CSC) housing is partially mediated by adrenal mechanisms , 2008, Stress.

[17]  Scott J. Russo,et al.  Molecular Adaptations Underlying Susceptibility and Resistance to Social Defeat in Brain Reward Regions , 2007, Cell.

[18]  M. Riva,et al.  The interaction between the internal clock and antidepressant efficacy , 2007 .

[19]  W. Falk,et al.  Adrenal insufficiency and colonic inflammation after a novel chronic psycho-social stress paradigm in mice: implications and mechanisms. , 2007, Endocrinology.

[20]  S. Higuchi,et al.  Chronobiological disturbances with hyperthermia and hypercortisolism induced by chronic mild stress in rats , 2006, Behavioural Brain Research.

[21]  W. Falk,et al.  Chronic intermittent psychosocial stress (social defeat/overcrowding) in mice increases the severity of an acute DSS-induced colitis and impairs regeneration. , 2006, Endocrinology.

[22]  B. L. Langille,et al.  Endothelium-Independent Flow-Induced Dilation in the Mouse Carotid Artery , 2006, Journal of Vascular Research.

[23]  Danielle L. Graham,et al.  Essential Role of BDNF in the Mesolimbic Dopamine Pathway in Social Defeat Stress , 2006, Science.

[24]  S. Kasper,et al.  Actigraphy in Patients with Seasonal Affective Disorder and Healthy Control Subjects Treated with Light Therapy , 2005, Biological Psychiatry.

[25]  R. Dantzer,et al.  Social factors and individual vulnerability to chronic stress exposure , 2005, Neuroscience & Biobehavioral Reviews.

[26]  D. Nutt,et al.  Invited review: the evolution of antidepressant mechanisms , 2004, Fundamental & clinical pharmacology.

[27]  Z. Tóth,et al.  Role of hypothalamic inputs in maintaining pituitary-adrenal responsiveness in repeated restraint. , 2003, American journal of physiology. Endocrinology and metabolism.

[28]  W. Falk,et al.  Contrasting activity of cytosin–guanosin dinucleotide oligonucleotides in mice with experimental colitis , 2003, Clinical and experimental immunology.

[29]  A. Johnson,et al.  Behavioral and cardiovascular changes in the chronic mild stress model of depression , 2003, Physiology & Behavior.

[30]  P. Meerlo,et al.  Intermittent Exposure to Social Defeat and Open-field Test in Rats: Acute and Long-term Effects on ECG, Body Temperature and Physical Activity , 2002, Stress.

[31]  Steven A. Brown,et al.  Resetting of circadian time in peripheral tissues by glucocorticoid signaling. , 2000, Science.

[32]  H. Westenberg,et al.  Anxiety disorders: a review of tricyclic antidepressants and selective serotonin reuptake inhibitors , 2000, Acta psychiatrica Scandinavica. Supplementum.

[33]  S. Levenstein,et al.  Stress and exacerbation in ulcerative colitis: a prospective study of patients enrolled in remission , 2000, American Journal of Gastroenterology.

[34]  Y Sakaki,et al.  Resetting central and peripheral circadian oscillators in transgenic rats. , 2000, Science.

[35]  R. Hirschfeld History and evolution of the monoamine hypothesis of depression. , 2000, The Journal of clinical psychiatry.

[36]  F. Holsboer,et al.  Behavioural profiles of two Wistar rat lines selectively bred for high or low anxiety-related behaviour , 1998, Behavioural Brain Research.

[37]  J. Volaufova,et al.  Effect of restraint stress on food intake and body weight is determined by time of day. , 1997, American journal of physiology. Regulatory, integrative and comparative physiology.

[38]  F. Chaouloff,et al.  Differential effects of social stress on central serotonergic activity and emotional reactivity in Lewis and spontaneously hypertensive rats , 1997, Neuroscience.

[39]  M. Papp,et al.  Effect of chronic mild stress on circadian rhythms in the locomotor activity in rats , 1996, Pharmacology Biochemistry and Behavior.

[40]  J. Moreau,et al.  Chronic mild stress‐induced anhedonia model of depression: sleep abnormalities and curative effects of electroshock treatment , 1995, Behavioural pharmacology.

[41]  B. Natelson,et al.  Repeated stress persistently elevates morning, but not evening, plasma corticosterone levels in male rats , 1994, Physiology & Behavior.

[42]  K. Miczek,et al.  Long-term impairment of autonomic circadian rhythms after brief intermittent social stress , 1993, Physiology & Behavior.

[43]  D. Lesieur,et al.  Novel naphthalenic ligands with high affinity for the melatonin receptor. , 1992, Journal of medicinal chemistry.

[44]  N. Sachser,et al.  Social stress in guinea pigs , 1989, Physiology & Behavior.

[45]  C. Bowden,et al.  Rethinking depression and the actions of antidepressants: uncovering the links between the neural and behavioral elements. , 2010, Journal of affective disorders.

[46]  P. Buckley Essential Role of BDNF in the Mesolimbic Dopamine Pathway in Social Defeat StressBerton O, McClung CA, DiLeone RJ, et al (Univ of Texas Southwestern Med Ctr, Dallas; Tufts Univ School of Medicine, Boston) Science 311:864–868, 2006§ , 2007 .

[47]  M. Sánchez,et al.  Neuroendocrine and immunocytochemical demonstrations of decreased hypothalamo-pituitary-adrenal axis responsiveness to restraint stress after long-term social isolation. , 1998, Endocrinology.

[48]  I. Heuser,et al.  Diurnal activity and pulsatility of the hypothalamus-pituitary-adrenal system in male depressed patients and healthy controls. , 1997, The Journal of clinical endocrinology and metabolism.

[49]  T. Byers,et al.  Relevance of major stress events as an indicator of disease activity prevalence in inflammatory bowel disease. , 1991, Behavioral medicine.

[50]  P. Willner Animal models of depression: an overview. , 1990, Pharmacology & therapeutics.

[51]  J. Meyerhoff,et al.  Diurnal variation in neuroendocrine response to stress in rats: plasma ACTH, beta-endorphin, beta-LPH, corticosterone, prolactin and pituitary cyclic AMP responses. , 1986, Neuroendocrinology.

[52]  J. Meyerhoff,et al.  Diurnal Variation in Neuroendocrine Response to Stress in Rats: Plasma ACTH, β-Endorphin, β-LPH, Corticosterone, Prolactin and Pituitary Cyclic AMP Responses , 1986 .