4.5 Article

Decreased response to social defeat stress in μ-opioid-receptor knockout mice

期刊

PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR
卷 99, 期 4, 页码 676-682

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbb.2011.06.008

关键词

Chronic social defeat stress; mu-opioid-receptor knockout; Behavior; Hippocampus; Brain-derived neurotrophic factor

资金

  1. Ministry of Health, Labor and Welfare of Japan
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan [17022007, 18023007]
  3. National Institute on Drug Abuse (NIH/DHHS, USA)
  4. Grants-in-Aid for Scientific Research [17022007, 18023007] Funding Source: KAKEN

向作者/读者索取更多资源

Substantial evidence exists that opioid systems are involved in stress response and that changes in opioid systems in response to stressors affect both reward and analgesia. Reportedly, mice suffering chronic social defeat stress subsequently show aversion to social contact with unfamiliar mice. To further examine the role of opioid systems in stress response, the behavioral and neurochemical effects of chronic social defeat stress (psychosocial stress) were evaluated in mu-opioid-receptor knockout (MOR-KO) mice. Aversion to social contact was induced by chronic social defeat stress in wild-type mice but was reduced in MOR-KO mice. Moreover, basal expression of brain-derived neurotrophic factor (BDNF) mRNA in MOR-KO mice hippocampi was significantly lower than in wild-type mice. Psychosocial stress significantly decreased BDNF mRNA expression in wild-type mice but did not affect BDNF expression in MOR-KO mice; no difference in basal levels of plasma corticosterone was observed. These results suggest that the mu-opioid receptor is involved in the behavioral sequelae of psychosocial stress and consequent regulation of BDNF expression in the hippocampus, and may play an important role in psychiatric disorders for which stress is an important predisposing or precipitating factor, such as depression, posttraumatic stress disorder, and social anxiety disorder. (C) 2011 Elsevier Inc. All rights reserved.

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