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Enhanced Up‐Regulation of Corticotropin‐Releasing Hormone Gene Expression in Response to Restraint Stress in the Hypothalamic Paraventricular Nucleus of Oxytocin Gene‐Deficient Male Mice
Author(s) -
Nomura M.,
Saito J.,
Ueta Y.,
Muglia L. J.,
Pfaff D. W.,
Ogawa S.
Publication year - 2003
Publication title -
journal of neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.062
H-Index - 116
eISSN - 1365-2826
pISSN - 0953-8194
DOI - 10.1046/j.1365-2826.2003.01095.x
Subject(s) - oxytocin , endocrinology , medicine , supraoptic nucleus , vasopressin , corticotropin releasing hormone , hypothalamus , neuropeptide , gene expression , in situ hybridization , biology , hormone , oxytocin receptor , gene , receptor , biochemistry
Abstract The neuropeptide oxytocin is released not only into the blood, but also within the brain in response to various stressors. Accumulating evidence suggests that central oxytocin may play a major role in the regulation of neuroendocrine responses to stress. In the present study, using the oxytocin knockout mouse model, we tested whether oxytocin might act to attenuate stress‐induced up‐regulation of corticotropin‐releasing hormone (CRH) mRNA expression in the brain. The expression of CRH mRNA in the paraventricular nucleus (PVN) after 4 h of restraint stress was examined in oxytocin gene‐deficient (OTKO), wild‐type and heterozygous male mice using in situ hybridization histochemistry. We found that basal levels of CRH mRNA were not different among the three genotypes. Although restraint stress resulted in a significant increase of CRH mRNA expression in the PVN regardless of genotype, the degree of stress induced‐up‐regulation was significantly higher in OTKO mice than in wild‐type mice. The effects of restraint stress on the expression of the arginine vasopressin (AVP) and the oxytocin genes were also examined. Unlike CRH mRNA, basal expression (in nonstressed control groups) of AVP mRNA in OTKO mice, as well as oxytocin mRNA in heterozygous mice, was significantly lower in the PVN and the supraoptic nucleus than in wild‐type mice. After restraint stress, the expression of AVP mRNA was significantly increased in the PVN of OTKO mice compared to the nonstressed control group, whereas the expression of both AVP and oxytocin mRNA were unchanged in the PVN and the supraoptic nucleus of wild‐type and heterozygous mice. Finally, in a separate set of mice, restraint stress‐induced Fos expression was also examined in several brain regions involved in stress response, including the lateral septum, the bed nucleus of the stria terminalis (BNST), the medial preoptic area, the PVN, the medial and central amygdala using immunohistochemistry. After 90 min of restraint stress, the number of Fos‐expressing cells significantly increased in all brain regions examined regardless of genotype. However, the number of stress‐induced Fos‐expressing cells in the BNST and the medial amygdala of OTKO mice was significantly lower than in wild‐type mice. Collectively, the findings in the present study suggest that oxytocin may regulate stress‐induced CRH gene expression in the PVN. Furthermore, neuronal activity in the BNST and the medial amygdala may be involved in this neuroendocrine regulatory system.