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Am J Physiol Endocrinol Metab 291: E147-E151, 2006. First published February 7, 2006; doi:10.1152/ajpendo.00005.2006
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Attenuated stress-induced catecholamine release in mice lacking the vasopressin V1b receptor

Shuji Itoh,1 Sakiko Yamada,1 Toyoki Mori,1 Takashi Miwa,1 Katsura Tottori,1 Yasufumi Uwahodo,1 Yoshitaka Yamamura,1 Meiko Fukuda,2 Koji Yamamoto,2 Akito Tanoue,3 and Gozoh Tsujimoto4

1Research Institute of Pharmacological and Therapeutical Development; 2Department of Toxicology, Tokushima Research Institute, Otsuka Pharmaceutical, Kagasuno, Tokushima; 3Department of Pharmacology, National Research Institute for Child Health and Development, Okura, Tokyo; and 4Department of Genomic Drug Discovery Science, Graduate School of Pharmaceutical Sciences, Kyoto University Faculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto, Japan

Submitted 6 January 2006 ; accepted in final form 30 January 2006

Vasopressin V1b receptor is specifically expressed in the pituitary and mediates adrenocorticotropin release, thereby regulating stress responses via its corticotropin releasing factor-like action. In the present study we examined catecholamine release in response to two types of stress in mice lacking the V1b receptor gene (V1bR–/– mice) vs. wild-type mice. There were no significant differences in the basal plasma levels of catecholamines between the two genotypes. In response to stress induced by forced swimming, norepinephrine (NE), but not epinephrine (E) or dopamine (DA), was increased in wild-type mice, whereas the increases in NE and DA were not observed in V1bR–/– mice. In wild-type mice, E, but not NE or DA, was increased in response to social isolation stress, whereas the increase in E was not observed in V1bR–/– mice. These results suggest that the V1b receptor regulates stress-induced catecholamine release. Because it has been suggested that arginine-vasopressin (AVP) is related to the development of depression, we also evaluated immobility time in the forced swimming test, and we found no significant change in V1bR–/– mice. Taken together, these findings suggest that, in addition to the previously elucidated effect on the hypothalamic-pituitary-adrenal axis, vasopressin activity via V1b receptors regulates stress-induced catecholamine release.

V1b receptor knockout mice; norepinephrine; epinephrine; dopamine; immobility time in the forced swimming test



Address for reprint requests and other correspondence: T. Mori, Research Institute of Pharmacological and Therapeutical Development, Otsuka Pharmaceutical, Ltd., 463–10, Kagasuno, Kawauchi-cho, Tokushima 771–0192, Japan (e-mail: to_mori{at}research.otsuka.co.jp)




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[Abstract] [Full Text] [PDF]




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