Impaired arginine-vasopressin-induced aldosterone release from adrenal gland cells in mice lacking the vasopressin V1A receptor

被引:17
作者
Birumachi, Jun-ichi
Hiroyama, Masami
Fujiwara, Yoko
Aoyagi, Toshinori
Sanbe, Atsushi
Tanoue, Akito
机构
[1] Department of Pharmacology, National Research Institute for Child Health and Development, Setagaya-ku, Tokyo, 157-8535
关键词
arginine-vasopressin; vasopressin V-1A receptor-deficient mice; aldosterone; adrenal gland cells;
D O I
10.1016/j.ejphar.2007.03.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We examined aldosterone release in response to stimulation with arginine-vasopressin (AVP) using adrenal gland cells. AVP caused a significant increase in aldosterone release from the dispersed adrenal gland cells of wild-type mice (V1AR+/+) at concentrations from 0.1 mu M to 1 mu M. In contrast, AVP-induced aldosterone release was impaired in adrenal gland cells from mice lacking the vasopressin V-1A receptor (V1AR-/-), while adrenocorticotropic hormone (ACTH)-induced aldosterone release in V1AR-/- mice was not significantly different from that in V1AR+/+ mice. In addition, a vasopressin V-1A receptor-selective antagonist 1-[1[4-(3-acetylaminopropoxy)benzoyl]-4-pipeiidyl]-3,4-dihydro-2(1H)-quinolinone (OPC-21268) potently inhibited AVP-induced aldosterone release. Thus, our study clearly demonstrates that AVP-induced aldosterone release from adrenal gland cells is mediated via the vasopressin V-1A receptor in mice. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:226 / 230
页数:5
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