Mechanisms underlying enhanced contractile response to endothelin-1 in diabetic rat basilar artery

被引:39
|
作者
Matsumoto, T [1 ]
Yoshiyama, S [1 ]
Kobayashi, T [1 ]
Kamata, K [1 ]
机构
[1] Hoshi Univ, Inst Med Chem, Dept Physiol & Morphol, Shinagawa Ku, Tokyo 1428501, Japan
关键词
basilar artery; contraction; diabetes; endothelin; nitric oxide; streptozotocin;
D O I
10.1016/j.peptides.2004.07.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated the influence of streptozotocin-induced diabetes on the responsiveness of the rat basilar artery to endothelin-1 (ET-1) and nitric oxide (NO), which is known to counteract ET-1. In basilar arteries isolated from diabetic rats: (a) the ET-1-induced contraction was enhanced, (b) the contraction induced by N-G-nitro-L-arginine [a nitric oxide synthase (NOS) inhibitor] was weaker, and (c) the levels of the mRNAs for ETA/ETB receptors and prepro-ET-1, but not for NOS, were significantly elevated (all versus age-matched controls). These data indicate that ET-1-induced vasoconstriction may be increased in the diabetic rat basilar artery, and that this hyper-reactivity to ET-1 may be due to an overproduction of ET-1, an up-regulation of ETA/ETB receptors, and a defect in the bioavailability of NO. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1985 / 1994
页数:10
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