Ghrelin improves endothelial dysfunction through growth hormone-independent mechanisms in rats

被引:127
作者
Shimizu, Y
Nagaya, N [1 ]
Teranishi, Y
Imazu, M
Yamamoto, H
Shokawa, T
Kangawa, K
Kohno, N
Yoshizumi, M
机构
[1] Natl Cardiovasc Ctr, Dept Internal Med, Osaka, Japan
[2] Hiroshima Univ, Grad Sch Biomed Sci, Dept Mol & Internal Med, Hiroshima, Japan
[3] Hiroshima Univ, Grad Sch Biomed Sci, Dept Neurophysiol, Hiroshima, Japan
[4] Natl Cardiovasc Ctr, Inst Res, Dept Biochem, Osaka, Japan
[5] Hiroshima Univ, Grad Sch Biomed Sci, Dept Cardiovasc Physiol & Med, Hiroshima, Japan
关键词
endothelium; growth substances; nitric oxide; nitric oxide synthase; vasorelaxation;
D O I
10.1016/j.bbrc.2003.09.085
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
Ghrelin is a novel growth hormone (GH)-releasing peptide which was isolated from the stomach. We have reported that ghrelin causes vasorelaxation in rats through GH-independent mechanisms. We investigated whether ghrelin improves endothelial dysfunction. Ghrelin was subcutaneously administered to GH-deficient rats for three weeks. After isolation of the thoracic aorta, aortic ring tension was measured to evaluate vasorelaxation. Acetylcholine-induced vasorelaxation was impaired in GH-deficient rats given placebo compared to that in normal rats given placebo. GH-deficient rats treated with ghrelin, however, showed a significant increase in the maximal relaxation as compared with those given placebo. This improvement by ghrelin was inhibited by N-G-nitro-L-arginine methyl ester, a nonselective nitric oxide synthase (NOS) inhibitor. Western blot analysis demonstrated that treatment with ghrelin increased endothelial NOS (eNOS) expression in the aorta of GH-deficient rats. These results suggest that administration of ghrelin improves endothelial dysfunction and increases eNOS expression in rats through GH-independent mechanisms. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:830 / 835
页数:6
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