Effects of endothelin-1 and nitric oxide on proliferation of cultured guinea pig bronchial smooth muscle cells

被引:15
作者
Kizawa, Y [1 ]
Ohuchi, N [1 ]
Saito, K [1 ]
Kusama, T [1 ]
Murakami, H [1 ]
机构
[1] Nihon Univ, Coll Pharm, Dept Physiol & Anat, Funabashi, Chiba 2748555, Japan
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 2001年 / 128卷 / 04期
关键词
endothelin-1; NO; mitogenesis; EGF; SIN-1; ODQ; BQ-123; BQ-788; bronchus; smooth muscle; guinea pig;
D O I
10.1016/S1532-0456(01)00172-7
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
The proliferative effects of endothelin-1 (ET-1), both alone and in combination with epidermal growth factor (EGF), and the effect of nitric oxide (NO) on the cell proliferation were investigated in cultured guinea pig bronchial smooth muscle cells. ET-I (10-100 nM) alone augmented cell proliferation. and was additive to the effect of EGF (0.48 nM) in a concentration-dependent manner. An ETA antagonist, BQ-123 (10 muM) reduced the cell-proliferative effect of ET-I. whereas an ETB antagonist, BQ-788 (10 muM), did not influence the effect. A NO donor, SIN-I (10 nM-1 muM), reduced the cell-proliferative effect of ET-I in a concentration-dependent manner. The effect of SIN-1 (1 muM) was partly, but significantly, reversed by a soluble guanylyl cyclase inhibitor, ODQ(1 muM) These results suggest that ET-1 acts not only as a co-mitogen with EGF but also as a mitogen alone, and that its action is mediated through activation of ETA receptors. Therefore, ET-I may contribute to airway remodeling, a pathophysiological hallmark of asthma. In addition, NO, which is produced mainly in the airway epithelium and is partly mediated through cGMP-dependent pathway, may reduce the phenomenon. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:495 / 501
页数:7
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