NONOates regulate KCl cotransporter-1 and-3 mRNA expression in vascular smooth muscle cells

被引:20
作者
Di Fulvio, M
Lauf, PK
Shah, SL
Adragna, NC
机构
[1] Wright State Univ, Sch Med, Dept Pharmacol & Toxicol, Dayton, OH 45435 USA
[2] Wright State Univ, Sch Med, Dept Physiol & Biophys, Dayton, OH 45435 USA
[3] Wright State Univ, Sch Med, Dept Cardiol, Dayton, OH 45435 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2003年 / 284卷 / 05期
关键词
nitric oxide; soluble guanylyl cyclase;
D O I
10.1152/ajpheart.00710.2002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nitric oxide (NO) donors regulate KCl cotransport (KCC) activity and cotransporter-1 and -3 (KCC1 and KCC3) mRNA expression in sheep erythrocytes and in primary cultures of rat vascular smooth muscle cells (VSMCs), respectively. In this study, we used NONOates as rapid and slow NO releasers to provide direct evidence implicating NO as a regulator of KCC3 gene expression at the mRNA level. In addition, we used the expression of KCC3 mRNA to further investigate the mechanism of action of these NO donors at the cellular level. Treatment of VSMCs with rapid NO releasers, like NOC-5 and NOC-9, as well as with the direct NO-independent soluble guanylyl cyclase (sGC) stimulator YC-1, acutely increased KCC3 mRNA expression in a concentration- and time-dependent manner. The slow NO releaser NOC-18 had no effect on KCC3 gene expression. A specific NO scavenger completely prevented the NONOate-induced KCC3 mRNA expression. Inhibition of sGC with LY-83583 blocked the NONOate- and YC-1-induced KCC3 mRNA expression. This study shows that in primary cultures of rat VSMCs, the fast NO releasers NOC-9 and NOC-5, but not the slow NO releaser NOC-18, acutely upregulate KCC3 mRNA expression in a NO/sGC-dependent manner.
引用
收藏
页码:H1686 / H1692
页数:7
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