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环磷酸鸟苷(cGMP)依赖性蛋白激酶I介导cGMP在小鼠心肌中的负性肌力作用。

cGMP-dependent protein kinase I mediates the negative inotropic effect of cGMP in the murine myocardium.

作者信息

Wegener Jörg W, Nawrath Hermann, Wolfsgruber Wiebke, Kühbandner Susanne, Werner Claudia, Hofmann Franz, Feil Robert

机构信息

Pharmakologisches Institut, Universität Mainz, Germany.

出版信息

Circ Res. 2002 Jan 11;90(1):18-20. doi: 10.1161/hh0102.103222.

Abstract

To study the role of cGMP-dependent protein kinase I (cGKI) for cardiac contractility, force of contraction (F(c)) was studied in electrically driven heart muscle from wild-type (WT) mice and from conventional and conditional cGKI knockout mice. Both 8-Br-cGMP and 8-pCPT-cGMP reduced Fc in cardiac muscle from juvenile WT but not from juvenile cGKI-null mutants. Similarly, the cGMP analogues reduced F(c) in forskolin-stimulated ventricular muscle from WT mice but not from cGKI-null mutants. In contrast, carbachol reduced F(c) in both groups of animals. 8-Br-cGMP reduced F(c) also in heart muscle from adult WT mice but not from adult cardiomyocyte-specific cGKI-knockout mice. These results demonstrate that cGKI mediates the negative inotropic effect of cGMP in the myocardium of juvenile and adult mice.

摘要

为研究环磷酸鸟苷依赖性蛋白激酶I(cGKI)对心脏收缩性的作用,我们在野生型(WT)小鼠以及常规和条件性cGKI基因敲除小鼠的电驱动心肌中研究了收缩力(F(c))。8-溴环磷酸鸟苷(8-Br-cGMP)和8-对氯苯硫基环磷酸鸟苷(8-pCPT-cGMP)均可降低幼年WT小鼠心肌的Fc,但对幼年cGKI基因敲除突变体无效。同样,cGMP类似物可降低WT小鼠福斯高林刺激的心室肌中的F(c),但对cGKI基因敲除突变体无效。相反,卡巴胆碱可降低两组动物的F(c)。8-Br-cGMP也可降低成年WT小鼠心肌的F(c),但对成年心肌细胞特异性cGKI基因敲除小鼠无效。这些结果表明,cGKI介导了cGMP在幼年和成年小鼠心肌中的负性变力作用。

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