Wegener Jörg W, Nawrath Hermann, Wolfsgruber Wiebke, Kühbandner Susanne, Werner Claudia, Hofmann Franz, Feil Robert
Pharmakologisches Institut, Universität Mainz, Germany.
Circ Res. 2002 Jan 11;90(1):18-20. doi: 10.1161/hh0102.103222.
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.
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。