尼可地尔(SG-75)刺激冠状动脉鸟苷酸环化酶作为其血管舒张作用的机制。

K Schmidt, R Reich, W R Kukovetz
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引用次数: 0

摘要

由于有证据表明尼可地尔(sg75)通过增加cGMP水平来放松冠状动脉平滑肌,因此更密切地研究了这种血管扩张剂对牛冠状动脉可溶性鸟苷酸环化酶的影响。结果发现,尼可地尔对鸟苷酸环化酶的刺激呈剂量依赖性(3-30 mM),达到对照值的100倍。与硝普钠不同的是,与硝化甘油类似,半胱氨酸(0.5- 20mm)也需要获得这种刺激。除硫代水杨酸能部分模拟半胱氨酸的作用外,其他所研究的硫醇均无效。从时间过程研究中可以看出,尼可地尔诱导的鸟苷酸环化酶的刺激具有滞后期的特征,这可以通过与尼可地尔预孵育来避免。在亚甲基蓝、铁氰化物或对苯二酚的存在下,尼可地尔的刺激作用减弱。这些结果进一步证明:a)尼可拉地尔通过刺激鸟苷酸环化酶发挥其血管扩张作用;b)硝酸酯,如硝酸甘油或尼可拉地尔,至少在体外,仅在半胱氨酸或较小程度上的硫代水杨酸存在时才刺激酶。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stimulation of coronary guanylate cyclase by nicorandil (SG-75) as a mechanism of its vasodilating action.

Since there is evidence suggesting that nicorandil (SG-75) relaxes coronary arterial smooth muscle by increasing cGMP levels, the effects of this vasodilator on soluble guanylate cyclase from bovine coronary arteries were studied more closely. It was found that nicorandil stimulated guanylate cyclase dose-dependently (3-30 mM) up to 100-fold the control value. Similar to nitroglycerin but in contrast to sodium nitroprusside, cysteine (0.5-20 mM) was required to obtain this stimulation. All other investigated thiols, except thiosalicylic acid which was partially able to mimic the cysteine effect, were ineffective. As evident from time course studies, nicorandil induced stimulation of guanylate cyclase was characterized by a lag-phase which could be avoided by preincubating the enzyme with nicorandil. The stimulatory effect of nicorandil was diminished in the presence of methylene blue, ferricyanide or hydroquinone. These results give further evidence that a) nicorandil exerts its vasodilating effect via stimulation of guanylate cyclase and b) nitrate esters, such as nitroglycerin or nicorandil, stimulate the enzyme, at least in vitro, only in the presence of cysteine or, to a lesser extent, thiosalicylic acid.

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