Increase in activating ability of human platelet guanylate cyclase during aggregation.

Biochemistry international Pub Date : 1992-12-01
I S Severina, N N Belushkina
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Abstract

The dynamics of changes in the stimulation of human platelet guanylate cyclase by some activators in aggregating platelets was studied. It was shown that ADP-induced aggregation of human platelets (donors) is accompanied by the enhancement of the intensity of guanylate cyclase activation by sodium nitroprusside, L-arginine, protoporphyrin IX and arachidonic acid and also by the increase in cGMP content. Immediately after the induction of aggregation the intensity of guanylate cyclase activation and cGMP content begin to increase. The rise reaches its maxima within several minutes, then followed by a fall to the initial level. The peaks of the enhanced capacity for guanylate cyclase activation by the above compounds coincide in time and intensity. On the basis of the proposed hypothetical scheme of cGMP action as a regulator of platelet aggregation a possible mechanism of enhancing the capacity of guanylate cyclase to be stimulated by various activators in aggregating platelets is suggested.

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人血小板鸟苷酸环化酶在聚集过程中的激活能力增强。
研究了血小板聚集过程中几种活化剂对人血小板鸟苷酸环化酶刺激的动态变化。结果表明,adp诱导的人血小板(供体)聚集伴随着硝普钠、l -精氨酸、原卟啉IX和花生四烯酸对鸟苷酸环化酶激活强度的增强以及cGMP含量的增加。在诱导聚集后,鸟苷酸环化酶的激活强度和cGMP含量立即开始增加。上升在几分钟内达到最大值,然后又回落到初始水平。上述化合物增强鸟苷酸环化酶激活能力的峰值在时间和强度上是一致的。在cGMP作为血小板聚集调节剂的假设方案的基础上,提出了提高鸟苷酸环化酶在血小板聚集过程中受各种活化剂刺激的能力的可能机制。
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