A primer for measuring cGMP signaling and cGMP-mediated vascular relaxation.

A primer for measuring cGMP signaling and cGMP-mediated vascular relaxation.
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DOI:
10.1016/j.niox.2021.09.008
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发表时间:
2021-12-01
影响因子:
3.9
通讯作者:
Beuve, Annie
Beuve, Annie
中科院分区:
生物学2区
文献类型:
--
作者:
Straub, Adam C.;Beuve, Annie

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可溶性鸟苷酸环化酶(sGC,也称为GC 1)是一氧化氮(NO)的主要受体,催化第二信使分子3′5′环鸟苷酸(cGMP)的产生,导致血管舒张,并抑制白细胞募集和血小板聚集。通过sGC激动或通过磷酸二酯酶抑制抑制cGMP分解来增强cGMP水平,已经获得FDA批准用于治疗心血管和肺部疾病的几种cGMP调节剂疗法。虽然基础研究继续提高我们对cGMP信号的理解,随着新疗法的发展,以提高cGMP水平,我们提供了一个简短的方法学引物测量cGMP和cGMP介导的血管舒张的研究人员。
Soluble guanylyl cyclase (sGC, also called GC1) is the main receptor for nitric oxide (NO) that catalyzes the production of the second messenger molecule, 3′5′ cyclic guanosine monophosphate (cGMP) leading to vaso-relaxation, and inhibition of leukocyte recruitment and platelet aggregation. Enhancing cGMP levels, through sGC agonism or inhibition of cGMP breakdown via phosphodiesterase inhibition, has yielded FDA approval for several cGMP modifier therapies for treatment of cardiovascular and pulmonary diseases. While basic research continues to improve our understanding of cGMP signaling and as new therapies evolve to elevate cGMP levels, we provide a short methodological primer for measuring cGMP and cGMP-mediated vascular relaxation for investigators.
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