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巯基参与血管平滑肌中一氧化氮的螯合及一氧化氮诱导的鸟苷酸环化酶激活。

Sulfhydryl involvement in nitric oxide sequestration and nitric oxide induced guanylyl cyclase activation in vascular smooth muscle.

作者信息

Liu Z G, McLaughlin B E, Marks G S, Brien J F, Nakatsu K

机构信息

Department of Pharmacology and Toxicology, Queen's University, Kingston, ON, Canada.

出版信息

Can J Physiol Pharmacol. 1995 Aug;73(8):1144-8. doi: 10.1139/y95-163.

Abstract

In the present study, the role of vascular smooth muscle sulhydryl groups was investigated with respect to sequestration of nitric oxide (NO) and activation of soluble guanylyl cyclase by NO. Vascular smooth muscle 100,000 x g supernatant (soluble) fraction was prepared in phosphate buffer, using the medial layer of bovine pulmonary artery. The soluble fraction was incubated with 100 pmol NO for 5 min in a sealed flask at 37 degree C under anerobic conditions in the presence or absence of the sulfhydryl reagent, N-ethylmaleimide (NEM, 5 mM). NO sequestration by the soluble fraction was measured as an indicator of NO binding. Total thiol content was measured in the soluble fraction with and without exposure to NEM. Guanylyl cyclase activity was measured in the soluble fraction with and without exposure to NO and a combination of NO and NEM. NEM decreased total thiol content in the soluble fraction from 103.59 nmol/mL to undetectable levels, and decreased guanylyl cyclase activity to below basal levels. The percentage of NO sequestered by the soluble fraction was inhibited by NEM by approximately 25% from a control value of 26.52 +/- 9.39 to 18.72 +/- 8.52, n = 13, p < 0.05. The data indicate that sulfhydryl groups are essential for guanylyl cyclase activation by NO, and are also involved in the sequestration of NO by the vascular smooth muscle soluble fraction.

摘要

在本研究中,研究了血管平滑肌巯基在一氧化氮(NO)螯合以及NO激活可溶性鸟苷酸环化酶方面的作用。使用牛肺动脉中层在磷酸盐缓冲液中制备血管平滑肌100,000 x g上清液(可溶性)部分。在有或没有巯基试剂N-乙基马来酰亚胺(NEM,5 mM)存在的情况下,将可溶性部分在37℃下于密封烧瓶中在厌氧条件下与100 pmol NO孵育5分钟。将可溶性部分对NO的螯合作为NO结合的指标进行测量。在有和没有暴露于NEM的情况下,测量可溶性部分中的总硫醇含量。在有和没有暴露于NO以及NO和NEM组合的情况下,测量可溶性部分中的鸟苷酸环化酶活性。NEM将可溶性部分中的总硫醇含量从103.59 nmol/mL降低到无法检测的水平,并将鸟苷酸环化酶活性降低到基础水平以下。NEM将可溶性部分螯合的NO百分比从26.52 +/- 9.39的对照值抑制了约25%,降至18.72 +/- 8.52,n = 13,p <0.05。数据表明,巯基对于NO激活鸟苷酸环化酶至关重要,并且还参与血管平滑肌可溶性部分对NO的螯合。

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