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诱导型一氧化氮合酶基因在膈肌和骨骼肌中的表达。

Expression of the inducible nitric oxide synthase gene in diaphragm and skeletal muscle.

作者信息

Thompson M, Becker L, Bryant D, Williams G, Levin D, Margraf L, Giroir B P

机构信息

Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas 75235-9063, USA.

出版信息

J Appl Physiol (1985). 1996 Dec;81(6):2415-20. doi: 10.1152/jappl.1996.81.6.2415.

Abstract

Nitric oxide (NO) is a pluripotent molecule that can be secreted by skeletal muscle through the activity of the neuronal constitutive isoform of NO synthase. To determine whether skeletal muscle and diaphragm might also express the macrophage-inducible form of NO synthase (iNOS) during provocative states, we examined tissue from mice at serial times after intravenous administration of Escherichia coli endotoxin. In these studies, iNOS mRNA was strongly expressed in the diaphragm and skeletal muscle of mice 4 h after intravenous endotoxin and was significantly diminished by 8 h after challenge. Induction of iNOS mRNA was followed by expression of iNOS immunoreactive protein on Western immunoblots. Increased iNOS activity was demonstrated by conversion of arginine to citrulline. Immunochemical analysis of diaphragmatic explants exposed to endotoxin in vitro revealed specific iNOS staining in myocytes, in addition to macrophages and endothelium. These results may be important in understanding the pathogenesis of respiratory pump failure during septic shock, as well as skeletal muscle injury during inflammation or metabolic stress.

摘要

一氧化氮(NO)是一种多能分子,可通过神经元型组成性一氧化氮合酶的活性由骨骼肌分泌。为了确定在激发状态下骨骼肌和膈肌是否也可能表达巨噬细胞诱导型一氧化氮合酶(iNOS),我们在静脉注射大肠杆菌内毒素后的连续时间点检查了小鼠组织。在这些研究中,静脉注射内毒素后4小时,iNOS mRNA在小鼠的膈肌和骨骼肌中强烈表达,攻击后8小时显著减少。iNOS mRNA的诱导之后是免疫印迹上iNOS免疫反应蛋白的表达。通过精氨酸向瓜氨酸的转化证明了iNOS活性的增加。体外暴露于内毒素的膈肌外植体的免疫化学分析显示,除了巨噬细胞和内皮细胞外,心肌细胞中也有特异性iNOS染色。这些结果对于理解脓毒性休克期间呼吸泵衰竭的发病机制以及炎症或代谢应激期间的骨骼肌损伤可能具有重要意义。

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