Increased Inducible Nitric Oxide Synthase in Skeletal Muscle Biopsies from Patients with Chronic Heart Failure

Volker Adams, Jiangtao Yu, Sven Möbius-Winkler, Axel Linke, Claudia Weigl, Lutz Hilbrich, Gerhard Schuler, Rainer Hambrecht
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引用次数: 63

Abstract

In addition to left ventricular pump failure and low cardiac output, structural and metabolic alterations of skeletal muscle are thought to contribute to exercise intolerance seen in patients with CHF. Studies using cardiac myocytes have implicated nitric oxide elaborated by inducible nitric oxide synthase (iNOS) as a potential agent associated with the genesis of dilated cardiomyopathy. The present study was designed to locate iNOS in the working skeletal muscle of patients with congestive heart failure. Specific antibodies were used to detect iNOS by immunohistochemistry in skeletal muscle biopsies (m. vastus lateralis) of 37 patients with left ventricular pump failure and 8 normal controls. The expression was restricted to skeletal muscle myocytes and was increased five- to ninefold in patients with chronic heart failure. There was no statistically significant difference in iNOS expression between patients with dilated cardiomyopathy and those with ischemic cardiomyopathy. The finding of a locally increased expression of iNOS and the experimental evidence that NO attenuates the contractile performance of the skeletal muscle suggest that the expression of iNOS may be responsible for the exercise intolerance seen in patients with chronic heart failure.

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慢性心力衰竭患者骨骼肌活检中诱导型一氧化氮合酶升高
除了左心室泵衰竭和心输出量低外,骨骼肌的结构和代谢改变被认为是导致CHF患者运动不耐受的原因。对心肌细胞的研究表明,由诱导型一氧化氮合酶(iNOS)合成的一氧化氮可能与扩张型心肌病的发生有关。本研究旨在定位充血性心力衰竭患者工作骨骼肌中的iNOS。采用免疫组化方法对37例左心室泵衰竭患者和8例正常对照的骨骼肌活检(股外侧肌)进行iNOS特异性抗体检测。这种表达仅限于骨骼肌肌细胞,在慢性心力衰竭患者中增加5 - 9倍。扩张型心肌病患者与缺血性心肌病患者iNOS表达差异无统计学意义。局部iNOS表达增加的发现以及NO降低骨骼肌收缩性能的实验证据表明,iNOS的表达可能是慢性心力衰竭患者运动不耐受的原因。
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