一氧化氮对人体骨骼肌特性的影响。

J. Folland, H. Maas, D. Jones
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引用次数: 14

摘要

我们研究了外源性一氧化氮(NO)对体内工作的人体骨骼肌的强度和收缩特性的作用。测量股四头肌的最大等长自主收缩力(MVC),并使用叠加电刺激来估计激活水平和“真实最大力”(TMF)。确定力-频率关系以评估肌肉收缩特性的变化。实验组(E, n=10)的受试者在治疗前和治疗期间分别使用不同剂量的三硝酸甘油(NO供体)作为透皮贴剂,分别给予100 (GTN100)或200 (GTN200)微h-1。对照组(C, n=6)在服用口服安慰剂的同时,在两个相似的时间段内进行测量。GTN200的强度显著增加(MVC: +5)。15%;TMF: + 3.87%)。c组的肌力没有变化。GTN治疗有降低次最大频率肌力的趋势,但最显著的变化是GTN100治疗肌力下降(约12%,P < 0.05),并且在整个研究过程中仍处于抑制状态。对照组c的收缩特性未见变化。目前的结果表明,GTN治疗增加了最大自主强度,但降低了抽搐张力。时间过程和剂量反应特征表明,这是一氧化氮在体内对人体肌肉的两种独立作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of nitric oxide on in vivo human skeletal muscle properties.
We have investigated the action of exogenous nitric oxide (NO) on the strength and contractile properties of human skeletal muscle working in vivo. Maximum isometric voluntary contraction force (MVC) of the quadriceps was measured and superimposed electrical stimulation was used to estimate the level of activation and 'true maximum force' (TMF). Force-frequency relationships were determined to assess changes in contractile properties of the muscle. Subjects in the experimental group (E, n=10) were measured before and during two separate periods of treatment with different doses of glyceryl trinitrate, a NO donor, delivering 100 (GTN100) or 200 (GTN200) microg h-1 as a trans-dermal patch. A control group (C, n=6) was measured during two similar periods whilst taking an oral placebo. There was a significant increase in strength with GTN200 (MVC: +5. 15%; TMF: +3.87%). There was no change in the strength of group C. There was a trend towards reduced forces at submaximal frequencies with GTN administration but the most notable change was a decline in twitch force (approximately 12%, P < 0.05) with GTN100 treatment and this remained depressed throughout the study. No changes were seen in the contractile properties of the control group C. The present results show that GTN treatment increased maximum voluntary strength but decreased twitch tension. The time course and dose-response characteristics indicate that these are two separate actions of NO on human muscle working in vivo.
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