盐酸克仑特罗治疗去神经肌肉萎缩的随机、双盲、安慰剂对照试验。

ISRN Pharmaceutics Pub Date : 2011-01-01 Epub Date: 2011-08-15 DOI:10.5402/2011/981254
Guang-Liang Jiang, Yu-Dong Gu, Li-Yin Zhang, Li-Ying Shen, Cong Yu, Jian-Guang Xu
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引用次数: 8

摘要

目标。β(2)-肾上腺素能激动剂,如瘦肉精,已被证明可以促进健康骨骼肌的肥大,并改善动物和人类在一些病理条件下的肌肉萎缩。本研究旨在探讨盐酸克仑特罗减轻去神经支配性肌肉萎缩的临床疗效。方法。采用双盲、安慰剂对照、平行和随机试验。71例臂丛神经损伤患者分别给予盐酸克仑特罗(60 μg, bid)或安慰剂治疗3个月。在研究之前和结束时,对患者进行体格检查、肱二头肌活检、肌电图(emg)和其他实验室检查。结果。与安慰剂治疗相比,盐酸克仑特罗显著缓解了ⅰ型和ⅱ型肌纤维横截面面积的减少,减轻了纤颤电位幅度的减少,无不良反应。结论。盐酸克仑特罗在该队列中安全改善失神经性肌肉萎缩;因此,鼓励对这种或其他β(2)激动剂治疗去神经支配引起的肌肉萎缩进行更大规模的临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Randomized, double-blind, and placebo-controlled trial of clenbuterol in denervated muscle atrophy.

Randomized, double-blind, and placebo-controlled trial of clenbuterol in denervated muscle atrophy.

Randomized, double-blind, and placebo-controlled trial of clenbuterol in denervated muscle atrophy.

Randomized, double-blind, and placebo-controlled trial of clenbuterol in denervated muscle atrophy.

Objectives. β(2)-adrenergic agonists, such as clenbuterol, have been shown to promote the hypertrophy of healthy skeletal muscles and to ameliorate muscle wasting in a few pathological conditions in both animals and humans. We intended to investigate the clinical efficacy of clenbuterol on attenuating denervation-induced muscle atrophy. Methods. A double-blind, placebo-controlled, parallel, and randomized trial was employed. 71 patients, suffering from brachial plexus injuries, were given either clenbuterol (60 μg, bid) or placebo for 3 months. Before and at the end of the study, patients were given physical examinations, biopsies of biceps brachii, electromyograms (EMGs), and other laboratory tests. Results. Compared with placebo treatment, clenbuterol significantly mitigated the decreases in cross-sectional areas of type I and II muscle fibers and alleviated the reduction in fibrillation potential amplitudes, without any adverse effects. Conclusions. Clenbuterol safely ameliorated denervated muscle atrophy in this cohort; thus larger clinical studies are encouraged for this or other β(2) agonists on denervation-induced muscle atrophy.

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