Human Performance Laboratory, Faculty of Kinesiology, University of Calgary, 2500 University Drive NW, Calgary, AB, Canada T2N 1N4.
J Biomech. 2013 Sep 27;46(14):2426-33. doi: 10.1016/j.jbiomech.2013.07.028. Epub 2013 Jul 26.
Onabotulinum toxin A (BTX-A) is a frequently used treatment modality to relax spastic muscles by preventing acetylcholine release at the motor nerve endings. Although considered safe, previous studies have shown that BTX-A injections cause muscle atrophy and deterioration in target and non-target muscles. Ideally, muscles should fully recover following BTX-A treatments, so that muscle strength and performance are not affected in the long-term. However, systematic, long-term data on the recovery of muscles exposed to BTX-A treatments are not available, thus practice guidelines on the frequency and duration of BTX-A injections, and associated recovery protocols, are based on clinical experience with little evidence-based information. Therefore, the purpose of this study was to investigate muscle recovery following a six months, monthly BTX-A injection (3.5 U/kg) protocol. Twenty seven skeletally mature NZW rabbits were divided into 5 groups: Control (n=5), zero month recovery - BTX-A+0M (n=5), one month recovery - BTX-A+1M (n=5), three months recovery - BTX-A+3M (n=5), and six months recovery - BTX-A+6M (n=7). Knee extensor strength, muscle mass and percent contractile material in injected and contralateral non-injected muscles was measured at each point of recovery. Strength and muscle mass were partially and completely recovered in injected and contralateral non-injected muscles for BTX-A+6M group animals, respectively. The percent of contractile material partially recovered in the injected, but did not recover in the contralateral non-injected muscles. We conclude from these results that neither target nor non-target muscles fully recover within six months of a BTX-A treatment protocol and that clinical studies on muscle recovery should be pursued.
肉毒毒素 A(BTX-A)是一种通过防止运动神经末梢乙酰胆碱释放来松弛痉挛肌肉的常用治疗方法。尽管被认为是安全的,但先前的研究表明,BTX-A 注射会导致肌肉萎缩和目标肌肉及非目标肌肉的恶化。理想情况下,肌肉在接受 BTX-A 治疗后应完全恢复,从而不会对肌肉力量和功能产生长期影响。然而,目前缺乏关于暴露于 BTX-A 治疗后的肌肉恢复的系统、长期数据,因此,关于 BTX-A 注射的频率和持续时间以及相关恢复方案的实践指南是基于临床经验,而证据基础信息较少。因此,本研究的目的是调查接受六个月、每月 BTX-A 注射(3.5 U/kg)方案后的肌肉恢复情况。27 只骨骼成熟的 NZW 兔分为 5 组:对照组(n=5)、零月恢复组-BTX-A+0M(n=5)、一月恢复组-BTX-A+1M(n=5)、三月恢复组-BTX-A+3M(n=5)和六月恢复组-BTX-A+6M(n=7)。在每次恢复时测量伸膝肌力量、肌肉质量和注射肌肉及对侧非注射肌肉的收缩物质百分比。BTX-A+6M 组动物的注射肌肉和对侧非注射肌肉的力量和肌肉质量部分和完全恢复。注射肌肉的收缩物质百分比部分恢复,但对侧非注射肌肉未恢复。从这些结果我们得出结论,在 BTX-A 治疗方案结束后六个月内,目标肌肉和非目标肌肉均未完全恢复,应该开展关于肌肉恢复的临床研究。