Neurological Unit 1, Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta, 20133, Milan, Italy.
Biochemical Science Department University of Padua, 35121, Padova, Italy.
Toxicon. 2020 May;179:84-91. doi: 10.1016/j.toxicon.2020.02.020. Epub 2020 Mar 14.
The Botulinum NeuroToxin (BoNT) comprises several serotypes with distinct properties, mechanisms of action, sensitivity and duration of effect in different species. The serotype A (BoNT/A) is the prevalent neurotoxin applied in human's disease. In this paper we present an overview of the current knowledge regarding the duration of effect and the neuromuscular sprouting of different BoNT serotypes in humans. Then, we report the original results of a study in healthy subjects treated with BoNT/A, B, C and F using different neurophysiological techniques. Twelve healthy volunteers (7 men, 5 women) are treated with BoNT/A, B, C and F or placebo in Abductor digiti minimi (ADM) muscle of the hand. Before and after injections, an extensive neurophysiological study is performed with the CMAP amplitude variation, Multi-Motor Unit Action Potentials (MUAPs) analysis, the Turns/Amplitude ratio of interference pattern (IP) and determination of jitter and Fiber Density (FD) at single-fiber electromyography (SFEMG), at week 2 (w2), 4 (w4), 6 (w6) and 8 (w8). A maximal neuromuscular block is obtained at w2 for all the serotypes. Afterwards, the CMAP trend appear similar for BoNT/A, B, and C while, BoNT/F shows a faster recover. Multi-MUAPs analysis and IP detect mild changes at w2 for all serotypes, except for BoNT/F that shows a greater change since w4. SFEMG have minimal changes in FD while, Jitter increase at w2 with a slower decrease over the time for all BoNTs. In conclusion, BoNT/F has earlier sprouting and complete recovery at w8. Other serotypes present a slower and similar profile. The EMG appear useful to study the functional recovery in humans, and these results should provide new evidence for assessing different serotypes. These findings improve our knowledge regarding the methods to evaluate duration of effects and dose equivalents in different serotypes, that in the future could change the clinicians strategy for disease-tailored BoNT therapies.
肉毒神经毒素(BoNT)由几种具有不同特性、作用机制、在不同物种中的敏感性和作用持续时间的血清型组成。血清型 A(BoNT/A)是应用于人类疾病的主要神经毒素。本文综述了不同 BoNT 血清型在人类中的作用持续时间和神经肌肉再生的最新知识。然后,我们报告了一项在健康受试者中使用不同神经生理学技术治疗 BoNT/A、B、C 和 F 的原始研究结果。12 名健康志愿者(7 名男性,5 名女性)在手的外展小指肌(ADM)中接受 BoNT/A、B、C 和 F 或安慰剂治疗。在注射前后,使用 CMAP 幅度变化、多运动单位动作电位(MUAP)分析、干扰模式(IP)的转数/幅度比和单纤维肌电图(SFEMG)中的抖动和纤维密度(FD)的测定进行广泛的神经生理学研究,在第 2 周(w2)、4 周(w4)、6 周(w6)和 8 周(w8)。所有血清型在 w2 时均可获得最大的神经肌肉阻滞。之后,CMAP 趋势对于 BoNT/A、B 和 C 来说相似,而 BoNT/F 则显示出更快的恢复。多 MUAPs 分析和 IP 在所有血清型中均在 w2 时检测到轻微变化,除了 BoNT/F,从 w4 开始变化更大。SFEMG 在 FD 中变化最小,而 Jitter 在 w2 时增加,随着时间的推移,所有 BoNTs 的减少速度都较慢。总之,BoNT/F 在 w8 时出现更早的发芽和完全恢复。其他血清型则呈现出较慢且相似的形态。肌电图可用于研究人类的功能恢复,这些结果应为评估不同血清型提供新的证据。这些发现提高了我们对不同血清型中评估作用持续时间和剂量等效性的方法的认识,这可能会改变临床医生针对疾病的 BoNT 治疗策略。