Üstün Ramazan, Oğuz Elif Kaval, Delilbaşı Çağrı, Şeker Ayşe, Taşpınar Filiz, Öncü Mehmet Reşit, Oğuz Ahmet Regaip
a Department of Physiology, Faculty of Medicine, Neuroscience Research Unit , Van Yuzuncu Yil University , Van , Turkey.
b Department of Science Education, Faculty of Education , Van Yuzuncu Yil University , Van , Turkey.
Somatosens Mot Res. 2017 Dec;34(4):248-257. doi: 10.1080/08990220.2017.1421160. Epub 2018 Jan 15.
Ankaferd Blood Stopper (ABS), a licenced medicinal herbal extract, is commonly used as an effective topical haemostatic agent. This study is designed to investigate whether topical ABS application may cause peripheral nerve degeneration and neuromuscular dysfunction in a mouse sciatic nerve model.
Twenty mice were randomly divided into two groups; an ABS treated experimental group and a saline-treated control group. Left sciatic nerves were treated with 0.3 ml of ABS in the experimental group and 0.3 ml of sterile saline in the control group for 5 min. Peripheral nerve degeneration and neuromuscular dysfunction were evaluated by behavioural tests, electrophysiological analysis and weight ratio comparison of target muscles.
The motor function, assessed by the sciatic function index, was significantly impaired in ABS-treated animals as compared to the animals treated with saline. Motor coordination, evaluated with the rotarod test, was significantly decreased (-42%) in ABS-treated animals compared to the saline-treated animals. The degree of pain, assessed by the reaction latency to thermal stimuli (hot-plate test), was significantly prolonged (313%) in ABS-treated mice when compared to the saline-treated mice. ABS-treated mice showed a significant reduction in motor nerve conduction velocity (MNCV) (-52%) and the compound muscle action potential (CMAP) (-47%); however, it significantly prolonged onset latency (23%). The gastrocnemius muscles weight ratio of the ABS group was considerably lower than that of the control group.
These findings demonstrate that ABS triggers peripheral nerve degeneration and functional impairment and, thus promotes a deterioration of sciatic nerves.
安卡非德止血剂(ABS)是一种已获许可的药草提取物,通常用作有效的局部止血剂。本研究旨在调查局部应用ABS是否会在小鼠坐骨神经模型中导致周围神经变性和神经肌肉功能障碍。
将20只小鼠随机分为两组;一组为接受ABS治疗的实验组,另一组为接受生理盐水治疗的对照组。实验组用0.3毫升ABS处理左坐骨神经,对照组用0.3毫升无菌生理盐水处理左坐骨神经,持续5分钟。通过行为测试、电生理分析和目标肌肉重量比比较来评估周围神经变性和神经肌肉功能障碍。
与用生理盐水处理的动物相比,用ABS处理的动物的坐骨神经功能指数评估的运动功能明显受损。与用生理盐水处理的动物相比,用旋转棒试验评估的用ABS处理的动物的运动协调性明显降低(-42%)。与用生理盐水处理的小鼠相比,用热刺激反应潜伏期(热板试验)评估的用ABS处理的小鼠的疼痛程度明显延长(313%)。用ABS处理的小鼠的运动神经传导速度(MNCV)明显降低(-52%),复合肌肉动作电位(CMAP)明显降低(-47%);然而,其起始潜伏期明显延长(23%)。ABS组的腓肠肌重量比明显低于对照组。
这些发现表明,ABS引发周围神经变性和功能损害,从而促进坐骨神经的恶化。