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川芎嗪拮抗链霉素耳毒性作用及其离子通道机制
引用本文:崔桂英,石丽娟,汤浩.川芎嗪拮抗链霉素耳毒性作用及其离子通道机制[J].听力学及言语疾病杂志,2007,15(2):129-131.
作者姓名:崔桂英  石丽娟  汤浩
作者单位:中国医科大学基础医学院生理学教研室/听觉研究室,沈阳,110001
摘    要:目的 研究川芎嗪(tetraethylplyrazine,TMP)拮抗链霉素耳毒性作用及其对耳蜗外毛细胞外向K^+通道的影响,寻求两者的相关性,旨在探讨川芎嗪拮抗耳中毒作用的离子通道机制。方法 选取豚鼠60只,随机分为6组,即对照组、链霉素组、川芎嗪低浓度组、川芎嗪高浓度组、川芎嗪低浓度+链霉素组和川芎嗪高浓度+链霉素组,分别注射生理盐水(2.5ml/kg)、链霉素(450mg/kg)、川芎嗪(12mg/kg)、川芎嗪(60ms/ks)、川芎嗪(12mg/kg)+链霉素(450mg/kg)、川芎嗪(60mg/kg)+链霉素(450mg/kg),用药10天后检测各组豚鼠ABR反应阈,并采用全细胞膜片钳技术观察川芎嗪对耳蜗外毛细胞Ca^2+敏感K^+电流和延迟外向K^+电流的影响。结果 结果表明川芎嗪明显降低链霉素所致的豚鼠ABR反应阈升高,提示川芎嗪具有明显的拮抗链霉素耳毒性作用;川芎嗪能明显增大豚鼠耳蜗外毛细胞Ca^2+敏感K^+电流和延迟外向K^+电流,并呈浓度依赖关系。结论 川芎嗪可能通过增大K^+通道电流而发挥其降低链霉素耳毒性作用,推测这是其抗耳毒性作用机制之一。

关 键 词:川芎嗪  外毛细胞  链霉素  K  通道
文章编号:1006-7299(2007)02-0129-03
收稿时间:2006-07-24
修稿时间:2006年7月24日

Reduction of Streptomycin Ototoxicity by Tetramethylpyrazine and its Ionic Channel Mechanism
Cui Guiying,Shi Lijuan,Tang Hao.Reduction of Streptomycin Ototoxicity by Tetramethylpyrazine and its Ionic Channel Mechanism[J].Journal of Audiology and Speech Pathology,2007,15(2):129-131.
Authors:Cui Guiying  Shi Lijuan  Tang Hao
Abstract:Objective To observe the effect of tetraethylplyrazine(TMP) on outward K~ channel of outer hair cells in guinea pig cochlea.Methods 60 guinea pigs were divided into 6 groups randomly in the experiment.Auditory brainstem response was used to monitor the change of ABR thresholds and patch clamp techniques to observe the effect of TMP on outward K~ channel.Results TMP decreased the elevated ABR threshold caused by streptomycin. The TMP increased the amplitudes of calcium sensitive potassium channels (I_ K(Ca) ) and delayed outward potassium channels (IK) of outer hair cells of guinea pig cochlea.Conclusion The study indicates that TMP may act as a protective agent against ototoxicity of streptomycin. The amplitudes of I_ K(Ca) and IK of outer hair cells are increased by the TMP,suggesting the possible mechanisms of reducing ototoxicity.
Keywords:Tetramethylpyrazine(TMP)  Outer hair cells  Streptomycin  K~  channel
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