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中国临床药理学与治疗学 ›› 2010, Vol. 15 ›› Issue (12): 1383-1387.

• 基础研究 • 上一篇    下一篇

A型肉毒毒素抑制乙酰胆碱诱发的大鼠离体幽门平滑肌的收缩

徐桂中1,2, 刘向文1, 侯一平1   

  1. 1兰州大学基础医学院神经科学研究所,人体解剖学与组织胚胎学研究所,兰州 730000,甘肃;
    2武汉市中心医院急诊科,武汉 430012,湖北
  • 收稿日期:2010-12-09 修回日期:2010-12-15 出版日期:2010-12-26 发布日期:2020-09-16
  • 通讯作者: 侯一平,男,教授,博士生导师,研究方向:神经毒素的作用机理及临床应用。Tel: 0931-8915886 E-mail: houyiping@lzu.edu.cn
  • 作者简介:徐桂中,男,硕士,住院医师,研究方向:神经毒素的作用机理。Tel: 13971377248 E-mail: 281824072@qq.com
  • 基金资助:
    甘肃省科技支撑计划(090NKCA112);兰州大学医学科研基金(LZUYX200605);甘肃省新药临床前重点研究实验室资助(KLPSGS0802)

Inhibitory effect of botulinum toxin type A on acetylcholine induced contractile response in rat pyloric smooth muscle in vitro

XU Gui-zhong1,2, LIU Xiang-wen1, HOU Yi-ping1   

  1. 1Department of Neuroscience, Anatomy, Histology and Embryology, School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, Gansu, China;
    2Emergency of Wuhan Central Hospital, Wuhan 430014, Hubei, China
  • Received:2010-12-09 Revised:2010-12-15 Online:2010-12-26 Published:2020-09-16

摘要: 目的: 观察A型肉毒毒素对内、外源性乙酰胆碱诱发的大鼠离体幽门平滑肌收缩的作用,并探讨其可能作用机制。方法: 利用电场刺激诱发大鼠离体幽门平滑肌释放乙酰胆碱或加入外源性乙酰胆碱诱发肌条收缩,比较A型肉毒毒素与阿托品对该诱发收缩的作用。结果: A型肉毒毒素抑制电场刺激诱发的大鼠离体胃幽门平滑肌的收缩(P<0.001)。阿托品和A型肉毒毒素均抑制乙酰胆碱诱发的大鼠离体胃幽门平滑肌的收缩(P<0.001),但A型肉毒毒素对乙酰胆碱诱发的收缩表现为不完全抑制。结论: A型肉毒毒素抑制电场刺激诱发内源性乙酰胆碱释放所产生的收缩作用,可能其裂解突触前膜上的SNAP-25蛋白而致;A型肉毒毒素抑制外源性乙酰胆碱诱发的肌条收缩作用类似阿托品,但机制尚不明,可能A型肉毒毒素作用于突触后膜受体或者平滑肌上的SNAP-25蛋白,而抑制肌条的收缩。

关键词: A型肉毒毒素, 乙酰胆碱, 离体, 幽门平滑肌

Abstract: AIM: To investigate the effect of botulinum toxin type A (BTX-A) on endogenous and exogenous acetylcholine (ACh) induced contractile response in rat pyloric smooth muscle in vitro.METHODS: The effects of BTX-A and atropine on pyloric contractility-induced respectively by electrical field stimulation (EFS), which is used to promote endogenous ACh release, and by ACh addition were comparatively evaluated.RESULTS: BTX-A inhibited the pyloric smooth muscle contractility-induced by EFS (P<0.001). Both of atropine and BTX-A significantly abolished pyloric contractility-induced by ACh (P<0.001), but BTX-A incompletely did it.CONCLUSION: The evidence of the inhibitory effect of BTX-A on pyloric contractility-induced by EFS suggests that BTX-A inhibits endogenous ACh release through cleaving SNAP-25 protein within presynaptic membrane. The result of the inhibition of BTX-A on ACh induced pyloric contractile response is similar to atropine, suggests that BTX-A probably acts on postsynaptic receptor or pyloric muscle directly.

Key words: Botulinum toxin type A, Acetylcholine, in vitro, Pyloric smooth muscle

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