Li L J, Liu C G
Institute of Pharmacology and Toxicology, Beijing 1100850, China.
Zhongguo Ying Yong Sheng Li Xue Za Zhi. 2001 May;17(2):133-6.
The effects of maitotoxin (MTX) on neuromuscular junction transmission in isolated non-uniformed stretched muscle preparation of rat diaphragms were studied using intracellular recording with microelectrodes.
(1) End-plate potentials (EPPs) were not induced abruptly after 18.0 min 10 microg/L MTX added to the chamber. Hereafter postsynaptic membrane potential was depolarized gradually, and the maximum depolarization value was 27.0 mV. The frequency of mEPP increased markedly after 70.3 min MTX administered, 32 folds compared with control. (2) 20 micromol/L verapamil was added to the chamber 20 min prior to 10 microg/L MTX. No evident effects of verapamil on the above parameters elicited by MTX was produced, except that it was 78.5 min when EPPs were not induced by train stimulation, which was longer than that was induced by MTX alone (P < 0.001).
The predominant effect of MTX on the neuromuscular junction transmission was that EPPs couldn't be elicited by indirect stimulation, and which could be inhibited partly by verapamil, a L-type calcium ion channel blocker. Postsynaptic membrane potential depolarization and mEPP frequency increasing induced by MTX couldn't be inhibited by verapamil.
采用微电极细胞内记录法,研究了海葵毒素(MTX)对大鼠膈肌非均匀拉伸肌肉标本神经肌肉接头传递的影响。
(1)在标本槽中加入10μg/L MTX 18.0分钟后,终板电位(EPPs)未突然诱发。此后突触后膜电位逐渐去极化,最大去极化值为27.0mV。给予MTX 70.3分钟后,微小终板电位(mEPP)频率显著增加,与对照组相比增加了32倍。(2)在加入10μg/L MTX前20分钟,向标本槽中加入20μmol/L维拉帕米。维拉帕米对MTX引起的上述参数无明显影响,只是在串刺激不诱发EPPs的时间为78.5分钟,比单独使用MTX时长(P<0.001)。
MTX对神经肌肉接头传递的主要作用是间接刺激不能诱发EPPs,且可被L型钙离子通道阻滞剂维拉帕米部分抑制。MTX引起的突触后膜电位去极化和mEPP频率增加不能被维拉帕米抑制。