Differences in Mode of Action of Cochinchinenin A and B on Tetrodotoxin-Resistant Sodium Channels

被引:1
|
作者
Chen Su [1 ,2 ]
Wu Shui-cai [1 ]
Zeng Yi
Liu Xiang-ming [2 ]
机构
[1] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing 100124, Peoples R China
[2] South Cent Univ Nationalities, Coll Biomed Engn, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Cochinchinenin; Tetrodotoxin-resistant sodium channel; Antagonistic interaction; Occupancy theory; Rate theory; DRAGONS BLOOD; COMBINATION; CURRENTS; NEURONS;
D O I
10.4314/tjpr.v12i3.17
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: To explore the mechanism of antagonistic interaction between cochinchinenin A and B in modulating tetrodotoxin-resistant (TTR-X) sodium currents. Methods: The time variation of the effects induced by cochinchinenin A and B on the TTX-R sodium currents in dorsal root ganglion (DRG) neurons of rats were observed using whole-cell patch clamp technique. Based on pharmacological fundamental theory, the modes of action of cochinchinenin A and B on TTX-R channels were distinguished. Results: The scatter diagram which reflected the time variation of inhibition effect on TTX-R sodium currents induced by cochinchinenin A fitted well with occupancy theory equation (goodness of fit test, p > 0.05), while that of cochinchinenin B fitted well with rate theory equation (p > 0.05). The rate constants for combination and dissociation between cochinchinenin A and TTX-R sodium channel were (198.7 +/- 39.9) x 10(-3) and (41.1 +/- 6.2) x 10(-3) respectively; while corresponding values for combination and association between cochinchinenin B and TTX-R sodium channel were (99.9 +/- 16.8) x 10(-3) and (5.3 +/- 0.4) x 10(-3) respectively. Conclusion: The main cause of the antagonistic interaction between cochinchinenin A and B may be attributed to the different modes of their action on TTX-R sodium channels.
引用
收藏
页码:385 / 391
页数:7
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