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

Chen Su^1,2 Wu Shui-cai¹ Zeng Yi and Liu Xiang-ming^2*

¹College of Life Science and Bioengineering, Beijing University of Technology, Beijing, 100124, ¹College of Biomedical Engineering, South-Central of University for Nationalities, Hubei, Wuhan, 430074, China. 

*For correspondence: Email: liu.xiangming@263.net  Tel: 86-027-67843892; Fax: 86-027-67841231 

Received:  13 August 2012                                                                            Revised accepted: 25 April 2013

Tropical Journal of Pharmaceutical Research, June 2013; 12(3): 385-391

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.