Inhibitory effect of mitragynine, an analgesic alkaloid from Thai herbal medicine, on neurogenic contraction of the vas deferens

被引:62
作者
Matsumoto, K
Yamamoto, LT
Watanabe, K
Yano, S
Shan, J
Pang, PKT
Ponglux, D
Takayama, H
Horie, S
机构
[1] Josai Int Univ, Fac Pharmaceut Sci, Dept Pharmacol, Togane, Chiba 2838555, Japan
[2] Chiba Univ, Grad Sch Pharmaceut Sci, Dept Chem Pharmacol, Chuo Ku, Chiba 2608675, Japan
[3] Chiba Univ, Grad Sch Pharmaceut Sci, Dept Mol Pharmacol & Pharmacotherapeut, Chuo Ku, Chiba 2608675, Japan
[4] Univ Alberta, Fac Med, Dept Physiol, Edmonton, AB T6G 2H7, Canada
[5] Chulalongkorn Univ, Fac Pharmaceut Sci, Dept Pharmacognosy, Bangkok 10330, Thailand
[6] Chiba Univ, Grad Sch Pharmaceut Sci, Dept Mol Struct & Biol Funct, Inage Ku, Chiba 2638522, Japan
关键词
mitragynine; morphine; vas deferens; Ca2+ channel; Mitragyna speciosa;
D O I
10.1016/j.lfs.2005.04.042
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The effect of an indole-alkaloid mitragynine isolated from the Thai medicinal herb kratom (Mitragyna speciosa) on neurogenic contraction of smooth muscle was studied in guinea-pig vas deferens. Mitragynine inhibited the contraction of the vas deferens produced by electrical transmural stimulation. On the other hand, mitragynine failed to affect the responses to norepinephrine and ATP. Mitragynine did not reduce KCl-induced contraction in the presence of tetrodotoxin, prazosin and alpha,beta-methylene ATP. Mitragynine inhibited nicotine- or tyramine-induced contraction. By using the patch-clamp technique, mitragynine was found to block T- and L-type Ca2+ channel currents in N1E-115 neuroblastoma cells. In the Ca2+ measurement by a fluorescent dye method, mitragynine reduced KCl-induced Ca2+ influx in neuroblastoma cells. The present results suggest that mitragynine inhibits the vas deferens contraction elicited by nerve stimulation, probably through its blockade of neuronal Ca2+ channels. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:187 / 194
页数:8
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