Fangchinoline inhibited the antinociceptive effect of morphine in mice

被引:23
作者
Fang, LH
Zhang, YH [1 ]
Ku, BS
机构
[1] Peking Univ, Sch Basic Med Sci, Dept Pharmacol, Beijing, Peoples R China
[2] Chinese Acad Med Sci, Inst Mat Med, Natl Ctr Pharmaceut Screening, Beijing 100050, Peoples R China
关键词
fangchinoline; Stephania tetrandra; morphine; serotonin; antinociception; tolerance;
D O I
10.1016/j.phymed.2003.06.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Fangchinoline (FAN), a non-specific calcium antagonist, is a major alkaloidal component of the creeper Stephania tetrandra S. Moore (or fenfangji). It has been shown to possess antagonistic activity on morphine-induced antinociception in mice. This study was undertaken to assess the antagonistic mechanism. The results demonstrated that FAN (IP) attenuated morphine (SC)-induced antinociception in a dose-dependent manner with significant effect at doses of 30 and 60 mg/kg body wt. (IP) in the tail-flick test but not the tail-pinch tests, carried out in mice. This antagonism was abolished by pretreatment with a serotonin precursor, 5-hydroxytryptophan (5-HTP, IP), but not by pretreatment with a noradrenaline precursor, L-dihydroxyphenylalanine (L-DOPA, IP) in the tail-flick test. On the other hand, the development of morphine-induced analgesic tolerance was not prevented by FAN. These results suggest that the serotonergic pathway may be involved in the antagonism of morphine-induced antinociception by FAN and, in agreement with other reports, also indicates the possible dissociation of the morphine analgesic effect from its tolerance-development mechanism. (c) 2004 Published by Elsevier GmbH.
引用
收藏
页码:183 / 188
页数:6
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