Antinociceptive effect of 7-hydroxymitragynine in mice:: Discovery of an orally active opioid analgesic from the Thai medicinal herb Mitragyna speciosa

被引:170
作者
Matsumoto, K
Horie, S
Ishikawa, H
Takayama, H
Aimi, N
Ponglux, D
Watanabe, K
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Chem Pharmacol Lab, Inage Ku, Chiba 2638522, Japan
[2] Chiba Univ, Grad Sch Pharmaceut Sci, Lab Mol Struct & Biol Funct, Inage Ku, Chiba 2638522, Japan
[3] Chulalongkorn Univ, Fac Pharmaceut Sci, Bangkok 10330, Thailand
关键词
mitragynine; 7-hydroxymitragynine; morphine; opioid receptor; analgesic; ileum;
D O I
10.1016/j.lfs.2003.09.054
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Mitragynine is an indole alkaloid isolated from the Thai medicinal plant Mitragyna speciosa. We previously reported the morphine-like action of mitragynine and its related compounds in the in vitro assays. In the present study, we investigated the opioid effects of 7-hydroxymitragynine, which is isolated as its novel constituent, on contraction of isolated ileum, binding of the specific ligands to opioid receptors and nociceptive stimuli in mice. In guinea-pig ileum, 7-hydroxymitragynine inhibited electrically contraction through the opioid receptors. Receptor-binding assays revealed that 7-hydroxymitragynine has a higher affinity for mu-opioid receptors relative to the other opioid receptors. Administration of 7-hydroxymitragynine (2.5-10 mg/kg, s.c.) induced dose-dependent antinociceptive effects in tail-flick and hot-plate tests in mice. Its effect was more potent than that of morphine in both tests. When orally administered, 7-hydroxymitragynine (5-10 mg/kg) showed potent antinociceptive activities in tail-flick and hot-plate tests. In contrast, only weak antinociception was observed in the case of oral administration of morphine at a dose of 20 mg/kg. It was found that 7-hydroxymitragynine is a novel opioid agonist that is structurally different from the other opioid agonists, and has potent analgesic activity when orally administered. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:2143 / 2155
页数:13
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