Antinociception, tolerance and withdrawal symptoms induced by 7-hydroxymitragynine, an alkaloid from the Thai medicinal herb Mitragyna speciosa

被引:90
作者
Matsumoto, K
Horie, S
Takayama, H
Ishikawa, H
Aimi, N
Ponglux, D
Murayama, T
Watanabe, K
机构
[1] Josai Int Univ, Fac Pharmaceut Sci, Pharmacol Lab, Chiba 2838555, 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 10300, Thailand
[4] Chiba Univ, Grad Sch Pharmaceut Sci, Chem Pharmacol Lab, Chuo Ku, Chiba 2608675, Japan
关键词
7-hydroxymitragynine; morphine; mu-opioid receptor; antinociception; tolerance; withdrawal;
D O I
10.1016/j.lfs.2004.10.086
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
7-Hydroxymitragynine is a potent opioid analgesic alkaloid isolated from the Thai medicinal herb Mitragyna speciosa, In the present study, we investigated the opioid receptor subtype responsible for the analgesic effect of this compound, [it addition. we tested whether development of tolerance, cross-tolerance to morphine and naloxone- induced withdrawal signs were observed in chronically 7-hydroxymitragynine-treated mice. Subcutaneous (s.c.) administration of 7-hydroxymitragynine produced a potent antinociceptive effect mainly through activation of mu-opioid receptors. Tolerance to the antinociceptive effect of 7-hydroxymitragynine developed as occurs to morphine, Cross-tolerance to morphine was evident in mice rendered tolerant to 7-hydroxymitragynine and vice versa. Naloxone-induced withdrawal signs were elicited equally in mice chronically treated with 7-hydroxymitragynine or morphine. 7-Hydroxymitragynine exhibited a potent antinociceptive effect based on activation of mu-opioid receptors and its morphine-like pharmacological character, but 7-hydroxymitragynine is structurally different from morphine. These interesting characters of 7-hydroxymitragynine promote further investigation of it as a novel lead compound for opioid studies, (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:2 / 7
页数:6
相关论文
共 22 条
[1]
Burkill I. H., 1935, DICT EC PRODUCTS MAL, V2, P1480
[2]
COWAN A, 1988, J PHARMACOL EXP THER, V246, P950
[3]
D'amour FE, 1941, J PHARMACOL EXP THER, V72, P74
[4]
Dhawan BN, 1996, PHARMACOL REV, V48, P567
[5]
Grewal KS, 1932, J PHARMACOL EXP THER, V46, P251
[6]
ETHNOPHARMACOLOGY OF KRATOM AND THE MITRAGYNA ALKALOIDS [J].
JANSEN, KLR ;
PRAST, CJ .
JOURNAL OF ETHNOPHARMACOLOGY, 1988, 23 (01) :115-119
[7]
ANTINOCICEPTIVE EFFECT OF LIPOPOLYSACCHARIDE FROM PANTOEA AGGLOMERANS ON STREPTOZOTOCIN-INDUCED DIABETIC MICE [J].
KAMEI, J ;
IWAMOTO, Y ;
SUZUKI, T ;
MISAWA, M ;
KASUYA, Y ;
NAGASE, H ;
OKUTOMI, T ;
SOMA, GI ;
MIZUNO, D .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1994, 251 (01) :95-98
[8]
Role of noradrenergic functions in the modification of naloxone-precipitated withdrawal jumping in morphine-dependent mice by diabetes [J].
Kamei, J ;
Ohsawa, M .
LIFE SCIENCES, 1997, 60 (15) :PL223-PL228
[9]
Antinociceptive effect of 7-hydroxymitragynine in mice:: Discovery of an orally active opioid analgesic from the Thai medicinal herb Mitragyna speciosa [J].
Matsumoto, K ;
Horie, S ;
Ishikawa, H ;
Takayama, H ;
Aimi, N ;
Ponglux, D ;
Watanabe, K .
LIFE SCIENCES, 2004, 74 (17) :2143-2155
[10]
Loss of morphine-induced analgesia, reward effect and withdrawal symptoms in mice lacking the mu-opioid-receptor gene [J].
Matthes, HWD ;
Maldonado, R ;
Simonin, F ;
Valverde, O ;
Slowe, S ;
Kitchen, I ;
Befort, K ;
Dierich, A ;
LeMeur, M ;
Dolle, P ;
Tzavara, E ;
Hanoune, J ;
Roques, BP ;
Kieffer, BL .
NATURE, 1996, 383 (6603) :819-823