YOKUKANSAN INHIBITS MORPHINE TOLERANCE AND PHYSICAL DEPENDENCE IN MICE: THE ROLE OF α2A-ADRENOCEPTOR

被引:25
作者
Nakagawa, T. [1 ]
Nagayasu, K. [1 ]
Nishitani, N. [1 ]
Shirakawa, H. [1 ]
Sekiguchi, K. [2 ]
Ikarashi, Y. [2 ]
Kase, Y. [2 ]
Kaneko, S. [1 ]
机构
[1] Kyoto Univ, Grad Sch Pharmaceut Sci, Dept Mol Pharmacol, Sakyo Ku, Kyoto 6068501, Japan
[2] Tsumura & Co, Tsumura Res Labs, Ami, Ibaraki 3001192, Japan
关键词
morphine; physical dependence; tolerance; yokukansan; alpha(2)-adrenoceptor; TRADITIONAL JAPANESE MEDICINE; NALOXONE-PRECIPITATED WITHDRAWAL; GEISSOSCHIZINE METHYL-ETHER; YI-GAN-SAN; OPIATE WITHDRAWAL; LOCUS-COERULEUS; PSYCHOLOGICAL SYMPTOMS; GLUTAMATE TRANSPORTER; AGGRESSIVE-BEHAVIOR; BRAIN-STEM;
D O I
10.1016/j.neuroscience.2012.09.079
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Yokukansan (YKS) is a traditional Japanese medicine consisting of seven medicinal herbs that is used for the treatment of neurosis, insomnia, and the behavioral/psychological symptoms of dementia. This study examined the effects of YKS on morphine tolerance and physical dependence in mice. Daily oral administration of YKS (0.5 or 1.0 g/kg) for 3 weeks significantly attenuated morphine tolerance and naloxone-precipitated morphine withdrawal signs (jumps and body weight loss) without affecting the analgesic effect of morphine. The inhibitory effect of YKS on withdrawal jumps in morphine-dependent mice was blocked by a single pretreatment with an alpha(2)-adrenoceptor antagonist, yohimbine, but not by an alpha(1)-adrenoceptor antagonist, prazosin. A similar inhibitory effect on withdrawal jumps was observed by repeated administration of yohimbine. The membrane expression of alpha(2A)-adrenoceptors in the pons/medulla was decreased in morphine withdrawn animals; this reduction was prevented by repeated administration of YKS or yohimbine. Competitive radioligand and [S-35]guanosine-5'-O-(3-thiotriphosphate) binding assays revealed that YKS and its constituent herbs, Glycyrrhiza (GR) and Uncaria hook (UH), had specific binding affinity for and antagonist activity against the alpha(2A)-adrenoceptor. Certain chemical constituents, including GR-derived glycyrrhizin and its metabolite, 18 beta-glycyrrhetinic acid, and UH-derived geissoschizine methyl ether (GME), shared such activities. Repeated administration of GR, UH, glycyrrhizin or GME significantly inhibited morphine withdrawal signs. These results suggest that YKS and its active constituents inhibit morphine tolerance and physical dependence, and that the latter is due at least in part to the prevention of the decreased membrane expression of the alpha(2A)-adrenoceptor in the brainstem by its prolonged blockade. (C) 2012 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:336 / 349
页数:14
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