Inhibitory effects of processed Aconiti tuber on morphine-induced conditioned place preference in rats

被引:13
|
作者
Wu, Guiyun [1 ]
Huang, Wenqi [1 ]
Zhang, Hui [1 ]
Li, Qiaobo [1 ]
Zhou, Jun [1 ]
Shu, Haihua [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Anesthesiol, Guangzhou 510080, Guangdong, Peoples R China
基金
高等学校博士学科点专项科研基金;
关键词
Processed Aconiti tuber; Morphine; Conditioned place preference; Kappa-opioid receptor; Dynorphin; KAPPA-OPIOID AGONIST; ANTINOCICEPTIVE TOLERANCE; DYNORPHIN A(1-13); COCAINE; REWARD; ACTIVATION; ADDICTION; RECEPTORS; PROLACTIN; MECHANISM;
D O I
10.1016/j.jep.2011.04.041
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Our previous studies indicated that processed Aconiti tuber (PAT), a traditional Chinese herbal medicine, had antinociceptive effects and inhibitory effects on morphine tolerance by activation of kappa-opioid receptor (KOR). Preclinical studies also demonstrated that KOR agonists functionally attenuate addictive behaviors of morphine, such as conditioned place preference (CPP). Therefore, we hypothesize that PAT may inhibit morphine-induced CPP in rats. Materials and methods: (1) Five groups of rats (n = 8 for each group) were alternately subcutaneous (s.c.) injected with morphine 10 mg/kg (one group receive normal saline as a control) and normal saline for 8 days and oral co-administrated with distilled water or PAT 0.3, 1.0, or 3.0 g/kg daily on days 2-9 during CPP training, respectively. (2) Other four groups of rats were randomly s.c. injected with norbinaltorphimine (nor-BNI; 5 mg/kg) or normal saline (as a control) 120 min before alternately s.c. with morphine and normal saline and oral co-administrated with distilled water or PAT 3.0 g/kg daily. Each rat was acquired pre-conditioning and post-conditioning CPP data and assayed dynorphin concentration:: by radioimmunoassay in rat's nucleus accumbens (NAc) after CPP training. Results: (1) PAT 1.0 or 3.0 g/kg dose-dependently decreased the morphine-induced increase of CPP scores. (2) Nor-BNI completely antagonized the inhibition of PAT on morphine-induced CPP. (3) PAT dose-dependently increased dynorphin content in rats' NAc after CPP training. Conclusions: (1) PAT dose-dependently inhibited morphine-induced CPP. (2) The inhibition of PAT on morphine-induced CPP was probably due to activation of KOR by increasing dynorphin release in rats' NAc. (C) 2011 Elsevier Ireland Ltd. All rights reserved,
引用
收藏
页码:254 / 259
页数:6
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