Mu-opioid receptor knockout mice are more sensitive to chlordiazepoxide-induced anxiolytic behavior

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• 作者：Kuo-Ching Wang^a ; ^b ; Yih-Jing Lee^b ; Lir-Wan Fan^c ; Pao-Pao Yang^d ; Pao-Luh Tao^d ; ^e ; Ing-Kang Ho^f ; ^g ; Lu-Tai Tien^b ; ^{068154@mail.fju.edu.tw}
• 关键词：Chlordiazepoxide ; Mu-opioid receptor knockout mice ; Elevated plus-maze test ; Western blot ; Glutamic acid decarboxylase
• 刊名：Brain Research Bulletin
• 出版年：2013
• 出版时间：January, 2013
• 年：2013
• 卷：90
• 期：Complete
• 页码：137-141
• 全文大小：485 K

文摘

We have previously demonstrated benzodiazepine binding in the cortex and hippocampus of mu-opioid receptor knockout (KO) mice. It is known that benzodiazepine receptors are involved in regulating anxiety-like behaviors. Thus, the present study was designed to examine whether there are changes in anxiety-like behavior in mice lacking mu-opioid receptors. To produce anxiolytic activity (less anxiety), the prototype benzodiazepine receptor agonist chlordiazepoxide (CDP, 5 mg/kg) was intraperitoneally administered in wild type (WT) and mu-opioid receptor KO mice. We found that compared to WT mice, mu-opioid receptor KO mice showed enhanced anxiolytic activity to CDP, including increased number of entries into open arm, increased percentage of the time spent in open arms, and decreased percentage of the time spent in enclosed arms in the elevated plus-maze test. We also assessed protein expression of the gamma-aminobutyric acid (GABA) synthetic enzyme (glutamic acid decarboxylase; GAD). Western blotting data indicated that neither the lack of mu-opioid receptors nor CDP treatment altered cortical or hippocampal GAD₆₅ or GAD₆₇ protein expression. These data indicate that compared with WT, mu-opioid receptor KO mice experienced less anxiety and exhibited enhanced anxiolytic activity to CDP treatment, and these effects were not dependent on GAD₆₅ or GAD₆₇ protein expression. Our previous and present data suggest that the anxiolytic activity displayed in mu-opioid receptor KO mice is associated with upregulation of the benzodiazepine receptor system.