周文华, 刘惠芬, 顾钧, 谢小虎, 唐甩恩, 杨国栋, 吴其夏. 吗啡依赖大鼠脊髓和脑干毒蕈碱受体亚型基因的表达J. 药学学报, 2002, 37(8): 611-615.
引用本文: 周文华, 刘惠芬, 顾钧, 谢小虎, 唐甩恩, 杨国栋, 吴其夏. 吗啡依赖大鼠脊髓和脑干毒蕈碱受体亚型基因的表达J. 药学学报, 2002, 37(8): 611-615.
ZHOU Wen-hua, LIU Hui-fen, GU Jun, XIE Xiao-hu, TANG Shuai-en, YANG Guo-dong, WU Qi-xia. mRNA EXPRESSION OF MUSCARINIC RECEPTORS IN SPINAL CORD AND BRAINSTEM IN MORPHINE DEPENDENT RATSJ. Acta Pharmaceutica Sinica, 2002, 37(8): 611-615.
Citation: ZHOU Wen-hua, LIU Hui-fen, GU Jun, XIE Xiao-hu, TANG Shuai-en, YANG Guo-dong, WU Qi-xia. mRNA EXPRESSION OF MUSCARINIC RECEPTORS IN SPINAL CORD AND BRAINSTEM IN MORPHINE DEPENDENT RATSJ. Acta Pharmaceutica Sinica, 2002, 37(8): 611-615.

吗啡依赖大鼠脊髓和脑干毒蕈碱受体亚型基因的表达

mRNA EXPRESSION OF MUSCARINIC RECEPTORS IN SPINAL CORD AND BRAINSTEM IN MORPHINE DEPENDENT RATS

  • 摘要: 目的观察吗啡依赖大鼠脊髓和脑干毒蕈碱型乙酰胆碱受体m1~5的表达。方法以β-actin为内标,用RT-PCR方法检测m1~5的表达。结果吗啡依赖大鼠脊髓m1~5受体和脑干中m1和m2表达较正常对照组明显升高,注射纳洛酮1 h后脊髓m1~4和脑干m1表达较依赖组减少。东莨菪碱(0.5 mg·kg-1,ip)或呱伦西平(10 mg·kg-1,ip)明显减少吗啡戒断症状,呱伦西平处理后脊髓m1,m2,m3和m5表达较戒断对照组增加,东莨菪碱处理后脊髓m2,m3和m4表达增加。结论脊髓M受体适应性改变是吗啡戒断症状表达的生物学基础。

     

    Abstract: AIMTo observe mRNA expression of muscarinic acetylcholine receptors in spinal cord and brainstem in morphine dependent or withdrawal rats. METHODSThe mRNA expression level of m1, m2, m3, m4 and m5 were determined by RT-PCR, the β-actin mRNA expression was used as internal control. RESULTSThe mRNA level of m1, m2, m3, m4 and m5 in spinal cord and m1 and m2 in brainstem were increased significantly during morphine dependence, and the levels of m1, m2, m3 and m4 in spinal cord and m1 in brainstem were decreased 1 h after the injection of naloxone (4 mg·kg-1, ip) in morphine dependent rats. Either scopolamine (0.5 mg·kg-1) or pirenzepine (10 mg·kg-1) was shown to significantly decrease the morphine withdrawal symptoms in rats. The levels of m1, m2, m3 and m5 in spinal cord were increased by pretreatment with pirenzepine and the levels of m2, m3 and m4 in spinal cord were increased by pretreatment with scopolamine. CONCLUSIONThe adaptive expression of muscarinic receptors at spinal and supraspinal levels play important role in mediating morphine dependence and withdrawal in rats.

     

/

返回文章
返回