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作 者:刘秀芬[1] 吴新民[1] 刘毓和[1] 左萍萍[2] 杨楠[2]
机构地区:[1]北京大学第一医院麻醉科,北京100034 [2]中国医学科学院基础医学研究所药理室,北京100005
出 处:《中国新药杂志》2009年第20期1975-1978,1982,共5页Chinese Journal of New Drugs
摘 要:目的:观察静脉持续输注丙泊酚(P)于给药后不同时间对老年大鼠大脑海马组织中胆碱能毒蕈碱样受体(M-R)和N-甲基-D-天门冬氨酸受体(NMDA-R)的影响。方法:在18月龄雄性或雌性SD大鼠,尾静脉注射丙泊酚10mg·kg-1诱导麻醉,然后恒速输注25或45mg·kg-1·h-1维持2h或4h;于丙泊酚给药后1d(近期影响组)或6,12d(远期影响组)急性处死大鼠,分离脑组织海马,用放射配体结合分析法测定M-R与[3H]-QNB以及NMDA-R与[3H]-MK-801的特异性结合量。结果:近期影响组和远期影响组分别与其对照组比较,M-R与[3H]-QNB特异性结合量及NMDA-R与[3H]-MK-801特异性结合量均无统计学差异。结论:丙泊酚静脉给药对老年大鼠海马M-R与[3H]-QNB特异性结合量及NMDA-R与[3H]-MK-801特异性结合量无近期和远期影响。Objective:To investigate the transient and permanent effect of continuous intravenous infusion of propofol at different doses on muscarinic receptor (M-R) and N-methy-D-aspartate receptor (NMDA-R) in the brain of aged rats.Methods:In 18-months-old male or female SD rats,anesthesia was induced by intravenous injection of propofol (10 mg·kg^-1) through tail vein,and maintained by small or large dose (25 or 45 mg·kg^-1·h^-1) for different time length (2h or 4h).Rats were decapitated and the hippocampus was removed 1d (for transient effect),or 6d and 12d (for permanent effect) after administration.The binding capacities of M-R with [3H]-QNB and NMDA-R with [3H]-MK-801 were measured by radiant ligand binding analysis.Results:In transient and permanent effect groups,the binding capacities of M-R with [3H]-QNB and NMDA-R with [3H]-MK-801 were not significantly different as compared with corresponding control.Conclusion:Intravenous propofol has neither transient nor permanent effect on the binding capacities of M-R with [3H]-QNB and NMDA-R with [3H]-MK-801 in the hippocampus of aged rats.
关 键 词:丙泊酚 老年 受体 毒蕈碱 N-甲基-D-天门冬氨酸
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