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出 处:《中华实验外科杂志》2015年第7期1510-1512,共3页Chinese Journal of Experimental Surgery
摘 要:目的 观察异丙酚对大鼠脊髓γ-氨基丁酸A(GABAA)、N-甲基-D天门冬氨酸受体(NMDA)表达的影响.方法 健康雄性SD大鼠40只,体质量220~ 250 g.随机分为空白对照组(C)、生理盐水组(NS)、异丙酚组(P组),P组分为P1、P2、P3组.生理盐水组(NS组),腹腔注射生理盐水;异丙酚组,腹腔注射异丙酚5 mg/kg(P1组)、30 mg/kg(P2组)、100 mg/kg(P3组).5 min后大鼠右侧后肢趾部皮下注射5%的福马林100μl建立疼痛模型,记录大鼠缩腿、舔爪累计时间.2h后处死大鼠,取脊髓使用免疫组织化学方法测定GABAA、NMDA的积分吸光度(IA)值.结果 C组没有缩腿、舔爪反应,与NS组[(1 326.56±198.32)s]比较,P组累计时间明显缩短(P<0.05);P3组(170.34±1.21) GABAA的IA值明显的高于其余4组,C组(85.86 ±0.47)最低.与C组比较,N、P组显著增高(P<0.05);C组(92.17 ±0.81) NMDA的IA值最低,NS组(190.43±1.20)最高,P组中P3最低.组间比较差异有统计学意义(P<0.05).结论 脊髓GABAA、NMDA受体参与了异丙酚的镇痛作用.Objective To observe the effects of propofol on the expression of N methyl D aspartate receptor (NMDA) and gamma aminobutyric acid A (GABAA) in the spinal cord of rats.Methods Healthy SD rats were randomly divided into 5 groups:control group (n =8) without given any treatment,normal saline group (n =8),and propofol group [n =24,subdividing 3 propofol subgroups (n =8 each)]:concentrations of propofol 5,30 and 100 mg/kg respectively).Five min later,5% formalin (100 μl) was injected subcutaneously into the planta region of right hindpaw.Rats were killed after 2 h and lumbar spinal cord was removed.The expression of GABAA and NMDA receptor proteins in the spinal cord dorsal horn was detected.Results The expression of GABAA protein in propofol 100 mg/kg subgroup (170.34 ± 1.21) was significantly higher than that of the rest 4 groups with the highest expression in control group (85.86 ± 0.47).As compared with control group,the GABAA protein expression was significantly increased in normal saline group and propofol group (P < 0.05).Integral absorbance of NMDA in control group was lowest (92.17 ± 0.81),and that normal saline group was highest (190.43 ± 1.20).The expression of NMDA protein was highest in propofol 100 mg/kg subgroup,and there was significant difference among three propofol subgroups (P < 0.05).Conclusion Spinal GABAAR and NMDAR receptors may participate in the analgesic effect of propofol.
关 键 词:异丙酚 γ-氨基丁酸A N-甲基-D天门冬氨酸受体
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