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作 者:赵以林[1] 罗爱林[1] 金小高[1] 王金韬[1] 谭蕾[1] 施庆余[1] 李世勇[1]
机构地区:[1]华中科技大学同济医学院附属同济医院麻醉科,武汉市430030
出 处:《中华麻醉学杂志》2011年第6期714-716,共3页Chinese Journal of Anesthesiology
基 金:国家自然科学基金(30772086)
摘 要:目的探讨异氟醚麻醉对新生大鼠海马激活肌细胞增强因子2(MEF2)信号通路的影响。方法取出生5d的SD大鼠24只,雌雄不拘,体重10-13g,采用随机数字表法,将大鼠随机分为2组(n=12):对照组(c组)和异氟醚组(I组)。I组大鼠放置在密闭箱中,吸入1.5%异氟醚和纯氧,吸入时间6h,C组不做任何处理。于异氟醚麻醉2、4、6h和麻醉结束后24h(T1-4)时(C组于相应时点)分别取3只大鼠,断头处死,取海马组织,采用RT-PCR法测定MEF2mRNA、synGAPImRNA和ArcmRNA及突触素ImRNA的表达水平,采用Westrnblot法测定突触素I蛋白的表达水平。结果与C组比较,I组T1-3时海马MEF2mRNA、synGAPImRNA、ArcmRNA和突触素ImRNA、T2-4。时海马突触素I蛋白表达水平均上调(P〈0.05)。结论吸人麻醉浓度的异氟醚可能通过激活新生大鼠海马MEF2信号通路从而影响发育期突触的形成。Objective To investigate the effects of isoflurane anenthesia on myocyte enhancer factor 2 (MElt2) signaling pathway in neonatal rat hippocampus. Methods Twenty-four 5-day-old SD rats of both sexes, weighing 10-13 g, were randomly divided into 2 groups ( n = 12 each) : control group (group C) and isoflurane group (group I). In group I, 1.5% isoflurane in 100% 02 was inhaled for 6 h. Group C received no treatment. Three rats in each group were sacrificed at 2, 4, 6 h of isoflurane anenthesia and 24 h after isoflurane anenthesia (T1-4), and the hippocampi removed for determination of MEF2 mRNA, synGAP I mRNA, Arc mRNA and synapsin I mRNA expression (by PT-PCR) and synapsin I protein expression (by Western blot). Results Compared with group C, the expression of MEF2 mRNA, synGAP I mRNA, Arc mRNA and synapsin I mRNA at T1-3 and synapsin I protein at T2-4 was up-regulated in group I ( P 〈 0.05). Conclusion Inhalation of anaesthetic concentration of isoflurane may affect synapse formation during the development of central nervous system by activating hippocampal MEF2 signaling pathways in neonatal rats.
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