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作 者:谭蕾[1] 罗爱林[1] 向强[1] 赵以林[1] 何璇[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学教研室,湖北武汉430030
出 处:《第四军医大学学报》2009年第5期405-407,共3页Journal of the Fourth Military Medical University
基 金:国家自然科学基金(30772086)
摘 要:目的:探讨氯胺酮、咪达唑仑及丙泊酚对大鼠发育期海马神经元细胞内钙浓度的影响.方法:将原代培养第5日的大鼠海马神经元用10μmol/L的Ca2+指示剂Fluo-4共孵育30 min洗涤后,分别加入150μmol/L氯胺酮,咪达唑仑3μmol/L,丙泊酚10μmol/L,采用激光共聚焦显微镜选定多个细胞分别测定荧光强度的变化.结果:氯胺酮使体外培养第5日的海马神经元代表钙浓度的荧光强度明显下降[(987±307)vs(766±226),P<0.05],咪达唑仑,丙泊酚均使体外培养5 d的海马神经元荧光强度明显升高[(1707±514)vs(2663±572),(1057±353)vs(1749±708),P<0.05].结论:阻滞NMDA受体的氯胺酮降低发育期海马神经元细胞内钙浓度,而兴奋GABAA受体的咪达唑仑,丙泊酚则会升高细胞内钙浓度.AIM : To investigate the effect of ketamine, midazo- lam and propofol on intraceflular Ca2+ in developing primary hippoeampus neurons of rats. METHODS: On the fifth day, the cultured hippocampal neurons were co-incubated with 10 μmol/L Fluo-4 AM for 30 min at 37℃. Excess dye was removed with three rinses of DMEM. Fluorescence imaging of intracellular Ca2. was performed to detect a number of neurons selected when the hippoeampal neurons were exposed to 150μmol/L ketamine, 3 μmol/L midazolam or 10 μmol/L propofol respectively. RESULTS: After exposed to 150 μmolfL ketamine, the intracel- lular calcium concentration of the developing neurons decreased significantly and fluorescence intensity of the neurons decreased from (987 ± 307) to (766 ± 226) (P 〈 0.05 ). When exposed to 3 μmol/L midazolam or 10 μmol/L propofol, the cytosolie Ca2 +of the neurons increased significantly and fluorescence intensity of the neurons exposed to midazolam increased from( 1707 ± 514 ) to (2663 ± 572) ( P 〈 0.05 ). Fluorescence intensity of the neurons exposed to propofol increased from( 1057 ±353 ) to (1749 ±708) ( P 〈 0.05 ). CONCLUSION : Ketamine decreases the intracel- lular Ca2+ of rat developing primary hippocampus neurons while midazolam and propofol may increase the intracellular Ca2 + of the neurons.
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