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作 者:徐启华[1,2] 丁帆[1,2] 代中华[1,2] 徐海飞[1,2] 郝维[1,2] 曹济民[1,2]
机构地区:[1]中国医学科学院基础医学研究所 [2]北京协和医学院基础学院生理学和病理生理学系,100005
出 处:《医学研究杂志》2010年第7期26-29,共4页Journal of Medical Research
基 金:国家自然科学基金资助项目(30670863);国家"863"项目资助课题(2008AA02Z425)
摘 要:目的建立体外培养大鼠脑微血管内皮细胞ox-LDL损伤模型,探讨hexarelin对大鼠脑微血管内皮细胞的保护作用。方法分离并培养大鼠脑微血管内皮细胞,分成正常对照组(control)、ox-LDL组(ox-LDL)、hexarelin+ox-LDL组(hex+ox-LDL)3组。其中ox-LDL组在培养液中加入ox-LDL50mg/L;hex+ox-LDL组加入ox-LDL50mg/L和0.1μmol/Lhexarelin;正常对照组加入等量PBS。各组细胞无血清培养12h,MTT法检测细胞存活率,TUNEL法检测细胞凋亡情况,Western blot法检测内皮细胞eNOS蛋白表达情况以及蛋白质硝基化情况。结果 50mg/Lox-LDL作用12h可明显诱导内皮细胞凋亡,减少eNOS蛋白表达,促进蛋白质的硝基化。而用0.1μmol/Lhexarelin和50mg/Lox-LDL共同孵育,可明显减少内皮细胞的凋亡,提高eNOS的表达水平,减少蛋白质的硝基化程度。结论 hexarelin能有效抑制由ox-LDL引起的脑微血管内皮细胞损伤,提示hexarelin对脑动脉粥样硬化可能有一定抑制作用。ObjectiveTo investigate the protective effects of hexarelin on ox-LDL induced endothelial injury in rat cerebral microvasculature. MethodsThe endothelial cells of rat cerebral microvasculature were isolated and cultured with serum-free culture medium for 12 hours at 37℃. The cultured endothelial cells were treated with either 50mg/L ox-LDL (ox-LDL group) or with 0.1μmol/L hexarelin and 50mg/L ox-LDL (hex+ox-LDL group). Control cells were treated with PBS (control group). Cell viability was assessed by MTT assay and apoptosis was evaluated by TUNEL. The expression levels of endothelial nitric oxide synthase (eNOS) and protein nitrification in endothelial cells were measured by Western blot. ResultsCompared with the control cells, the apoptotic rate and protein nitrification level increased, and the eNOS expression level decreased in the ox-LDL treated endothelial cells. In cells with hexarelin + ox-LDL treatment, however, the apoptotic rate and protein nitrification significantly decreased and eNOS expression significantly increased compared with the ox-LDL treated cells. ConclusionHexarelin effectively protected the ox-LDL induced endothelial injuries in rat cerebral microvasculature. These effects suggest that hexarelin may have a potential in treating cerebral atherosclerosis.
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