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作 者:张婷婷[1] 任鹏宇[1] 刘嘉祺[1] 翟凤国[1] 关利新[1] ZHANG Ting -ting etal(Department of pharmacology, Mudanjiang Medical University, Mudanjiang, Heilongjiang 157011, China)
机构地区:[1]牡丹江医学院药理教研室,黑龙江牡丹江157011
出 处:《牡丹江医学院学报》2017年第1期28-30,80,共4页Journal of Mudanjiang Medical University
基 金:国家自然科学基金课题(81374007;81641125);黑龙江省自然科学基金课题(H201379);黑牡丹江医学院研究生创新科研课题(2014YJSCX-14)
摘 要:目的探讨西洋参茎叶皂苷对PC12细胞在氧糖剥夺损伤中的保护作用及可能机制。方法以缺氧缺糖诱导PC12细胞损伤模型(OGD)模拟脑缺血病理的改变,应用MTT法检测细胞存活率,分光光度计检测乳酸脱氢酶(LDH)释放量、超氧化物歧化酶(SOD)活性、丙二醛(MDA)及一氧化氮(NO)含量,研究西洋参茎叶皂苷对该氧糖剥夺损伤模型的影响。结果与正常对照组比较,模型组PC12细胞在OGD损伤后细胞存活率和SOD活性显著下降(P<0.01),LDH释放量显著增加(P<0.01),MDA和NO水平均明显升高(P<0.01)。与模型组比较,西洋参茎叶皂苷高、中剂量组可明显提高细胞的存活率(P<0.01)和SOD活性(P<0.01),减少LDH释放(P<0.01),降低MDA和NO水平(P<0.01),差异具有统计学意义。结论西洋参茎叶皂苷对PC12细胞氧糖剥夺损伤具有保护作用,其保护机制可能与PQS稳定细胞膜,抗氧化损伤及清除自由基的作用有关。Objective To investigate the protective effect of Panax quinquefolium saponins from steams and leaves (PQS) on PC12 cell injured by oxygen - glucose deprivation(OGD) as well as the possible mechanisms. Methods A pheochromocytoma cell in- jury model was induced by OGD to simulate the cerebral isehemic changes. The protective effects of PQS were investigated in this mod- el. The MTT assay and the lactate dehydrogenase (LDH) release were used to evaluate the protective effects of PQS. Superoxide dis- mutase (SOD), malondialdehyde (MDA) and nitric oxide (NO) were determined by speetrophotometry using commercial kits. Re- sults Compared with the control group, oxygen -glucose deprivation injury model group significantly reduce the cell survival rate and SOD activities( P 〈 0.01 ) ,increased the LDH leakage rate( P 〈 0.01 ), enhanced the content of MDA and NO( P 〈 0.01 ). Treatment with PQS (200, 1 oo μg·mL^-1) significantly enhanced the cell viability and SOD activities (P 〈 0.01 ), reduced LDH release (P 〈 0.01 ) , decreased the content of MDA and NO( P 〈0.01 )of the pheochromocytoma ceils compared with the OGD group. Conclusion PQS offers protective effect against OGD- induced injury in PC12 cells, and the possible mechanism may be associated with the im- provement of cell antioxidant capacity and scavenging free radical.
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