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黄精多糖预处理对乳鼠心肌细胞缺氧/复氧损伤的保护作用
引用本文:朱烨丰,刘季春,何明.黄精多糖预处理对乳鼠心肌细胞缺氧/复氧损伤的保护作用[J].矿产勘查,2010(3):29-32.
作者姓名:朱烨丰  刘季春  何明
作者单位:[1]南昌大学研究生院医学部2007级,南昌330006 [2]南昌大学第一附属医院胸外科,南昌330006 [3]南昌大学医学院药理教研室,南昌330006
摘    要:目的研究黄精多糖(Polygona-Polysaccharose,PSP)预处理对乳鼠心肌细胞缺氧/复氧(anoxia/reoxygen-ation,A/R)损伤的保护作用及与其抗氧化作用的关系。方法实验用SD新生大鼠(出生1~3 d)20只,雌雄不拘,常规方法培养心肌细胞,在培养48 h后按随机数字表法分为4组(每组重复实验6次):正常对照组(Control组)、A/R组、缺氧预处理(anoxia preconditioning,APC)组(APC+AR组,3次短暂缺氧复氧,再进行A/R操作)、PSP预处理组(PSP+A/R组)。对以下指标进行检测:细胞存活率(MTT法),培养液中乳酸脱氢酶(LDH)活性、脂质过氧化产物丙二醛(MDA)含量以及超氧化物歧化酶(SOD)活性;心肌细胞凋亡率(流式细胞仪)。结果与对照组比较,A/R组心肌细胞存活率、细胞培养液中SOD活性均明显降低(均P〈0.01),而细胞培养液中MDA含量、LDH活性及心肌细胞凋亡率均明显增加(均P〈0.01)。与A/R组比较,APC+A/R组与PSP+A/R组心肌细胞存活率、细胞培养液中SOD活性均明显增加(均P〈0.01),同时细胞培养液中MDA含量、LDH活性及心肌细胞凋亡率均明显降低(均P〈0.01)。与APC+A/R组比较,PSP+A/R组心肌细胞存活率、细胞培养液中MDA含量及LDH、SOD活性和心肌细胞凋亡率差异均无统计学意义(均P〉0.05)。结论 PSP预处理可减轻心肌细胞A/R损伤,具有模拟APC作用,其机制可能与PSP的抗氧化作用有关。

关 键 词:黄精多糖  心肌细胞  缺氧/复氧损伤  预适应  氧自由基  原代培养  动物  实验  大鼠

Study of Preconditioning with Polygona-Polysaccharose Protects Cultured Neonatal Rat Myocardial Cells against Anoxia/Reoxygenation Injury
ZHU Ye-fenga,LIU Ji-chunb,HE Ming.Study of Preconditioning with Polygona-Polysaccharose Protects Cultured Neonatal Rat Myocardial Cells against Anoxia/Reoxygenation Injury[J].Mineral Exploration,2010(3):29-32.
Authors:ZHU Ye-fenga  LIU Ji-chunb  HE Ming
Affiliation:c(a.2007 Grade of Medical Department of Graduate School;b.Department ofChest Surgery,the First Affiliated Hospital;c.Department of Pharmacology,Medical College,Nanchang University,Nanchang 330006,China)
Abstract:Objective To explore the protective effects of Polygona-Polysaccharose(PSP) on neonatal rat myocardial cells with anoxia/reoxygenation(A/R) injury and the mechanisms.Methods The myocardial cells were isolated from 20 SD neonatal rats and cultured,followed by random table method divided into four groups after being cultured for 48 hours(the experiment was duplicated 6 times in each groups),namely:normal control group,A/R group,anoxia preconditioning(APC)group(APC+A/R group),PSP preconditioning group(PSP+A/R group).Various techniques were adopted to detect the cells and cellular products:the levels of myocardial cells viability rate was assay by MTT colorimetric method;the levels of culture fluid of released lactate dehydrogenase(LDH),superoxide dismutase(SOD),and malondialde hyde(MAD);the ratio of myocardial cells apoptosis was detected by Annexin-V/PI assays with flow cytometry.Results Compared with the control group,the myocardial cells viability,the levels of culture fluid of released SOD of A/R group significantly decreased(all P0.01),whereas levels of culture fluid of released MDA,LDH,and the ratio of apoptosis significantly increased(all P0.01).Compared with A/R group,the myocardial cells viability and the levels of intracellular SOD of APC+A/R group and PSP+A/R group were significantly increased(all P0.01),while levels of culture fluid of released MDA,LDH,and the ratio of apoptosis significantly decreased(P0.01,respectively).Compared with APC+A/R group,the myocardial cells viability and the levels of intracellular SOD,MDA,LDH,and the ratio of apoptosis were not statistically significant(all P0.05).Conclusion It suggests that PSP could protect myocardial cells against A/R injury,the mechanisms of which lie in that PSP could increase activities of endogenous antioxidants.
Keywords:Polygona-Polysaccharose  myocardial cells  anoxia/reoxygenation injury  preconditioning  oxygen free radical  primary culture  animals  laboratory  rats
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