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出 处:《中华中医药杂志》2011年第10期2282-2284,共3页China Journal of Traditional Chinese Medicine and Pharmacy
基 金:贵州省高层次人才科研条件特助经费项目[No.TZJF(2006)12]~~
摘 要:目的:探讨银杏达莫(GBE)对家兔缺血再灌注(I/R)心肌细胞凋亡、凋亡基因及左心室功能的影响。方法:24只家兔分为对照组、缺血再灌注组(I/R)及银杏达莫组(GBE)各8只,缺血再灌注180min后,TUNEL法观察心肌细胞凋亡,免疫组化观察bcl-2、caspase-3蛋白表达,半定量RT-PCR法检测caspase-3 mRNA、bcl-2 mRNA表达,超声测量家兔左心室Tei及LVEF值。结果:与对照组比较,I/R组和GBE组凋亡细胞灰度值、caspase-3表达、Tei值增高(P<0.05),bcl-2表达、LVEF值降低(P<0.05);与I/R组相比较,GBE组bcl-2表达、LVEF值增高(P<0.01,P<0.05),凋亡心肌灰度值、caspase-3表达及Tei值减少(P<0.01,P<0.05)。结论:GBE可减少I/R心肌凋亡,改善左心室功能,上调抑凋亡基因bcl-2,下调促凋亡基因caspase-3。Objective: To study the effect of Ginkgo biloba extract(GBE) on cardiac myocyte apoptosis,the expression of bcl-2,caspase-3 and the left ventricular function in rabbits with myocardial Ischemia/reperfusion.Methods: 24 rabbits were divided into 3 groups randomly(8 rabbits per group),namely Sham-operated group(Sham);ischemia reperfusion group(I/R) and Ginkgo biloba extract group(GBE).At the moment of 180 minutes after reperfusion,Using TUNEL,immunohistochemical and RT-PCR method for detecting myocardium cell apoptosis,expression of protein bcl-2,and caspase-3 and expression of mRNA bcl-2 and caspase-3;UCG was used and Tei index and ejection fraction(LVEF) of the left ventricular were examined to assess the left ventricular total and systolic function in rabbits.Results: Results cardiac myocyte apoptosis,expression of caspase-3,Tei in rabbits with I/R group and GBE group were higher than those of controls(P〈0.05).Results: the expression of bcl-2,caspase-3 and LVEF in rabbits with I/R group and GBE group were lower than those of controls(P〈0.05).Cardiac myocyte apoptosis and the express of caspase-3 in GBE group decreased significantly(P〈0.01,P〈0.05) and the express of bcl-2 in GBE group increased significantly compared with the I/R group.The left ventricular function in GBE improved significantly(P〈0.05) compared with the I/R group.Conclusions: GBE could decrease cardiomyocyte apoptosis significantly and improve left ventricular function significantly.Up-regulating the protein expression of bcl-2 and down-regulating the protein expression of caspase-3 in cardiomyocytes during I/R course may be one of the mechanisms of GBE.
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