期刊文献+

黄芪总黄酮对高糖培养下牛视网膜血管周细胞凋亡的影响 被引量:16

Effect of total flavonoids of Astragalus on apoptosis of cultured bovine retinal capillary pericytes under high glucose
下载PDF
导出
摘要 目的:探讨黄芪总黄酮对高糖培养下的牛视网膜血管周细胞凋亡的影响。方法:以在体外培养3代融合的牛视网膜血管周细胞为对象,分为正常对照组、高糖组(25 mmol/L)、干预组不同浓度黄芪总黄酮组(0.25、0.5、1.0、2.0 mg/ml),孵育6d,采用TUNEL法检测培养后周细胞凋亡率;硫代巴比妥酸检测培养液丙二醛(MDA)水平;黄嘌呤氧化酶反应系统检测培养液超氧化物歧化酶(SOD)水平。结果:与高糖组比较,黄芪总黄酮0.5、1.0、2.0mg/ml组周细胞MDA含量、SOD活力、MDA含量/SOD活力比值及凋亡率均降低(P<0.01);MDA含量/SOD活力与周细胞凋亡率二者呈正相关(r=0.921,P<0.01);黄芪总黄酮2.0 mg/ml组周细胞氧化应激水平及凋亡率明显低于其他各组(P<0.05)。结论:一定浓度黄芪总黄酮对高糖培养下的牛视网膜血管周细胞凋亡有明显的抑制作用,呈剂量依赖性。 Objective: To study the effects of total flavonoids of Astragalus on apoptosis of bovine retinal capillary pericytes (BRPs) under high glucose. Methods: The third generation of nearly symphysic bovine retinal vessel pericytes cultivated in vitro were divided into normal control group, high glucose group, and Astragalus total flavonoids groups (0.25, 0.5, 1.0, 2.0 mg/ml) at random. After being incubated for 6 days, apoptosis of BRPs were detected by TUNEL method. TBA method was used to detect the eontents of MDA. Xanthine oxidase method was used to detect the SOD activities. Results: Compared with high glucose group, the apoptosis, MDA contents, SOD activity, MDA content/SOD activity of BRPs reduced markedly in total flavonoids of Astragalus groups(0.5, 1.0, 2.0mg/ml) (P 〈 0.01). The MDA content/SOD activity of BRPs correlated positively with the apoptotic rate of BRPs( r = 0.921, P 〈 0.01 ). The oxidative stress levels and apoptosis of BRPs in each total flavonoids group was lower than that of other groups( P 〈 0.05). Conclusion: Certain concentration of the total flavonoids of Astragalus can decrease the apoptosis and oxidative stress of BRPs in a dose-dependent manner.
出处 《中华中医药杂志》 CAS CSCD 北大核心 2008年第3期250-252,共3页 China Journal of Traditional Chinese Medicine and Pharmacy
基金 国家中医药管理局资助项目(No.06-07JP14)
关键词 糖尿病视网膜病变 周细胞 黄芪总黄酮 细胞凋亡 Diabetic retinopat hy Pericytes Total flavonoids of Astragalus Apoptosis
  • 相关文献

参考文献7

二级参考文献23

共引文献212

同被引文献236

引证文献16

二级引证文献159

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部