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作 者:杨威[1] 郑丽丽[1] 李冲[1] 李珊[1] 王志芳[1] 王小红[1] 张毅[2]
机构地区:[1]郑州大学第一附属医院内分泌科,450052 [2]郑州大学第一附属医院生物细胞治疗中心,450052
出 处:《中华内分泌代谢杂志》2013年第9期809-811,共3页Chinese Journal of Endocrinology and Metabolism
摘 要:在正常糖浓度(5.5mmol/L)和高糖(33mmol/L)培养的人脐静脉内皮细胞(HUVECs)分别加入不同浓度的艾塞那肽并干预不同时间后,噻唑蓝(MTT)法检测细胞活力,应用流式细胞仪检测细胞早期凋亡率,Western印迹法检测蛋白激酶B(Akt)磷酸化、Bcl-2和Bax蛋白表达水平。结果显示.HUVECs经高糖培养48和72h后,细胞活力明显下降(P〈0.01)。经1、10和100nmol/L艾塞那肽干预48h后,细胞活力明显增加,并呈浓度依赖性(P〈0.01)。与正常糖浓度组比较,高糖组细胞凋亡率升高.Akt磷酸化和Bcl-2蛋白表达水平下降,Bax蛋白表达增加,Bcl-2/Bax比值降低(P〈0.01)。艾塞那肽干预后,细胞凋亡率下降,Akt磷酸化和Bcl-2蛋白表达增加,Bax蛋白表达下降,Bcl-2/Bax比值升高(P〈0.01),而艾塞那肽的作用可被磷酸肌醇3激酶(P13K)抑制剂LY294002所对抗(P〈0.01)。提示艾塞那肽可通过P13k/Akt信号通路调节Bcl-2/Bax蛋白表达来抑制高糖诱导的内皮细胞凋亡,起到保护内皮细胞的作用。After human umbilical vein endothelial cells (HUVECs) were incubated with various concentrations of exenatide for 24,48, and 72 h under the conditions of 5.5 and 33 nlmol/L glucose, the cell viability was detected by MTT assay. The apoptosis rate of endothelial cells was measured by flow cytometry. Protein kinase B (Akt) phosphorylation, Bcl-2, and Bax protein expression were detected by Western blotting. The results showed that the cell viability was decreased after HUVECs were incubated with high glucose for48 and 72 h ( P〈O. O1 ). Treatment with 1, 10, and 100 nmol/L exenatide for 48 h significantly increased the cell viability in the presence of high glucose, in a dose-dependent manner (P〈0.01). High glucose inhibited Akt phosphorylation and Bcl-2 protein expression, stimulated Bax protein expression, with decreased Bcl-2/Bax ratio and increased apoptosis ratio of cells. After treatment with exenatide, the cell apoptosis reduced, Akt phosphorylation and Bcl-2 protein expression increased, and Bax protein expression decreased, with increased Bcl-2/Bax ratio ( P 〈 0. 01 ). These effects of exenatide on endothelial cell were abrogated by an inhibitor of phosphotylinosital 3 kinase (PI3K) LY294002 (P〈 0. 01 ), suggesting that the exenatide may regulate Bcl-2/Bax protein expression and inhibit endothelial cell apoptosis induced by high glucose through PI3k/Akt signal pathway, and thus may protect endothelial cells.
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