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儿茶素清除超氧阴离子对血管紧张素II诱导的内皮祖细胞中NO和eNOS表达及细胞凋亡的影响

[Effects of clearance of superoxide anion by catechin on the expression of NO and eNOS and apoptosis in endothelial progenitor cells induced by angiotensin II].

作者信息

Wu Li-Yuan, Dang Xi-Qiang, He Xiao-Jie, Yi Zhu-Wen

机构信息

Department of Pediatrics, Second Xiangya Hospital, Central South University, Changsha 410011, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2009 Jun;11(6):476-80.

Abstract

OBJECTIVE

To evaluate the effect of clearance of superoxide anion by catechin on the expression of nitrogen monoxidum (NO) and endothelial nitricoxide synthase (eNOS) and apoptosis in endothelial progenitor cells (EPCs) induced by angiotensin II (Ang II).

METHODS

The marrow endothelial progenitor cells of Sprague-Dawley rats were isolated and assigned to control (no treatment), Ang II treatment and Ang II + catechin treatment groups. After 48 hrs of culture, the concentration of O2*- in the supernate was measured by the NBT method, and NO concentration in the supernate was measured by the nitrate reductase method; the apoptosis rate of EPCs was detected by the TUNEL method; the mRNA expression of eNOS was detected by RT-PCR; the protein expression of eNOS was detected by Western blot analysis.

RESULTS

Ang II of 10-6 mol/L was determined as the suitable concentration for cell induction by the MTT test. Catechin of 400 mg/L was determined as an advisable intervention dosage. The apoptosis rate of EPCs in the control, the Ang II and the Ang II+catechin treatment groups were 2.48+/-0.12%, 54.18+/-0.77% and 16.87+/-0.35%, respectively, and there were significant differences among the three groups (P<0.01). The O2*- concentration in the Ang II and the Ang II+catechin treatment groups (81.7+/- 3.6 and 62.3+/- 2.2 U/L respectively) was significantly higher than that in the control group (33.7+/- 2.8 U/L) (P<0.01). An increased NO concentration was also found in the Ang II (189. 8+/- 9.0 micromol/L) and the Ang II+catechin treatment groups (276.4+/- 10.1 micromol/L) compared with that in the control group (105.8+/- 9.8 micromol/L) (P<0.01). There were significant differences in the concentrations of O2*- and NO between the Ang II and the Ang II+catechin treatment groups (P<0.05). The mRNA (P<0.05) and protein expression (P<0.01) of eNOS in the Ang II and the Ang II+catechin treatment groups increased significantly compared with those in the control group. The Ang II+catechin treatment group showed increased eNOS protein expression compared with the Ang II group (P<0.05).

CONCLUSIONS

Ang II may induce the generation of O2*-, inactivate NO and increase gene and protein expression of eNOS in EPCs. Catechin might decrease the apoptosis of EPCs through the effective clearance of O2*-and the reduction of NO inactivation and of eNOS protein uncoupling.

摘要

目的

评估儿茶素清除超氧阴离子对血管紧张素II(Ang II)诱导的内皮祖细胞(EPCs)中一氧化氮(NO)、内皮型一氧化氮合酶(eNOS)表达及细胞凋亡的影响。

方法

分离Sprague-Dawley大鼠骨髓内皮祖细胞,分为对照组(未处理)、Ang II处理组和Ang II+儿茶素处理组。培养48小时后,采用NBT法测定上清液中O2*-浓度,采用硝酸还原酶法测定上清液中NO浓度;采用TUNEL法检测EPCs凋亡率;采用RT-PCR检测eNOS的mRNA表达;采用蛋白质印迹分析检测eNOS的蛋白表达。

结果

通过MTT试验确定10-6 mol/L的Ang II为合适的细胞诱导浓度。确定400 mg/L的儿茶素为适宜的干预剂量。对照组、Ang II处理组和Ang II+儿茶素处理组EPCs的凋亡率分别为2.48±0.12%、54.18±0.77%和16.87±0.35%,三组间差异有统计学意义(P<0.01)。Ang II处理组和Ang II+儿茶素处理组的O2*-浓度(分别为81.7±3.6和62.3±2.2 U/L)显著高于对照组(33.7±2.8 U/L)(P<0.01)。与对照组(105.8±9.8 μmol/L)相比,Ang II处理组(189.8±9.0 μmol/L)和Ang II+儿茶素处理组(276.4±10.1 μmol/L)的NO浓度也升高(P<0.01)。Ang II处理组和Ang II+儿茶素处理组之间的O2*-和NO浓度差异有统计学意义(P<0.05)。与对照组相比,Ang II处理组和Ang II+儿茶素处理组中eNOS的mRNA(P<0.05)和蛋白表达(P<0.01)显著增加。与Ang II组相比,Ang II+儿茶素处理组的eNOS蛋白表达增加(P<0.05)。

结论

Ang II可能诱导EPCs中O2*-的生成,使NO失活,并增加eNOS的基因和蛋白表达。儿茶素可能通过有效清除O2*-、减少NO失活和eNOS蛋白解偶联来减少EPCs的凋亡。

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