首页> 外文期刊>Pharmacological reports: PR >Protective effect of alpha-lipoic acid on oxidized low density lipoprotein-induced human umbilical vein endothelial cell injury.
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Protective effect of alpha-lipoic acid on oxidized low density lipoprotein-induced human umbilical vein endothelial cell injury.

机译:α-硫辛酸对氧化的低密度脂蛋白诱导的人脐静脉内皮细胞损伤的保护作用。

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摘要

The present study investigated the effect and possible mechanisms of alpha-lipoic acid (LA) in preventing endothelial cell injury induced by oxidized low-density lipoprotein (oxLDL). A model of human umbilical vein endothelial cell (HUVEC) injury was established by incubating the HUVECs with 200 mug/ml oxLDL. HUVECs were pre-treated with 0.1, 0.2 or 0.5 mmol/l of LA in the presence of oxLDL for 24 h. Apoptosis and cellular surface ceramide content were investigated separately by flow cytometry and by LC-MS/MS. LOX-1, Bcl-2 and CRP protein expression levels were evaluated by western blotting. LOX-1 mRNA expression was evaluated by RT-PCR assay. The results showed that oxLDL induced cytotoxicity in both concentration-dependent and time-dependent manners. LA boosted the cell survival rate and significantly reduced the content of MDA and lactate dehydrogenase (LDH) leakage. Apoptotic rates were significantly reduced by the addition of LA compared to oxLDL group. LA might also have inhibited ceramide generation induced by oxLDL in a dose-dependent manner. Furthermore, LA down-regulated LOX-1 protein and mRNA expression and up-regulated Bcl-2 protein expression levels in a dose-dependent manner. Expression of CRP protein was weak and undetectable. These results suggested that LA exhibited cytoprotective effects against oxLDL by decreasing apoptotic rates and decreasing cellular surface ceramide content, two effects that are related to decreased LOX-1 expression, and also by stimulating the expression of Bcl-2 protein. The cytoprotective effects are not thought to be due to inhibited C-reactive protein (CRP) protein expression in HUVECs.
机译:本研究调查了α-硫辛酸(LA)在预防氧化低密度脂蛋白(oxLDL)诱导的内皮细胞损伤中的作用及其可能的机制。通过将HUVEC与200杯/毫升oxLDL孵育,建立了人脐静脉内皮细胞(HUVEC)损伤的模型。在oxLDL存在下,用0.1、0.2或0.5 mmol / l的LA对HUVEC进行预处理24小时。通过流式细胞术和LC-MS / MS分别研究细胞凋亡和细胞表面神经酰胺含量。通过蛋白质印迹评估LOX-1,Bcl-2和CRP蛋白表达水平。通过RT-PCR测定评估LOX-1 mRNA的表达。结果表明oxLDL以浓度依赖性和时间依赖性方式诱导细胞毒性。 LA可提高细胞存活率,并显着降低MDA含量和乳酸脱氢酶(LDH)泄漏。与oxLDL组相比,添加LA可显着降低细胞凋亡率。 LA可能还以剂量依赖性方式抑制了oxLDL诱导的神经酰胺生成。此外,LA以剂量依赖性方式下调LOX-1蛋白和mRNA表达,并上调Bcl-2蛋白表达水平。 CRP蛋白的表达较弱且无法检测。这些结果表明,LA通过降低细胞凋亡率和降低细胞表面神经酰胺含量,对oxLDL表现出细胞保护作用,这两种作用与LOX-1表达降低以及刺激Bcl-2蛋白表达有关。认为细胞保护作用不是由于HUVEC中C反应蛋白(CRP)蛋白表达受抑制所致。

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