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α-硫辛酸对过氧化氢诱导的胰腺β细胞氧化应激的剂量相关细胞保护作用。

Dose-related cytoprotective effect of alpha-lipoic acid on hydrogen peroxide-induced oxidative stress to pancreatic beta cells.

作者信息

Lee Byung Wan, Kwon Soo Jin, Chae Hee Young, Kang Jun Goo, Kim Chul Sik, Lee Seong Jin, Yoo Hyung Joon, Kim Jae Hyeon, Park Kyong Soo, Ihm Sung-Hee

机构信息

Department of Internal Medicine, Hallym University College of Medicine, Chuncheon, Republic of Korea.

出版信息

Free Radic Res. 2009 Jan;43(1):68-77. doi: 10.1080/10715760802590400.

Abstract

alpha-Lipoic acid (alpha-LA), an antioxidant used for diabetic polyneuropathy, was reported to induce AMP-activated protein kinase activation and reductions in insulin secretion in pancreatic beta-cells at high concentrations (> or = 500 micromol/l). This study investigated whether alpha-LA has a protective role under oxidative stress in beta-cells and its effect is dose-related. In INS-1 cells treated with alpha-LA (150-1200 micromol/l) for 24 h, alpha-LA itself (> or = 300 micromol/l) induced apoptotic death dose-dependently. However, pre-treatment with 150 and 300 micromol/l alpha-LA reduced the hydrogen peroxide-induced apoptosis in INS-1 cells and isolated islets. alpha-LA alleviated hydrogen peroxide-induced reactive oxygen species production, mitochondrial membrane depolarization and c-JNK activation in beta-cells. alpha-LA induced phosphoinositide 3-kinase-dependent Akt phosphorylation in INS-1 cells. While alpha-LA is harmful to beta-cells at high concentrations in vitro, it has potential cytoprotective effects on beta-cells under oxidative stress as in diabetes by its antioxidant properties and possibly by Akt phosphorylation at clinically relevant concentrations.

摘要

α-硫辛酸(α-LA)是一种用于治疗糖尿病性多发性神经病变的抗氧化剂,据报道,高浓度(≥500微摩尔/升)时,它会诱导胰腺β细胞中AMP激活的蛋白激酶活化并减少胰岛素分泌。本研究调查了α-LA在β细胞氧化应激状态下是否具有保护作用及其效应是否与剂量相关。在用α-LA(150 - 1200微摩尔/升)处理24小时的INS-1细胞中,α-LA本身(≥300微摩尔/升)会剂量依赖性地诱导凋亡性死亡。然而,用150和300微摩尔/升的α-LA预处理可减少过氧化氢诱导的INS-1细胞和分离胰岛的凋亡。α-LA减轻了过氧化氢诱导的β细胞中活性氧的产生、线粒体膜去极化和c-JNK活化。α-LA在INS-1细胞中诱导了磷酸肌醇3激酶依赖性的Akt磷酸化。虽然α-LA在体外高浓度时对β细胞有害,但在糖尿病等氧化应激状态下,它通过其抗氧化特性以及可能在临床相关浓度下通过Akt磷酸化对β细胞具有潜在的细胞保护作用。

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