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脂联素诱导的内源性和外源性凋亡途径的抑制可保护胰岛β细胞免受凋亡。

Adiponectin-induced inhibition of intrinsic and extrinsic apoptotic pathways protects pancreatic β-cells against apoptosis.

机构信息

Department of Endocrinology, The First Affiliated Hospital, Chongqing Medical University, Chongqing, China.

出版信息

Horm Metab Res. 2013 Aug;45(8):561-6. doi: 10.1055/s-0033-1341500. Epub 2013 May 13.

DOI:10.1055/s-0033-1341500
PMID:23670348
Abstract

Apoptosis is the main form of β-cell death in type 2 diabetes mellitus. There are 2 major pathways leading to apoptosis, 'intrinsic and extrinsic pathways'. Adiponectin is an adipocyte-derived hormone, which plays an important role in glucose and lipid metabolism. The main aims of this study were to investigate related apoptotic pathways in diabetes and the anti-apoptosis effects of adiponectin on pancreatic β-cell and the underlying mechanisms. Diabetic mice were generated by intraperitoneal injection of streptozotocin (STZ, 50 mg/kg/d for 5 days) and high-fat diet. Adiponectin overexpressing mice were developed by injecting lentivirus expressing mouse full length adiponectin (plenti-acdc-EGFP) through tail vein. Fourteen days after plenti-acdc-EGFP lentivirus injection, plasma adiponectin protein levels were increased 2-fold. Plasma triglyceride and glucose levels, but not total cholesterol, were significantly reduced in plenti-acdc-EGFP-treated mice. Pancreatic β-cell apoptotic numbers and the expression of caspase-8, -9, -3 in islet increased in diabetic mice, which was reversed by elevated adiponectin in plenti-acdc-EGFP-treated mice. These results suggest that both intrinsic and extrinsic apoptotic pathways have an important role in diabetic β-cell apoptosis. Adiponectin has antidiabetic and anti-apoptotic effects by regulating glucose and lipid metabolisms and inhibiting intrinsic and extrinsic apoptotic pathway in pancreatic β-cells.

摘要

细胞凋亡是 2 型糖尿病β细胞死亡的主要形式。有 2 条主要途径导致细胞凋亡,即“内在途径和外在途径”。脂联素是一种脂肪细胞衍生的激素,在葡萄糖和脂质代谢中发挥重要作用。本研究的主要目的是研究糖尿病相关的凋亡途径以及脂联素对胰岛β细胞的抗凋亡作用及其潜在机制。通过腹腔注射链脲佐菌素(STZ,50mg/kg/d 连续 5 天)和高脂饮食诱导建立糖尿病小鼠模型。通过尾静脉注射表达全长脂联素的慢病毒(plenti-acdc-EGFP)构建脂联素过表达小鼠。plenti-acdc-EGFP 慢病毒注射 14 天后,血浆脂联素蛋白水平增加 2 倍。plenti-acdc-EGFP 处理的小鼠血浆三酰甘油和葡萄糖水平显著降低,而总胆固醇水平没有变化。糖尿病小鼠胰岛细胞中细胞凋亡数量增加,caspase-8、-9、-3 的表达增加,而 plenti-acdc-EGFP 处理的小鼠中升高的脂联素可逆转这些变化。这些结果表明,内在途径和外在途径在糖尿病β细胞凋亡中都发挥了重要作用。脂联素通过调节葡萄糖和脂质代谢以及抑制胰岛β细胞内、外在凋亡途径发挥抗糖尿病和抗凋亡作用。

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