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Autophagy protects pancreatic beta cell mass and function in the setting of a high-fat and high-glucose diet

机译:自噬可在高脂高糖饮食的情况下保护胰腺β细胞质量和功能

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Autophagy is a major regulator of pancreatic beta cell homeostasis. Altered autophagic activity has been implicated in the beta cells of patients with type 2 diabetes, and in the beta cells of obese diabetic rodents. Here, we show that autophagy was induced in beta cells by either a high-fat diet or a combined high-fat and high-glucose diet, but not by high-glucose alone. However, a high-glucose intake alone did increase beta cell mass and insulin secretion moderately. Depletion of Atg7, a necessary component of the autophagy pathway, in beta cells by pancreatic intra-ductal AAV8-shAtg7 infusion in C57BL/6 mice, resulted in decreased beta cell mass, impaired glucose tolerance, defective insulin secretion, and increased apoptosis when a combined high-fat and high-glucose diet was given, seemingly due to suppression of autophagy. Taken together, our findings suggest that the autophagy pathway may act as a protective mechanism in pancreatic beta cells during a high-calorie diet.
机译:自噬是胰腺β细胞稳态的主要调节剂。自噬活性的改变与2型糖尿病患者的β细胞以及肥胖的啮齿类动物的β细胞有关。在这里,我们显示高脂饮食或高脂高糖饮食联合诱导了β细胞的自噬,但高糖饮食并没有。但是,仅高糖摄入确实会适度增加β细胞质量和胰岛素分泌。胰管内AAV8-shAtg7输注C57BL / 6小鼠后,β细胞中Atg7(自噬途径的必要成分)的消耗减少,导致β细胞质量下降,葡萄糖耐量降低,胰岛素分泌缺陷和凋亡增加。似乎是由于抑制了自噬,所以高脂和高糖饮食相结合。综上所述,我们的发现表明自噬途径可能在高热量饮食期间充当胰腺β细胞的保护机制。

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