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肠道果糖代谢产生的甘油酸可诱导胰岛细胞损伤和葡萄糖不耐受。

Glycerate from intestinal fructose metabolism induces islet cell damage and glucose intolerance.

机构信息

Department of Prosthodontics, School and Hospital of Stomatology, Wuhan University, Wuhan, Hubei 430079, China; Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708, USA.

Department of Biomedical Engineering, Pratt School of Engineering, Duke University, Durham, NC 27708, USA; Department of Pharmacology & Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

Cell Metab. 2022 Jul 5;34(7):1042-1053.e6. doi: 10.1016/j.cmet.2022.05.007. Epub 2022 Jun 9.

Abstract

Dietary fructose, especially in the context of a high-fat western diet, has been linked to type 2 diabetes. Although the effect of fructose on liver metabolism has been extensively studied, a significant portion of the fructose is first metabolized in the small intestine. Here, we report that dietary fat enhances intestinal fructose metabolism, which releases glycerate into the blood. Chronic high systemic glycerate levels induce glucose intolerance by slowly damaging pancreatic islet cells and reducing islet sizes. Our findings provide a link between dietary fructose and diabetes that is modulated by dietary fat.

摘要

饮食中的果糖,尤其是在高脂肪的西方饮食环境下,与 2 型糖尿病有关。尽管果糖对肝脏代谢的影响已经得到广泛研究,但很大一部分果糖首先在小肠中代谢。在这里,我们报告说,饮食中的脂肪会增强肠道果糖代谢,从而将甘油酸释放到血液中。慢性高全身性甘油酸水平通过缓慢损伤胰岛细胞和减小胰岛大小,导致葡萄糖耐量降低。我们的发现为饮食果糖与糖尿病之间提供了联系,而这种联系受到饮食脂肪的调节。

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