Tajima Kazuki, Shirakawa Jun, Okuyama Tomoko, Kyohara Mayu, Yamazaki Shunsuke, Togashi Yu, Terauchi Yasuo
Department of Endocrinology and Metabolism, Graduate School of Medicine, Yokohama City University, Yokohama, Japan.
Department of Endocrinology and Metabolism, Graduate School of Medicine, Yokohama City University, Yokohama, Japan
Am J Physiol Endocrinol Metab. 2017 Sep 1;313(3):E367-E380. doi: 10.1152/ajpendo.00447.2016. Epub 2017 May 16.
Metformin has been widely used for the treatment of type 2 diabetes. However, the effect of metformin on pancreatic β-cells remains controversial. In this study, we investigated the impacts of treatment with metformin on pancreatic β-cells in a mouse model fed a high-fat diet (HFD), which triggers adaptive β-cell replication. An 8-wk treatment with metformin improved insulin resistance and suppressed the compensatory β-cell hyperplasia induced by HFD-feeding. In contrast, the increment in β-cell mass arising from 60 wk of HFD feeding was similar in mice treated with and those treated without metformin. Interestingly, metformin suppressed β-cell proliferation induced by 1 wk of HFD feeding without any changes in insulin resistance. Metformin directly suppressed glucose-induced β-cell proliferation in islets and INS-1 cells in accordance with a reduction in mammalian target of rapamycin phosphorylation. Taken together, metformin suppressed HFD-induced β-cell proliferation independent of the improvement of insulin resistance, partly via direct actions.
二甲双胍已被广泛用于治疗2型糖尿病。然而,二甲双胍对胰腺β细胞的作用仍存在争议。在本研究中,我们在喂食高脂饮食(HFD)的小鼠模型中研究了二甲双胍治疗对胰腺β细胞的影响,高脂饮食会引发适应性β细胞复制。二甲双胍治疗8周可改善胰岛素抵抗,并抑制高脂饮食喂养诱导的代偿性β细胞增生。相比之下,在接受二甲双胍治疗和未接受二甲双胍治疗的小鼠中,高脂饮食喂养60周引起的β细胞质量增加相似。有趣的是,二甲双胍抑制了高脂饮食喂养1周诱导的β细胞增殖,而胰岛素抵抗没有任何变化。二甲双胍直接抑制了胰岛和INS-1细胞中葡萄糖诱导的β细胞增殖,这与雷帕霉素哺乳动物靶点磷酸化的降低相一致。综上所述,二甲双胍抑制高脂饮食诱导的β细胞增殖,与胰岛素抵抗的改善无关,部分是通过直接作用实现的。