Camporez João Paulo G, Asrih Mohamed, Zhang Dongyan, Kahn Mario, Samuel Varman T, Jurczak Michael J, Jornayvaz François R
Department of Internal MedicineHoward Hughes Medical InstituteYale University School of Medicine, New Haven, Connecticut 06536, USAService of EndocrinologyDiabetes and Metabolism, Lausanne University Hospital, Rue du Bugnon 46, 1011 Lausanne CHUV, Switzerland.
Department of Internal MedicineHoward Hughes Medical InstituteYale University School of Medicine, New Haven, Connecticut 06536, USAService of EndocrinologyDiabetes and Metabolism, Lausanne University Hospital, Rue du Bugnon 46, 1011 Lausanne CHUV, Switzerland Department of Internal MedicineHoward Hughes Medical InstituteYale University School of Medicine, New Haven, Connecticut 06536, USAService of EndocrinologyDiabetes and Metabolism, Lausanne University Hospital, Rue du Bugnon 46, 1011 Lausanne CHUV, Switzerland.
J Endocrinol. 2015 Sep;226(3):207-17. doi: 10.1530/JOE-15-0136. Epub 2015 Jul 22.
Fibroblast growth factor 21 (FGF21) is an important regulator of hepatic glucose and lipid metabolism and represents a potential pharmacological agent for the treatment of type 2 diabetes and obesity. Mice fed a ketogenic diet (KD) develop hepatic insulin resistance in association with high levels of FGF21, suggesting a state of FGF21 resistance. To address the role of FGF21 in hepatic insulin resistance, we assessed insulin action in FGF21 whole-body knock-out (FGF21 KO) male mice and their littermate WT controls fed a KD. Here, we report that FGF21 KO mice have hepatic insulin resistance and increased hepatic glucose production associated with an increase in plasma glucagon levels. FGF21 KO mice are also hypometabolic and display increased fat mass compared with their WT littermates. Taken together, these findings support a major role of FGF21 in regulating energy expenditure and hepatic glucose and lipid metabolism, and its potential role as a candidate in the treatment of diseases associated with insulin resistance.
成纤维细胞生长因子21(FGF21)是肝脏葡萄糖和脂质代谢的重要调节因子,是治疗2型糖尿病和肥胖症的潜在药物。喂食生酮饮食(KD)的小鼠会出现肝脏胰岛素抵抗,并伴有高水平的FGF21,提示存在FGF21抵抗状态。为了研究FGF21在肝脏胰岛素抵抗中的作用,我们评估了喂食KD的FGF21全身敲除(FGF21 KO)雄性小鼠及其同窝野生型(WT)对照小鼠的胰岛素作用。在此,我们报告FGF21 KO小鼠存在肝脏胰岛素抵抗,且肝脏葡萄糖生成增加,同时血浆胰高血糖素水平升高。与同窝WT小鼠相比,FGF21 KO小鼠代谢率也较低,且脂肪量增加。综上所述,这些发现支持FGF21在调节能量消耗、肝脏葡萄糖和脂质代谢中起主要作用,以及其作为治疗与胰岛素抵抗相关疾病的候选药物的潜在作用。