Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; Clinic Center of Human Gene Research, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Department of Cardiovascular Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Biochem Biophys Res Commun. 2018 May 15;499(3):403-409. doi: 10.1016/j.bbrc.2018.03.052. Epub 2018 Apr 3.
Metabolic disorders, including obesity, non-alcoholic fatty liver disease (NAFLD), metabolic syndrome and diabetes, are complex and progressive diseases. Enoyl coenzyme A hydratase 1 (Ech1) is an enzyme that participates in mitochondrial fatty acid β-oxidation; however, little is known regarding the significance of Ech1 in the pathogenesis of metabolic disorders. Here, we report that high-fat-diet (HFD)-induced and genetic obesity could increase Ech1 expression in mouse liver. The overexpression of Ech1 using adeno-associated virus (AAV2/8) ameliorated HFD-induced liver lipid accumulation and accompanying liver injury. Additionally, Ech1 overexpression resulted in improved dyslipidemia and insulin resistance in HFD-fed mice. Further, the studies revealed that Ech1 could directly inhibit lipogenesis gene expressions and attenuate the insulin pathway induced by an HFD. Together, our results demonstrate that Ech1 protects against HFD-induced hepatic steatosis and insulin resistance and that its inhibitory effects on lipogenesis and insulin signaling may partly explain its role in metabolic disorders.
代谢紊乱包括肥胖、非酒精性脂肪性肝病(NAFLD)、代谢综合征和糖尿病,是复杂且进展性的疾病。烯酰辅酶 A 水合酶 1(Ech1)是参与线粒体脂肪酸β氧化的一种酶,但对于 Ech1 在代谢紊乱发病机制中的意义知之甚少。在这里,我们报告高脂肪饮食(HFD)诱导和遗传肥胖可增加小鼠肝脏中 Ech1 的表达。使用腺相关病毒(AAV2/8)过表达 Ech1 可改善 HFD 诱导的肝脏脂质积累和伴随的肝损伤。此外,Ech1 的过表达导致 HFD 喂养小鼠的血脂异常和胰岛素抵抗得到改善。进一步的研究表明,Ech1 可直接抑制脂肪生成基因的表达,并减弱 HFD 诱导的胰岛素通路。总之,我们的研究结果表明,Ech1 可预防 HFD 诱导的肝脂肪变性和胰岛素抵抗,其对脂肪生成和胰岛素信号的抑制作用可能部分解释了其在代谢紊乱中的作用。