Tanaka Naoki, Takahashi Shogo, Fang Zhong-Ze, Matsubara Tsutomu, Krausz Kristopher W, Qu Aijuan, Gonzalez Frank J
Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA; Department of Toxicology, School of Public Health, Tianjin Medical University, Tianjin, China.
Biochim Biophys Acta. 2014 Nov;1841(11):1596-607. doi: 10.1016/j.bbalip.2014.08.015. Epub 2014 Aug 29.
Methionine- and choline-deficient diet (MCD) is a model for nonalcoholic steatohepatitis (NASH) in rodents. However, the mechanism of NASH development by dietary methionine/choline deficiency remains undetermined. To elucidate the early metabolic changes associated with MCD-NASH, serum metabolomic analysis was performed using mice treated with MCD and control diet for 3 days and 1 week, revealing significant increases in oleic and linoleic acids after MCD treatment. These increases were correlated with reduced body weight and white adipose tissue (WAT) mass, increased phosphorylation of hormone-sensitive lipase, and up-regulation of genes encoding carboxylesterase 3 and β2-adrenergic receptor in WAT, indicating accelerated lipolysis in adipocytes. The changes in serum fatty acids and WAT by MCD treatment were reversed by methionine supplementation, and similar alterations were detected in mice fed a methionine-deficient diet (MD), thus demonstrating that dietary methionine deficiency enhances lipolysis in WAT. MD treatment decreased glucose and increased fibroblast growth factor 21 in serum, thus exhibiting a similar metabolic phenotype as the fasting response. Comparison between MCD and choline-deficient diet (CD) treatments suggested that the addition of MD-induced metabolic alterations, such as WAT lipolysis, to CD-induced hepatic steatosis promotes liver injury. Collectively, these results demonstrate an important role for dietary methionine deficiency and WAT lipolysis in the development of MCD-NASH.
蛋氨酸和胆碱缺乏饮食(MCD)是啮齿动物非酒精性脂肪性肝炎(NASH)的一种模型。然而,饮食中蛋氨酸/胆碱缺乏导致NASH发展的机制仍未明确。为了阐明与MCD-NASH相关的早期代谢变化,对用MCD和对照饮食处理3天和1周的小鼠进行了血清代谢组学分析,结果显示MCD处理后油酸和亚油酸显著增加。这些增加与体重和白色脂肪组织(WAT)质量的降低、激素敏感性脂肪酶磷酸化的增加以及WAT中编码羧酸酯酶3和β2-肾上腺素能受体的基因上调相关,表明脂肪细胞中的脂解加速。补充蛋氨酸可逆转MCD处理引起的血清脂肪酸和WAT的变化,并且在喂食蛋氨酸缺乏饮食(MD)的小鼠中也检测到了类似的改变,从而证明饮食中蛋氨酸缺乏会增强WAT中的脂解。MD处理降低了血清中的葡萄糖并增加了成纤维细胞生长因子21,因此表现出与禁食反应相似的代谢表型。MCD和胆碱缺乏饮食(CD)处理之间的比较表明,在CD诱导的肝脂肪变性基础上增加MD诱导的代谢改变(如WAT脂解)会促进肝损伤。总体而言,这些结果证明了饮食中蛋氨酸缺乏和WAT脂解在MCD-NASH发展中的重要作用。