Role of white adipose lipolysis in the development of NASH induced by methionine- and choline-deficient diet |
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Authors: | Naoki Tanaka Shogo Takahashi Zhong-Ze Fang Tsutomu Matsubara Kristopher W. Krausz Aijuan Qu Frank J. Gonzalez |
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Affiliation: | 1. Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA;2. Department of Toxicology, School of Public Health, Tianjin Medical University, Tianjin, China;3. Department of Anatomy and Regenerative Biology, Osaka City University, Osaka, Japan |
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Abstract: | 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. |
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Keywords: | Acaca, acetyl-coenzyme A carboxylase alpha Acly, ATP citrate lyase Adrb, β-adrenergic receptor ALT, alanine aminotransferase Apob, apolipoprotein B ATGL, adipose triglyceride lipase CD, choline-deficient diet Ces3, carboxylesterase 3 Dgat, diacylglycerol O-acyltransferase Emr1, EGF-like module containing, mucin-like, hormone receptor-like sequence 1 ER, endoplasmic reticulum eWAT, epididymal white adipose tissue FA, fatty acid Fasn, fatty acid synthase FGF, fibroblast growth factor Glut4, glucose transporter type 4 GSH, glutathione HETE, hydroxyeicosatetraenoic acid HSL, hormone-sensitive lipase IL, interleukin Itgam, integrin alpha M Lcat, lecithin cholesterol acyltransferase Lpl, lipoprotein lipase MCD, methionine- and choline-deficient diet MCS, methionine- and choline-supplemented MCD diet MD, methionine-deficient diet Mttp, microsomal triglyceride transfer protein NAFLD, nonalcoholic fatty liver disease NASH, nonalcoholic steatohepatitis NEFA, non-esterified fatty acid OPLS, orthogonal projection to latent structure PCA, principal component analysis Pnpla2, patatin-like phospholipase domain containing 2 PPAR, peroxisome proliferator-activated receptor qPCR, quantitative polymerase chain reaction ROS, reactive oxygen species Scd1, stearoyl-coenzyme A desaturase 1 SS, simple steatosis TG, triglyceride TNF, tumor necrosis factor UPLC-ESI-QTOFMS, ultra-performance liquid chromatography-electrospray ionization-quadrupole time-of-flight mass spectrometry VLDL, very-low-density lipoprotein WAT, white adipose tissue |
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