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Role of white adipose lipolysis in the development of NASH induced by methionine- and choline-deficient diet
Authors:Naoki Tanaka  Shogo Takahashi  Zhong-Ze Fang  Tsutomu Matsubara  Kristopher W. Krausz  Aijuan Qu  Frank J. Gonzalez
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
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.
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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