The effects of brewers' spent grain on high-fat diet-induced fatty liver

被引:6
作者
Pei, Ya [1 ]
Balogun, Olugbenga [2 ]
Otieno, Dammah [2 ]
Parks, John S. [3 ]
Kang, Hye Won [1 ]
机构
[1] North Carolina Agr & Tech State Univ, Dept Family & Consumer Sci, Food & Nutr Sci, Greensboro, NC 27411 USA
[2] North Carolina Agr & Tech State Univ, Appl Sci & Technol, Greensboro, NC 27411 USA
[3] Wake Forest Sch Med, Dept Internal Med, Sect Mol Med, Winston Salem, NC 27157 USA
基金
美国农业部;
关键词
Brewers' spent grain; Hepatic steatosis; Cholesterol; Bile acids; INSULIN-RESISTANCE; CHOLESTEROL; FIBER;
D O I
10.1016/j.bbrc.2022.05.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Obesity drives nonalcoholic fatty liver disease (NAFLD). This study investigated the effects of dietary brewers' spent grain (BSG) supplementation on obesity-induced NAFLD. Mice fed a high-fat diet supplemented with 30% BSG (HFD30) had reduced body weight and decreased plasma total cholesterol (TC) concentrations compared with HFD-fed mice. Retroperitoneal white adipose tissue (RWAT) and liver weights were reduced. Consistent with reduced hepatic triacylglycerol, TC, and non-esterified fatty acid concentrations, HFD30-fed mice showed reduced hepatic steatosis. 3-hydroxy-3-methylglutaryl-CoA reductase and low-density lipoprotein receptor genes were increased, whereas carnitine palmitoyltransferase 1 alpha, ATP-binding cassette subfamily A member 1 (Abca1), and cholesterol 7 alphahydroxylase genes were upregulated in the liver of HFD30-fed mice. Abca1 gene expression was also increased in epididymal WAT and RWAT of HFD30-fed mice. BSG supplementation increased and decreased fecal fat and bile acid concentrations, respectively. Taken together, BSG supplementation reduced HFD-induced hepatic lipid accumulation by increasing fatty acid oxidation and bile acid synthesis in the liver as well as decreasing lipid absorption in the intestine. (C) 2022 The Authors. Published by Elsevier Inc.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 21 条
[1]   Pathogenesis of Insulin Resistance and Atherogenic Dyslipidemia in Nonalcoholic Fatty Liver Disease [J].
Akhtar, Daud H. ;
Iqbal, Umair ;
Vazquez-Montesino, Luis Miguel ;
Dennis, Brittany B. ;
Ahmed, Aijaz .
JOURNAL OF CLINICAL AND TRANSLATIONAL HEPATOLOGY, 2019, 7 (04) :362-370
[2]   Technological Properties and Consumer Acceptability of Bakery Products Enriched with Brewers' Spent Grains [J].
Amoriello, Tiziana ;
Mellara, Francesco ;
Galli, Vincenzo ;
Amoriello, Monica ;
Ciccoritti, Roberto .
FOODS, 2020, 9 (10)
[3]   Role of the hepatic ABCA1 transporter in modulating intrahepatic cholesterol and plasma HDL cholesterol concentrations [J].
Basso, F ;
Freeman, L ;
Knapper, CL ;
Remaley, A ;
Stonik, J ;
Neufeld, EB ;
Tansey, T ;
Amar, MJA ;
Fruchart-Najib, J ;
Duverger, N ;
Santamarina-Fojo, S ;
Brewer, HB .
JOURNAL OF LIPID RESEARCH, 2003, 44 (02) :296-302
[4]   Consumption of barley β-glucan ameliorates fatty liver and insulin resistance in mice fed a high-fat diet [J].
Choi, Joo Sun ;
Kim, Hyunsook ;
Jung, Myeong Ho ;
Hong, Shinhee ;
Song, Jihyun .
MOLECULAR NUTRITION & FOOD RESEARCH, 2010, 54 (07) :1004-1013
[5]  
Favari E, 2015, HANDB EXP PHARMACOL, V224, P181, DOI 10.1007/978-3-319-09665-0_4
[6]  
Hales Craig M, 2017, NCHS Data Brief, P1
[7]   Composition and Nutrient Value Proposition of Brewers Spent Grain [J].
Ikram, Sana ;
Huang, LianYan ;
Zhang, Huijuan ;
Wang, Jing ;
Yin, Meng .
JOURNAL OF FOOD SCIENCE, 2017, 82 (10) :2232-2242
[8]   Effects of long-term soluble vs. insoluble dietary fiber intake on high-fat diet-induced obesity in C57BL/6J mice [J].
Isken, Frank ;
Klaus, Susanne ;
Osterhoff, Martin ;
Pfeiffer, Andreas F. H. ;
Weickert, Martin O. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2010, 21 (04) :278-284
[9]   Thioesterase superfamily member 2/acyl-CoA thioesterase 13 (Them2/Acot13) regulates hepatic lipid and glucose metabolism [J].
Kang, Hye Won ;
Niepel, Michele W. ;
Han, Shuxin ;
Kawano, Yuki ;
Cohen, David E. .
FASEB JOURNAL, 2012, 26 (05) :2209-2221
[10]   Regulatory role for phosphatidylcholine transfer protein/StarD2 in the metabolic response to peroxisome proliferator activated receptor alpha (PPARα) [J].
Kang, Hye Won ;
Kanno, Keishi ;
Scapa, Erez F. ;
Cohen, David E. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2010, 1801 (04) :496-502