Oyster extracts attenuate pathological changes in non-alcoholic steatohepatitis (NASH) mouse model

被引:17
作者
Watanabe, Mitsugu [1 ]
Fuda, Hirotoshi [2 ]
Okabe, Hiroaki [2 ]
Joko, Sae [2 ]
Miura, Yusuke [2 ]
Hui, Shu-Ping [2 ]
Yimin [3 ]
Hamaoka, Naohiro [4 ]
Miki, Emiko [1 ]
Chiba, Hitoshi [2 ]
机构
[1] Watanabe Oyster Lab Co Ltd, 490-3 Shimoongata Cho, Hachioji, Tokyo 1920154, Japan
[2] Hokkaido Univ, Fac Hlth Sci, Sapporo, Hokkaido 0600812, Japan
[3] Hokkaido Univ, Grad Sch Med, Sapporo, Hokkaido 0608638, Japan
[4] Hokkaido Res Org, Food Proc Res Ctr, Ebetsu, Hokkaido 0690836, Japan
基金
日本学术振兴会;
关键词
Pacific oyster; Obesity; Insulin resistance; Polyphenol; Antioxidant; FATTY LIVER-DISEASE; CULTURED HUMAN HEPATOCYTES; GREEN TEA POLYPHENOL; PHENOLIC ANTIOXIDANT; HEPATIC STEATOSIS; METABOLIC SYNDROME; CRASSOSTREA-GIGAS; OXIDATIVE STRESS; PPAR-GAMMA; CELL-DEATH;
D O I
10.1016/j.jff.2015.11.029
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The phenolic compound 3,5-dihydroxy-4-methoxybenzyl alcohol (DHMBA) is a natural antioxidant recently isolated from the Pacific oyster. DHMBA, up to a concentration of 500 mu M, has demonstrated a strong in vitro hepatocyte-protective effect from oxidative stress without any cytotoxicity. This study investigated the in vivo potential of DHMBA-rich oyster extracts (DOE) for prevention or attenuation of non-alcoholic steatohepatitis (NASH). NASH-model mice, developed by supplementation of a high-fat diet for 23 weeks and intravenous injections of oxidised low-density lipoproteins, exhibited obesity, insulin resistance, hepatic steatosis, inflammation, fibrosis, and apoptosis. These changes were significantly moderated by supplementation of DOE. The search for an underlying mechanism determined that DOE significantly improved the redox status of DNA, proteins, and lipids. Moreover, DOE suppressed the increase of hepatic expression of PPARy and CD36 (fatty acid transporter) in the NASH-model mice. DOE might serve as a functional food for people at elevated risk for NASH. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:516 / 531
页数:16
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