Omega-3 polyunsaturated fatty acids as a treatment strategy for nonalcoholic fatty liver disease

被引:103
|
作者
Jump, Donald B. [1 ]
Lytle, Kelli A. [1 ]
Depner, Christopher M. [1 ]
Tripathy, Sasmita [1 ]
机构
[1] Oregon State Univ, Mol Nutr & Diabet Res Lab, Sch Biol & Populat Hlth Sci, 107A Milam Hall, Corvallis, OR 97331 USA
基金
美国国家卫生研究院; 美国食品与农业研究所;
关键词
ELEMENT-BINDING PROTEIN; LEUCINE ZIPPER PROTEIN; GLYCATION END-PRODUCTS; TOLL-LIKE RECEPTORS; DOCOSAHEXAENOIC ACID; EICOSAPENTAENOIC ACID; GENE-EXPRESSION; AMERICAN ASSOCIATION; PRACTICE GUIDELINE; WESTERN DIET;
D O I
10.1016/j.pharmthera.2017.07.007
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Obese and type 2 diabetic (T2DM) patients have a high prevalence of nonalcoholic fatty liver disease (NAFLD). NAFLD is a continuum of chronic liver diseases ranging from benign hepatosteatosis to nonalcoholic steatohepatitis (NASH), cirrhosis and primary hepatocellular cancer (HCC). Because of its strong association with the obesity epidemic, NAFLD is rapidly becoming a major public health concern worldwide. Surprisingly, there are no FDA approved NAFLD therapies; and current therapies focus on the co-morbidities associated with NAFLD, namely, obesity, hyperglycemia, dyslipidemia, and hypertension. The goal of this review is to provide background on the disease process, discuss human studies and preclinical models that have examined treatment options. We also provide an in-depth rationale for the use of dietary omega 3 polyunsaturated fatty acid (w3 PUFA) supplements as a treatment option for NAFLD. This focus is based on recent studies indicating that NASH patients and preclinical mouse models of NASH have low levels of hepatic C20-22 omega 3 PUFA. This decline in hepatic PUFA may account for the major phenotypic features associated with NASH, including steatosis, inflammation and fibrosis. Finally, our discussion will address the strengths and limitations of omega 3 PUFA supplements use in NAFLD therapy. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:108 / 125
页数:18
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