Abstract

The purpose of this study was to clarify the hepatoprotective mechanisms of fish oil in ethanol-fed rats based on lipid metabolism. Thirty eight-week-old male Wistar rats were divided into six groups: C (control), CF25 (control diet with 25% fish oil substitution), CF57 (control diet with 57% fish oil substitution), E (ethanol-containing diet) group, EF25 (ethanol-containing diet with 25% fish oil substitution), and EF57 (ethanol-containing diet with 57% fish oil substitution) groups. All of the groups were pair-fed an isoenergetic diet based on E group. Rats were sacrificed after eight weeks. When compared with C group, the plasma aspartate transaminase (AST) activity and hepatic steatosis and inflammatory cell infiltration were significantly higher, while plasma adiponectin level and hepatic AMP-activated protein kinase α (AMPKα) protein expression was significantly lower in the E group. However, the hepatic damage, including steatosis and inflammation were ameliorated in the EF25 and EF57 groups. Moreover, mRNA levels of fatty acid-oxidative enzymes, such as medium-chain acyl-coenzyme A dehydrogenase (MCAD) and carnitine palmitoyltransferase I (CPT-1) were significantly elevated in the EF57 group than those in E group. Partial replacement with fish oil might improve the fatty acid oxidation by raising mRNA levels of downstream transcription factors, finally inhibit the ethanol-induced hepatic steatosis in rats.

Highlights

  • Alcohol abuse, alcohol dependence, and other alcohol-related health problems are important public health issues worldwide [1]

  • We found that the replacement of olive oil with fish oil for (25% or 57%) in the diet significantly decreased plasma and hepatic TG and total cholesterol (TC) levels, thereby improving hepatic steatosis in rats fed with an ethanol-containing liquid diet for eight weeks [7]

  • A previous study indicated that after feeding on a fish oil-containing diet (10% w/w; eicosapentaenoic acid (EPA):docosahexaenoic acid (DHA) = 4:3) for 16 weeks, hepatic sterol response element-binding protein (SREBP)-1c expression and the downstream gene mRNA level significantly decreased in SD rats [21]

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Summary

Introduction

Alcohol dependence, and other alcohol-related health problems are important public health issues worldwide [1]. Chronic ethanol intake can cause fatty liver, hepatitis, cirrhosis, and even hepatoma. In Taiwan, hepatitis B and C are the main reasons for chronic liver disease. Patients with hepatitis B or C may exacerbate their liver disease and increase the mortality rates by consuming alcohol [2]. Alcoholic liver disease (ALD) needs to garner greater attention in Taiwan. Fish oil contains abundant amounts of n-3 polyunsaturated fatty acids (PUFAs), such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which were found to play important roles in lipid metabolism, antioxidative status, and immune function [3].

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