Abstract

Hepatic lipid accumulation and oxidative stress are crucial pathophysiological mechanisms for non-alcoholic fatty liver disease (NAFLD). Thus, we examined the effect of a combination of flaxseed oil (FO) and astaxanthin (ASX) on hepatic lipid accumulation and oxidative stress in rats fed a high-fat diet. ASX was dissolved in flaxseed oil (1 g/kg; FO + ASX). Animals were fed diets containing 20% fat, where the source was lard, or 75% lard and 25% FO + ASX, or 50% lard and 50% FO + ASX, or FO + ASX, for 10 weeks. Substitution of lard with FO + ASX reduced steatosis and reduced hepatic triacylglycerol and cholesterol. The combination of FO and ASX significantly decreased hepatic sterol regulatory element-binding transcription factor 1 and 3-hydroxy-3-methylglutaryl-CoA reductase but increased peroxisome proliferator activated receptor expression. FO + ASX significantly suppressed fatty acid synthase and acetyl CoA carboxylase but induced carnitine palmitoyl transferase-1 and acyl CoA oxidase expression. FO + ASX also significantly elevated hepatic SOD, CAT and GPx activity and GSH, and markedly reduced hepatic lipid peroxidation. Thus, FO and ASX may reduce NAFLD by reversing hepatic steatosis and reducing lipid accumulation and oxidative stress.

Highlights

  • Nonalcoholic fatty liver disease (NAFLD), which includes benign hepatic steatosis and cirrhosis, has been shown to be associated with obesity, hyperlipidemia and type II diabetes [1,2]

  • ALA can compete with linoleic acid to reduce arachidonic acid or act as a precursor for longer chain n-3 PUFAs, or it can directly interact with nuclear receptors and ion channels to produce positive effects [8]

  • Western blot was performed with the following antibodies: β-actin mAb (#3700, Cell Signaling, Danvers, MA, USA), peroxisome proliferator activated receptor α (PPARα) pAb, sterol regulatory element-binding transcription factor 1 (SREBP1)

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Summary

A Combination of Flaxseed Oil and Astaxanthin

Jiqu Xu 1,2,3,† , Shuang Rong 4,† , Hui Gao 5 , Chang Chen 6,7 , Wei Yang 5 , Qianchun Deng 1,2,3 , Qingde Huang 1,2,3 , Lingyun Xiao 8 and Fenghong Huang 1,2,3, *. Hubei Key Laboratory of Lipid Chemistry and Nutrition, Oil Crops Research Institute, Chinese Academy of Agricultural Sciences, 2 Xudong Second Road, Wuhan 430062, China. Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, 2 Xudong. Functional Oil Laboratory Associated by Oil Crops Research Institute, Chinese Academy of Agricultural.

Introduction
Chemical Sources
Animals and Diets
Tissue Preparation
Liver Histology
Liver Lipid Content
Western Blot
Quantitative Real-Time PCR
Assay of Hepatic Antioxidant Activity and Lipid Peroxidation
2.11. Statistical Analyses
Effects of FO and ASX Combination on Hepatic Enzymes in Plasma
Rats fed a high‐fat diet for diet
Effects of FO and ASX on Liver Lipids
Effects of FO and ASX on Liver
Effects of FO and ASX on Liver mRNA Expression
Effects of FO and ASX on Liver Antioxidant Capacity and Lipid Peroxidation
Discussion
Conclusions
Full Text
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