Biomol Ther.  2016 Nov;24(6):650-658. 10.4062/biomolther.2016.176.

Protective Effects of Ecklonia stolonifera Extract on Ethanol-Induced Fatty Liver in Rats

Affiliations
  • 1Department of Preventive Pharmacy and Toxicology, College of Pharmacy, Kyung Hee University, Seoul 02447, Republic of Korea. sychoung@khu.ac.kr
  • 2Department of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
  • 3Department of Food Science and Nutrition, Pukyong National University, Busan 48513, Republic of Korea.

Abstract

Chronic alcohol consumption causes alcoholic liver disease, which is associated with the initiation of dysregulated lipid metabolism. Recent evidences suggest that dysregulated cholesterol metabolism plays an important role in the pathogenesis of alcoholic fatty liver disease. Ecklonia stolonifera (ES), a perennial brown marine alga that belongs to the family Laminariaceae, is rich in phlorotannins. Many studies have indicated that ES has extensive pharmacological effects, such as antioxidative, hepatoprotective, and antiinflammatory effects. However, only a few studies have investigated the protective effect of ES in alcoholic fatty liver. Male Sprague-Dawley rats were randomly divided into normal diet (ND) (fed a normal diet for 10 weeks) and ethanol diet (ED) groups. Rats in the ED group were fed a Lieber-DeCarli liquid diet (containing 5% ethanol) for 10 weeks and administered ES extract (50, 100, or 200 mg/kg/day), silymarin (100 mg/kg/day), or no treatment for 4 weeks. Each treatment group comprised of eight rats. The supplementation with ES resulted in decreased serum levels of triglycerides (TGs), total cholesterol, alanine aminotransferase, and aspartate aminotransferase. In addition, there were decreases in hepatic lipid and malondialdehyde levels. Changes in liver histology, as analyzed by Oil Red O staining, showed that the ES treatment suppressed adipogenesis. In addition, the ES treatment increased the expression of fatty acid oxidation-related genes (e.g., PPAR-α and CPT-1) but decreased the expression of SREBP 1, which is a TG synthesis-related gene. These results suggest that ES extract may be useful in preventing fatty acid oxidation and reducing lipogenesis in ethanol-induced fatty liver.

Keyword

Ecklonia stolonifera; Hepatoprotective effect; Fatty liver; PPAR-alpha; SREBP-1; Ethanol

MeSH Terms

Adipogenesis
Alanine Transaminase
Alcohol Drinking
Animals
Aspartate Aminotransferases
Cholesterol
Diet
Ethanol
Fatty Liver*
Fatty Liver, Alcoholic
Humans
Lipid Metabolism
Lipogenesis
Liver
Liver Diseases, Alcoholic
Male
Malondialdehyde
Metabolism
Rats*
Rats, Sprague-Dawley
Silymarin
Triglycerides
Alanine Transaminase
Aspartate Aminotransferases
Cholesterol
Ethanol
Malondialdehyde
Silymarin
Triglycerides
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