A functional chicken‐liver hydrolysate‐based supplement ameliorates alcohol liver disease via regulation of antioxidation, anti‐inflammation, and antiapoptosis

Author:

Wu Yi‐Hsieng Samuel12,Lin Yi‐Ling13,Kao Yi‐Feng4,Chen Jr‐Wei5,Chen Yi‐Chou6,Chen Yi‐Chen17ORCID

Affiliation:

1. Department of Animal Science and Technology National Taiwan University Taipei City Taiwan

2. Institute of Food Safety and Health Risk Assessment National Yang Ming Chiao Tung University Taipei City Taiwan

3. Undergraduate and Graduate Programs of Nutrition Science National Taiwan Normal University Taipei City Taiwan

4. Seafood Technology Division, Fisheries Research Institute Ministry of Agriculture Keelung City Taiwan

5. Department of Animal Industry Ministry of Agriculture Taipei City Taiwan

6. Great Billion Biotech Co., Limited. New Taipei City Taiwan

7. Master Program in Global Agriculture Technology and Genomic Science International College, National Taiwan University Taipei City Taiwan

Abstract

AbstractTons of broiler livers are produced yearly in Taiwan but always considered waste. Our team has successfully patented and characterized a chicken‐liver hydrolysate (CLH) with several biofunctions. Chronic alcohol consumption causes hepatosteatosis or even hepatitis, cirrhosis, and cancers. This study was to investigate the hepatoprotection of CLH‐based supplement (GBHP01™) against chronic alcohol consumption. Results showed that GBHP01™ could reduce (p < .05) enlarged liver size, lipid accumulation/steatosis scores, and higher serum AST, ALT, γ‐GT, triglyceride, and cholesterol levels induced by an alcoholic liquid diet. GBHP01™ reduced liver inflammation and apoptosis in alcoholic liquid‐diet‐fed mice via decreasing TBARS, interleukin‐6, interleukin‐1β, and tumor necrosis factor‐α levels, increasing reduced GSH/TEAC levels and activities of SOD, CAT and GPx, as well as downregulating CYP2E1, BAX/BCL2, Cleaved CASPASE‐9/Total CASPASE‐9 and Active CASPASE‐3/Pro‐CASPASE‐3 (p < .05). Furthermore, GBHP01™ elevated hepatic alcohol metabolism (ADH and ALDH activities) (p < .05). In conclusion, this study prove the hepatoprotection of GBHP01™ against alcohol consumption.

Funder

Ministry of Science and Technology, Taiwan

National Taiwan University

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Management, Monitoring, Policy and Law,Toxicology,General Medicine

Reference49 articles.

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