Author/Authors :
Ye, Manhong College of Bioscience and Biotechnology - Yangzhou University - Yangzhou 225009 - Jiangsu Province, China , Xu, Mengting College of Bioscience and Biotechnology - Yangzhou University - Yangzhou 225009 - Jiangsu Province, China , Ding, Mengmeng College of Bioscience and Biotechnology - Yangzhou University - Yangzhou 225009 - Jiangsu Province, China , Ji, Chao Fubiao Biotech Co - Ltd, Huai-an 211799 - Jiangsu Province, China , Ji, Jian Fubiao Biotech Co - Ltd, Huai-an 211799 - Jiangsu Province, China , Ji, Fubiao Fubiao Biotech Co - Ltd, Huai-an 211799 - Jiangsu Province, China , Wei, Wanhong Joint International Research Laboratory of Agricultural & Agri-Product Safety - Yangzhou University - Yangzhou 225009 - Jiangsu Province, China , Yang, Shengmei Joint International Research Laboratory of Agricultural & Agri-Product Safety - Yangzhou University - Yangzhou 225009 - Jiangsu Province, China , Zhou, Bin College of Animal Science and Technology - Yangzhou University - Yangzhou 225009 - Jiangsu Province, China
Abstract :
Objective(s): The current study investigated the potential hepatoprotective effects of the ethanolic
extracts of Chinese propolis (EECP) on ethanol-induced fatty liver in mice.
Materials and Methods: C57BL/6J mice were orally gavaged with 50% ethanol alone or coadministrated
with EECP at the dose of 0.2 ml/kg bodyweight for eight weeks. The dose for ethanol
was 6 ml/kg bodyweight for the first two experimental weeks, and then increased to 8, 10, and 12
ml/kg bodyweight every two experimental weeks. Alterations in the hepatic transcriptome due to
concomitant administration of EECP were investigated using RNA-Seq technique.
Results: Our results showed that the main EECP-responsive genes were involved in lipid syntheses,
which were significantly down-regulated in both female and male mice co-administrated with EECP.
In female mice, these differentially expressed genes (DEGs) were mainly associated with fatty acid
biosynthesis. While in male mice, these DEGs were mainly involved in the steroid metabolic process
and cholesterol biosynthetic process. Despite the sex-associated responses in lipid metabolism, EECP
also exerted other beneficial effects in female mice through modulation of the cytokine-cytokine
receptor interaction pathway that helped explaining its hepato-protective effectiveness.
Conclusion: Our findings indicated that the mechanism regarding the hepato-protective effects of
EECP was gender-dependent, which is worthy of further investigation during the development of
therapeutic interventions using EECP to reduce the adverse influences of ethanol.
Keywords :
Alcoholic , Chinese propolis , Fatty liver , Inbred C57BL , Lipid metabolism , Mice