Your browser doesn't support javascript.
loading
Gender associated effects of the ethanolic extracts of Chinese propolis on the hepatic transcriptome in ethanol-treated mice.
Ye, Manhong; Xu, Mengting; Ding, Mengmeng; Ji, Chao; Ji, Jian; Ji, Fubiao; Wei, Wanhong; Yang, Shengmei; Zhou, Bin.
Afiliación
  • Ye M; College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
  • Xu M; College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
  • Ding M; College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
  • Ji C; Fubiao Biotech Co, Ltd, Huai-an 211799, Jiangsu Province, China.
  • Ji J; Fubiao Biotech Co, Ltd, Huai-an 211799, Jiangsu Province, China.
  • Ji F; Fubiao Biotech Co, Ltd, Huai-an 211799, Jiangsu Province, China.
  • Wei W; Joint International Research Laboratory of Agricultural & Agri-Product Safety, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
  • Yang S; Joint International Research Laboratory of Agricultural & Agri-Product Safety, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
  • Zhou B; College of Animal Science and Technology, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
Iran J Basic Med Sci ; 22(10): 1211-1217, 2019 Oct.
Article en En | MEDLINE | ID: mdl-31998465
ABSTRACT

OBJECTIVES:

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 co-administrated 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.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Iran J Basic Med Sci Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Iran J Basic Med Sci Año: 2019 Tipo del documento: Article