Ye Manhong, Xu Mengting, Ding Mengmeng, Ji Chao, Ji Jian, Ji Fubiao, Wei Wanhong, Yang Shengmei, Zhou Bin
College of Bioscience and Biotechnology, Yangzhou University, Yangzhou 225009, Jiangsu Province, China.
Fubiao Biotech Co, Ltd, Huai-an 211799, Jiangsu Province, China.
Iran J Basic Med Sci. 2019 Oct;22(10):1211-1217. doi: 10.22038/ijbms.2019.37348.8886.
The current study investigated the potential hepatoprotective effects of the ethanolic extracts of Chinese propolis (EECP) on ethanol-induced fatty liver in mice.
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.
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.
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.
本研究调查了中华蜂胶乙醇提取物(EECP)对小鼠乙醇诱导性脂肪肝的潜在肝脏保护作用。
将C57BL/6J小鼠单独口服50%乙醇,或与剂量为0.2 ml/kg体重的EECP共同给药,持续八周。乙醇剂量在前两个实验周为6 ml/kg体重,随后每两个实验周增加至8、10和12 ml/kg体重。使用RNA-Seq技术研究因同时给予EECP而导致的肝脏转录组变化。
我们的结果表明,主要的EECP反应基因参与脂质合成,在同时给予EECP的雌性和雄性小鼠中均显著下调。在雌性小鼠中,这些差异表达基因(DEGs)主要与脂肪酸生物合成相关。而在雄性小鼠中,这些DEGs主要参与类固醇代谢过程和胆固醇生物合成过程。尽管在脂质代谢中存在性别相关反应,但EECP还通过调节细胞因子-细胞因子受体相互作用途径在雌性小鼠中发挥了其他有益作用,这有助于解释其肝脏保护效果。
我们的研究结果表明,EECP肝脏保护作用的机制具有性别依赖性,这在开发使用EECP减少乙醇不良影响的治疗干预措施过程中值得进一步研究。