Institut des Maladies Métaboliques et Cardiovasculaires, INSERM U1048, Toulouse, France.
Université de Toulouse, Université Paul Sabatier, Toulouse, France.
Endocrine. 2018 Apr;60(1):112-121. doi: 10.1007/s12020-018-1536-1. Epub 2018 Feb 1.
Apelin treatment has been shown to improve insulin sensitivity in insulin resistant mice by acting in skeletal muscles. However, the effects of systemic apelin on the hepatic energy metabolism have not been addressed. We thus aimed to determine the effect of chronic apelin treatment on the hepatic lipid metabolism in insulin resistant mice. The apelin receptor (APJ) expression was also studied in this context since its regulation has only been reported in severe liver pathologies.
Mice were fed a high-fat diet (HFD) in order to become obese and insulin resistant compared to chow fed mice (CD). HFD mice then received a daily intraperitoneal injection of apelin (0.1 µmol/kg) or PBS during 28 days.
Triglycerides content and the expression of different lipogenesis-related genes were significantly decreased in the liver of HFD apelin-treated compared to PBS-treated mice. Moreover, at this stage of insulin resistance, the beta-oxidation was increased in liver homogenates of HFD PBS-treated mice compared to CD mice and reduced in HFD apelin-treated mice. Finally, APJ expression was not up-regulated in the liver of insulin resistant mice. In isolated hepatocytes from chow and HFD fed mice, apelin did not induce significant effect.
Altogether, these results suggest that systemic apelin treatment decreases steatosis in insulin resistant mice without directly targeting hepatocytes.
已有研究表明,阿片肽可作用于骨骼肌,改善胰岛素抵抗小鼠的胰岛素敏感性。然而,系统阿片肽对肝脏能量代谢的影响尚未得到阐明。因此,我们旨在确定慢性阿片肽治疗对胰岛素抵抗小鼠肝脏脂质代谢的影响。在这方面,我们还研究了阿片肽受体(APJ)的表达,因为其调节仅在严重的肝脏病理中报道过。
通过高脂饮食(HFD)使小鼠肥胖并对胰岛素产生抵抗,与正常饮食(CD)喂养的小鼠相比。然后,HFD 小鼠在 28 天内每天接受一次腹腔内注射阿片肽(0.1 μmol/kg)或 PBS。
与 PBS 处理的 HFD 小鼠相比,HFD 阿片肽处理的小鼠肝脏中的甘油三酯含量和不同脂肪生成相关基因的表达显著降低。此外,在胰岛素抵抗的这个阶段,HFD PBS 处理的小鼠的肝匀浆中的β氧化增加,而 CD 小鼠的β氧化减少,HFD 阿片肽处理的小鼠的β氧化减少。最后,胰岛素抵抗小鼠的肝脏中未上调 APJ 表达。在正常饮食和高脂饮食喂养的小鼠的分离肝细胞中,阿片肽没有引起明显的作用。
综上所述,这些结果表明,系统阿片肽治疗可减少胰岛素抵抗小鼠的脂肪变性,而无需直接针对肝细胞。