Laboratory of Aquaculture Nutrition and Environmental Health (LANEH), School of Life Sciences, East China Normal University, Shanghai, China.
Sci Rep. 2017 Jan 31;7:41706. doi: 10.1038/srep41706.
Peroxisome proliferation activated receptor α (PPARα) is an important transcriptional regulator of lipid metabolism and is activated by high-fat diet (HFD) and fibrates in mammals. However, whether nutritional background affects PPARα activation and the hypolipidemic effects of PPARα ligands have not been investigated in fish. In the present two-phase study of Nile tilapia (Oreochromis niloticus), fish were first fed a HFD (13% fat) or low-fat diet (LFD; 1% fat) diet for 10 weeks, and then fish from the first phase were fed the HFD or LFD supplemented with 200 mg/kg body weight fenofibrate for 4 weeks. The results indicated that the HFD did not activate PPARα or other lipid catabolism-related genes. Hepatic fatty acid β-oxidation increased significantly in the HFD and LFD groups after the fenofibrate treatment, when exogenous substrates were sufficiently provided. Only in the HFD group, fenofibrate significantly increased hepatic PPARα mRNA and protein expression, and decreased liver and plasma triglyceride concentrations. This is the first study to show that body fat deposition and dietary lipid content affects PPARα activation and the hypolipidemic effects of fenofibrate in fish, and this could be due to differences in substrate availability for lipid catabolism in fish fed with different diets.
过氧化物酶体增殖物激活受体 α(PPARα)是脂质代谢的重要转录调节剂,在哺乳动物中可被高脂肪饮食(HFD)和贝特类药物激活。然而,营养背景是否会影响 PPARα 的激活以及 PPARα 配体的降血脂作用,在鱼类中尚未得到研究。本研究采用尼罗罗非鱼(Oreochromis niloticus)进行了两阶段实验,首先将鱼饲喂高脂肪饮食(HFD;13%脂肪)或低脂肪饮食(LFD;1%脂肪)10 周,然后第一阶段的鱼再用 HFD 或 LFD 补充 200mg/kg 体重的非诺贝特进行 4 周的喂养。结果表明,HFD 并未激活 PPARα 或其他与脂质分解代谢相关的基因。在用非诺贝特处理后,当外源性底物充足时,HFD 和 LFD 组的肝脂肪酸β-氧化显著增加。只有在 HFD 组中,非诺贝特显著增加了肝 PPARα mRNA 和蛋白表达,并降低了肝和血浆甘油三酯浓度。这是首次研究表明,体脂沉积和膳食脂质含量会影响鱼类中 PPARα 的激活和非诺贝特的降血脂作用,这可能是由于不同饮食喂养的鱼类在脂质分解代谢的底物可用性方面存在差异。