School of Nutrition and Health Sciences, Taipei Medical University, Taipei 11031, Taiwan.
Research Center of Geriatric Nutrition, College of Nutrition, Taipei Medical University, Taipei 11031, Taiwan.
Nutrients. 2018 Jun 22;10(7):802. doi: 10.3390/nu10070802.
The purpose of this study was to clarify the hepatoprotective mechanisms of fish oil in ethanol-fed rats based on lipid metabolism. Thirty eight-week-old male Wistar rats were divided into six groups: C (control), CF25 (control diet with 25% fish oil substitution), CF57 (control diet with 57% fish oil substitution), E (ethanol-containing diet) group, EF25 (ethanol-containing diet with 25% fish oil substitution), and EF57 (ethanol-containing diet with 57% fish oil substitution) groups. All of the groups were pair-fed an isoenergetic diet based on E group. Rats were sacrificed after eight weeks. When compared with C group, the plasma aspartate transaminase (AST) activity and hepatic steatosis and inflammatory cell infiltration were significantly higher, while plasma adiponectin level and hepatic AMP-activated protein kinase α (AMPKα) protein expression was significantly lower in the E group. However, the hepatic damage, including steatosis and inflammation were ameliorated in the EF25 and EF57 groups. Moreover, mRNA levels of fatty acid-oxidative enzymes, such as medium-chain acyl-coenzyme A dehydrogenase (MCAD) and carnitine palmitoyltransferase I (CPT-1) were significantly elevated in the EF57 group than those in E group. Partial replacement with fish oil might improve the fatty acid oxidation by raising mRNA levels of downstream transcription factors, finally inhibit the ethanol-induced hepatic steatosis in rats.
本研究旨在基于脂质代谢阐明鱼油对乙醇喂养大鼠的肝保护机制。将 38 周龄雄性 Wistar 大鼠分为六组:C(对照组)、CF25(对照组中 25%的鱼油替代物)、CF57(对照组中 57%的鱼油替代物)、E(含乙醇饮食组)、EF25(含乙醇饮食中 25%的鱼油替代物)和 EF57(含乙醇饮食中 57%的鱼油替代物)。所有组均根据 E 组进行等能量喂养。八周后处死大鼠。与 C 组相比,E 组大鼠的血浆天冬氨酸转氨酶(AST)活性、肝脂肪变性和炎症细胞浸润明显升高,而血浆脂联素水平和肝 AMP 激活蛋白激酶α(AMPKα)蛋白表达明显降低。然而,EF25 和 EF57 组大鼠的肝损伤,包括脂肪变性和炎症均有所改善。此外,EF57 组大鼠的脂肪酸氧化酶,如中链酰基辅酶 A 脱氢酶(MCAD)和肉碱棕榈酰转移酶 I(CPT-1)的 mRNA 水平明显高于 E 组。部分用鱼油替代可能通过提高下游转录因子的 mRNA 水平来改善脂肪酸氧化,最终抑制乙醇诱导的大鼠肝脂肪变性。