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鱼油对慢性乙醇喂养大鼠脂代谢及其分子生物学调节物的影响。

Effects of Fish Oil on Lipid Metabolism and Its Molecular Biological Regulators in Chronic Ethanol-Fed Rats.

机构信息

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.

出版信息

Nutrients. 2018 Jun 22;10(7):802. doi: 10.3390/nu10070802.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ced5/6073669/401b19c0b154/nutrients-10-00802-g001.jpg

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