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油酸可保护肝细胞及非酒精性脂肪性肝炎大鼠中饱和脂肪酸介导的脂毒性。

Oleic acid protects saturated fatty acid mediated lipotoxicity in hepatocytes and rat of non-alcoholic steatohepatitis.

机构信息

Key Laboratory of Transplant Engineering and Immunology, National Health and Family Planning Commission (NHFPC), Regenerative Medicine Research Center, West China Hospital, Sichuan University, Chengdu, PR China.

Animal Center, West China Hospital, Sichuan University, Chengdu, PR China.

出版信息

Life Sci. 2018 Jun 15;203:291-304. doi: 10.1016/j.lfs.2018.04.022. Epub 2018 Apr 27.

Abstract

UNLABELLED

Aim This study aims to demonstrate the protective effects of monounsaturated oleic acid (OA) against saturated palmitic acid (PA) induced cellular lipotoxicity in hepatocytes and rats with non-alcoholic steatohepatitis (NASH).

MAIN METHODS

Human hepatoma cell line HepG2 cells and neonatal rat primary hepatocytes were treated with PA or/and OA for 24 h. SD rats were fed with high fat diet (HFD) to induce NASH. From the 16th w, the HFD was full or half replaced by olive oil to observe the protective effects.

KEY FINDINGS

In vitro, OA substantially alleviated PA induced cellular apoptosis, oxidative stress, ER stress, mitochondrial dysfunction, as well as inflammation in hepatocytes. In vivo, only olive oil supplementation had no detrimental effects, while HFD developed NASH in normal rats. Full replacement of HFD with olive oil had profoundly reversed NASH. Noteworthily, half replacement of HFD with olive oil (a mixed diet) has ameliorated NASH injury as well. It strikingly changed the hepatic histology from macrovesicular-steatosis into entire microvesicular-steatosis, and significantly reduced inflammation, ballooning and fibrosis.

SIGNIFICANCE

Our study has demonstrated in both hepatocytes and NASH rats that oleic acids had great potential to combat the saturated fatty acids induced hepatic lipotoxicity. Only half replacement of HFD by monounsaturated fatty acids rich diet still had significant therapeutic outcome in NASH rats. Redirecting the toxic saturated fatty acids into triglyceride storage and reduction of cholesterol accumulation might be the possible explanation of OA driven protection in this scenario.

摘要

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目的 本研究旨在证明单不饱和油酸(OA)对肝细胞和非酒精性脂肪性肝炎(NASH)大鼠中饱和棕榈酸(PA)诱导的细胞脂肪毒性的保护作用。

主要方法

用人肝癌细胞系 HepG2 细胞和新生大鼠原代肝细胞用 PA 或/和 OA 处理 24 小时。SD 大鼠给予高脂肪饮食(HFD)诱导 NASH。从第 16 周开始,用橄榄油完全或半替代 HFD 观察保护作用。

主要发现

在体外,OA 显著减轻了 PA 诱导的肝细胞凋亡、氧化应激、内质网应激、线粒体功能障碍和炎症。在体内,只有橄榄油补充剂没有不良影响,而 HFD 在正常大鼠中发展为 NASH。用橄榄油完全替代 HFD 可显著逆转 NASH。值得注意的是,用橄榄油半替代 HFD(混合饮食)也改善了 NASH 损伤。它显著地将肝组织学从大泡性脂肪变性转变为整个微泡性脂肪变性,并显著减少炎症、气球样变和纤维化。

意义

我们的研究在肝细胞和 NASH 大鼠中表明,油酸具有对抗饱和脂肪酸诱导的肝脂肪毒性的巨大潜力。只有用富含单不饱和脂肪酸的 HFD 半替代仍能在 NASH 大鼠中产生显著的治疗效果。将毒性饱和脂肪酸转向甘油三酯储存和减少胆固醇积累可能是 OA 驱动保护作用的可能解释。

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