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二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)对代谢综合征中神经酰胺脂毒性的影响。

The impact of EPA and DHA on ceramide lipotoxicity in the metabolic syndrome.

作者信息

Walchuk Chelsey, Wang Yidi, Suh Miyoung

机构信息

Department of Food and Human Nutritional Sciences, University of Manitoba, Winnipeg, Manitoba, R3T 2N2, Canada.

Division of Neurodegenerative Disorders (DND) & Canadian Centre for Agri-Food Research in Health and Medicine (CCARM), St. Boniface Hospital Albrechtsen Research Centre, Winnipeg, Manitoba, R2H 2A6, Canada.

出版信息

Br J Nutr. 2021 Apr 28;125(8):863-875. doi: 10.1017/S0007114520003177. Epub 2020 Aug 14.

Abstract

The metabolic syndrome (MetS) is a cluster of cardiovascular risk factors including obesity, insulin resistance (IR) and dyslipidaemia. Consumption of a high-fat diet (HFD) enriched in SFA leads to the accumulation of ceramide (Cer), the central molecule in sphingolipid metabolism. Elevations in plasma and tissue Cer are found in obese individuals, and there is evidence to suggest that Cer lipotoxicity contributes to the MetS. EPA and DHA have shown to improve MetS parameters including IR, inflammation and hypertriacylglycerolaemia; however, whether these improvements are related to Cer is currently unknown. This review examines the potential of EPA and DHA to improve Cer lipotoxicity and MetS parameters including IR, inflammation and dyslipidaemia in vitro and in vivo. Current evidence from cell culture and animal studies indicates that EPA and DHA attenuate palmitate- or HFD-induced Cer lipotoxicity and IR, whereas evidence in humans is greatly lacking. Overall, there is intriguing potential for EPA and DHA to improve Cer lipotoxicity and related MetS parameters, but more research is warranted.

摘要

代谢综合征(MetS)是一组心血管危险因素,包括肥胖、胰岛素抵抗(IR)和血脂异常。食用富含饱和脂肪酸(SFA)的高脂饮食(HFD)会导致神经酰胺(Cer)的积累,神经酰胺是鞘脂代谢的核心分子。肥胖个体的血浆和组织中神经酰胺水平会升高,并且有证据表明神经酰胺的脂毒性与代谢综合征有关。二十碳五烯酸(EPA)和二十二碳六烯酸(DHA)已被证明可改善代谢综合征的参数,包括胰岛素抵抗、炎症和高甘油三酯血症;然而,这些改善是否与神经酰胺有关目前尚不清楚。本综述探讨了二十碳五烯酸和二十二碳六烯酸在体外和体内改善神经酰胺脂毒性以及代谢综合征参数(包括胰岛素抵抗、炎症和血脂异常)的潜力。目前来自细胞培养和动物研究的证据表明,二十碳五烯酸和二十二碳六烯酸可减轻棕榈酸或高脂饮食诱导的神经酰胺脂毒性和胰岛素抵抗,而人体研究证据则极为缺乏。总体而言,二十碳五烯酸和二十二碳六烯酸在改善神经酰胺脂毒性和相关代谢综合征参数方面具有诱人的潜力,但仍需要更多的研究。

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