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代谢综合征中磷脂脂肪酸重排的综合研究:与器官功能障碍的相关性。

A comprehensive study of phospholipid fatty acid rearrangements in metabolic syndrome: correlations with organ dysfunction.

机构信息

Laboratoire "Lipotoxicity and Channelopathies (LitCh) - ConicMeds", Université de Poitiers, 1, rue Georges Bonnet, 86073 Poitiers, France.

Laboratoire "Signalisation et Transports Ioniques Membranaires (STIM; EA 7349)", Université de Poitiers, 1, rue Georges Bonnet, 86073 Poitiers, France.

出版信息

Dis Model Mech. 2020 Jun 15;13(6):dmm043927. doi: 10.1242/dmm.043927.

Abstract

The balance within phospholipids (PLs) between saturated fatty acids and monounsaturated or polyunsaturated fatty acids is known to regulate the biophysical properties of cellular membranes. As a consequence, in many cell types, perturbing this balance alters crucial cellular processes, such as vesicular budding and the trafficking/function of membrane-anchored proteins. The worldwide spread of the Western diet, which is highly enriched in saturated fats, has been clearly correlated with the emergence of a complex syndrome known as metabolic syndrome (MetS). MetS is defined as a cluster of risk factors for cardiovascular diseases, type 2 diabetes and hepatic steatosis; however, no clear correlations have been established between diet-induced fatty acid redistribution within cellular PLs and the severity/chronology of the symptoms associated with MetS or the function of the targeted organs. To address this issue, in this study we analyzed PL remodeling in rats exposed to a high-fat/high-fructose diet (HFHF) over a 15-week period. PL remodeling was analyzed in several organs, including known MetS targets. We show that fatty acids from the diet can redistribute within PLs in a very selective manner, with phosphatidylcholine being the preferred sink for this redistribution. Moreover, in the HFHF rat model, most organs are protected from this redistribution, at least during the early onset of MetS, at the expense of the liver and skeletal muscles. Interestingly, such a redistribution correlates with clear-cut alterations in the function of these organs.This article has an associated First Person interview with the first author of the paper.

摘要

磷脂(PL)中饱和脂肪酸与单不饱和或多不饱和脂肪酸之间的平衡,已知可以调节细胞膜的生物物理特性。因此,在许多细胞类型中,破坏这种平衡会改变关键的细胞过程,如囊泡出芽和膜锚定蛋白的运输/功能。富含饱和脂肪的西方饮食在全球范围内的广泛传播,与一种被称为代谢综合征(MetS)的复杂综合征的出现明显相关。MetS 被定义为心血管疾病、2 型糖尿病和肝脂肪变性风险因素的集群;然而,饮食诱导的细胞 PL 内脂肪酸再分布与 MetS 相关症状的严重程度/病程或靶向器官的功能之间,尚未建立明确的相关性。为了解决这个问题,在这项研究中,我们分析了暴露于高脂肪/高果糖饮食(HFHF)15 周的大鼠中的 PL 重塑。在几个器官中分析了 PL 重塑,包括已知的 MetS 靶标。我们表明,饮食中的脂肪酸可以以非常选择性的方式在 PL 内再分布,其中磷脂酰胆碱是这种再分布的首选汇。此外,在 HFHF 大鼠模型中,大多数器官至少在 MetS 早期发病时免受这种再分布的影响,以牺牲肝脏和骨骼肌为代价。有趣的是,这种再分布与这些器官功能的明显改变相关。本文有该论文第一作者的相关第一人称采访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/455c/7328154/1c14c6c0025b/dmm-13-043927-g1.jpg

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