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饮食诱导的遗传多样性合作杂交小鼠非酒精性脂肪性肝病肝酯化脂肪酸组成的脂质组学分析。

Lipidomic profiling of the hepatic esterified fatty acid composition in diet-induced nonalcoholic fatty liver disease in genetically diverse Collaborative Cross mice.

机构信息

Division of Biochemical Toxicology, FDA-National Center for Toxicological Research, Jefferson, Arkansas, USA.

Office of Pharmacovigilance and Epidemiology, FDA-Center for Drug Evaluation and Research, Silver Spring, Maryland, USA.

出版信息

J Nutr Biochem. 2022 Nov;109:109108. doi: 10.1016/j.jnutbio.2022.109108. Epub 2022 Jul 17.

Abstract

Non-alcoholic fatty liver disease (NAFLD), one of the most common forms of chronic liver disease, is characterized by the excessive accumulation of lipid species in hepatocytes. Recent studies have indicated that in addition to the total lipid quantities, changes in lipid composition are a determining factor in hepatic lipotoxicity. Using ultra-high performance liquid chromatography coupled with electrospray tandem mass spectrometry, we analyzed the esterified fatty acid composition in 24 strains of male and female Collaborative Cross (CC) mice fed a high fat/high sucrose (HF/HS) diet for 12 weeks. Changes in lipid composition were found in all strains after the HF/HS diet, most notably characterized by increases in monounsaturated fatty acids (MUFA) and decreases in polyunsaturated fatty acids (PUFA). Similar changes in MUFA and PUFA were observed in a choline- and folate-deficient (CFD) mouse model of NAFLD, as well as in hepatocytes treated in vitro with free fatty acids. Analysis of fatty acid composition revealed that alterations were accompanied by an increase in the estimated activity of MUFA generating SCD1 enzyme and an estimated decrease in the activity of PUFA generating FADS1 and FADS2 enzymes. PUFA/MUFA ratios were inversely correlated with lipid accumulation in male and female CC mice fed the HF/HS diet and with morphological markers of hepatic injury in CFD diet-fed mouse model of NAFLD. These results demonstrate that different models of NAFLD are characterized by similar changes in the esterified fatty acid composition and that alterations in PUFA/MUFA ratios may serve as a diagnostic marker for NAFLD severity.

摘要

非酒精性脂肪性肝病(NAFLD)是最常见的慢性肝病之一,其特征是肝细胞内脂质物质的过度积累。最近的研究表明,除了总脂质量外,脂质组成的变化也是肝毒性的决定因素。我们使用超高效液相色谱-电喷雾串联质谱联用技术,分析了饲喂高脂肪/高蔗糖(HF/HS)饮食 12 周的 24 只雄性和雌性协同杂交(CC)小鼠的酯化脂肪酸组成。在 HF/HS 饮食后,所有品系的脂质组成都发生了变化,最明显的特征是单不饱和脂肪酸(MUFA)增加,多不饱和脂肪酸(PUFA)减少。胆碱和叶酸缺乏(CFD)NAFLD 小鼠模型以及体外用游离脂肪酸处理的肝细胞中也观察到 MUFA 和 PUFA 的相似变化。脂肪酸组成分析表明,这些变化伴随着 MUFA 生成 SCD1 酶的估计活性增加和 PUFA 生成 FADS1 和 FADS2 酶的估计活性降低。在饲喂 HF/HS 饮食的雄性和雌性 CC 小鼠中,PUFA/MUFA 比值与脂质积累呈负相关,与 CFD 饮食喂养的 NAFLD 小鼠模型中肝损伤的形态学标志物呈负相关。这些结果表明,不同的 NAFLD 模型的酯化脂肪酸组成具有相似的变化,而 PUFA/MUFA 比值的改变可能是 NAFLD 严重程度的诊断标志物。

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