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Metabolomic profiling in liver of adiponectin-knockout mice uncovers lysophospholipid metabolism as an important target of adiponectin action

机译:脂联素敲除小鼠肝脏的代谢组学分析揭示溶血磷脂代谢是脂联素作用的重要靶标

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摘要

Adiponectin mediates anti-diabetic effects via increasing hepatic insulin sensitivity and direct metabolic effects. In the present study, we conducted a comprehensive and unbiased metabolomic profiling of liver tissue from AdKO (adiponectin-knockout) mice, with and without adiponectin supplementation, fed on an HFD (high-fat diet) to derive insight into the mechanisms and consequences of insulin resistance. Hepatic lipid accumulation and insulin resistance induced by the HFD were reduced by adiponectin. The HFD significantly altered levels of 147 metabolites, and bioinformatic analysis indicated that one of the most striking changes was the profile of increased lysophospholipids. These changes were largely corrected by adiponectin, at least in part via direct regulation of PLA2 (phospholipase A2) as palmitate-induced PLA2 activation was attenuated by adiponectin in primary hepatocytes. Notable decreases in several glycerolipids after the HFD were reversed by adiponectin, which also corrected elevations in several diacyglycerol and ceramide species. Our data also indicate that stimulation of ω-oxidation of fatty acids by the HFD is enhanced by adiponectin. In conclusion, this metabolomic profiling approach in AdKO mice identified important targets of adiponectin action, including PLA2, to regulate lysophospholipid metabolism and ω-oxidation of fatty acids.
机译:脂联素通过增加肝胰岛素敏感性和直接代谢作用来介导抗糖尿病作用。在本研究中,我们进行了HFD(高脂饮食)喂养的,添加或不添加脂联素的AdKO(脂联素敲除)小鼠肝脏组织的代谢组学分析,并且无偏见胰岛素抵抗。脂联素降低了HFD诱导的肝脂质蓄积和胰岛素抵抗。 HFD显着改变了147种代谢物的水平,生物信息学分析表明,最显着的变化之一是溶血磷脂含量增加。这些变化在很大程度上被脂联素纠正,至少部分是通过直接调节PLA2(磷脂酶A2)来实现的,因为棕榈酸酯诱导的PLA2活化被脂联素在原代肝细胞中减弱了。脂联素逆转了HFD后,几种甘油脂的显着下降,这也纠正了几种双甘油和神经酰胺的升高。我们的数据还表明,脂联素增强了HFD对脂肪酸ω-氧化的刺激作用。总之,AdKO小鼠的这种代谢组学分析方法确定了脂联素作用的重要靶点,包括PLA2,以调节溶血磷脂代谢和脂肪酸的ω-氧化。

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