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An ethanolic extract of Artemisia scoparia inhibits lipolysis in vivo and has antilipolytic effects on murine adipocytes in vitro

机译:蒿的乙醇提取物在体内抑制脂肪分解并在体外对鼠类脂肪细胞具有抗脂肪分解作用

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摘要

An ethanolic extract of Artemisia scoparia (SCO) has metabolically favorable effects on adipocyte development and function in vitro and in vivo. In diet-induced obese mice, SCO supplementation significantly reduced fasting glucose and insulin levels. Given the importance of adipocyte lipolysis in metabolic health, we hypothesized that SCO modulates lipolysis in vitro and in vivo. Free fatty acids and glycerol were measured in the sera of mice fed a high-fat diet with or without SCO supplementation. In cultured 3T3-L1 adipocytes, the effects of SCO on lipolysis were assessed by measuring glycerol and free fatty acid release. Microarray analysis, qPCR, and immunoblotting were used to assess gene expression and protein abundance. We found that SCO supplementation of a high-fat diet in mice substantially reduces circulating glycerol and free fatty acid levels, and we observed a cell-autonomous effect of SCO to significantly attenuate tumor necrosis factor-α (TNFα)-induced lipolysis in cultured adipocytes. Although several prolipolytic and antilipolytic genes were identified by microarray analysis of subcutaneous and visceral adipose tissue from SCO-fed mice, regulation of these genes did not consistently correlate with SCO’s ability to reduce lipolytic metabolites in sera or cell culture media. However, in the presence of TNFα in cultured adipocytes, SCO induced antilipolytic changes in phosphorylation of hormone-sensitive lipase and perilipin. Together, these data suggest that the antilipolytic effects of SCO on adipose tissue play a role in the ability of this botanical extract to improve whole body metabolic parameters and support its use as a dietary supplement to promote metabolic resiliency.
机译:蒿的乙醇提取物(SCO)在体内外对脂肪细胞的发育和功能具有代谢上有利的影响。在饮食诱发的肥胖小鼠中,补充SCO可以显着降低空腹血糖和胰岛素水平。考虑到脂肪细胞脂解在代谢健康中的重要性,我们假设SCO在体外和体内均可调节脂解。在高脂饮食中添加或不添加SCO的小鼠血清中测量游离脂肪酸和甘油。在培养的3T3-L1脂肪细胞中,通过测量甘油和游离脂肪酸的释放来评估SCO对脂解的影响。微阵列分析,qPCR和免疫印迹用于评估基因表达和蛋白质丰度。我们发现SCO补充高脂饮食在小鼠中可显着降低循环甘油和游离脂肪酸水平,并且我们观察到SCO的细胞自主作用可显着减弱培养的脂肪细胞中肿瘤坏死因子-α(TNFα)诱导的脂解作用。尽管通过SCO喂养的小鼠的皮下和内脏脂肪组织的微阵列分析鉴定出了几种促脂和抗脂解基因,但是这些基因的调控与SCO减少血清或细胞培养基中脂解代谢产物的能力并没有始终相关。但是,在培养的脂肪细胞中存在TNFα的情况下,SCO可以诱导激素敏感性脂酶和周脂素磷酸化的抗脂解作用变化。总之,这些数据表明,SCO对脂肪组织的抗脂解作用在这种植物提取物改善全身代谢参数的能力中起作用,并支持其用作膳食补充剂以促进代谢弹性。

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