DA-6034 可改善高脂饮食诱导的肥胖小鼠的肝脏脂肪变性和炎症。

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Journal of Yeungnam medical science Pub Date : 2024-04-01 Epub Date: 2024-03-15 DOI:10.12701/jyms.2023.01389
Hong Min Kim, Mi-Hye Kwon, Eun Soo Lee, Kyung Bong Ha, Choon Hee Chung
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引用次数: 0

摘要

背景:非酒精性脂肪肝(NAFLD)的特征是肝脏甘油三酯含量增加,以及炎性巨噬细胞通过肝脏中的 C-C motif 趋化因子受体(CCR)5 通路浸润增加。DA-6034(7-羧甲基氧基-3',4',5-三甲氧基黄酮)是 eupatilin 的合成衍生物,在炎症性肠病中具有抗炎活性。然而,DA-6034 对非酒精性脂肪肝炎症反应的影响尚未得到很好的阐明。因此,我们旨在确定 DA-6034 对肝脏脂肪变性和炎症的影响:将 40 只雄性 C57BL/6J 小鼠分为以下四组:(1)普通饮食组(RD);(2)添加 DA-6034 的普通饮食组;(3)高脂饮食组(HFD);(4)添加 DA-6034 的高脂饮食组。所有小鼠均在实验开始 12 周后处死。使用 RAW264.7 细胞评估 DA-6034 对巨噬细胞的影响:结果:DA-6034 不仅降低了高密度脂蛋白喂养小鼠的肝脏甘油三酯水平和脂质积累,还降低了巨噬细胞浸润和促炎细胞因子。荧光激活细胞分拣机分析显示,DA-6034 降低了高密度脂蛋白喂养小鼠肝脏中 CD8+ T 细胞的比例。DA-6034还能降低CCR5的表达,减少HFD喂养小鼠肝脏巨噬细胞的迁移,并抑制CCR2配体和CCR4配体刺激巨噬细胞的迁移:总之,DA-6034可通过调节巨噬细胞中CCR5的表达减轻肥胖症的肝脏脂肪变性和炎症反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DA-6034 ameliorates hepatic steatosis and inflammation in high fat diet-induced obese mice.

Background: Nonalcoholic fatty liver disease (NAFLD) is characterized by an increase in hepatic triglyceride content and increased inflammatory macrophage infiltration through the C-C motif chemokine receptor (CCR) 5 pathway in the liver. DA-6034 (7-carboxymethyloxy-3',4',5-trimethoxy flavone), is a synthetic derivative of eupatilin that exhibits anti-inflammatory activity in inflammatory bowel disease. However, the effect of DA-6034 on the inflammatory response in NAFLD is not well elucidated. Therefore, we aimed to determine the effect of DA-6034 on hepatic steatosis and inflammation.

Methods: Forty male C57BL/6J mice were divided into the following four groups: (1) regular diet (RD), (2) RD with DA-6034, (3) high fat diet (HFD), and (4) HFD with DA-6034. All mice were sacrificed 12 weeks after the start of the experiment. The effects of DA-6034 on macrophages were assessed using RAW264.7 cells.

Results: DA-6034 not only reduced hepatic triglyceride levels and lipid accumulation but also macrophage infiltration and proinflammatory cytokines in HFD-fed mice. According to fluorescence-activated cell sorter analysis, DA-6034 reduced the CD8+ T cell fraction in the liver of HFD-fed mice. DA-6034 also reduced CCR5 expression and the migration of liver macrophages in HFD-fed mice and inhibited CCR2 ligand and CCR4 ligand, which stimulated the migration of macrophages.

Conclusion: Overall, DA-6034 attenuates hepatic steatosis and inflammation in obesity by regulating CCR5 expression in macrophages.

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