Peiyu Xue , Xinyong You , Li Ren , Weiming Yue , Zheng Ma
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引用次数: 0
摘要
山奈酚可通过调节各种信号通路发挥生物功能。本研究利用油酸和棕榈酸处理的 HepG2 细胞和高脂饮食小鼠,评估了山奈酚对脂质积累的改善作用。体外油红 O 染色显示,山奈酚处理可改善脂质积累(TG 含量 p < 0.001,TC 含量 p < 0.05)。免疫荧光、Western印迹分析和RT-qPCR表明,山奈酚能促进PPARγ的核转位,降低PPARγ、C/EBPβ和SREBP-1c的表达。山奈酚膳食干预可减少高密度脂蛋白胆固醇(HFD)喂养小鼠肝细胞的脂质积累和炎症细胞浸润,并降低其血清中 IL-6 和 TNF-α 的水平(山奈酚 60 mg/kg/d 时,IL-6 的 p < 0.001,TNF-α 的 p < 0.01)。同时,组织病理学检查显示,在实验剂量下,包括心、肺、肾和脾在内的器官没有实质性损伤或明显的炎症病变。上述研究结果可作为进一步临床前研究山奈酚缓解脂质积累潜力的参考。
PPARγ-mediated amelioration of lipid metabolism abnormality by kaempferol
Kaempferol can exert biological functions by regulating various signaling pathways. This study evaluated the ameliorative effect of kaempferol on lipid accumulation using oleic acid and palmitic acid-treated HepG2 cells and high-fat diet mice. In vitro oil red O staining showed that kaempferol treatment improved lipid accumulation (p < 0.001 for TG content and p < 0.05 for TC content). Immunofluorescence, Western blot analysis and RT-qPCR showed that kaempferol could promote nuclear translocation of PPARγ and reduce the expression of PPARγ, C/EBPβ, and SREBP-1c. Dietary intervention with kaempferol could reduce the lipid accumulation in hepatocytes and inflammatory cell infiltration, as well as attenuated serum levels of IL-6 and TNF-α in HFD-fed mice (p < 0.001 for IL-6 and p < 0.01 for TNF-α at kaempferol 60 mg/kg/d). Meanwhile, histopathological examination revealed that there was no substantial damage or distinct inflammation lesions in organs at the experimental dose, including the heart, lung, kidney, and spleen. The aforementioned research findings can serve as references for further preclinical investigations on the potential of kaempferol to mitigate lipid accumulation.
期刊介绍:
Archives of Biochemistry and Biophysics publishes quality original articles and reviews in the developing areas of biochemistry and biophysics.
Research Areas Include:
• Enzyme and protein structure, function, regulation. Folding, turnover, and post-translational processing
• Biological oxidations, free radical reactions, redox signaling, oxygenases, P450 reactions
• Signal transduction, receptors, membrane transport, intracellular signals. Cellular and integrated metabolism.