首页> 美国卫生研究院文献>Mediators of Inflammation >Antilipotoxicity Activity of Osmanthus fragrans and Chrysanthemum morifolium Flower Extracts in Hepatocytes and Renal Glomerular Mesangial Cells
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Antilipotoxicity Activity of Osmanthus fragrans and Chrysanthemum morifolium Flower Extracts in Hepatocytes and Renal Glomerular Mesangial Cells

机译:桂花和菊花提取物对肝细胞和肾小球系膜细胞的抗脂活性

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摘要

The excess influx of free fatty acids (FFAs) into nonadipose tissues, such as those of liver and kidney, induces lipotoxicity leading to hepatic steatosis and renal dysfunction. The aim of this study was to investigate the protective effects of methanolic flower extracts of Osmanthus fragrans (OF) and Chrysanthemum morifolium (CM) against FFA-induced lipotoxicity in hepatocytes (human HepG2 cells) and renal glomerular mesangial cells (mouse SV40-Mes13 cells). The results showed that OF and CM significantly suppressed FFA-induced intracellular triacylglycerol accumulation via partially inhibiting the gene expression of sterol regulatory element-binding protein-1c (SREBP-1c) and glycerol-3-phosphate acyltransferase (GPAT) in HepG2 cells. Both extracts inhibited reactive oxygen species (ROS) generation by FFA-stimulated HepG2 cells. OF and CM also suppressed the mRNA expression of interleukin- (IL-) 1β, IL-6, IL-8, tumor necrosis factor- (TNF-) α, and transforming growth factor- (TGF-) β by HepG2 cells treated with conditioned medium derived from lipopolysaccharide-treated THP-1 monocytes. Furthermore, OF and CM effectively inhibited oleate-induced cellular lipid accumulation, TGF-β secretion, and overexpression of fibronectin in mesangial cells. In conclusion, OF and CM possess hepatoprotective activity by inhibiting hepatic fat load and inflammation and renal protection by preventing FFA-induced mesangial extracellular matrix formation.
机译:游离脂肪酸(FFA)大量流入非脂肪组织(如肝和肾组织)会引起脂毒性,导致肝脂肪变性和肾功能障碍。这项研究的目的是调查桂花(OF)和菊花菊花(CM)的甲醇花提取物对FFA诱导的肝细胞(人HepG2细胞)和肾小球系膜细胞(小鼠SV40-Mes13细胞)的脂毒性的保护作用)。结果表明,OF和CM通过部分抑制HepG2细胞中的固醇调节元件结合蛋白1c(SREBP-1c)和3-磷酸甘油酰基转移酶(GPAT)的基因表达来显着抑制FFA诱导的细胞内三酰甘油的积累。两种提取物均抑制了FFA刺激的HepG2细胞产生的活性氧(ROS)。 OF和CM还抑制了用HepG2处理的HepG2细胞的白介素(IL-)1β,IL-6,IL-8,肿瘤坏死因子(TNF-)α和转化生长因子(TGF-)β的mRNA表达。脂多糖处理的THP-1单核细胞衍生的条件培养基。此外,OF和CM可有效抑制油酸诱导的系膜细胞中脂质的蓄积,TGF-β的分泌以及纤连蛋白的过度表达。总之,OF和CM通过抑制肝脂肪负荷和炎症具有保肝活性,并通过阻止FFA诱导的系膜细胞外基质形成来保护肾脏和保护肾脏。

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