Department of Infection, Immunity, and Inflammation, University of LeicesterLeicester, UK; College of Nursing, University of RaparinRanya, Iraq.
Department of Sport, Health, and Exercise Science, University of Hull Hull, UK.
Front Cell Dev Biol. 2016 Jun 22;4:61. doi: 10.3389/fcell.2016.00061. eCollection 2016.
Low grade endotoxemia is a feature of obesity which is linked to development of steatohepatitis in non-alcoholic fatty liver disease. In this study, macrophages (J774) and hepatocytes (HepG2) were stimulated with lipopolysaccharide (LPS) from E. coli 0111: B4 and analyzed for modulation of this response when preconditioned or stimulated subsequent to LPS, with different doses of Vitamin D3 or docosahexaenoic acid (DHA) over a time period of 1 and 5 days. Pro-inflammatory TNFα and pro-fibrotic TGFβ released into the supernatants were measured by ELISA; qPCR was performed for Srebp-1c and PPARα mRNA (genes for products involved in fatty acid synthesis and catabolism, respectively). Vitamin D3 and DHA exerted a consistent, dose dependent anti-inflammatory effect, and increased PPARα relative to Srebp-1c in both cell types. By contrast, addition of free fatty acids (FFA, oleic acid/palmitic acid 2:1) caused aggravation of LPS-induced inflammatory reaction and an increase of Srebp-1c relative to PPARα. Our results argue in favor of dietary supplementation of Vitamin D3 or DHA (and avoidance of monounsaturated/saturated fatty acids) to alleviate development of fatty liver disease.
低度内毒素血症是肥胖的一个特征,与非酒精性脂肪性肝病中的脂肪性肝炎的发展有关。在这项研究中,用大肠杆菌 0111:B4 的脂多糖 (LPS) 刺激巨噬细胞 (J774) 和肝细胞 (HepG2),并分析当用不同剂量的维生素 D3 或二十二碳六烯酸 (DHA) 预处理或在 LPS 刺激后预处理时,这种反应的调节作用,时间为 1 天和 5 天。通过 ELISA 测量上清液中释放的促炎 TNFα 和促纤维化 TGFβ;通过 qPCR 进行 Srebp-1c 和 PPARα mRNA(分别为参与脂肪酸合成和分解代谢产物的基因)的检测。维生素 D3 和 DHA 表现出一致的、剂量依赖性的抗炎作用,与 Srebp-1c 相比,两种细胞类型中的 PPARα 均增加。相比之下,添加游离脂肪酸 (FFA,油酸/棕榈酸 2:1) 会加重 LPS 诱导的炎症反应,并增加 Srebp-1c 与 PPARα 的比值。我们的结果支持通过膳食补充维生素 D3 或 DHA(并避免单不饱和/饱和脂肪酸)来减轻脂肪肝疾病的发展。