Department of Nutrition, Georgia State University, Atlanta, Georgia, USA.
Department of Pathobiology, Auburn University, Auburn, Alabama, USA.
Obesity (Silver Spring). 2019 Aug;27(8):1305-1313. doi: 10.1002/oby.22534. Epub 2019 Jun 17.
Methionine restriction (MR) decreases inflammation and improves markers of metabolic disease in rodents. MR also increases hepatic and circulating concentrations of fibroblast growth factor 21 (FGF21). Emerging evidence has suggested that FGF21 exerts anti-inflammatory effects. The purpose of this study was to determine the role of FGF21 in mediating the MR-induced reduction in inflammation.
Wild-type and Fgf21 mice were fed a high-fat (HF) control or HF-MR diet for 8 weeks. In a separate experiment, mice were fed a HF diet (HFD) for 10 weeks. Vehicle or recombinant FGF21 (13.6 µg/d) was administered via osmotic minipump for an additional 2 weeks. Inflammation and metabolic parameters were measured.
Fgf21 mice were more susceptible to HFD-induced inflammation, and MR reduced inflammation in white adipose tissue (WAT) and liver of Fgf21 mice. MR downregulated activity of signal transducer and activator of transcription 3 in WAT of both genotypes. FGF21 administration reduced hepatic lipids and blood glucose concentrations. However, there was little effect of FGF21 on inflammatory gene expression in liver or adipose tissue or circulating cytokines.
MR reduces inflammation independent of FGF21 action. Endogenous FGF21 is important to protect against the development of HFD-induced inflammation in liver and WAT, yet administration of low-dose FGF21 has little effect on markers of inflammation.
甲硫氨酸限制(MR)可降低啮齿动物的炎症反应,并改善代谢性疾病的标志物。MR 还会增加肝脏和循环中的成纤维细胞生长因子 21(FGF21)浓度。新出现的证据表明,FGF21 具有抗炎作用。本研究旨在确定 FGF21 在介导 MR 诱导的炎症减少中的作用。
野生型和 Fgf21 小鼠分别用高脂肪(HF)对照或 HF-MR 饮食喂养 8 周。在另一个实验中,小鼠用 HF 饮食(HFD)喂养 10 周。通过渗透微型泵额外给予载体或重组 FGF21(13.6µg/d)2 周。测量炎症和代谢参数。
Fgf21 小鼠更容易发生 HFD 诱导的炎症,MR 可降低 Fgf21 小鼠白色脂肪组织(WAT)和肝脏的炎症。MR 下调了两种基因型 WAT 中信号转导和转录激活因子 3 的活性。FGF21 给药可降低肝脂质和血糖浓度。然而,FGF21 对肝脏或脂肪组织中炎症基因表达或循环细胞因子的影响很小。
MR 可降低炎症,与 FGF21 作用无关。内源性 FGF21 对于防止 HFD 诱导的肝和 WAT 炎症很重要,但给予低剂量 FGF21 对炎症标志物几乎没有影响。