Jiangxi Provincial Key Laboratory for Animal Health, Institute of Animal Population Health, College of Animal Science and Technology, Jiangxi Agricultural University, No. 1101 Zhimin Avenue, Economic and Technological Development District, Nanchang, 330045, Jiangxi, P.R. China.
Sci Rep. 2019 Jul 12;9(1):10141. doi: 10.1038/s41598-019-46183-y.
Fatty liver haemorrhagic syndrome (FLHS) is a widespread metabolic disease in laying hens that causes a decrease in egg production and even death. Insulin resistance is a major contributor to the pathogenesis of nonalcoholic fatty liver disease. However, the relationship between FLHS and the insulin resistance mechanisms underlying FLHS is not well elucidated. Therefore, we established an FLHS model induced by feeding a high-energy low-protein diet. In the current study, we found that the fasting glucose and insulin concentrations were elevated in the FLHS group compared with the control group during the experimental period. The results of the oral glucose tolerance test (OGTT) and insulin sensitivity test (IST) showed a high level of insulin resistance in the FLHS model. InsR, 4EBP-1, Glut-1 and Glut-3 mRNA expression were decreased, and TOR, S6K1, and FOXO1 were elevated (P < 0.05). Metabolomic analysis with GC/MS identified 46 differentially expressed metabolites between these two groups, and of these, 14 kinds of metabolism molecules and 32 kinds of small metabolism molecules were decreased (P < 0.05). Further investigation showed that glucose, lipid and amino acid metabolism blocks in the progression of FLHS by GO functional and pathway analysis. Overall, these results suggest that insulin resistance participated in FLHS; comprehensively, metabolites participated in the dysregulated biological process.
脂肪肝出血综合征(FLHS)是一种广泛存在于产蛋母鸡中的代谢性疾病,可导致产蛋量下降,甚至死亡。胰岛素抵抗是导致非酒精性脂肪肝发病的主要原因之一。然而,FLHS 与 FLHS 相关的胰岛素抵抗机制之间的关系尚未得到很好的阐明。因此,我们建立了一种通过喂养高能低蛋白饮食诱导的 FLHS 模型。在本研究中,我们发现与对照组相比,FLHS 组在实验期间空腹血糖和胰岛素浓度升高。口服葡萄糖耐量试验(OGTT)和胰岛素敏感性试验(IST)的结果显示 FLHS 模型存在高水平的胰岛素抵抗。InsR、4EBP-1、Glut-1 和 Glut-3mRNA 的表达降低,而 TOR、S6K1 和 FOXO1 升高(P<0.05)。GC/MS 的代谢组学分析鉴定出这两组之间有 46 种差异表达的代谢物,其中 14 种代谢物和 32 种小代谢物减少(P<0.05)。进一步研究表明,GO 功能和途径分析显示葡萄糖、脂质和氨基酸代谢在 FLHS 的进展中受阻。总的来说,这些结果表明胰岛素抵抗参与了 FLHS;综合来看,代谢物参与了失调的生物学过程。