Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hang Zhou 310058, PR China.
Department of Veterinary Medicine, College of Animal Sciences, Zhejiang University, Hang Zhou 310058, PR China.
Int Immunopharmacol. 2019 Jun;71:382-391. doi: 10.1016/j.intimp.2019.03.048. Epub 2019 Apr 2.
Previous investigation showed that intravenous injection of ginsenoside Rg1 had a therapeutic effect on Escherichia coli lipopolysaccharide-induced mastitis in lactating goats and it protected animals from lipopolysaccharide challenge via toll-like receptor 4 signaling pathway. The present study was to use proteomic approach to explore the anti-inflammatory mechanisms of Rg1. Nine dairy goats were randomly divided into three groups with 3 animals in each: groups 1 and 2 received intra-mammary infusion of lipopolysaccharide and then intravenously injected with saline or Rg1 solution; animals in group 3 were first intramammarily and then intravenously administered saline solution, and served as a control group. Milk whey at 6 h post lipopolysaccharide challenge was prepared for tandem mass tags based quantitative proteomic analysis. The results showed that 791 proteins were totally identified from the whey. Of them, 98 proteins between groups 1 (lipopolysaccharide + Saline) and 3 (Saline + Saline), and 34 proteins between groups 2 (lipopolysaccharide + Rg1) and 1 were significantly different. Group 1 than group 3 had significantly more inflammatory factors such as interleukin 6, acute phase proteins, blood coagulation factors, complement proteins, and oxidative stress markers while these factors were reduced in group 2 treated with Rg1. In addition, proteins in group 2 associated with peroxisome-proliferator-activated receptor γ activation and recovery of milk fat and production were upregulated compared to group 1. Therefore, Rg1 may exert its anti-inflammatory effect on lipopolysaccharide-induced mastitis in goats via modulating expression of proteins relating to peroxisome-proliferator-activated receptor γ and toll-like receptor 4 signaling pathway.
先前的研究表明,人参皂苷 Rg1 静脉注射对哺乳期山羊大肠杆菌脂多糖诱导的乳腺炎具有治疗作用,它通过 toll 样受体 4 信号通路保护动物免受脂多糖的挑战。本研究采用蛋白质组学方法探讨 Rg1 的抗炎机制。将 9 只奶山羊随机分为 3 组,每组 3 只:第 1 和 2 组接受乳内注射脂多糖,然后静脉注射生理盐水或 Rg1 溶液;第 3 组先乳内给药,然后静脉注射生理盐水,作为对照组。脂多糖挑战后 6 h 制备乳清进行串联质量标签定量蛋白质组学分析。结果从乳清中共鉴定出 791 种蛋白质。其中,第 1 组(脂多糖+生理盐水)和第 3 组(生理盐水+生理盐水)之间的 98 种蛋白质,以及第 2 组(脂多糖+Rg1)和第 1 组之间的 34 种蛋白质差异显著。第 1 组比第 3 组有更多的炎症因子,如白细胞介素 6、急性期蛋白、凝血因子、补体蛋白和氧化应激标志物,而这些因子在第 2 组用 Rg1 治疗后减少。此外,与过氧化物酶体增殖物激活受体 γ 激活和恢复乳脂和产量相关的蛋白质在第 2 组中上调,与第 1 组相比。因此,Rg1 可能通过调节与过氧化物酶体增殖物激活受体 γ 和 toll 样受体 4 信号通路相关的蛋白质的表达,对山羊脂多糖诱导的乳腺炎发挥抗炎作用。