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Synergistic effects of Lactobacillus rhamnosus culture supernatant and bone marrow mesenchymal stem cells on the development of alcoholic steatohepatitis in mice

机译:鼠李糖乳杆菌培养物上清液和骨髓间充质干细胞对小鼠酒精性脂肪性肝炎发展的协同作用

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摘要

The gut microbiota has been shown to play an important role in chronic liver disease. It has been found that both Lactobacillus rhamnosus and its culture supernatant have the potential to mitigate alcoholic steatohepatitis. However, the exact mechanism is still not fully understood. Bone marrow mesenchymal stem cells have immunosuppressive effects with few side effects. The synergistic effect between Lactobacillus rhamnosus culture supernatant and bone marrow mesenchymal stem cells (BMMSCs) deserves further observation. In this study, a mouse model of chronic alcoholic hepatitis was established by eight weeks of Lieber-DeCarli liquid diet feeding; and LGG-s, BMMSCs or a combination of the two were used to explore a new therapeutic method for alcoholic liver disease and to study the mechanism. The results showed that the combined LGG-s and BMMSC treatment might have a synergistic effect and could improve the symptoms of alcoholic hepatitis by regulating inflammation, autophagy and lymphocyte subsets through the PI3k/NF-kB and PI3K/mTOR pathways. With the treatment, the autophagy rate accelerated, and alcohol-induced natural killer B (NKB) cell and follicular helper T (TFH) cell numbers decreased. These findings suggest that the development of alcoholic hepatitis may occur via PI3K/NF-kB and PI3K/mTOR pathway overactivation as well as through NKB and TFH cell imbalances. Moreover, LGG-s and BMMSCs can regulate these factors and alleviate the disease.
机译:肠道菌群已显示在慢性肝病中起重要作用。已经发现鼠李糖乳杆菌及其培养物上清液均具有减轻酒精性脂肪性肝炎的潜力。但是,确切的机制仍未完全理解。骨髓间充质干细胞具有免疫抑制作用,几乎没有副作用。鼠李糖乳杆菌培养物上清液与骨髓间充质干细胞(BMMSCs)之间的协同作用值得进一步观察。在这项研究中,通过八个星期的Lieber-DeCarli流质饮食喂养建立了慢性酒精性肝炎的小鼠模型。和LGG-s,BMMSC或两者的组合被用来探索一种治疗酒精性肝病的新方法并研究其机理。结果表明,LGG-s和BMMSC联合治疗可能具有协同作用,并可以通过PI3k / NF-kB和PI3K / mTOR途径调节炎症,自噬和淋巴细胞亚群,从而改善酒精性肝炎的症状。通过这种治疗,自噬速度加快,酒精诱导的自然杀手B(NKB)细胞和滤泡辅助性T(TFH)细胞数量减少。这些发现表明,酒精性肝炎的发生可能通过PI3K / NF-kB和PI3K / mTOR途径过度激活以及NKB和TFH细胞失衡而发生。此外,LGG-s和BMMSC可以调节这些因素并减轻疾病。

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