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GG通过调节肠道微生物群和代谢途径减轻MASLD/MASH的进展。

GG attenuates MASLD/MASH progression by modulating gut microbiota and metabolic pathways.

作者信息

Wang Shi-Long, Liang Si, Li Si-Yu, Fu Jin-Wen, Wang Zi-Yi-Ru, Zhu Dong-Qing, Chen Nan

机构信息

School of Basic Medical Sciences, Hebei University, Baoding, China.

Department of Anesthesiology, Affiliated Hospital of Hebei University, Baoding, China.

出版信息

Front Microbiol. 2025 Jul 24;16:1586678. doi: 10.3389/fmicb.2025.1586678. eCollection 2025.

Abstract

INTRODUCTION

Non-alcoholic fatty liver disease (MASLD) is a common liver condition with a global prevalence of approximately 25%, often associated with overweight, obesity, and abnormalities in glucose and lipid metabolism. Its histological hallmark is hepatic steatosis. Non-alcoholic steatohepatitis (MASH), an advanced form of MASLD, can lead to cirrhosis and liver cancer. Dysbiosis of the gut microbiota plays a significant role in chronic liver diseases, making probiotic treatment a focal point in MASLD research. Studies have shown that GG (LGG) can improve gut microbiota, reduce hepatic fat accumulation, and lower blood lipid levels in MASLD model mice. However, the role of LGG in the progression from MASLD to MASH remains unclear.

METHODS

In this study, we constructed MASLD and MASH models using a high-fructose, high-fat diet combined with carbon tetrachloride (CCl4) induction to explore the effects of LGG on disease progression. Our findings revealed that in the MASLD model, LGG improved lipid metabolism and inflammatory responses by modulating the gut microbiota (e.g., increasing the abundance of Bacteroidetes) and promoting the production of short-chain fatty acids (SCFAs). Additionally, LGG reduced the expression of genes related to lipogenesis, further alleviating MASLD.

RESULTS

In the MASH model, LGG primarily exerted its effects by inhibiting the TGF-β/SMAD signaling pathway and reducing the expression of pro-inflammatory factors (e.g., IL-1β, IL-6, TNF-α), thereby mitigating liver fibrosis and inflammation. Furthermore, LGG restored intestinal barrier function, reduced intestinal permeability, and prevented harmful substances like endotoxins from entering the liver, further alleviating hepatic inflammation and fibrosis.

DISCUSSION

Although LGG shows promise in the treatment of MASLD and MASH, its mechanisms of action and long-term effects require further investigation. Future research should focus on optimizing the types, dosages, and treatment regimens of probiotics, as well as monitoring their long-term impact on gut microbiota balance, to ensure their safety and efficacy in clinical applications.

摘要

引言

代谢功能障碍相关脂肪性肝病(MASLD)是一种常见的肝脏疾病,全球患病率约为25%,常与超重、肥胖以及糖脂代谢异常相关。其组织学特征为肝脂肪变性。非酒精性脂肪性肝炎(MASH)是MASLD的一种晚期形式,可导致肝硬化和肝癌。肠道微生物群失调在慢性肝病中起重要作用,使益生菌治疗成为MASLD研究的一个重点。研究表明,鼠李糖乳杆菌GG(LGG)可改善肠道微生物群,减少MASLD模型小鼠的肝脏脂肪堆积并降低血脂水平。然而,LGG在MASLD向MASH进展过程中的作用仍不清楚。

方法

在本研究中,我们使用高糖高脂饮食联合四氯化碳(CCl4)诱导构建了MASLD和MASH模型,以探讨LGG对疾病进展的影响。我们的研究结果显示,在MASLD模型中,LGG通过调节肠道微生物群(如增加拟杆菌门的丰度)和促进短链脂肪酸(SCFAs)的产生来改善脂质代谢和炎症反应。此外,LGG降低了与脂肪生成相关基因的表达,进一步减轻了MASLD。

结果

在MASH模型中,LGG主要通过抑制TGF-β/SMAD信号通路并降低促炎因子(如IL-1β、IL-6、TNF-α)的表达发挥作用,从而减轻肝纤维化和炎症。此外,LGG恢复了肠道屏障功能,降低了肠道通透性,并防止内毒素等有害物质进入肝脏,进一步减轻肝脏炎症和纤维化。

讨论

尽管LGG在MASLD和MASH的治疗中显示出前景,但其作用机制和长期影响仍需进一步研究。未来的研究应侧重于优化益生菌的类型、剂量和治疗方案,以及监测它们对肠道微生物群平衡的长期影响,以确保其在临床应用中的安全性和有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8792/12328336/efc15d7558e5/fmicb-16-1586678-g001.jpg

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