1. Academic Validation
  2. Metformin attenuated sepsis-related liver injury by modulating gut microbiota

Metformin attenuated sepsis-related liver injury by modulating gut microbiota

  • Emerg Microbes Infect. 2022 Dec;11(1):815-828. doi: 10.1080/22221751.2022.2045876.
Huoyan Liang 1 2 Heng Song 1 2 Xiaojuan Zhang 1 Gaofei Song 1 2 Yuze Wang 1 Xianfei Ding 1 Xiaoguang Duan 1 Lifeng Li 3 Tongwen Sun 1 2 Quancheng Kan 4
Affiliations

Affiliations

  • 1 General ICU, The First Affiliated Hospital of Zhengzhou University, Henan Key Laboratory of Critical Care Medicine, Zhengzhou Key Laboratory of Sepsis, Henan Engineering Research Center for Critical Care Medicine, Zhengzhou, People's Republic of China.
  • 2 Academy of Medical Sciences, Zhengzhou University, Zhengzhou, People's Republic of China.
  • 3 Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Internet Medical and System Applications of National Engineering Laboratory, Zhengzhou, People's Republic of China.
  • 4 Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, People's Republic of China.
Abstract

Increased evidence shows that gut microbiota acts as the primary regulator of the liver; however, its role in sepsis-related liver injury (SLI) in the elderly is unclear. This study assessed whether metformin could attenuate SLI by modulating gut microbiota in septic-aged rats. Cecal ligation and puncture (CLP) was used to induce SLI in aged rats. Fecal microbiota transplantation (FMT) was used to validate the roles of gut microbiota in these pathologies. The composition of gut microbiota was analysed by 16S rRNA sequencing. Moreover, the liver and colon tissues were analysed by histopathology, immunofluorescence, immunohistochemistry, and reverse transcription polymerase chain reaction (RT-PCR). Metformin improved liver damage, colon barrier dysfunction in aged SLI rats. Moreover, metformin improved sepsis-induced liver inflammation and damage under gut microbiota. Importantly, FMT assay showed that rats gavaged with faeces from metformin-treated SLI rats displayed less severe liver damage and colon barrier dysfunctions than those gavaged with faeces from SLI rats. The gut microbiota composition among the sham-operated, CLP-operated and metformin-treated SLI rats was different. In particular, the proportion of Klebsiella and Escherichia_Shigella was higher in SLI rats than sham-operated and metformin-treated SLI rats; while metformin could increase the proportion of Bifidobacterium, Muribaculaceae, Parabacteroides_distasonis and Alloprevitella in aged SLI rats. Additionally, Klebsiella and Escherichia_Shigella correlated positively with the inflammatory factors in the liver. Our findings suggest that metformin may improve liver injury by regulating the gut microbiota and alleviating colon barrier dysfunction in septic-aged rats, which may be an effective therapy for SLI.

Keywords

CLP; Sepsis-related liver injury; aged rats; gut microbiota; metformin.

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