Gut microbiota regulates hepatic ischemia–reperfusion injury‐induced cognitive dysfunction via the HDAC2‐ACSS2 axis in mice

Abstract

AimsHepatic ischemia–reperfusion injury (HIRI) resulting from hepatic inflow occlusion, which is a common procedure in liver surgery is inevitable. Previous research has confirmed that the cognitive dysfunction induced by HIRI is closely related to dysbiosis of the gut microbiota. This research aims to investigate the mechanisms underlying this complication.MethodsC57BL/6 mice underwent hepatic ischemia experimentally through the occlusion of the left hepatic artery and portal vein. To assess the HDAC2‐ACSS2 axis, gut microbiota transplantation. Enzyme‐linked immunosorbent assay and LC/MS short‐chain fatty acid detection were utilized.ResultsThe findings indicated a notable decline in ACSS2 expression in the hippocampus of mice experiencing hepatic ischemia–reperfusion injury, emphasizing the compromised acetate metabolism in this particular area. Furthermore, the cognitive impairment phenotype and the dysregulation of the HDAC2‐ACSS2 axis could also be transmitted to germ‐free mice via fecal microbial transplantation. Enzyme‐linked immunosorbent assay revealed reduced Acetyl‐coenzyme A (acetyl‐CoA) and Acetylated lysine levels in the hippocampus.ConclusionThese findings suggest that acetate metabolism is impaired in the hippocampus of HIRI‐induced cognitive impairment mice and related to dysbiosis, leading to compromised histone acetylation.