Paralleling the increasing prevalence of obesity, diabetes mellitus, and the metabolic syndrome in the general population, metabolic dysfunction-associated steatotic liver disease (MASLD) has become the most common cause of chronic liver disease worldwide.
MASLD represents a spectrum of long-term conditions characterised by fat deposition in the liver. In the UK, MASLD is the most prevalent cause of chronic liver disease, estimated to affect 1 in 3 adults.
The liver receives 75% of its blood flow directly from the intestinal portal circulation and due to the strong anatomical link between the gut and the liver, it is suggested that gut dysbiosis affects hepatic function and contributes to the pathogenesis of MASLD.
To this extent, the gut-liver axis has emerged as being critical to understanding the mechanisms and previously hidden aetiologies of liver disease progression. Early onset of MASLD and disease severity has been linked to high levels of TMAO, PAA, TCA and GCA in mice and humans. Investigating the impact of these gut metabolites and harmful bile acids in lipid accumulation is an important step for further understanding MASLD pathogenesis.
Led by
Dr David Sheridan
we have been working in exposing different MASLD models to gut metabolites. We have been optimising Precision cut liver slices (PCLS) from human liver samples. PCLS are an emerging state-of-the-art technology where thin slices are prepared from liver resections sustained in tissue culture. These slices are extremely versatile and an ideal tool to investigate MASLD development and progression.