期刊
JOURNAL OF CLINICAL MEDICINE
卷 10, 期 5, 页码 -出版社
MDPI
DOI: 10.3390/jcm10051081
关键词
cystathionine beta-synthase/cystathionine gamma-lyase (CBS/CSE) system; glutathione; H2S production; liver fibrosis; non-alcoholic steatohepatitis; sulfur metabolism
资金
- Novo Nordisk
- Novo Nordisk Foundation [NNF19OC0055001]
The prevalence of non-alcoholic fatty liver disease (NAFLD) is increasing globally, possibly related to obesity and metabolic syndrome. The transsulfuration pathway (TSP) plays a vital role in maintaining sulfur balance and optimal cellular function. While a causative link between TSP and NAFLD has not been established, dysfunctions in TSP and related pathways have been reported in NAFLD and liver cirrhosis, suggesting a need for further investigation.
The prevalence of non-alcoholic fatty liver disease (NAFLD) is increasing and approximately 25% of the global population may have NAFLD. NAFLD is associated with obesity and metabolic syndrome, but its pathophysiology is complex and only partly understood. The transsulfuration pathway (TSP) is a metabolic pathway regulating homocysteine and cysteine metabolism and is vital in controlling sulfur balance in the organism. Precise control of this pathway is critical for maintenance of optimal cellular function. The TSP is closely linked to other pathways such as the folate and methionine cycles, hydrogen sulfide (H2S) and glutathione (GSH) production. Impaired activity of the TSP will cause an increase in homocysteine and a decrease in cysteine levels. Homocysteine will also be increased due to impairment of the folate and methionine cycles. The key enzymes of the TSP, cystathionine beta-synthase (CBS) and cystathionine gamma-lyase (CSE), are highly expressed in the liver and deficient CBS and CSE expression causes hepatic steatosis, inflammation, and fibrosis in animal models. A causative link between the TSP and NAFLD has not been established. However, dysfunctions in the TSP and related pathways, in terms of enzyme expression and the plasma levels of the metabolites (e.g., homocysteine, cystathionine, and cysteine), have been reported in NAFLD and liver cirrhosis in both animal models and humans. Further investigation of the TSP in relation to NAFLD may reveal mechanisms involved in the development and progression of NAFLD.
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