Cytotoxic effect of 7α‐hydroxy‐4‐cholesten‐3‐one on HepG2 cells: Hypothetical role of acetaldehyde‐modified Δ4‐3‐ketosteroid‐5β‐reductase (the 37‐kd‐liver protein) in the pathogenesis of alcoholic liver injury in the rat
Renee C. Lin, Michael J. Fillenwarth, Xiangnan Du – 30 December 2003 – We recently identified ▵4‐3‐ketosteroid‐5β‐reductase as the 37 kd liver protein which is highly susceptible to acetaldehyde modification in rats continuously fed alcohol. The 5β‐reductase is a key enzyme involved in bile acid synthesis. We report here that the ability to degrade 7α‐hydroxy‐4‐cholesten‐3‐one (HCO) was lower in the liver cytosol of alcohol‐fed rats than in control animals, suggesting an inhibition of the 5β‐reductase enzyme activity by acetaldehyde modification.