Jiang_2026_Acta.Pharmacol.Sin__

Carboxylesterases CES1 and CES2 are the pivotal hepatic enzymes involved in triglyceride (TG) hydrolysis and prodrug metabolism, yet their expression and activity are suppressed in metabolic dysfunction-associated steatotic liver disease (MASLD). Liver X receptor alpha (LXRalpha) is known to play a crucial role in maintaining the constitutive expression of CES1 in human liver cells. Oridonin (ORI) is a diterpene derived from a traditional Chinese herb that possesses antitumor, anti-inflammatory, and antimicrobial activities. We previously demonstrated that ORI, as a natural LXRalpha agonist, activated the LXRalpha-ATGL/EPT1 pathway, correcting the TG/phosphatidylethanolamine (PE) lipid imbalance induced by obesity and thereby improving MASLD. Here, we investigated the regulatory role of LXRalpha on CES1/CES2 expression in MASLD liver and elucidated the underlying molecular mechanisms of ORI's lipid-lowering effects. A high-fat diet (HFD)-induced steatosis model was established in mice. The mice were treated with ORI (100 mg.kg(-)(1).d(-)(1), i.g.) from the 16th to the 24th week. RNA-seq analysis in MASLD patients demonstrated that LXRalpha is a key transcriptional regulator of CES1 and CES2. LXRalpha knockout (LXRalpha(-)(/)(-)) mice exhibited aggravated HFD-induced steatosis and impaired metabolic conversion of the CES1/CES2 substrates, oseltamivir and irinotecan. This deficiency resulted in a corresponding increase in their drug exposure (AUC) by 154.5% and 26.2%, respectively. Mechanistically, LXRalpha directly bound to liver X receptor response elements (LXREs) in the promoter regions of CES1 (-183/-165 bp) and CES2 (-1870/-1852 bp) to drive transcription in HepG2 cells. Furthermore, ORI (2.5, 5, 10 microM) dose-dependently restored CES1/CES2 expression and activity, reducing lipid accumulation. Silencing of CES1 or CES2 abolished ORI's lipid-lowering effect, confirming their essential roles. These findings establish the LXRalpha-CES1/CES2 pathway as a pivotal node integrating hepatic lipid homeostasis and drug metabolism, positioning ORI as a promising therapeutic agent for MASLD.