Chenodeoxycholic acid-mediated activation of the farnesoid X receptor negatively regulates hydroxysteroid sulfotransferase

Drug Metab Pharmacokinet. 2006 Aug;21(4):315-23. doi: 10.2133/dmpk.21.315.

Abstract

Hydroxysteroid sulfotransferase catalyzing bile acid sulfation plays an essential role in protection against lithocholic acid (LCA)-induced liver toxicity. Hepatic levels of Sult2a is up to 8-fold higher in farnesoid X receptor-null mice than in the wild-type mice. Thus, the influence of FXR ligand (chenodeoxycholic acid (CDCA) and LCA) feeding on hepatic Sult2a expression was examined in FXR-null and wild-type mice. Hepatic Sult2a protein content was elevated in FXR-null and wild-type mice fed a LCA (1% and 0.5%) diet. Treatment with 0.5% CDCA diet decreased hepatic Sult2a to 20% of the control in wild-type mice, but increased the content in FXR-null mice. Liver Sult2a1 (St2a4) mRNA levels were reduced to 26% in wild-type mice after feeding of a CDCA diet, while no decrease was observed on Sult2a1 mRNA levels in FXR-null mice after CDCA feeding. A significant inverse relationship (r(2)=0.523) was found between hepatic Sult2a protein content and small heterodimer partner (SHP) mRNA level. PCN-mediated increase in Sult2a protein levels were attenuated by CDCA feeding in wild-type mice, but not in FXR-null mice. Human SULT2A1 protein and mRNA levels were decreased in HepG2 cells treated with the FXR agonists, CDCA or GW4064 in dose-dependent manners, although SHP mRNA levels were increased. These results suggest that SULT2A is negatively regulated through CDCA-mediated FXR activation in mice and humans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Chenodeoxycholic Acid / metabolism
  • Chenodeoxycholic Acid / pharmacology*
  • DNA-Binding Proteins / agonists*
  • DNA-Binding Proteins / deficiency
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation / drug effects*
  • Female
  • Gene Expression Regulation, Enzymologic / drug effects
  • Humans
  • Lithocholic Acid / metabolism
  • Liver / drug effects
  • Liver / enzymology
  • Mice
  • Pregnenolone Carbonitrile / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Cytoplasmic and Nuclear / agonists*
  • Receptors, Cytoplasmic and Nuclear / deficiency
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Sulfotransferases / antagonists & inhibitors*
  • Sulfotransferases / genetics
  • Sulfotransferases / metabolism*
  • Transcription Factors / agonists*
  • Transcription Factors / deficiency
  • Transcription Factors / metabolism*

Substances

  • DNA-Binding Proteins
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • nuclear receptor subfamily 0, group B, member 2
  • farnesoid X-activated receptor
  • Chenodeoxycholic Acid
  • Pregnenolone Carbonitrile
  • Lithocholic Acid
  • Sulfotransferases
  • alcohol sulfotransferase