Ascorbic acid deficiency decreases hepatic cytochrome P-450, especially CYP2B1/2B2, and simultaneously induces heme oxygenase-1 gene expression in scurvy-prone ODS rats

Biosci Biotechnol Biochem. 2014;78(6):1060-6. doi: 10.1080/09168451.2014.910105. Epub 2014 May 28.

Abstract

The mechanisms underlying the decrease in hepatic cytochrome P-450 (CYP) content in ascorbic acid deficiency was investigated in scurvy-prone ODS rats. First, male ODS rats were fed a diet containing sufficient ascorbic acid (control) or a diet without ascorbic acid (deficient) for 18 days, with or without the intraperitoneal injection of phenobarbital. Ascorbic acid deficiency decreased hepatic microsomal total CYP content, CYP2B1/2B2 protein, and mitochondrial cytochrome oxidase (COX) complex IV subunit I protein, and simultaneously increased heme oxygenase-1 protein in microsomes and mitochondria. Next, heme oxygenase-1 inducers, that is lipopolysaccharide and hemin, were administered to phenobaribital-treated ODS rats fed sufficient ascorbic acid. The administration of these inducers decreased hepatic microsomal total CYP content, CYP2B1/2B2 protein, and mitochondrial COX complex IV subunit I protein. These results suggested that the stimulation of hepatic heme oxygenase-1 expression by ascorbic acid deficiency caused the decrease in CYP content in liver.

Keywords: CYP2B1/2B2; ODS rat; ascorbic acid; cytochrome P-450; heme oxygenase-1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aryl Hydrocarbon Hydroxylases / metabolism*
  • Cytochrome P-450 CYP2B1 / metabolism*
  • Disease Susceptibility
  • Electron Transport Complex IV / metabolism
  • Gene Expression Regulation, Enzymologic*
  • Heme Oxygenase-1 / genetics*
  • Lipopolysaccharides / pharmacology
  • Liver / drug effects
  • Liver / enzymology*
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology
  • Phenobarbital / pharmacology
  • Rats
  • Scurvy / enzymology*
  • Scurvy / genetics*
  • Scurvy / metabolism
  • Steroid Hydroxylases / metabolism*

Substances

  • Lipopolysaccharides
  • Steroid Hydroxylases
  • Aryl Hydrocarbon Hydroxylases
  • Cytochrome P-450 CYP2B1
  • steroid 16-beta-hydroxylase
  • Heme Oxygenase-1
  • Electron Transport Complex IV
  • Phenobarbital