Induction and regulation of cytochrome P450 K-5 (lauric acid hydroxylase) in rat renal microsomes by starvation

Biochim Biophys Acta. 1990 Oct 12;1036(1):18-23. doi: 10.1016/0304-4165(90)90208-e.

Abstract

The effects of starvation on rat renal cytochrome P-450s were studied. The content of spectrally measured cytochrome P-450 in the renal microsomes of male rats increased 2-fold with 72 h starvation, but cytochrome b5 and NADPH-cytochrome P-450 reductase were not induced. 7-Ethoxycoumarin O-dealkylation and aniline hydroxylation activities of the renal microsomes of control male rats were very low but were induced 2.5-3-fold by 72 h starvation. Aminopyrine N-demethylation and lauric acid hydroxylation activities were induced 1.5-2-fold by 72 h starvation. The changes in catalytic activities suggested that the contents of individual cytochrome P-450s in the renal microsomes were altered by starvation. The contents of some cytochrome P-450s were measured by Western blotting. P450 DM (P450IIE1), a typical form of cytochrome P-450 induced by starvation in rat liver, was barely detected in rat kidney and was induced 2-fold by 72 h starvation. P450 K-5, a typical renal cytochrome P-450 and lauric acid hydroxylase, accounted for 81% of the spectrally measured cytochrome P-450 in the renal microsomes of control male rats and was induced 2-fold by 72 h starvation. P450 K-5 was not induced in rat kidney by treatment with chemicals such as acetone or clofibrate. The renal microsomes of male rats contained 6-times as much P450 K-5 as those of female rats. These results suggest that P450 K-5 is regulated by an endocrine factor.

MeSH terms

  • Animals
  • Cytochrome P-450 CYP4A
  • Cytochrome P-450 Enzyme System / analysis
  • Cytochrome P-450 Enzyme System / biosynthesis*
  • Enzyme Induction
  • Fatty Acids / metabolism
  • Kidney / enzymology*
  • Microsomes / enzymology*
  • Mixed Function Oxygenases / analysis
  • Mixed Function Oxygenases / biosynthesis*
  • Rats
  • Rats, Inbred Strains
  • Starvation / enzymology*

Substances

  • Fatty Acids
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP4A