Requirement for omega and (omega;-1)-hydroxylations of fatty acids by human cytochromes P450 2E1 and 4A11

J Lipid Res. 1999 Nov;40(11):1990-7.

Abstract

Human liver microsomes and recombinant human P450 have been used as enzyme source in order to better understand the requirement for the optimal rate of omega and (omega;-1)-hydroxylations of fatty acids by cytochromes P450 2E1 and 4A. Three parameters were studied: alkyl chain length, presence and configuration of double bond(s) in the alkyl chain, and involvement of carboxylic function in the fatty acid binding inside the access channel of P450 active site. The total rate of metabolite formation decreased when increasing the alkyl chain length of saturated fatty acids (from C12 to C16), while no hydroxylated metabolite was detected when liver microsomes were incubated with stearic acid. However, unsaturated fatty acids, such as oleic, elaidic and linoleic acids, were omega and (omega;-1)-hydroxylated with an efficiency at least similar to palmitic acid. The (omega;-1)/omega ratio decreased from 2.8 to 1 with lauric, myristic and palmitic acids as substrates, while the reverse was observed for unsaturated C18 fatty acids which are mainly omega-hydroxylated, except for elaidic acid showing a metabolic profile quite similar to those of saturated fatty acids. The double bond configuration did not significantly modify the ability of hydroxylation of fatty acid, while the negatively charged carboxylic group allowed a configuration energetically favourable for omega and (omega;-1)-hydroxylation inside the access channel of active site.

MeSH terms

  • Chromatography, High Pressure Liquid
  • Cytochrome P-450 CYP2E1 / metabolism*
  • Cytochrome P-450 CYP4A
  • Cytochrome P-450 Enzyme System / metabolism*
  • Fatty Acids / analysis
  • Fatty Acids / metabolism
  • Fatty Acids, Unsaturated / analysis
  • Fatty Acids, Unsaturated / metabolism*
  • Genetic Engineering
  • Humans
  • Hydroxylation
  • Kinetics
  • Microsomes, Liver / enzymology
  • Mixed Function Oxygenases / metabolism*
  • Palmitates / metabolism
  • Recombinant Proteins
  • Transfection

Substances

  • Fatty Acids
  • Fatty Acids, Unsaturated
  • Palmitates
  • Recombinant Proteins
  • Cytochrome P-450 Enzyme System
  • methyl palmitate
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP2E1
  • Cytochrome P-450 CYP4A