Cytochrome P450 4A, peroxisomal enzymes and nicotinamide cofactors in koala liver.

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Ngo S, Kong S, Kirlich A, McKinnon RA, Stupans I

Cytochrome P450 4A, peroxisomal enzymes and nicotinamide cofactors in koala liver.

Comp Biochem Physiol C Toxicol Pharmacol. 2000 Dec;127(3):327-34.

PubMed ID
11246504 [ View in PubMed
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Abstract

We have examined hepatic levels of microsomal lauric acid hydroxylase activity and cyanide-insensitive palmitoyl coenzyme A oxidative activity in koala (Phascolarctos cinereus) and tammar wallaby (Macropus eugenii) and compared our results to those determined in rat. Microsomal lauric acid hydroxylation was significantly higher in koala than in tammar wallaby or rat. However, cyanide-insensitive palmitoyl-CoA oxidation was absent in the koala. We have also determined the hepatic nicotinamide cofactors in these species. Hepatic nicotinamide-adenine dinucleotide (NAD) and the ratio of NAD/nicotinamide-adenine dinucleotide phosphate (NADP) were higher in koala than in tammar wallaby and rat liver. Reverse transcription of koala liver mRNA, followed by polymerase chain reaction using primers based on highly conserved areas in the CYP4A family led to the cloning of a partial, near full length, cDNA clone with approximately 70% nucleotide and deduced amino acid sequence identity to human CYP4A11. The CYP has been named CYP4A15.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
NADHCytochrome P450 4A11ProteinHumans
Unknown
Not AvailableDetails