Cytochrome P450 1A1/2 induction by antiparasitic drugs: dose-dependent increase in ethoxyresorufin O-deethylase activity and mRNA caused by quinine, primaquine and albendazole in HepG2 cells.

Article Details

Citation

Bapiro TE, Andersson TB, Otter C, Hasler JA, Masimirembwa CM

Cytochrome P450 1A1/2 induction by antiparasitic drugs: dose-dependent increase in ethoxyresorufin O-deethylase activity and mRNA caused by quinine, primaquine and albendazole in HepG2 cells.

Eur J Clin Pharmacol. 2002 Nov;58(8):537-42. Epub 2002 Oct 2.

PubMed ID
12451431 [ View in PubMed
]
Abstract

OBJECTIVE: To investigate the inductive effects of twenty-four antiparasitic drugs on cytochrome P450 (CYP) 1A1 and 1A2 enzyme activities. METHODS: Human hepatoma (HepG2) cells were exposed to antiparasitic drugs for 24 h, and the ethoxyresorufin O-deethylase (EROD) activity, indicative of CYP1A enzyme activity, was measured fluorometrically. In addition, the CYP1A1 and CYP1A2 mRNA expression levels were determined by means of quantitative reverse-transcriptase polymerase chain reaction. RESULTS: Quinine, albendazole and primaquine caused a dose-dependent increase in EROD activity of 5.5, 4.0 and 7.5-fold, at concentrations eliciting maximal induction, respectively. 2,3,7,8-tetrachlorodibenzo- p-dioxin, used as a positive control at a final concentration of 1.5 nM, caused a 30-fold increase in EROD activity. The induction of EROD activity was accompanied by an increase in CYP1A1 and CYP1A2 mRNA expression levels. Niclosamide, 4-chlorophenylbiguanide, dapsone, amodiaquine and desethylamodiaquine caused slight increases in EROD activity. No effect on CYP1A was observed for artemisinin, suramin, diethylcarbamazine, pyrimethamine, metrifonate, ivermectin, pyrantel artesunate, cycloguanil, atovaquone, melarsoprol, praziquantel, proguanil and dihydroartemisinin. CONCLUSIONS: Quinine, albendazole and primaquine induce CYP1A1 and CYP1A2 at the transcriptional level. Considering the plasma concentrations (C(max)) achieved in vivo after administration of a therapeutic dose, induction by quinine and albendazole might be of clinical significance. The induction by primaquine, however, may not be of pharmacological or toxicological significance as concentrations at which it occurs are much higher than those attained in vivo.

DrugBank Data that Cites this Article

Drugs
Drug Enzymes
DrugEnzymeKindOrganismPharmacological ActionActions
AlbendazoleCytochrome P450 1A1ProteinHumans
Unknown
Inducer
Details
AlbendazoleCytochrome P450 1A2ProteinHumans
Unknown
Inducer
Details
PrimaquineCytochrome P450 1A1ProteinHumans
Unknown
Inducer
Details
PrimaquineCytochrome P450 1A2ProteinHumans
Unknown
Substrate
Inducer
Details
QuinineCytochrome P450 1A1ProteinHumans
Unknown
Inhibitor
Inducer
Details
Pharmaco-transcriptomics
DrugDrug GroupsGeneGene IDChangeInteractionChromosome
AlbendazoleApproved Vet ApprovedCYP1A11543
upregulated
Albendazole results in increased expression of CYP1A1 mRNA15q24.1
AlbendazoleApproved Vet ApprovedCYP1A21544
upregulated
Albendazole results in increased expression of CYP1A2 mRNA15q24.1
PrimaquineApprovedCYP1A11543
upregulated
Primaquine results in increased expression of CYP1A1 mRNA15q24.1
PrimaquineApprovedCYP1A21544
upregulated
Primaquine results in increased expression of CYP1A2 mRNA15q24.1
QuinineApprovedCYP1A11543
upregulated
Quinine results in increased expression of CYP1A1 mRNA15q24.1
QuinineApprovedCYP1A21544
upregulated
Quinine results in increased expression of CYP1A2 mRNA15q24.1