Abstract
Almotriptan is a novel highly selective 5-hydroxytryptamine1B/1D agonist developed for the acute oral treatment of migraine. The in vitro metabolism of almotriptan has been investigated using human liver subcellular fractions and cDNA-expressed human enzymes, to study the metabolic pathways and identify the enzymes responsible for the formation of the major metabolites. Specific enzymes were identified by correlation analysis, chemical inhibition studies, and incubation with various cDNA expressed human enzymes. Human liver microsomes and S9 fraction metabolize almotriptan by 2-hydroxylation of the pyrrolidine group to form a carbinolamine metabolite intermediate, a reaction catalyzed by CYP3A4 and CYP2D6. This metabolite is further oxidized by aldehyde dehydrogenase to the open ring γ-aminobutyric acid metabolite. Almotriptan is also metabolized at the dimethylaminoethyl group byN-demethylation, a reaction that is carried out by five different cytochrome P450s, flavin monooxygenase-3 mediated N-oxidation, and MAO-A catalyzed oxidative deamination to form the indole acetic acid and the indole ethyl alcohol derivatives of almotriptan. The use of human liver mitochondria confirmed the contribution of MAO-A to the metabolism of almotriptan. Both, the γ-aminobutyric acid and the indole acetic acid metabolites have been found to be the major in vivo metabolites of almotriptan in humans. In addition, different clinical trials conducted to study the effects of CYP3A4, CYP2D6, and MAO-A on the pharmacokinetics of almotriptan confirmed the involvement of these enzymes in the metabolic clearance of this drug and that no dose changes are required in the presence of inhibitors of these enzymes.
Footnotes
- Abbreviations used are::
- Almotriptan
- 3-(2-dimethylaminoethyl)-5-(1-pyrrodinylsulfonylmethyl)-1H-indole
- 5HT
- 5-hydroxytryptamine
- P450
- cytochrome P450
- MAO
- monoamine oxidase
- LAS-31936
- 3-[1-methyl-4-piperidinyl]-N-methyl-1H-indole-3-ethanesulfonamide
- PMSF
- phenylmethylsulfonyl fluoride
- disulfiram
- tetraethylthiuram disulfide
- DDTC
- diethyldithiocarbamate
- HPLC
- high performance liquid chromatography
- FMO
- flavin monooxygenase
- AO
- aldehyde oxidase
- XO
- xanthine oxidase
- Received September 5, 2002.
- Accepted December 18, 2002.
- The American Society for Pharmacology and Experimental Therapeutics
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