DEXTROMETHORPHAN METABOLISM IN RAT - INTERSTRAIN DIFFERENCES AND THE FATE OF INDIVIDUALLY ADMINISTERED OXIDATIVE METABOLITES

Citation
F. Bochner et al., DEXTROMETHORPHAN METABOLISM IN RAT - INTERSTRAIN DIFFERENCES AND THE FATE OF INDIVIDUALLY ADMINISTERED OXIDATIVE METABOLITES, Xenobiotica, 24(6), 1994, pp. 543-552
Citations number
20
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
00498254
Volume
24
Issue
6
Year of publication
1994
Pages
543 - 552
Database
ISI
SICI code
0049-8254(1994)24:6<543:DMIR-I>2.0.ZU;2-6
Abstract
1. Dextromethorphan undergoes O- and N-demethylation, with the resulta nt metabolites being further N- and O-demethylated respectively to 5-h ydroxymorphinan. The polymorphically expressed O-demethylation reactio n is catalysed by P4502D1 in the Sprague-Dawley (SD) rat. The Dark-Ago uti (DA) rat lacks this enzyme. 2. The aims were: (1) to determine if there were strain differences also in the Hooded Wistar (HW) and Albin o Wister (AW) rats with respect to the four demethylation reactions af ter dextromethorphan 20 mg/kg intraperitoneally; (2) to investigate th e inhibition of the demethylation reactions by quinine and quinidine ( each 40 mg/kg i.p.) in the above strains; and (3) to investigate the f ate of separately administered metabolites (5 mg/kg i.p.) of dextromet horphan in the SD strain. 3. The total recovery of dextromethorphan an d metabolites in the four strains ranged from 38 to 64% of the dose. T he O-demethylation ratios (expressed as the ratio of urinary total dex trorphan divided by dextromethorphan) in the AW and DA strains were si milar but less than in the SD/HW strains; the N-demethylation ratios ( expressed as the ratio of urinary total 3-hydroxymorphinan plus 5-meth oxymorphinan divided by dextromethorphan) in the DA and SD strains wer e similar but greater than in the AW and HW strains. Quinine and quini dine significantly reduced the O-demethylation ratio in the SD and DA rat strains, and the N-demethylation ratio in the SD strain. 4. In the SD rat the major metabolic route was via O-demethylation to dextrorph an. The source of 3-hydroxymorphinan is primarily from N-demethylation of dextromethorphan to 3-methoxymorphinan and its subsequent O-demeth ylation to 3-hydroxymorphinan. The O-demethylation metabolic ratio for dextromethorphan should be calculated as the quotient of urinary tota l dextrorphan divided by dextromethorphan.