Document Detail


Metabolism, distribution and excretion of a selective N-methyl-D-aspartate receptor antagonist, traxoprodil, in rats and dogs.
MedLine Citation:
PMID:  17496205     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Disposition of traxoprodil ({1-[2-hydroxy-2-(4-hydroxy-phenyl)-1-methyl-ethyl]-4-phenyl-piperidin-4-ol}mesylate; TRX), a selective antagonist of the N-methyl-d-aspartate class of glutamate receptors, was investigated in rats and dogs after administration of a single i.v. bolus dose of [(14)C]TRX. Total mean recoveries of the radiocarbon were 92.5 and 88.2% from rats and dogs, respectively. Excretion of radioactivity was rapid and nearly complete within 48 h after dosing in both species. Whole-body autoradioluminography study suggested that TRX radioactivity was retained more by uveal tissues, kidney, and liver than by other tissues. TRX is extensively metabolized in rats and dogs since only 8 to 15% of the administered radioactivity was excreted as unchanged drug in the urine of these species. The metabolic pathways included aromatic hydroxylation at the phenylpiperidinol moiety, hydroxylation at the hydroxyphenyl ring, and O-glucuronidation. There were notable species-related qualitative and quantitative differences in the metabolism of TRX in rats and dogs. The hydroxylation at the 3-position of the phenol ring followed by methylation of the resulting catechol intermediate and subsequent conjugation were identified as the main metabolic pathways in dogs. In contrast, formation of the major metabolites in rats was due to oxidation at the 4'-position of the phenylpiperidinol moiety followed by further oxidation and phase II conjugation. TRX glucuronide conjugate was identified as the major circulating component in rats, whereas the glucuronide and sulfate conjugates of O-methyl catechol metabolite were the major metabolites in dog plasma. The site of conjugation of regioisomeric glucuronides was established from the differences in the collision-induced dissociation product ion spectra of their methylated products.
Authors:
Chandra Prakash; Donghui Cui; Michael J Potchoiba; Todd Butler
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Publication Detail:
Type:  Journal Article     Date:  2007-05-11
Journal Detail:
Title:  Drug metabolism and disposition: the biological fate of chemicals     Volume:  35     ISSN:  0090-9556     ISO Abbreviation:  Drug Metab. Dispos.     Publication Date:  2007 Aug 
Date Detail:
Created Date:  2007-07-20     Completed Date:  2007-11-02     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9421550     Medline TA:  Drug Metab Dispos     Country:  United States    
Other Details:
Languages:  eng     Pagination:  1350-64     Citation Subset:  IM    
Affiliation:
Department of Pharmacokinetics, Pfizer Global Research and Development, Groton, Connecticut 06340, USA. chandra.prakash@pfizer.com
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MeSH Terms
Descriptor/Qualifier:
Animals
Bile / metabolism
Chromatography, High Pressure Liquid
Dogs
Feces / chemistry
Female
Glucuronic Acid / metabolism
Glucuronides / analysis,  biosynthesis
Injections, Intravenous
Male
Microsomes, Liver / metabolism
Molecular Structure
Neuroprotective Agents / administration & dosage,  chemistry,  pharmacokinetics
Piperidines / blood,  metabolism*,  pharmacokinetics*
Rats
Rats, Long-Evans
Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors*
Sex Factors
Tandem Mass Spectrometry
Tissue Distribution
Urine / chemistry
Chemical
Reg. No./Substance:
0/Glucuronides; 0/Neuroprotective Agents; 0/Piperidines; 0/Receptors, N-Methyl-D-Aspartate; 0/traxoprodil mesylate; 576-37-4/Glucuronic Acid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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