Abstract
Disposition and metabolism of the new anticonvulsant 2,6-dimethylbenzamide N-(5-methyl-3-isoxazolyl) (D2916) was studied in male and female rats after oral administration of14C-labeled material. D2916 was well absorbed in both sexes and distributed to all tissues, with maximal drug concentrations found in elimination and metabolization organs, as well as in fatty tissues. Striking differences in pharmacokinetic parameters of total radioactivity were observed between males and females: females had higher brain concentrations and longer blood and tissue half-lives. The study of blood, bile, urine, and brain metabolites showed that D2916 follows two degradation pathways related to hydroxylation of methyl groups. Males prefer to hydroxylate one of the methyl groups of the phenyl ring, and females prefer to hydroxylate the methyl of the isoxazolyl ring forming the active metabolite D3187. These findings suggest a sex difference in the location of the hydroxylation of the D2916 molecule and can explain the longer anticonvulsant effect observed in the female rat that is related both to an orientation of the metabolism toward the formation of the active metabolite and to a better ability to this metabolite to cross the blood-brain barrier, compared with the unchanged drug.
Footnotes
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Send reprint requests to: Dr. J. C. Maurizis, Unité INSERM U71, Rue Montalembert, BP 184, 63005 Clermont-Ferrand, Cedex 1, France.
- Abbreviations used are::
- D2916
- 2,6-dimethylbenzamide N-(5-methyl-3-isoxazolyl)
- MES
- maximal electroshock
- D3187
- 2,6-dimethylbenzamideN-(5-hydroxymethyl-3-isoxazolyl)
- D3269
- 3-(2,6-dimethylbenzoylamino)-5-isoxazolecarboxylic acid
- D3342
- 7-methyl-1(3H)-isofuranone
- D3389
- 7-hydroxymethyl-1(3H)-isofuranone
- t1/2
- elimination half-life
- AUC
- area under the curve
- Received February 19, 1996.
- Accepted September 26, 1996.
- The American Society for Pharmacology and Experimental Therapeutics
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