Cyclosporin metabolism by the gastrointestinal mucosa.
Open Access
- 1 March 1991
- journal article
- Published by Wiley in British Journal of Clinical Pharmacology
- Vol. 31 (3) , 344-346
- https://doi.org/10.1111/j.1365-2125.1991.tb05540.x
Abstract
The intestinal mucosal metabolism of the immunosuppressant cyclosporin (CsA) has been studied in vitro using the Ussing chamber technique. Histologically normal colon was obtained from six patients undergoing resections. The mucosal sheets were mounted between two perspex chambers. Three hours after addition of [3H]-CsA (0.2 microCi; 10 microM) to the mucosal chamber, more than 90% of the radioactivity was present in that chamber. Metabolite analysis, by high performance liquid chromatography, indicated that 77.6 +/- 9.2% (mean +/- s.d.) of the drug present was CsA, 9.9 +/- 4.4% and 8.7 +/- 4.7% were the oxidative metabolites M17 and M21 respectively (metabolites identified by co-chromatography with authentic standards). Total metabolite production in tissues from the six individuals was variable (10.1-30.6% at 3 h) and increased over the time period of the study. A different pattern of metabolism was obtained from a single sample of gastric mucosa. More than 20% of CsA was metabolised although neither M17 nor M21 were detected. The results of this study suggest that the gut wall is involved in the first pass metabolism of CsA in vivo and that this could be a contributory factor to the poor systemic availability of CsA seen in some patients.Keywords
This publication has 14 references indexed in Scilit:
- CyclosporineNew England Journal of Medicine, 1989
- Calcium channel antagonists and cyclosporine metabolism: in vitro studies with human liver microsomes.British Journal of Clinical Pharmacology, 1989
- Comparative effects of two antimycotic agents, ketoconazole and terbinafine on the metabolism of tolbutamide, ethinyloestradiol, cyclosporin and ethoxycoumarin by human liver microsomes in vitro.British Journal of Clinical Pharmacology, 1989
- Glutathione S-transferase, cytochrome P450, and uridine 5′-diphosphate-glucuronosyltransferase in human small intestine and liverGastroenterology, 1989
- Metabolism of the contraceptive steroid desogestrel by the intestinal mucosa.British Journal of Clinical Pharmacology, 1989
- Clinical pharmacokinetics of cyclosporinPharmacology & Therapeutics, 1989
- Cyclosporine metabolism in human liver: Identification of a cytochrome P-450III gene family as the major cyclosporine-metabolizing enzyme explains interactions of cyclosporine with other drugsClinical Pharmacology & Therapeutics, 1988
- Intestinal metabolism of ethinyloestradiol and paracetamol in vitro: studies using Ussing chambers.British Journal of Clinical Pharmacology, 1987
- Clinical Pharmacokinetics of CyclosporinClinical Pharmacokinetics, 1986
- INDIVIDUALIZATION OF CYCLOSPORINE THERAPY USING PHARMACOKINETIC AND PHARMACODYNAMIC PARAMETERSTransplantation, 1985