Caffeine metabolism before and after liver transplantation
Autor: | S Hrusovsky, P. R. Bechtel, Gilles Paintaud, Hervé Le-Louët, Y. C. Bechtel, M P Brientini, G. Mantion, Jean-Philippe Miguet |
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Rok vydání: | 2001 |
Předmět: |
Adult
Male Xanthine Oxidase medicine.medical_specialty medicine.medical_treatment Azathioprine Urine Liver transplantation Biology Mixed Function Oxygenases Cytochrome P-450 CYP2A6 chemistry.chemical_compound Cytochrome P-450 Enzyme System Liver Function Tests Pharmacokinetics Cytochrome P-450 CYP1A2 Reference Values Caffeine Internal medicine medicine Humans Pharmacology (medical) Uracil Aged Pharmacology medicine.diagnostic_test CYP1A2 Middle Aged Liver Transplantation Transplantation Endocrinology Liver chemistry Case-Control Studies Cyclosporine Female Aryl Hydrocarbon Hydroxylases Liver function tests Immunosuppressive Agents medicine.drug |
Zdroj: | Europe PubMed Central |
ISSN: | 0946-1965 |
Popis: | Aim To study drug metabolism in patients before and after liver transplantation using caffeine as a probe drug. Forty-five patients undergoing liver transplantation for various liver diseases and who had well documented dossiers were selected for the study. Before the liver transplantation and 1 month, 1 year, and 6 years after liver transplantation, they were given 200 mg of caffeine by the oral route in the morning after voiding their bladder. Twenty-four-hour urine samples were collected and caffeine and metabolites were determined by HPLC: 1-methylurate (1U), 1-methylxanthine (1X), 1.7-dimethylurate (17U), 1.7-dimethylxanthine (17X), 7-methylxanthine (7X), 3-methylxanthine (3X), 1.3-dimethylurate (13U), 3.7-dimethylxanthine (37X), 1.3-dimethylxanthine (13X), 1.3.7-trimethylxanthine = caffeine (137X). Indices of enzyme activities were calculated from the following urinary elimination ratios: (AFMU+1U+1X)/17U for CYP1A2, 17U/17X for CYP2A6, 1U/1X for xanthine oxidase (XO), AFMU/(AFMU+1U+1X) for N-acetyltransferase (NAT-2). Results Compared with results obtained in a group of 70 healthy subjects, caffeine metabolism before liver transplantation was deeply depressed with a decreased elimination rate in the case of all metabolites and a decreased CYP1A2 activity. Caffeine metabolism began to return to the control values one month after transplantation. One year and 6 years after liver transplantation, quantitatively, the metabolism of caffeine was stable and not different from control, but with qualitative modifications. CYP1A2 activity was decreased with reduced urinary elimination rates of 1X and 17X. XO and CYP2A6 activities and 1U and 17U urinary elimination rates were increased. Immunosuppressive treatment was possibly responsible for the metabolic pathway changes. Almost the same modifications were observed in 9 patients after bone marrow transplantation who had been treated with the same immunosuppressive drugs, cyclosporine and azathioprine. During severe rejection phases in 6 of the liver transplant patients, caffeine metabolism was progressively decreased when the usual liver function tests showed moderate but uniform changes. Conclusion Despite an apparent normal drug-metabolic function, immunosuppressive treatment induces stable variations in drugmetabolic pathways after liver transplantation which can be detected from the changes in caffeine metabolism. |
Databáze: | OpenAIRE |
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