Metabolic disposition of tacrine in primary suspensions of rat hepatocyte and in single-pass perfused liver:in vitro/in vivocomparisons
Autor: | S Bezek, W. F. Pool, M Kukan, T F Woolf |
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Rok vydání: | 1994 |
Předmět: |
Male
medicine.medical_specialty Liver cytology Health Toxicology and Mutagenesis Metabolite In Vitro Techniques Biology Toxicology Biochemistry chemistry.chemical_compound In vivo Internal medicine medicine Animals Carbon Radioisotopes Rats Wistar Pharmacology General Medicine Metabolism Prognosis In vitro Rats Perfusion Endocrinology medicine.anatomical_structure Liver chemistry Tacrine Hepatocyte Toxicity medicine.drug |
Zdroj: | Xenobiotica. 24:1107-1117 |
ISSN: | 1366-5928 0049-8254 |
DOI: | 10.3109/00498259409038670 |
Popis: | 1. Incubations of tacrine (1,2,3,4-tetrahydro-9-acridinamine monohydrochloride monohydrate, THA) with a primary suspension of rat hepatocytes for 2 min resulted in formation of the 1-hydroxy derivative as the major metabolite with smaller amounts of the 2- and 4-hydroxy metabolites. 2. Apparent Vmax and Km for THA metabolism were 12.4 +/- 3.3 nmol/min/g liver and 0.98 +/- 0.34 microM respectively. 3. Incubations of THA for longer time-periods (10 min) resulted in irreversible binding of THA-derived radioactivity to hepatocellular protein. The apparent maximal rate of irreversible binding (Bmax) was 76.7 +/- 30.5 pmol equivalents bound/h/mg cell protein, whereas the apparent Kb for binding was 2.8 +/- 1.4 microM. 4. The kinetic parameters, Vmax and Km, were used to predict steady-state extraction ratios (ERSS) for various THA input concentrations (Cin) in single-pass perfused rat liver. At low input concentrations (0.72-0.85 microM; CinKm), ERSS of THA was approximately 1. For higher Cin (14.05, 20.72, 20.88 microM; CinKm), the calculated ERSS was markedly decreased with 0.300, 0.296 and 0.261, respectively. 5. The intrinsic clearance of THA (Cli) estimated from in vitro hepatocyte data was 6.7 ml/min/g liver while the apparent oral THA clearance (Cloral) calculated from in vivo rat data was 6.6 ml/min/g liver. |
Databáze: | OpenAIRE |
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