Uptake, subcellular distribution and biotransformation of 3H-labelled astemizole in cultured rat hepatocytes
| Autor: | Yves-Jacques Schneider, Christine Waterkeyn, Willem Meuldermans, André Trouet, Pierre M. Laduron |
|---|---|
| Rok vydání: | 1987 |
| Předmět: |
Male
Endosome Mitochondria Liver Biology Centrifugation Isopycnic Endoplasmic Reticulum Biochemistry Cytosol medicine Animals Receptors Histamine H1 Receptor Biotransformation Cells Cultured Chromatography High Pressure Liquid Pharmacology Differential centrifugation Cathepsin Endoplasmic reticulum Cell Membrane Chloroquine Astemizole Ligand (biochemistry) Culture Media Rats Kinetics Liver Microsomes Liver Benzimidazoles Lysosomes medicine.drug |
| Zdroj: | Biochemical pharmacology. 36(23) |
| ISSN: | 0006-2952 |
| Popis: | When incubated with 3H-astemizole, a potent antagonist of H1 receptor, cultured rat hepatocytes, which do not express specific receptors for this ligand, avidly take up 3H-label proportionally to the drug concentration. HPLC analysis indicates that at 10 ng 3H-astemizole/ml, cells almost entirely deplete the culture medium of the drug within 4 hr of incubation. At 37 degrees, astemizole is metabolized and released into the culture medium mainly under the form of glucuronoconjugated metabolites. Differential centrifugation of homogenates from hepatocytes incubated with 3H-astemizole indicates that astemizole and unconjugated metabolites are found in the particulate fraction, whereas astemizole and conjugated metabolites are present in the cytosol. Isopycnic centrifugation on sucrose gradient shows that the major part of the 3H-label in the particulate fraction distributes like phospholipids and NADPH cytochrome c reductase, suggesting an association with membranes and, in particular, with the endoplasmic reticulum. Chloroquine, a drug accumulating within lysosomes and acidic endosomes, decreases the uptake of 3H-astemizole by hepatocytes and induces, during isopycnic centrifugation of a particulate fraction, a shift of the 3H-label towards lower densities where it closely accompanies cathepsin B. This suggests that a minor part of astemizole accumulated in the hepatocytes could be trapped within lysosomes. These results could support the hypothesis that aspecific binding of astemizole to cellular membranes and, to a lesser extent, trapping in lysosomes could play a role in the pharmacokinetics of the drug. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|