Back to Search
Start Over
[Cytochrome P450 3A4 and Benzodiazepines].
- Source :
-
Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica [Seishin Shinkeigaku Zasshi] 2003; Vol. 105 (5), pp. 631-42. - Publication Year :
- 2003
-
Abstract
- Cytochrome P450(CYP)3A4 is one of the CYP enzymes catalyzing oxidative metabolism, and involved in the metabolism of many drugs. Among benzodiazepines, alprazolam, triazolam, brotizolam and midazolam are mainly metabolished by CYP3A4, and quazepam, diazepam and flunitrazepam are partly metabolised by this enzyme. Azole antifungals, macrolide antibiotics, calcium antagonists and grapefruit juice inhibit CYP3A4 activity, while antiepileptics and rifampicin induce the activity. The drugs affecting CYP3A4 activity inhibit or induce the metabolism of the benzodiazepines metabolised by this enzyme, and induce side effects or reduce therapeutic effects of these drugs. Therefore, the combination of the two groups of drugs should be avoided, and if it is unavoidable the dose of benzodiazepines should be adjusted.
- Subjects :
- Anti-Bacterial Agents pharmacology
Anticonvulsants pharmacology
Antifungal Agents pharmacology
Azoles pharmacology
Benzodiazepines
Calcium Channel Blockers pharmacology
Cytochrome P-450 CYP3A
Cytochrome P-450 Enzyme Inhibitors
Drug Interactions
Food-Drug Interactions
Humans
Macrolides
Rifampin pharmacology
Anti-Anxiety Agents metabolism
Cytochrome P-450 Enzyme System physiology
Subjects
Details
- Language :
- Japanese
- ISSN :
- 0033-2658
- Volume :
- 105
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Seishin shinkeigaku zasshi = Psychiatria et neurologia Japonica
- Publication Type :
- Academic Journal
- Accession number :
- 12875231