COMPARATIVE METABOLISM OF LORAZEPAM IN MAN AND 4 ANIMAL SPECIES
- 1 January 1978
- journal article
- research article
- Vol. 39 (10), 11-15
Abstract
The metabolic disposition of lorazepam (Wy-4036) in man, dog, cat, rat and miniature swine is compared. Except in the cat, absorption of lorazepam is rapid in these species. Absorption in humans is nearly complete. Lorazepam glucuronide is the major metabolite in all species except the rat in which a dihydrodiol derivative is the main product of lorazepam biotransformation. Lorazepam glucuronide, which has no demonstrable CNS activity, is also present in the plasma of all species investigated. The concentrations of lorazepam in rat brain correlate well with those in plasma but are about 3 times higher. The urinary route of excretion predominates in man, dog and miniature swine while in the rat the bulk of the drug-related material is eliminated with the feces as a consequence of biliary excretion. [The benzodiazepines, of which lorazepam is one, have previously been shown to have psychoactive properties.].This publication has 2 references indexed in Scilit:
- N‐Desmethyldiazepam: A new metabolite of chlordiazepoxide in manClinical Pharmacology & Therapeutics, 1976
- Clinical pharmacokinetics of lorazepamClinical Pharmacology & Therapeutics, 1976