Studies on the conversion of haloperidol and its tetrahydropyridine dehydration product to potentially neurotoxic pyridinium metabolites by human liver microsomes.

Abstract

The neuroleptic agent haloperidol (HP) and its tetrahydropyridine dehydration product HPTP are biotransformed to the potentially neurotoxic HP pyridinium species HPP+ and the reduced HP pyridinium species RHPP+ in humans and rodents. The studies reported here were designed to identify the specific form(s) of human cytochrome P450 that catalyze(s) these transformations. Fifteen human liver microsomal preparations all catalyzed the oxidation of HP and HPTP to HPP+ and HPTP to RHPP+. Values for kcat/KM averaged 6.71 and 1.24 min-1 mM-1 for HPP+ and RHPP+ formation, respectively. The rates of conversion of HP and HPTP to HPP+ correlated well with testosterone 6 beta-hydroxylase activity, a marker of P450 3A activity. Microsomes prepared from a human lymphoblastoid cell line co-expressing human P450 3A4 and cytochrome P450 reductase also catalyzed the formation of HPP+ from HP and HPTP. Troleandomycin and ketoconazole, potent P450 3A inhibitors, and antibodies against P450 3A were effective inhibitors of HPP+ formation. We conclude that the conversions of HP and HPTP to potentially neurotoxic pyridinium metabolite HPP+ are catalyzed selectively by P450 3A4 in human liver microsomes.

• Authors: E Usuki, R Pearce, A Parkinson, N Castagnol Jr
• Journal: Chemical research in toxicology (Chem Res Toxicol) Vol. 9 Issue 4 Pg. 800-6 (Jun 1996) ISSN: 0893-228X [Print] United States
• PMID: 8831826 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Antibodies
• Antipsychotic Agents
• Enzyme Inhibitors
• Pyridinium Compounds
• Cytochrome P-450 Enzyme System
• 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
• Steroid Hydroxylases
• steroid hormone 6-beta-hydroxylase
• Haloperidol

Topics

• 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine (chemistry)
• Animals
• Antibodies (metabolism)
• Antipsychotic Agents (chemistry, metabolism)
• Calibration
• Chromatography, High Pressure Liquid
• Cytochrome P-450 Enzyme System (immunology, metabolism)
• Dose-Response Relationship, Drug
• Enzyme Inhibitors (metabolism)
• Haloperidol (chemistry, metabolism)
• Humans
• Kinetics
• Microsomes, Liver (enzymology, metabolism)
• Oxidation-Reduction
• Pyridinium Compounds (metabolism)
• Rats
• Spectrometry, Fluorescence
• Steroid Hydroxylases (metabolism)