Transport, Metabolism, and in Vivo Population Pharmacokinetics of the Chloro Benztropine Analogs, a Class of Compounds Extensively Evaluated in Animal Models of Drug Abuse
No Thumbnail Available
Date
2007
Authors
Journal Title
Journal ISSN
Volume Title
Publisher
THE JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
Abstract
Recently, extensive behavioral research has been conducted on the benztropine (BZT) analogs with the goal of developing successful therapeutics for cocaine abuse. The present study was conducted to characterize the contribution of dispositional factors in mediating the behavioral differences among the chloro BZT analogs and to identify cytochrome P450 enzymes involved in their metabolism. Bidirectional transport and efflux studies of four of the chloro BZT analogs were conducted.
Screening with a panel of human and rat Supersomes was performed for 4 ,4 -diCl BZT. In addition, pharmacokinetic and brain distribution studies for 4 -Cl and 4 ,4 -diCl BZT in
Sprague-Dawley rats were conducted. The permeability of the chloro analogs ranged from 8.26 to 32.23 and from 1.37 to 21.65 10 6 cm/s, whereas the efflux ratios ranged from 2.1 to 6.9 and from 3.3 to 28.4 across Madin-Darby canine kidneymultidrug
resistance 1 (MDCK-MDR1) and Caco-2 monolayers, respectively. The P-glycoprotein (P-gp) inhibitor verapamil reduced the efflux ratios and enhanced the absorptive transport of the chloro BZT analogs. 4 ,4 -diCl BZT was a substrate of human CYP2D6 and 2C19 and rat 2C11 and 3A1. The brain uptake for 4 -Cl and 4 ,4 -diCl BZT was comparable and higher than previously reported for cocaine (brain-to-plasma partition
coefficient 4.6–4.7 versus 2.1 for cocaine). The rank order for t1/2 was 4 ,4 -diCl BZT 4 -Cl BZT cocaine and for steadystate volume of distribution was 4 -Cl BZT 4 ,4 -diCl BZT cocaine. In conclusion, the chloro analogs differ significantly in their clearance and duration of action, which correlates to their behavioral profiles and abuse liability. Furthermore, these results suggest that the distinctive behavioral profile of these
analogs is not due to limited brain exposure.
Description
Keywords
Staff Publication - SoP
Citation
JPET, Vol. 320, No. 1, 2007