![]() |
|
|
Drug Metabolism Research Pharmacia & Upjohn
The selectivity of inhibition for four dopamine receptor agonists
(pramipexole, ropinirole, pergolide, and bromocriptine) on six human
cytochrome P450 enzyme activities were evaluated using a simple
in vitro inhibition screen. Drug-P450 interactions characterized as potent (i.e. greater than 50% inhibition
of control enzyme activity) were then further examined to determine an
IC50 for the interaction. Of the dopamine
receptor agonists tested, three drugs, ropinirole, pergolide, and
bromocriptine, were found to inhibit the activity of at least one human
cytochrome P450 enzyme, while the remaining dopamine agonist,
pramipexole, was devoid of any potent P450 interaction. None of the
agonists tested inhibited the P450 marker activities of 2C9, 2C19, and
2E1. However, partial inhibition was observed between ropinirole and
CYP1A2 and pergolide and CYP3A4. In contrast, potent interactions were observed between CYP2D6 and pergolide and ropinirole, as well as with
CYP3A4 and bromocriptine. The results of this study indicate several
drug P450 interactions; however, the likelihood of an in
vivo interaction with these drugs remains to be established.
This article has been cited by other articles:
![]() |
A. Nath, Y. V. Grinkova, S. G. Sligar, and W. M. Atkins Ligand Binding to Cytochrome P450 3A4 in Phospholipid Bilayer Nanodiscs: THE EFFECT OF MODEL MEMBRANES J. Biol. Chem., September 28, 2007; 282(39): 28309 - 28320. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Ekins, J. Berbaum, and R. K. Harrison GENERATION AND VALIDATION OF RAPID COMPUTATIONAL FILTERS FOR CYP2D6 AND CYP3A4 Drug Metab. Dispos., September 1, 2003; 31(9): 1077 - 1080. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. A. Wynalda, J. M. Hutzler, M. D. Koets, T. Podoll, and L. C. Wienkers IN VITRO METABOLISM OF CLINDAMYCIN IN HUMAN LIVER AND INTESTINAL MICROSOMES Drug Metab. Dispos., July 1, 2003; 31(7): 878 - 887. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. C. Wienkers and M. A. Wynalda Multiple Cytochrome P450 Enzymes Responsible for the Oxidative Metabolism of the Substituted (S)-3-Phenylpiperidine, (S,S)-3-[3-(Methylsulfonyl)phenyl]-1-propylpiperidine Hydrochloride, in Human Liver Microsomes Drug Metab. Dispos., December 1, 2002; 30(12): 1372 - 1377. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Gao, D. L. Johnson, S. Ekins, J. Janiszewski, K. G. Kelly, R. D. Meyer, and M. West Optimizing Higher Throughput Methods to Assess Drug-Drug Interactions for CYP1A2, CYP2C9, CYP2C19, CYP2D6, rCYP2D6, and CYP3A4 In Vitro Using a Single Point IC50 J Biomol Screen, August 1, 2002; 7(4): 373 - 382. [Abstract] [PDF] |
||||
![]() |
D. M. Stresser, A. P. Blanchard, S. D. Turner, J. C. L. Erve, A. A. Dandeneau, V. P. Miller, and C. L. Crespi Substrate-Dependent Modulation of CYP3A4 Catalytic Activity: Analysis of 27 Test Compounds with Four Fluorometric Substrates Drug Metab. Dispos., April 13, 2001; 28(12): 1440 - 1448. [Abstract] [Full Text] |
||||
![]() |
M. A. Wynalda, M. J. Hauer, and L. C. Wienkers Oxidation of the Novel Oxazolidinone Antibiotic Linezolid in Human Liver Microsomes Drug Metab. Dispos., September 1, 2000; 28(9): 1014 - 1017. [Abstract] [Full Text] |
||||
![]() |
L. C. Wienkers, C. Allievi, M. J. Hauer, and M. A. Wynalda Cytochrome P-450-Mediated Metabolism of the Individual Enantiomers of the Antidepressant Agent Reboxetine in Human Liver Microsomes Drug Metab. Dispos., November 1, 1999; 27(11): 1334 - 1340. [Abstract] [Full Text] |
||||