Mechanisms and Consequences of Drug-Drug Interactions

被引:14
作者
Greenblatt, David J. [1 ]
机构
[1] Tufts Univ, Sch Med, Program Pharmacol & Expt Therapeut, Boston, MA 02111 USA
关键词
drug metabolism; drug interactions; induction; inhibition; in vitro models; IN-VITRO DATA; KIDNEY-TRANSPLANT RECIPIENTS; PREGNANE-X-RECEPTOR; ENZYME-INDUCTION; RISK-ASSESSMENT; TIME-COURSE; CYTOCHROME-P450; ENZYMES; QUANTITATIVE PREDICTION; METABOLIC INHIBITION; CONCENTRATIVE UPTAKE;
D O I
10.1002/cpdd.339
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Medications used to treat human immunodeficiency virus (HIV) and hepatitis C virus (HCV) infections present a special challenge with respect to the management of potential and actual drug-drug interactions (DDIs). The HIV and HCV treatments may interact with each other, and also interact with drugs of abuse and/or with medications used to treat substance abuse. Possible mechanisms of these DDIs generally include induction or inhibition of activity/expression of human cytochromes P450, glucuronosyl transferases, or energy-dependent transport proteins. These DDIs can be complex and time-dependent in nature. Because time and resources available for new drug development are necessarily limited, not all potential DDIs can be evaluated via clinical pharmacokinetic studies in the course of development of HIV, HCV, and substance abuse treatments. Strategies are needed to refine existing in vitro models and screening techniques to allow more efficient targeting of resources to those clinical studies having the highest impact in terms of enhancing medication effectiveness and patient safety.
引用
收藏
页码:118 / 124
页数:7
相关论文
共 69 条
[1]   Efficacy and safety of low-dose ketoconazole (50 mg) to reduce the cost of cyclosporine in renal allograft recipients [J].
Abraham, MA ;
Thomas, PP ;
John, GT ;
Job, V ;
Shankar, V ;
Jacob, CK .
TRANSPLANTATION PROCEEDINGS, 2003, 35 (01) :215-216
[2]   Drug interactions in primary care: Impact of a new algorithm on risk determination [J].
Bergk, V ;
Gasse, C ;
Rothenbacher, D ;
Loew, M ;
Brenner, H ;
Haefeli, WE .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2004, 76 (01) :85-96
[3]   Prediction of in vivo drug-drug interactions from in vitro data -: Factors affecting prototypic drug-drug interactions involving CYP2C9, CYP2D6 and CYP3A4 [J].
Brown, Hayley S. ;
Galetin, Aleksandra ;
Hallifax, David ;
Houston, J. Brian .
CLINICAL PHARMACOKINETICS, 2006, 45 (10) :1035-1050
[4]   The induction of cytochrome P450 3A5 (CYP3A5) in the human liver and intestine is mediated by the xenobiotic sensors pregnane X receptor (PXR) and constitutively activated receptor (CAR) [J].
Burk, O ;
Koch, I ;
Raucy, J ;
Hustert, E ;
Eichelbaum, M ;
Brockmöller, J ;
Zanger, UM ;
Wojnowski, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (37) :38379-38385
[5]  
CONNEY AH, 1967, PHARMACOL REV, V19, P317
[6]   INFLUENCE OF BARBITURATES ON COUMARIN PLASMA LEVELS AND PROTHROMBIN RESPONSE [J].
DAYTON, PG ;
WEINER, M ;
TARCAN, Y ;
CHENKIN, T .
JOURNAL OF CLINICAL INVESTIGATION, 1961, 40 (10) :1797-&
[7]   Cobicistat: A Review of Its Use as a Pharmacokinetic Enhancer of Atazanavir and Darunavir in Patients with HIV-1 Infection [J].
Deeks, Emma D. .
DRUGS, 2014, 74 (02) :195-206
[8]   Evaluation of Various Static and Dynamic Modeling Methods to Predict Clinical CYP3A Induction Using In Vitro CYP3A4 mRNA Induction Data [J].
Einolfl, H. J. ;
Chen, L. ;
Fahmi, O. A. ;
Gibson, C. R. ;
Obach, R. S. ;
Shebley, M. ;
Silva, J. ;
Sinz, M. W. ;
Unadkat, J. D. ;
Zhang, L. ;
Zhao, P. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2014, 95 (02) :179-188
[9]   A prospective, randomized study of coadministration of ketoconazole and cyclosporine A in kidney transplant recipients: Ten-year follow-up [J].
El-Agroudy, AE ;
Sobh, MA ;
Hamdy, AF ;
Ghoneim, MA .
TRANSPLANTATION, 2004, 77 (09) :1371-1376
[10]   Time response of cytochrome P450 1A2 activity on cessation of heavy smoking [J].
Faber, MS ;
Fuhr, U .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2004, 76 (02) :178-184