The evolving role of drug metabolism in drug discovery and development

被引:56
作者
Yengi, Lilian G. [1 ]
Leung, Louis [1 ]
Kao, John [1 ]
机构
[1] Wyeth Res, Drug Metab Div, Collegeville, PA 19426 USA
关键词
drug discovery and development; drug interactions clearance; drug metabolism; exposure; idiosyncratic drug toxicity; inhibition; integration of emerging sciences; pharmacogenetics; pharmacogenomics; transporters;
D O I
10.1007/s11095-006-9217-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Drug metabolism in pharmaceutical research has traditionally focused on the well-defined aspects of absorption, distribution, metabolism and excretion, commonly-referred to ADME properties of a compound, particularly in the areas of metabolite identification, identification of drug metabolizing enzymes (DMEs) and associated metabolic pathways, and reaction mechanisms. This traditional emphasis was in part due to the limited scope of understanding and the unavailability of in vitro and in vivo tools with which to evaluate more complex properties and processes. However, advances over the past decade in separate but related fields such as pharmacogenetics, pharmacogenomics and drug transporters, have dramatically shifted the drug metabolism paradigm. For example, knowledge of the genetics and genomics of DMEs allows us to better understand and predict enzyme regulation and its effects on exogenous (pharmacokinetics) and endogenous pathways as well as biochemical processes (pharmacology). Advances in the transporter area have provided unprecedented insights into the role of transporter proteins in absorption, distribution, metabolism and excretion of drugs and their consequences with respect to clinical drug-drug and drug-endogenous substance interactions, toxicity and interindividual variability in pharmacokinetics. It is therefore essential that individuals involved in modern pharmaceutical research embrace a fully integrated approach and understanding of drug metabolism as is currently practiced. The intent of this review is to reexamine drug metabolism with respect to the traditional as well as current practices, with particular emphasis on the critical aspects of integrating chemistry and biology in the interpretation and application of metabolism data in pharmaceutical research.
引用
收藏
页码:842 / 858
页数:17
相关论文
共 199 条
[1]   STEADY-STATE PLASMA LEVELS OF NORTRIPTYLINE INTWINS - INFLUENCE OF GENETIC FACTORS AND DRUG THERAPY [J].
ALEXANDERSON, B ;
EVANS, DAP ;
SJOQVIST, F .
BMJ-BRITISH MEDICAL JOURNAL, 1969, 4 (5686) :764-+
[2]   Assessment of drug interactions in hepatobiliary transport using rhodamine 123 in sandwich-cultured rat hepatocytes [J].
Annaert, PP ;
Brouwer, KLR .
DRUG METABOLISM AND DISPOSITION, 2005, 33 (03) :388-394
[3]  
Annaert PP, 2001, DRUG METAB DISPOS, V29, P1277
[4]  
[Anonymous], 2006, GUID IND DRUG INT ST
[5]   EVIDENCE FOR SUPEROXIDE GENERATION BY NADPH-CYTOCHROME-C REDUCTASE OF RAT-LIVER MICROSOMES [J].
AUST, SD ;
ROERIG, DL ;
PEDERSON, TC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1972, 47 (05) :1133-&
[6]  
AXELROD JULIUS, 1955, JOUR BIOL CHEM, V214, P753
[7]   Transporters and their impact on drug disposition [J].
Beringer, PM ;
Slaughter, RL .
ANNALS OF PHARMACOTHERAPY, 2005, 39 (06) :1097-1108
[8]   Apparent mechanism-based inhibition of human CYP2D6 in vitro by paroxetine: Comparison with fluoxetine and quinidine [J].
Bertelsen, KM ;
Venkatakrishnan, K ;
Von Moltke, LL ;
Obach, RS ;
Greenblatt, DJ .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (03) :289-293
[9]   Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction [J].
Bertilsson, G ;
Heidrich, J ;
Svensson, K ;
Åsman, M ;
Jendeberg, L ;
Sydow-Bäckman, M ;
Ohlsson, R ;
Postlind, H ;
Blomquist, P ;
Berkenstam, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12208-12213
[10]   GEOGRAPHICAL INTERRACIAL DIFFERENCES IN POLYMORPHIC DRUG OXIDATION - CURRENT STATE OF KNOWLEDGE OF CYTOCHROMES P450 (CYP) 2D6 AND 2C19 [J].
BERTILSSON, L .
CLINICAL PHARMACOKINETICS, 1995, 29 (03) :192-209