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
[11]   The conduct of in vitro and in vivo drug-drug interaction studies: A Pharmaceutical Research and Manufacturers of America (PhRMA) perspective [J].
Bjornsson, TD ;
Callaghan, JT ;
Einolf, HJ ;
Fischer, V ;
Gan, L ;
Grimm, S ;
Kao, J ;
King, SP ;
Miwa, G ;
Ni, L ;
Kumar, G ;
McLeod, J ;
Obach, RS ;
Roberts, S ;
Roe, A ;
Shah, A ;
Snikeris, F ;
Sullivan, JT ;
Tweedie, D ;
Vega, JM ;
Walsh, J ;
Wrighton, SA .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (07) :815-832
[12]   Mechanism-based inactivation and reversibility: Is there a new trend in the inactivation of cytochrome P450 enzymes? [J].
Blobaum, AL .
DRUG METABOLISM AND DISPOSITION, 2006, 34 (01) :1-7
[13]   SXR, a novel steroid and xenobiotic-sensing nuclear receptor [J].
Blumberg, B ;
Sabbagh, W ;
Juguilon, H ;
Bolado, J ;
van Meter, CM ;
Ono, ES ;
Evans, RM .
GENES & DEVELOPMENT, 1998, 12 (20) :3195-3205
[14]   The role of multidrug, transporters in drug availability, metabolism and toxicity [J].
Bodó, A ;
Bakos, E ;
Szeri, F ;
Váradi, A ;
Sarkadi, B .
TOXICOLOGY LETTERS, 2003, 140 :133-143
[15]   Gene expression in two hepatic cell lines, cultured primary hepatocytes, and liver slices compared to the in vivo liver gene expression in rats:: Possible implications for toxicogenomics use of in vitro systems [J].
Boess, F ;
Kamber, M ;
Romer, S ;
Gasser, R ;
Muller, D ;
Albertini, S ;
Suter, L .
TOXICOLOGICAL SCIENCES, 2003, 73 (02) :386-402
[16]  
Brockmoller J, 2000, Pharmacogenomics, V1, P125, DOI 10.1517/14622416.1.2.125
[17]   DETOXICATION OF DRUGS AND OTHER FOREIGN COMPOUNDS BY LIVER MICROSOMES [J].
BRODIE, BB ;
AXELROD, J ;
COOPER, JR ;
GAUDETTE, L ;
LADU, BN ;
MITOMA, C ;
UDENFRIEND, S .
SCIENCE, 1955, 121 (3147) :603-604
[18]   Correlation between genotype and phenotype of the human arylamine N-acetyltransferase type 1 (NAT1) [J].
Bruhn, C ;
Brockmöller, J ;
Cascorbi, I ;
Roots, I ;
Borchert, HH .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (11) :1759-1764
[19]   Identification of the polymorphically expressed CYP2C19 and the wild-type CYP2C9-ILE359 allele as low-K-m catalysts of cyclophosphamide and ifosfamide activation [J].
Chang, TKH ;
Yu, L ;
Goldstein, JA ;
Waxman, DJ .
PHARMACOGENETICS, 1997, 7 (03) :211-221
[20]   AMINO TERMINAL SEQUENCE-ANALYSIS OF HUMAN-PLACENTA AROMATASE [J].
CHEN, S ;
SHIVELY, JE ;
NAKAJIN, S ;
SHINODA, M ;
HALL, PF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 135 (03) :713-719