Valproic acid pathway: pharmacokinetics and pharmacodynamics

被引:310
作者
Ghodke-Puranik, Yogita [1 ]
Thorn, Caroline F. [4 ]
Lamba, Jatinder K. [1 ,2 ]
Leeder, J. Steven [6 ]
Song, Wen [1 ]
Birnbaum, Angela K. [1 ,3 ]
Altman, Russ B. [4 ,5 ]
Klein, Teri E. [4 ]
机构
[1] Univ Minnesota Twin Cities, Dept Expt & Clin Pharmacol, Minneapolis, MN USA
[2] Univ Minnesota Twin Cities, PUMA Inst Personalized Med, Minneapolis, MN USA
[3] Univ Minnesota Twin Cities, Ctr Clin & Cognit Neuropharmacol, Minneapolis, MN USA
[4] Stanford Univ, Med Ctr, Dept Genet, Stanford, CA 94305 USA
[5] Stanford Univ, Med Ctr, Dept Bioengn, Stanford, CA 94305 USA
[6] Childrens Mercy Hosp & Clin, Div Clin Pharmacol & Therapeut Innovat, Kansas City, MO USA
关键词
pathway; pharmacodynamics; pharmacogenomics; pharmacokinetics; valproic acid; HUMAN LIVER-MICROSOMES; 2-NORMAL-PROPYL-4-PENTENOIC ACID; INDUCED HYPERAMMONEMIA; METABOLIC-ACTIVATION; IN-VIVO; IDENTIFICATION; CYP2C9; DRUG; POLYMORPHISM; ASSOCIATION;
D O I
10.1097/FPC.0b013e32835ea0b2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
[No abstract available]
引用
收藏
页码:236 / 241
页数:6
相关论文
共 39 条
[1]   New insights on the mechanisms of valproate-induced hyperammonemia: Inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoA [J].
Aires, Catia C. P. ;
van Cruchten, Arno ;
Ijlst, Lodewijk ;
de Almeida, Isabel Tavares ;
Duran, Marinus ;
Wanders, Ronald J. A. ;
Silva, Margarida F. B. .
JOURNAL OF HEPATOLOGY, 2011, 55 (02) :426-434
[2]   Influence of CYP2C9 polymorphism on metabolism of valproate and its hepatotoxin metabolite in Iranian patients [J].
Amini-Shirazi, Noushin ;
Ghahremani, Mohammad Hossein ;
Ahmadkhaniha, Reza ;
Mandegary, Ali ;
Dadgar, Armin ;
Abdollahi, Mohammad ;
Shadnia, Shahin ;
Pakdaman, Hossein ;
Kebriaeezadeh, Abbas .
TOXICOLOGY MECHANISMS AND METHODS, 2010, 20 (08) :452-457
[3]   Effect of Aging on Glucuronidation of Valproic Acid in Human Liver Microsomes and the Role of UDP-Glucuronosyltransferase UGT1A4, UGT1A8, and UGT1A10 [J].
Argikar, Upendra A. ;
Remmel, Rory P. .
DRUG METABOLISM AND DISPOSITION, 2009, 37 (01) :229-236
[5]  
Blanco-Serrano B, 1999, BIOPHARM DRUG DISPOS, V20, P233, DOI 10.1002/(SICI)1099-081X(199907)20:5<233::AID-BDD179>3.0.CO
[6]  
2-5
[7]   Histone deacetylases in acute myeloid leukaemia show a distinctive pattern of expression that changes selectively in response to deacetylase inhibitors [J].
Bradbury, C ;
Khanim, F ;
Hayden, R ;
Bunce, CM ;
White, DA ;
Drayson, MT ;
Craddock, C ;
Turner, BM .
LEUKEMIA, 2005, 19 (10) :1751-1759
[8]   Molecular and Therapeutic Potential and Toxicity of Valproic Acid [J].
Chateauvieux, Sebastien ;
Morceau, Franck ;
Dicato, Mario ;
Diederich, Marc .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2010,
[9]   Pharmacokinetic and pharmacodynamic interaction of lorazepam and valproic acid in relation to UGT2B7 genetic polymorphism in healthy subjects [J].
Chung, J-Y ;
Cho, J-Y ;
Yu, K-S ;
Kim, J-R ;
Lim, K. S. ;
Sohn, D-R ;
Shin, S-G ;
Jang, I-J .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2008, 83 (04) :595-600
[10]   The effect of valproic acid on drug and steroid glucuronidation by expressed human UDP-glucuronosyltransferases [J].
Ethell, BT ;
Anderson, GD ;
Burchell, B .
BIOCHEMICAL PHARMACOLOGY, 2003, 65 (09) :1441-1449