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Volumn 40, Issue 9, 2012, Pages 1778-1784

Metabolism of the active metabolite of quetiapine, N-desalkylquetiapine in vitro

Author keywords

[No Author keywords available]

Indexed keywords

7 HYDROXY N DESALKYLQUETIAPINE; BENZYLNIRVANOL; CYTOCHROME P450 1A2; CYTOCHROME P450 2C19; CYTOCHROME P450 2C9; CYTOCHROME P450 2D6; CYTOCHROME P450 3A4; CYTOCHROME P450 INHIBITOR; DESIPRAMINE; DRUG METABOLITE; ENZYME INHIBITOR; FLUVOXAMINE; KETOCONAZOLE; METHANOL; N DESALKYLQUETIAPINE; N DESALKYLQUETIAPINE SULFOXIDE; PROMAZINE; QUETIAPINE; QUINIDINE; SPARTEINE; SULFAPHENAZOLE; UNCLASSIFIED DRUG;

EID: 84865193567     PISSN: 00909556     EISSN: 1521009X     Source Type: Journal    
DOI: 10.1124/dmd.112.045237     Document Type: Article
Times cited : (37)

References (21)
  • 2
    • 79953170187 scopus 로고    scopus 로고
    • Pharmacokinetic variability of quetiapine and the active metabolite N-desalkylquetiapine in psychiatric patients
    • Bakken GV, Rudberg I, Molden E, Refsum H, and Hermann M (2011) Pharmacokinetic variability of quetiapine and the active metabolite N-desalkylquetiapine in psychiatric patients. Ther Drug Monit 33:222-226.
    • (2011) Ther Drug Monit , vol.33 , pp. 222-226
    • Bakken, G.V.1    Rudberg, I.2    Molden, E.3    Refsum, H.4    Hermann, M.5
  • 3
    • 0027406654 scopus 로고
    • Fluvoxamine is a potent inhibitor of cytochrome P4501A2
    • DOI 10.1016/0006-2952(93)90272-X
    • Brøsen K, Skjelbo E, Rasmussen BB, Poulsen HE, and Loft S (1993) Fluvoxamine is a potent inhibitor of cytochrome P4501A2. Biochem Pharmacol 45:1211-1214. (Pubitemid 23098317)
    • (1993) Biochemical Pharmacology , vol.45 , Issue.6 , pp. 1211-1214
    • Brosen, K.1    Skjelbo, E.2    Rasmussen, B.B.3    Polsen, H.E.4    Loft, S.5
  • 4
    • 0345490845 scopus 로고    scopus 로고
    • Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450
    • Busby WF Jr, Ackermann JM, and Crespi CL (1999) Effect of methanol, ethanol, dimethyl sulfoxide, and acetonitrile on in vitro activities of cDNA-expressed human cytochromes P-450. Drug Metab Dispos 27:246-249. (Pubitemid 29072079)
    • (1999) Drug Metabolism and Disposition , vol.27 , Issue.2 , pp. 246-249
    • Busby Jr., W.F.1    Ackermann, J.M.2    Crespi, C.L.3
  • 5
    • 0026787192 scopus 로고
    • The effect of selective serotonin re-uptake inhibitors on cytochrome P4502D6 (CYP2D6) activity in human liver microsomes
    • Crewe HK, Lennard MS, Tucker GT, Woods FR, and Haddock RE (1992) The effect of selective serotonin re-uptake inhibitors on cytochrome P4502D6 (CYP2D6) activity in human liver microsomes. Br J Clin Pharmacol 34:262-265.
    • (1992) Br J Clin Pharmacol , vol.34 , pp. 262-265
    • Crewe, H.K.1    Lennard, M.S.2    Tucker, G.T.3    Woods, F.R.4    Haddock, R.E.5
  • 6
    • 0031963279 scopus 로고    scopus 로고
    • 2 receptor blockade and plasma drug concentrations after discontinuation of quetiapine (Seroquel®) in patients with schizophrenia
    • DOI 10.1007/s002130050492
    • Gefvert O, Bergström M, Långström B, Lundberg T, Lindström L, and Yates R (1998) Time course of central nervous dopamine-D2 and 5-HT2 receptor blockade and plasma drug concentrations after discontinuation of quetiapine (Seroquel) in patients with schizophrenia. Psychopharmacology 135:119-126. (Pubitemid 28055494)
    • (1998) Psychopharmacology , vol.135 , Issue.2 , pp. 119-126
    • Gefvert, O.1    Bergstrom, M.2    Langstrom, B.3    Lundberg, T.4    Lindstrom, L.5    Yates, R.6
  • 7
    • 33644898140 scopus 로고    scopus 로고
    • Effects of cytochrome P450 3A modulators ketoconazole and carbamazepine on quetiapine pharmacokinetics
    • DOI 10.1111/j.1365-2125.2005.02507.x
    • Grimm SW, Richtand NM, Winter HR, Stams KR, and Reele SB (2006) Effects of cytochrome P450 3A modulators ketoconazole and carbamazepine on quetiapine pharmacokinetics. Br J Clin Pharmacol 61:58-69. (Pubitemid 43381238)
    • (2006) British Journal of Clinical Pharmacology , vol.61 , Issue.1 , pp. 58-69
    • Grimm, S.W.1    Richtand, N.M.2    Winter, H.R.3    Stams, K.R.4    Reele, S.B.5
  • 8
    • 0001711452 scopus 로고    scopus 로고
    • In vitro prediction of potential metabolic drug interactions for Seroquel
    • Abstract
    • Grimm SW, Stams KR, and Bui K (1997) In vitro prediction of potential metabolic drug interactions for Seroquel (Abstract). Schizophr Res 24:198.
    • (1997) Schizophr Res , vol.24 , pp. 198
    • Grimm, S.W.1    Stams, K.R.2    Bui, K.3
  • 9
    • 33745668220 scopus 로고    scopus 로고
    • In vitro studies on quetiapine metabolism using the substrate depletion approach with focus on drug-drug interactions
    • Hasselstrøm J and Linnet K (2006) In vitro studies on quetiapine metabolism using the substrate depletion approach with focus on drug-drug interactions. Drug Metabol Drug Interact 21: 187-211.
    • (2006) Drug Metabol Drug Interact , vol.21 , pp. 187-211
    • Hasselstrøm, J.1    Linnet, K.2
  • 10
    • 0034105896 scopus 로고    scopus 로고
    • In vitro-in vivo scaling of cyp kinetic data not consistent with the classical Michaelis-Menten model
    • Houston JB and Kenworthy KE (2000) In vitro-in vivo scaling of CYP kinetic data not consistent with the classical Michaelis-Menten model. Drug Metab Dispos 28:246-254. (Pubitemid 30137047)
    • (2000) Drug Metabolism and Disposition , vol.28 , Issue.3 , pp. 246-254
    • Houston, J.B.1    Kenworthy, K.E.2
  • 11
    • 49549104014 scopus 로고    scopus 로고
    • N-desalkylquetiapine, a potent norepinephrine reuptake inhibitor and partial 5-HT1A agonist, as a putative mediator of quetiapine's antidepressant activity
    • Jensen NH, Rodriguiz RM, Caron MG, Wetsel WC, Rothman RB, and Roth BL (2008) N-desalkylquetiapine, a potent norepinephrine reuptake inhibitor and partial 5-HT1A agonist, as a putative mediator of quetiapine's antidepressant activity. Neuropsychopharmacology 33:2303-2312.
    • (2008) Neuropsychopharmacology , vol.33 , pp. 2303-2312
    • Jensen, N.H.1    Rodriguiz, R.M.2    Caron, M.G.3    Wetsel, W.C.4    Rothman, R.B.5    Roth, B.L.6
  • 12
    • 4143108324 scopus 로고    scopus 로고
    • Substrate depletion approach for determining in vitro metabolic clearance: Time dependencies in hepatocyte and microsomal incubations
    • DOI 10.1124/dmd.104.000125
    • Jones HM and Houston JB (2004) Substrate depletion approach for determining in vitro metabolic clearance: time dependencies in hepatocyte and microsomal incubations. Drug Metab Dispos 32:973-982. (Pubitemid 39096058)
    • (2004) Drug Metabolism and Disposition , vol.32 , Issue.9 , pp. 973-982
    • Jones, H.M.1    Houston, J.B.2
  • 13
    • 14044254164 scopus 로고    scopus 로고
    • Metabolism of alfentanil by cytochrome P4503A (CYP3A) enzymes
    • DOI 10.1124/dmd.104.002709
    • Klees TM, Sheffels P, Dale O, and Kharasch ED (2005) Metabolism of alfentanil by cytochrome P4503a (cyp3a) enzymes. Drug Metab Dispos 33:303-311. (Pubitemid 40279928)
    • (2005) Drug Metabolism and Disposition , vol.33 , Issue.3 , pp. 303-311
    • Klees, T.M.1    Sheffels, P.2    Dale, O.3    Kharasch, E.D.4
  • 14
    • 0028237729 scopus 로고
    • Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: Studies with liver microsomes of 30 Japanese and 30 Caucasians
    • Shimada T, Yamazaki H, Mimura M, Inui Y, and Guengerich FP (1994) Interindividual variations in human liver cytochrome P-450 enzymes involved in the oxidation of drugs, carcinogens and toxic chemicals: studies with liver microsomes of 30 Japanese and 30 Caucasians. J Pharmacol Exp Ther 270:414-423. (Pubitemid 24229655)
    • (1994) Journal of Pharmacology and Experimental Therapeutics , vol.270 , Issue.1 , pp. 414-423
    • Shimada, T.1    Yamazaki, H.2    Mimura, M.3    Inui, Y.4    Guengerich, F.P.5
  • 15
    • 0034770465 scopus 로고    scopus 로고
    • Human drug metabolism and the cytochromes P450: Application and relevance of in vitro models
    • DOI 10.1177/00912700122012724
    • Venkatakrishnan K, Von Moltke LL, and Greenblatt DJ (2001) Human drug metabolism and the cytochromes P450: application and relevance of in vitro models. J Clin Pharmacol 41:1149-1179. (Pubitemid 32983216)
    • (2001) Journal of Clinical Pharmacology , vol.41 , Issue.11 , pp. 1149-1179
    • Venkatakrishnan, K.1    Von Moltke, L.L.2    Greenblatt, D.J.3
  • 16
    • 0028898816 scopus 로고
    • Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: Comparison with other selective serotonin reuptake inhibitor antidepressants
    • von Moltke LL, Greenblatt DJ, Court MH, Duan SX, Harmatz JS, and Shader RI (1995) Inhibition of alprazolam and desipramine hydroxylation in vitro by paroxetine and fluvoxamine: comparison with other selective serotonin reuptake inhibitor antidepressants. J Clin Psychopharmacol 15:125-131.
    • (1995) J Clin Psychopharmacol , vol.15 , pp. 125-131
    • Von Moltke, L.L.1    Greenblatt, D.J.2    Court, M.H.3    Duan, S.X.4    Harmatz, J.S.5    Shader, R.I.6
  • 17
    • 0345016882 scopus 로고    scopus 로고
    • 5 on drug oxidation activities of human cytochrome P450 (CYP) 3As: Similarity of CYP3A5 with CYP3A4 but not CYP3A7
    • DOI 10.1016/j.bcp.2003.08.004
    • Yamaori S, Yamazaki H, Suzuki A, Yamada A, Tani H, Kamidate T, Fujita K, and Kamataki T (2003) Effects of cytochrome b(5) on drug oxidation activities of human cytochrome P450 (CYP) 3As: similarity of CYP3A5 with CYP3A4 but not CYP3A7. Biochem Pharmacol 66:2333-2340. (Pubitemid 37456741)
    • (2003) Biochemical Pharmacology , vol.66 , Issue.12 , pp. 2333-2340
    • Yamaori, S.1    Yamazaki, H.2    Suzuki, A.3    Yamada, A.4    Tani, H.5    Kamidate, T.6    Fujita, K.-I.7    Kamataki, T.8
  • 20
    • 0029671251 scopus 로고    scopus 로고
    • Roles of cytochrome b5 in the oxidation of testosterone and nifedipine by recombinant cytochrome P450 3A4 and by human liver microsomes
    • Yamazaki H, Nakano M, Imai Y, Ueng YF, Guengerich FP, and Shimada T (1996) Roles of cytochrome b5 in the oxidation of testosterone and nifedipine by recombinant cytochrome P450 3A4 and by human liver microsomes. Arch Biochem Biophys 325:174-182.
    • (1996) Arch Biochem Biophys , vol.325 , pp. 174-182
    • Yamazaki, H.1    Nakano, M.2    Imai, Y.3    Ueng, Y.F.4    Guengerich, F.P.5    Shimada, T.6
  • 21
    • 70349386728 scopus 로고    scopus 로고
    • Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part I
    • Zhou SF (2009) Polymorphism of human cytochrome P450 2D6 and its clinical significance: Part I. Clin Pharmacokinet 48:689-723.
    • (2009) Clin Pharmacokinet , vol.48 , pp. 689-723
    • Zhou, S.F.1


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