메뉴 건너뛰기




Volumn 39, Issue 10, 2009, Pages 788-793

Effects of the CYP2C9*13 allele on the pharmacokinetics of losartan in healthy male subjects

Author keywords

CYP2C9; E3174; Lorartan; Pharmacokinetics; Polymorphism

Indexed keywords

2 BUTYL 4 CHLORO 1 [[2' (1H TETRAZOL 5 YL) 4 BIPHENYLYL]METHYL] 5 IMIDAZOLECARBOXYLIC ACID; CYTOCHROME P450 2C9; LOSARTAN; ANTIHYPERTENSIVE AGENT; CYP2C9 PROTEIN, HUMAN; IMIDAZOLE DERIVATIVE; TETRAZOLE DERIVATIVE; UNSPECIFIC MONOOXYGENASE;

EID: 70350658226     PISSN: 00498254     EISSN: 13665928     Source Type: Journal    
DOI: 10.1080/00498250903134435     Document Type: Article
Times cited : (36)

References (24)
  • 3
    • 0028849020 scopus 로고
    • Effects of cimetidine on pharmacokinetics and pharmacodynamics of Iosartan, an ATl-selective non-peptide angiotensin II receptor antagonist
    • Goldberg MR, Lo MW, Bradstreet TE, Ritter MA, Höglund P. (1995). Effects of cimetidine on pharmacokinetics and pharmacodynamics of Iosartan, an ATl-selective non-peptide angiotensin II receptor antagonist. Eur J Clin Pharmacol 49(1-2):115-119
    • (1995) Eur J Clin Pharmacol , vol.49 , Issue.1-2 , pp. 115-119
    • Goldberg, M.R.1    Lo, M.W.2    Bradstreet, T.E.3    Ritter, M.A.4    Höglund, P.5
  • 4
    • 28744439821 scopus 로고    scopus 로고
    • Catalytic activities of human cytochrome P450 2C9*1, 2C9*3 and 2C9*13
    • Guo Y, Wang Y, Si D, Fawcett PJ, Zhong D, Zhou H. (2004). Catalytic activities of human cytochrome P450 2C9*1, 2C9*3 and 2C9*13. Xenobiotica 35(9):853-861
    • (2004) Xenobiotica , vol.35 , Issue.9 , pp. 853-861
    • Guo, Y.1    Wang, Y.2    Si, D.3    Fawcett, P.J.4    Zhong, D.5    Zhou, H.6
  • 5
    • 18844392062 scopus 로고    scopus 로고
    • Role of CYP2C9 and its variants (CYP2C9*3 and CYP2C9*13) in the metabolism of lornoxicam in humans
    • Guo Y, Zhang Y, Wang Y, Chen X, Si D, Zhong D, Fawcett JP, Zhou H. (2005). Role of CYP2C9 and its variants (CYP2C9*3 and CYP2C9*13) in the metabolism of lornoxicam in humans. Drug Metab Dispos 33(6):749-753
    • (2005) Drug Metab Dispos , vol.33 , Issue.6 , pp. 749-753
    • Guo, Y.1    Zhang, Y.2    Wang, Y.3    Chen, X.4    Si, D.5    Zhong, D.6    Fawcett, J.P.7    Zhou, H.8
  • 6
    • 68849120724 scopus 로고    scopus 로고
    • Effect of silymarin on the pharmacokinetics of losartan and its active metabolite E-3174 in healthy Chinese volunteers
    • Han Y, Guo D, Chen Y, Chen Y, Tan ZR, Zhou HH. (2009). Effect of silymarin on the pharmacokinetics of losartan and its active metabolite E-3174 in healthy Chinese volunteers. Eur J Clin Pharmacol 65(6):585-591
    • (2009) Eur J Clin Pharmacol , vol.65 , Issue.6 , pp. 585-591
    • Han, Y.1    Guo, D.2    Chen, Y.3    Chen, Y.4    Tan, Z.R.5    Zhou, H.H.6
  • 7
    • 0031957174 scopus 로고    scopus 로고
    • Fluconazole but not itraconazole decreases the metabolism of losartan to E-3174
    • Kaukonen KM, Olkkola KT, Neuvonen PJ. (1998). Fluconazole but not itraconazole decreases the metabolism of losartan to E-3174. Eur J Clin Pharmacol 53(6):445-449
    • (1998) Eur J Clin Pharmacol , vol.53 , Issue.6 , pp. 445-449
    • Kaukonen, K.M.1    Olkkola, K.T.2    Neuvonen, P.J.3
  • 9
    • 0029588499 scopus 로고
    • Pharmacokinetics of losartan, an angiotensin II receptor antagonist, and its active metabolite EXP3174 in humans
    • Lo MW, Goldberg MR, McCrea JB, Lu H, Furtek CI, Bjornsson TD. (1995). Pharmacokinetics of losartan, an angiotensin II receptor antagonist, and its active metabolite EXP3174 in humans. Clin Pharmacol Ther 58(6):641-649
    • (1995) Clin Pharmacol Ther , vol.58 , Issue.6 , pp. 641-649
    • Lo, M.W.1    Goldberg, M.R.2    McCrea, J.B.3    Lu, H.4    Furtek, C.I.5    Bjornsson, T.D.6
  • 11
    • 0027509397 scopus 로고
    • Pharmacokinetics and biochemical efficacy after single and multiple oral administration of losartan, an orally active nonpeptide angiotensin II receptor antagonist in humans
    • Ohtawa M, Takayama F, Saitoh K, Yoshinaga T, Nakashima M. (1993). Pharmacokinetics and biochemical efficacy after single and multiple oral administration of losartan, an orally active nonpeptide angiotensin II receptor antagonist in humans. Br J Clin Pharmacol 35(3):290-297
    • (1993) Br J Clin Pharmacol , vol.35 , Issue.3 , pp. 290-297
    • Ohtawa, M.1    Takayama, F.2    Saitoh, K.3    Yoshinaga, T.4    Nakashima, M.5
  • 12
    • 0142092612 scopus 로고    scopus 로고
    • Simultaneous determination of losartan and EXP3174 in human plasma and urine utilizing liquid chromatography/tandem mass spectrometry
    • Polinko M, Riffel K, Song H, Lo MW. (2003). Simultaneous determination of losartan and EXP3174 in human plasma and urine utilizing liquid chromatography/tandem mass spectrometry. J Pharm Biomed Anal 33(1):73-84.
    • (2003) J Pharm Biomed Anal , vol.33 , Issue.1 , pp. 73-84
    • Polinko, M.1    Riffel, K.2    Song, H.3    Lo, M.W.4
  • 13
    • 13944274619 scopus 로고    scopus 로고
    • Clinical and toxicological relevance of CYP2C9: Drug-drug interactions and pharmacogenetics
    • Rettie AE, Jones JP. (2005). Clinical and toxicological relevance of CYP2C9: drug-drug interactions and pharmacogenetics. Annu Rev Pharmacol Toxicol 45:477-494
    • (2005) Annu Rev Pharmacol Toxicol , vol.45 , pp. 477-494
    • Rettie, A.E.1    Jones, J.P.2
  • 14
    • 3242760534 scopus 로고    scopus 로고
    • Identification of a novel variant CYP2C9 allele in Chinese
    • Si D, Guo Y, Zhang Y, Yang L, Zhou H, Zhong D. (2004). Identification of a novel variant CYP2C9 allele in Chinese. Pharmacogenetics 14(7):465-469
    • (2004) Pharmacogenetics , vol.14 , Issue.7 , pp. 465-469
    • Si, D.1    Guo, Y.2    Zhang, Y.3    Yang, L.4    Zhou, H.5    Zhong, D.6
  • 15
    • 0034061961 scopus 로고    scopus 로고
    • Active transport of the angiotensin-II antagonist losartan and its main metabolite EXP 3174 across MDCK-MDR1 and Caco-2 cell monolayers
    • Soldner A, Benet LZ, Mutschler E, Christians U. (2000). Active transport of the angiotensin-II antagonist losartan and its main metabolite EXP 3174 across MDCK-MDR1 and Caco-2 cell monolayers. Br J Pharmacol 129(6):1235-1243
    • (2000) Br J Pharmacol , vol.129 , Issue.6 , pp. 1235-1243
    • Soldner, A.1    Benet, L.Z.2    Mutschler, E.3    Christians, U.4
  • 16
    • 0028894286 scopus 로고
    • Biotransformation of losartan to its active carboxylic acid metabolite in human liver microsomes. Role of cytochrome P450 2C and 3A subfamily members
    • Stearns RA, Chakravarty PK, Chen R, Chiu SH. (1995). Biotransformation of losartan to its active carboxylic acid metabolite in human liver microsomes. Role of cytochrome P450 2C and 3A subfamily members. Drug Metab Dispos 23(2):207-215
    • (1995) Drug Metab Dispos , vol.23 , Issue.2 , pp. 207-215
    • Stearns, R.A.1    Chakravarty, P.K.2    Chen, R.3    Chiu, S.H.4
  • 19
    • 33745727111 scopus 로고    scopus 로고
    • Amodiaquine, its desethylated metabolite, or both, inhibit the metabolism of debrisoquine (CYP2D6) and losartan (CYP2C9) in vivo
    • Wennerholm A, Nordmark A, Pihlsgard M, Mahindi M, Bertilsson L, Gustafsson LL. (2006). Amodiaquine, its desethylated metabolite, or both, inhibit the metabolism of debrisoquine (CYP2D6) and losartan (CYP2C9) in vivo. Eur J Clin Pharmacol 62(7):539-546
    • (2006) Eur J Clin Pharmacol , vol.62 , Issue.7 , pp. 539-546
    • Wennerholm, A.1    Nordmark, A.2    Pihlsgard, M.3    Mahindi, M.4    Bertilsson, L.5    Gustafsson, L.L.6
  • 22
    • 47649110030 scopus 로고    scopus 로고
    • Disposition of a CYP2C9 phenotyping agent, losartan, is not influenced by the common 3435C>T variation of the drug transporter gene ABCB1 (MDR1)
    • Yasar U, Babaoglu MO, Bozkurt A. (2008). Disposition of a CYP2C9 phenotyping agent, losartan, is not influenced by the common 3435C>T variation of the drug transporter gene ABCB1 (MDR1). Basic Clin Pharmacol Toxicol 103(2):176-179
    • (2008) Basic Clin Pharmacol Toxicol , vol.103 , Issue.2 , pp. 176-179
    • Yasar, U.1    Babaoglu, M.O.2    Bozkurt, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.