Effects of uptake and efflux transporter inhibition on erythromycin breath test results

被引:44
作者
Frassetto, L. A.
Poon, S.
Tsourounis, C.
Valera, C.
Benet, L. Z. [1 ]
机构
[1] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Clin Res Ctr, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Clin Pharm, San Francisco, CA 94143 USA
关键词
D O I
10.1038/sj.clpt.6100148
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The erythromycin breath test (EBT) is a standard test used to evaluate the extent of CYP3A4 activity. This study examines whether presumed changes in CYP3A4 activity are in fact related to inhibition of an uptake organic anion transporter using rifampin and inhibition of the efflux hepatic P-glycoprotein transporter using lansoprazole. Three EBT tests in healthy adults were conducted: EBT alone, with lansoprazole, and with rifampin. For all subjects, lansoprazole treatment increased respiratory C-14 excretion by +0.257 +/- 0.51met/ h (P=0.07) and rifampin decreased C-14 excretion by - 0.447 +/- 0.40 met/h ( P < 0.001) compared with baseline. Comparing lansoprazole to rifampin, C-14 excretion increased by -0.697 +/- 0.50met/h ( P < 0.001). Only women had significant changes after drug infusion: C-14 excretion after rifampin -0.407 +/- 0.36met/h ( P < 0.018) and +0.47 +/- 0.44met/h ( P=0.018) after lansoprazole. Relying on EBT without considering transporter interactions can lead to errors in interpreting the degree of CYP3A4 metabolism.
引用
收藏
页码:828 / 832
页数:5
相关论文
共 20 条
  • [1] CLINICAL UTILITY OF BREATH TESTS FOR THE ASSESSMENT OF HEPATIC-FUNCTION
    BAKER, AL
    KOTAKE, AN
    SCHOELLER, DA
    [J]. SEMINARS IN LIVER DISEASE, 1983, 3 (04) : 318 - 329
  • [2] There are no useful CYP3A probes that quantitatively predict the in vivo kinetics of other CYP3A substrates and no expectation that one will be found
    Benet, LZ
    [J]. MOLECULAR INTERVENTIONS, 2005, 5 (02) : 79 - +
  • [3] Unmasking the dynamic interplay between efflux transporters and metabolic enzymes
    Benet, LZ
    Cummins, CL
    Wu, CY
    [J]. INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2004, 277 (1-2) : 3 - 9
  • [4] Sex-related differences in the clearance of cytochrome P450 3A4 substrates may be caused by P-glycoprotein
    Cummins, CL
    Wu, CY
    Benet, LZ
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2002, 72 (05) : 474 - 489
  • [5] Evaluation of the pharmacokinetics and pharmacodynamics of intravenous lansoprazole
    Freston, JW
    Pilmer, BL
    Chiu, YL
    Wang, Q
    Stolle, JC
    Griffin, JS
    Lee, CQ
    [J]. ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2004, 19 (10) : 1111 - 1122
  • [6] The erythromycin breath test reflects P-glycoprotein function independently of cytochrome P450 3A activity
    Kurnik, Daniel
    Wood, Alastair J. J.
    Wilkinson, Grant R.
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2006, 80 (03) : 228 - 234
  • [7] Hepatic microsome studies are insufficient to characterize in vivo hepatic metabolic clearance and metabolic drug-drug interactions: Studies of digoxin metabolism in primary rat hepatocytes versus microsomes
    Lam, JL
    Benet, LZ
    [J]. DRUG METABOLISM AND DISPOSITION, 2004, 32 (11) : 1311 - 1316
  • [8] In vitro and in vivo correlation of hepatic transporter effects on erythromycin metabolism: Characterizing the importance of transporter-enzyme interplay
    Lam, Justine L.
    Okochi, Hideaki
    Huang, Yong
    Benet, Leslie Z.
    [J]. DRUG METABOLISM AND DISPOSITION, 2006, 34 (08) : 1336 - 1344
  • [9] Ex situ inhibition of hepatic uptake and efflux significantly changes metabolism: Hepatic enzyme-transporter interplay
    Lau, YY
    Wu, CY
    Okochi, H
    Benet, LZ
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2004, 308 (03) : 1040 - 1045
  • [10] In silico and in vitro screening for inhibition of cytochrome P450CYP3A4 by comedications commonly used by patients with cancer
    Maréchal, JD
    Yu, JL
    Brown, S
    Kapelioukh, I
    Rankin, EM
    Wolf, CR
    Roberts, GCK
    Paine, MJI
    Sutcliffe, MJ
    [J]. DRUG METABOLISM AND DISPOSITION, 2006, 34 (04) : 534 - 538