Effects of Aspirin on the Bioavailability and Pharmacokinetics of Repaglinide: Possible Role of Cytochrome P450 3A Isoforms Inhibition by Aspirin

被引:0
作者
Jun Lu
Hong-Yan Ren
Jun-Shik Choi
Cheng Li
Jian-Peng Guo
机构
[1] Yanbian University Hospital,Department of Pharmacy
[2] Yanbian University,College of Integration Science
[3] Chosun University,College of Pharmacy
[4] Yanbian University,College of Medicine
[5] Yanbian University,College of Pharmacy
来源
Pharmaceutical Chemistry Journal | 2022年 / 55卷
关键词
repaglinide; bioavailability; pharmacokinetics; aspirin; CYP3A isoforms; blood glucose;
D O I
暂无
中图分类号
学科分类号
摘要
The purpose of this study was to investigate the effects of aspirin on the bioavailability and pharmacokinetics of repaglinide in rats. Repaglinide and aspirin interact with cytochrome P450 (CYP) 3A isoforms. Clinically, repaglinide and aspirin can be prescribed for the prevention or treatment of diabetes and cardiovascular disease as complications of diabetes. The effect of aspirin on P-glycoprotein (P-gp) and CYP3A4 activity was evaluated. The pharmacokinetic parameters of repaglinide and blood glucose concentrations were also determined in rats after oral (0.5 mg/kg) and intravenous (0.2 mg/kg) administration of repaglinide in the presence and absence of aspirin (5 and 20 mg/kg). Aspirin could inhibit CYP3A4 activity with an IC50 value of 15.0 μM, but aspirin did not inhibit P-gp activity by comparing with the relative cellular uptake of rhodamine-123. Compared to the oral control group, aspirin significantly increased the AUC0–∞ and the Cmax of repaglinide by 36.6% and 18.8%, respectively, while the CL/F ratio was significantly decreased by aspirin. Aspirin also increased the absolute bioavailability (A.B.) of repaglinide by 36.9% compared to the oral control group. Moreover, the relative bioavailability (R.B.) of repaglinide was 1.13 to 1.37 times greater than that in the control group. Oral aspirin (20 mg/kg) could significantly decrease the blood glucose concentrations after oral (0.5 mg/kg) administration of repaglinide compared to the oral control groups. Aspirin enhanced the oral bioavailability of repaglinide, which may be attributed to the inhibition of CYP3A isoform mediated metabolism in the small intestine and/or in the liver rather than to the inhibition of P-gp in the small intestine and/or the reduction of renal elimination of repaglinide by aspirin. The increase in the oral bioavailability of repaglinide should be taken into consideration as potential drug interaction when coadministering repaglinide and aspirin. Furthermore, the blood glucose concentration should be carefully monitored during their coadministration.
引用
收藏
页码:1151 / 1156
页数:5
相关论文
共 50 条
  • [11] Effects of Fluvastatin on the Pharmacokinetics of Repaglinide: Possible Role of CYP3A4 and P-glycoprotein Inhibition by Fluvastatin
    Lee, Chong-Ki
    Choi, Jun-Shik
    Bang, Joon Seok
    KOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, 2013, 17 (03) : 245 - 251
  • [12] Inhibition of cytochrome P450 3A by acetoxylated analogues of resveratrol in in vitro and in silico models
    Basheer, Loai
    Schultz, Keren
    Kerem, Zohar
    SCIENTIFIC REPORTS, 2016, 6
  • [13] Effects of efonidipine on the pharmacokinetics and pharmacodynamics of repaglinide: possible role of CYP3A4 and P-glycoprotein inhibition by efonidipine
    Li, Cheng
    Choi, Dong-Hyun
    Choi, Jun-Shik
    JOURNAL OF PHARMACOKINETICS AND PHARMACODYNAMICS, 2012, 39 (01) : 99 - 108
  • [14] Effects of efonidipine on the pharmacokinetics and pharmacodynamics of repaglinide: possible role of CYP3A4 and P-glycoprotein inhibition by efonidipine
    Cheng Li
    Dong-Hyun Choi
    Jun-Shik Choi
    Journal of Pharmacokinetics and Pharmacodynamics, 2012, 39 : 99 - 108
  • [15] Metabolism of Beclomethasone Dipropionate by Cytochrome P450 3A Enzymes
    Roberts, Jessica K.
    Moore, Chad D.
    Ward, Robert M.
    Yost, Garold S.
    Reilly, Christopher A.
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2013, 345 (02) : 308 - 316
  • [16] Involvement of P-glycoprotein and cytochrome P450 3A in the metabolism of florfenicol of rabbits
    Liu, N.
    Guo, M.
    Mo, F.
    Sun, Y. -H.
    Yuan, Z.
    Cao, L. -H.
    Jiang, S. -X.
    JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS, 2012, 35 (02) : 202 - 205
  • [17] Effects of lovastatin on the pharmacokinetics of diltiazem and its main metabolite, desacetyldiltiazem, in rats: possible role of cytochrome P450 3A4 and P-glycoprotein inhibition by lovastatin
    Hong, Soon-Pyo
    Yang, Joon-Seung
    Han, Jung-Yeon
    Ha, Sung-Il
    Chung, Joong-Wha
    Koh, Young-Youp
    Chang, Kyong-Sig
    Choi, Dong-Hyun
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2011, 63 (01) : 129 - 135
  • [18] Evaluation of the Effects of Maytenus ilicifolia on the Activities of Cytochrome P450 3A and P-glycoprotein
    do Nascimento, Sara Batista
    Nascimento, Mariana de Lima
    de Araujo, Lais Lobato
    de Oliveira, Flavio Martins
    Vieira, Maria do Carmo
    Duarte-Almeida, Joaquim Mauricio
    Siqueira, Joao Maximo
    Cesar, Isabela da Costa
    Derendorf, Hartmut
    de Castro, Whocely Victor
    CURRENT DRUG METABOLISM, 2020, 21 (04) : 281 - 290
  • [19] Effects of myricetin, an antioxidant, on the pharmacokinetics of losartan and its active metabolite, EXP-3174, in rats: possible role of cytochrome P450 3A4, cytochrome P450 2C9 and P-glycoprotein inhibition by myricetin
    Choi, Dong-Hyun
    Li, Cheng
    Choi, Jun-Shik
    JOURNAL OF PHARMACY AND PHARMACOLOGY, 2010, 62 (07) : 908 - 914
  • [20] Cytochrome P450 3A and P-glycoprotein drug-drug interactions with voclosporin
    Ling, Spencer Y.
    Huizinga, Robert B.
    Mayo, Patrick R.
    Larouche, Richard
    Freitag, Derrick G.
    Aspeslet, Launa J.
    Foster, Robert T.
    BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2014, 77 (06) : 1039 - 1050