Literature DB >> 34272690

Reversible Mechanisms of Enzyme Inhibition and Resulting Clinical Significance.

Barbara Ring1, Steven A Wrighton2, Michael Mohutsky3.   

Abstract

Inhibition of a drug-metabolizing enzyme by the reversible interaction of a drug with the enzyme, thus decreasing the metabolism of another drug, is a major cause of clinically significant drug-drug interactions. This chapter defines the four reversible mechanisms of inhibition exhibited by drugs: competitive, noncompetitive, uncompetitive, and mixed competitive/noncompetitive. An in vitro procedure to determine the potential of a drug to be a reversible inhibitor is also provided. Finally, a number of examples of clinically significant drug-drug interactions resulting from reversible inhibition are described.
© 2021. Springer Science+Business Media, LLC, part of Springer Nature.

Keywords:  Competitive inhibition; Ki value and IC50 value; Mixed competitive–noncompetitive inhibition; Noncompetitive inhibition; Reversible inhibition; Uncompetitive inhibition

Year:  2021        PMID: 34272690     DOI: 10.1007/978-1-0716-1554-6_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  56 in total

1.  Predictions of cytochrome P450-mediated drug-drug interactions using cryopreserved human hepatocytes: comparison of plasma and protein-free media incubation conditions.

Authors:  Jialin Mao; Michael A Mohutsky; John P Harrelson; Steven A Wrighton; Stephen D Hall
Journal:  Drug Metab Dispos       Date:  2012-01-06       Impact factor: 3.922

2.  In vitro inhibition of CYP1A2 by model inhibitors, anti-inflammatory analgesics and female sex steroids: predictability of in vivo interactions.

Authors:  Marjo J Karjalainen; Pertti J Neuvonen; Janne T Backman
Journal:  Basic Clin Pharmacol Toxicol       Date:  2008-08       Impact factor: 4.080

3.  Effect of common organic solvents on in vitro cytochrome P450-mediated metabolic activities in human liver microsomes.

Authors:  N Chauret; A Gauthier; D A Nicoll-Griffith
Journal:  Drug Metab Dispos       Date:  1998-01       Impact factor: 3.922

4.  Adverse drug events in the outpatient setting: an 11-year national analysis.

Authors:  Florence T Bourgeois; Michael W Shannon; Clarissa Valim; Kenneth D Mandl
Journal:  Pharmacoepidemiol Drug Saf       Date:  2010-09       Impact factor: 2.890

5.  In vitro glucuronidation using human liver microsomes and the pore-forming peptide alamethicin.

Authors:  M B Fisher; K Campanale; B L Ackermann; M VandenBranden; S A Wrighton
Journal:  Drug Metab Dispos       Date:  2000-05       Impact factor: 3.922

6.  Physicochemical Properties, Biotransformation, and Transport Pathways of Established and Newly Approved Medications: A Systematic Review of the Top 200 Most Prescribed Drugs vs. the FDA-Approved Drugs Between 2005 and 2016.

Authors:  Anitha Saravanakumar; Armin Sadighi; Rachel Ryu; Fatemeh Akhlaghi
Journal:  Clin Pharmacokinet       Date:  2019-10       Impact factor: 6.447

Review 7.  Prevalence of Non-Cytochrome P450-Mediated Metabolism in Food and Drug Administration-Approved Oral and Intravenous Drugs: 2006-2015.

Authors:  Matthew A Cerny
Journal:  Drug Metab Dispos       Date:  2016-04-15       Impact factor: 3.922

8.  A novel model for the prediction of drug-drug interactions in humans based on in vitro cytochrome p450 phenotypic data.

Authors:  Chuang Lu; Gerald T Miwa; Shimoga R Prakash; Liang-Shang Gan; Suresh K Balani
Journal:  Drug Metab Dispos       Date:  2006-10-04       Impact factor: 3.922

9.  Evaluation of CYP2C8 inhibition in vitro: utility of montelukast as a selective CYP2C8 probe substrate.

Authors:  Brooke M VandenBrink; Robert S Foti; Dan A Rock; Larry C Wienkers; Jan L Wahlstrom
Journal:  Drug Metab Dispos       Date:  2011-06-22       Impact factor: 3.922

10.  Multisite kinetic analysis of interactions between prototypical CYP3A4 subgroup substrates: midazolam, testosterone, and nifedipine.

Authors:  Aleksandra Galetin; Stephen E Clarke; J Brian Houston
Journal:  Drug Metab Dispos       Date:  2003-09       Impact factor: 3.922

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.