Literature DB >> 3061491

Role of the red blood cell in drug metabolism.

P A Cossum1.   

Abstract

Contrary to the belief that the RBC is not metabolically active towards pharmacologically active endogenous and exogenous substances, it is evident that the RBC contains moderate cytochrome P-450-like activity, in addition to the ability to catalyse various other transformations of a range of drugs. The list of drugs for which there is evidence of metabolism by RBC (Table 1) contains examples from several drug classes. However some major classes of drugs which are principally cleared in vivo by metabolism are missing (for example, benzodiazepines). Moreover, there is as yet no evidence for the RBC having the capacity for the more important drug conjugation reactions (glucuronidation, sulphation) although there is evidence of other conjugation reactions (methylation, acetylation, glutathione conjugation). It is conceivable that the RBC could be used as a convenient tissue to add to other metabolism screening procedures used in drug development. Already use has been made of the RBC in identifying fast and slow acetylators. Others have used RBC to identify a possible sex-based difference in drug metabolism. Hopefully, this review has stimulated interest in the ability of the RBC to metabolize drugs and this interest will result in further discoveries.

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Year:  1988        PMID: 3061491     DOI: 10.1002/bod.2510090402

Source DB:  PubMed          Journal:  Biopharm Drug Dispos        ISSN: 0142-2782            Impact factor:   1.627


  7 in total

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Journal:  J Chromatogr B Analyt Technol Biomed Life Sci       Date:  2013-09-23       Impact factor: 3.205

2.  Heat stabilization of blood spot samples for determination of metabolically unstable drug compounds.

Authors:  Daniel Blessborn; Karl Sköld; David Zeeberg; Karnrawee Kaewkhao; Olof Sköld; Martin Ahnoff
Journal:  Bioanalysis       Date:  2013-01       Impact factor: 2.681

3.  Detection of multiple globin monoadducts and cross-links after in vitro exposure of rat erythrocytes to S-(1,2-dichlorovinyl)-L-cysteine sulfoxide and after in vivo treatment of rats with S-(1,2-dichlorovinyl)-L-cysteine sulfoxide.

Authors:  Nella Barshteyn; Adnan A Elfarra
Journal:  Chem Res Toxicol       Date:  2008-08-06       Impact factor: 3.739

4.  Inactivation of apaziquone by haematuria: implications for the design of phase III clinical trials against non-muscle invasive bladder cancer.

Authors:  Roger M Phillips; Paul M Loadman; Guru Reddy
Journal:  Cancer Chemother Pharmacol       Date:  2019-03-13       Impact factor: 3.333

5.  A Multi-scale Computational Platform to Mechanistically Assess the Effect of Genetic Variation on Drug Responses in Human Erythrocyte Metabolism.

Authors:  Nathan Mih; Elizabeth Brunk; Aarash Bordbar; Bernhard O Palsson
Journal:  PLoS Comput Biol       Date:  2016-07-28       Impact factor: 4.475

6.  Formation primaquine-5,6-orthoquinone, the putative active and toxic metabolite of primaquine via direct oxidation in human erythrocytes.

Authors:  Pius S Fasinu; N P Dhammika Nanayakkara; Yan-Hong Wang; Narayan D Chaurasiya; H M Bandara Herath; James D McChesney; Bharathi Avula; Ikhlas Khan; Babu L Tekwani; Larry A Walker
Journal:  Malar J       Date:  2019-01-30       Impact factor: 2.979

7.  Light-controllable dithienylethene-modified cyclic peptides: photoswitching the in vivo toxicity in zebrafish embryos.

Authors:  Sergii Afonin; Oleg Babii; Aline Reuter; Volker Middel; Masanari Takamiya; Uwe Strähle; Igor V Komarov; Anne S Ulrich
Journal:  Beilstein J Org Chem       Date:  2020-01-07       Impact factor: 2.883

  7 in total

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