Role of ABC Transporters in Veterinary Medicine: Pharmaco- Toxicological Implications
-
Published:2019-05-14
Issue:7
Volume:26
Page:1251-1269
-
ISSN:0929-8673
-
Container-title:Current Medicinal Chemistry
-
language:en
-
Short-container-title:CMC
Author:
Virkel Guillermo1, Ballent Mariana1, Lanusse Carlos1, Lifschitz Adrián1
Affiliation:
1. Laboratorio de Farmacologia, Centro de Investigacion Veterinaria de Tandil (CIVETAN-CONICETCICPBA), Facultad de Ciencias Veterinarias, Universidad Nacional del Centro de la Provincia de Buenos Aires (FCV-UNCPBA), Campus Universitario (Los Ombues y Reforma Universitaria), (7000) Tandil, Prov. de Buenos Aires, Argentina
Abstract
Unlike physicians, veterinary practitioners must deal with a number of animal species with crucial differences in anatomy, physiology and metabolism. Accordingly, the pharmacokinetic behaviour, the clinical efficacy and the adverse or toxic effects of drugs may differ across domestic animals. Moreover, the use of drugs in food-producing species may impose a risk for humans due to the generation of chemical residues in edible products, a major concern for public health and consumer's safety. As is clearly known in human beings, the ATP binding cassette (ABC) of transport proteins may influence the bioavailability and elimination of numerous drugs and other xenobiotics in domestic animals as well. A number of drugs, currently available in the veterinary market, are substrates of one or more transporters. Therefore, significant drug-drug interactions among ABC substrates may have unpredictable pharmacotoxicological consequences in different species of veterinary interest. In this context, different investigations revealed the major relevance of P-gp and other transport proteins, like breast cancer resistance protein (BCRP) and multidrug resistance-associated proteins (MRPs), in both companion and livestock animals. Undoubtedly, the discovery of the ABC transporters and the deep understanding of their physiological role in the different species introduced a new paradigm into the veterinary pharmacology. This review focuses on the expression and function of the major transport proteins expressed in species of veterinary interest, and their impact on drug disposition, efficacy and toxicity.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry
Reference160 articles.
1. Stewart J, Gorman N. J Vet Intern Med, Multi-drug resistance genes in the management of neoplastic disease.,, 1991, 5,, 239-247, 2. Moore A, Leveille C, Reimann K, Shu H, Arias I. Cancer Invest, The expression of P-glycoprotein in canine lymphoma and its association with multidrug resistance.,, 1995, 13,, 475-479, 3. Mealey K, Bentjen S, Gay J, Cantor G. Pharmacogenetics, Ivermectin sensitivity in collies is associated with a deletion mutation of the mdr1 gene.,, 2001, 11,, 727-733, 4. Paul A, Tranquilli W, Seward R, Todd K, DiPietro J. Am J Vet Res, Clinical observations in collies given ivermectin orally.,, 1987, 48,, 684-685, 5. Tranquilli W, Paul A, Seward R. Am J Vet Res, Ivermectin plasma concentrations in collies sensitive to ivermectin-induced toxicosis.,, 1989, 50,, 769-770,
Cited by
30 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|