Literature DB >> 24731191

The effect of breed and sex on sulfamethazine, enrofloxacin, fenbendazole and flunixin meglumine pharmacokinetic parameters in swine.

J T Howard1, R E Baynes, J D Brooks, J L Yeatts, B Bellis, M S Ashwell, P Routh, A T O'Nan, C Maltecca.   

Abstract

Drug use in livestock has received increased attention due to welfare concerns and food safety. Characterizing heterogeneity in the way swine populations respond to drugs could allow for group-specific dose or drug recommendations. Our objective was to determine whether drug clearance differs across genetic backgrounds and sex for sulfamethazine, enrofloxacin, fenbendazole and flunixin meglumine. Two sires from each of four breeds were mated to a common sow population. The nursery pigs generated (n = 114) were utilized in a random crossover design. Drugs were administered intravenously and blood collected a minimum of 10 times over 48 h. A non-compartmental analysis of drug and metabolite plasma concentration vs. time profiles was performed. Within-drug and metabolite analysis of pharmacokinetic parameters included fixed effects of drug administration date, sex and breed of sire. Breed differences existed for flunixin meglumine (P-value<0.05; Cl, Vdss ) and oxfendazole (P-value<0.05, AUC0→∞ ). Sex differences existed for oxfendazole (P-value < 0.05; Tmax ) and sulfamethazine (P-value < 0.05, Cl). Differences in drug clearance were seen, and future work will determine the degree of additive genetic variation utilizing a larger population.
© 2014 John Wiley & Sons Ltd.

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Year:  2014        PMID: 24731191     DOI: 10.1111/jvp.12128

Source DB:  PubMed          Journal:  J Vet Pharmacol Ther        ISSN: 0140-7783            Impact factor:   1.786


  7 in total

1.  Human Food Safety Implications of Variation in Food Animal Drug Metabolism.

Authors:  Zhoumeng Lin; Christopher I Vahl; Jim E Riviere
Journal:  Sci Rep       Date:  2016-06-15       Impact factor: 4.379

2.  Gene co-expression network analysis identifies porcine genes associated with variation in metabolizing fenbendazole and flunixin meglumine in the liver.

Authors:  Jeremy T Howard; Melissa S Ashwell; Ronald E Baynes; James D Brooks; James L Yeatts; Christian Maltecca
Journal:  Sci Rep       Date:  2017-05-02       Impact factor: 4.379

3.  A study to assess the correlation between plasma, oral fluid and urine concentrations of flunixin meglumine with the tissue residue depletion profile in finishing-age swine.

Authors:  Jessica L Bates; Locke A Karriker; Suzanne M Rajewski; Zhoumeng Lin; Ronette Gehring; Mengjie Li; Jim E Riviere; Johann F Coetzee
Journal:  BMC Vet Res       Date:  2020-06-22       Impact factor: 2.741

4.  Modelling Shows the Negative Impact of Age Dependent Pharmacokinetics on the Efficacy of Oxytetracycline in Young Steers.

Authors:  Peter Hekman; Johan Schefferlie; Ronette Gehring
Journal:  Front Vet Sci       Date:  2022-01-28

5.  An Interactive Generic Physiologically Based Pharmacokinetic (igPBPK) Modeling Platform to Predict Drug Withdrawal Intervals in Cattle and Swine: A Case Study on Flunixin, Florfenicol, and Penicillin G.

Authors:  Wei-Chun Chou; Lisa A Tell; Ronald E Baynes; Jennifer L Davis; Fiona P Maunsell; Jim E Riviere; Zhoumeng Lin
Journal:  Toxicol Sci       Date:  2022-07-28       Impact factor: 4.109

6.  Differential Gene Expression across Breed and Sex in Commercial Pigs Administered Fenbendazole and Flunixin Meglumine.

Authors:  Jeremy T Howard; Audrey T O'Nan; Christian Maltecca; Ronald E Baynes; Melissa S Ashwell
Journal:  PLoS One       Date:  2015-09-14       Impact factor: 3.240

7.  Genetic Parameter Estimates for Metabolizing Two Common Pharmaceuticals in Swine.

Authors:  Jeremy T Howard; Melissa S Ashwell; Ronald E Baynes; James D Brooks; James L Yeatts; Christian Maltecca
Journal:  Front Genet       Date:  2018-02-13       Impact factor: 4.599

  7 in total

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