Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers

Over recent years, pigs have been promoted as potential animal model due to their anatomical and physiological similarities with humans. However, information about the contribution of distinct renal elimination processes [glomerular filtration rate (GFR), effective renal plasma flow (ERPF), tubular...

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Main Authors: Laura Dhondt, Siska Croubels, Peter De Paepe, Steven C. Wallis, Saurabh Pandey, Jason A. Roberts, Jeffrey Lipman, Pieter De Cock, Mathias Devreese
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-06-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphar.2020.00883/full
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language English
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author Laura Dhondt
Siska Croubels
Peter De Paepe
Steven C. Wallis
Saurabh Pandey
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jeffrey Lipman
Jeffrey Lipman
Jeffrey Lipman
Pieter De Cock
Pieter De Cock
Pieter De Cock
Mathias Devreese
spellingShingle Laura Dhondt
Siska Croubels
Peter De Paepe
Steven C. Wallis
Saurabh Pandey
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jeffrey Lipman
Jeffrey Lipman
Jeffrey Lipman
Pieter De Cock
Pieter De Cock
Pieter De Cock
Mathias Devreese
Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers
Frontiers in Pharmacology
piglet
renal function
animal model
iohexol
para-aminohippuric acid
pindolol
author_facet Laura Dhondt
Siska Croubels
Peter De Paepe
Steven C. Wallis
Saurabh Pandey
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jason A. Roberts
Jeffrey Lipman
Jeffrey Lipman
Jeffrey Lipman
Pieter De Cock
Pieter De Cock
Pieter De Cock
Mathias Devreese
author_sort Laura Dhondt
title Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers
title_short Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers
title_full Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers
title_fullStr Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers
title_full_unstemmed Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous Markers
title_sort conventional pig as animal model for human renal drug excretion processes: unravelling the porcine renal function by use of a cocktail of exogenous markers
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2020-06-01
description Over recent years, pigs have been promoted as potential animal model due to their anatomical and physiological similarities with humans. However, information about the contribution of distinct renal elimination processes [glomerular filtration rate (GFR), effective renal plasma flow (ERPF), tubular secretion, and reabsorption] in pigs is currently limited. Therefore, a cocktail of renal markers, consisting of iohexol (GFR), para-aminohippuric acid (ERPF and net tubular anion secretion), pindolol (net tubular cation secretion), and fluconazole (net tubular reabsorption) was administered intravenously to 7-week-old male conventional pigs. Plasma and urinary concentrations were determined using validated analytical methods. The clearance of iohexol (GFR) was 97.87 ± 16.05 ml/min/m² (mean ± SD). The ERPF, calculated as the renal clearance of PAH, was 226.77 ± 62.45 ml/min/m², whereas the net tubular secretion of PAH was 130.28 ± 52.62 ml/min/m². The net tubular secretion of R-pindolol and S-pindolol was 13.53 ± 12.97 and 18.01 ± 39.23 ml/min/m², respectively. The net tubular reabsorption of fluconazole was 78.32 ± 13.52 ml/min/m². Overall, this cocktail of renal markers was considered to be safe for use in pigs since no adverse effects were observed. Iohexol, PAH and fluconazole were considered suitable renal marker to assess the porcine renal function. Pindolol seems less appropriate due to the high degree of nonrenal clearance in pigs. The values of GFR, ERPF, and anion secretion are within the same range for both human and pig. Regarding the tubular reabsorption of fluconazole, slightly higher values were obtained for pigs. Nevertheless, these results indicate the conventional pig could be an appropriate animal model to study renal drug elimination processes in humans.
topic piglet
renal function
animal model
iohexol
para-aminohippuric acid
pindolol
url https://www.frontiersin.org/article/10.3389/fphar.2020.00883/full
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spelling doaj-84599fa3bea34f689996dc1c861429f82020-11-25T02:48:45ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122020-06-011110.3389/fphar.2020.00883544965Conventional Pig as Animal Model for Human Renal Drug Excretion Processes: Unravelling the Porcine Renal Function by Use of a Cocktail of Exogenous MarkersLaura Dhondt0Siska Croubels1Peter De Paepe2Steven C. Wallis3Saurabh Pandey4Jason A. Roberts5Jason A. Roberts6Jason A. Roberts7Jason A. Roberts8Jason A. Roberts9Jeffrey Lipman10Jeffrey Lipman11Jeffrey Lipman12Pieter De Cock13Pieter De Cock14Pieter De Cock15Mathias Devreese16Department of Pharmacology, Toxicology and Biochemistry, Ghent University, Merelbeke, BelgiumDepartment of Pharmacology, Toxicology and Biochemistry, Ghent University, Merelbeke, BelgiumHeymans Institute of Pharmacology, Ghent University, Ghent, BelgiumUQ Centre for Clinical Research, The University of Queensland, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaUQ Centre for Clinical Research, The University of Queensland, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaUQ Centre for Clinical Research, The University of Queensland, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaDepartment of Intensive Care Medicine, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaCentre for Translational Anti-Infective Pharmacodynamics, School of Pharmacy, The University of Queensland, Brisbane, QLD, AustraliaDepartment of Pharmacy, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaDivision of Anaesthesiology Critical Care Emergency and Pain Medicine, Nîmes University Hospital, University of Montpellier, Nîmes, FranceUQ Centre for Clinical Research, The University of Queensland, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaDepartment of Intensive Care Medicine, Royal Brisbane & Women's Hospital, Brisbane, QLD, AustraliaDivision of Anaesthesiology Critical Care Emergency and Pain Medicine, Nîmes University Hospital, University of Montpellier, Nîmes, FranceHeymans Institute of Pharmacology, Ghent University, Ghent, BelgiumDepartment of Pharmacy, Ghent University Hospital, Ghent, BelgiumDepartment of Paediatric Intensive Care, Ghent University Hospital, Ghent, BelgiumDepartment of Pharmacology, Toxicology and Biochemistry, Ghent University, Merelbeke, BelgiumOver recent years, pigs have been promoted as potential animal model due to their anatomical and physiological similarities with humans. However, information about the contribution of distinct renal elimination processes [glomerular filtration rate (GFR), effective renal plasma flow (ERPF), tubular secretion, and reabsorption] in pigs is currently limited. Therefore, a cocktail of renal markers, consisting of iohexol (GFR), para-aminohippuric acid (ERPF and net tubular anion secretion), pindolol (net tubular cation secretion), and fluconazole (net tubular reabsorption) was administered intravenously to 7-week-old male conventional pigs. Plasma and urinary concentrations were determined using validated analytical methods. The clearance of iohexol (GFR) was 97.87 ± 16.05 ml/min/m² (mean ± SD). The ERPF, calculated as the renal clearance of PAH, was 226.77 ± 62.45 ml/min/m², whereas the net tubular secretion of PAH was 130.28 ± 52.62 ml/min/m². The net tubular secretion of R-pindolol and S-pindolol was 13.53 ± 12.97 and 18.01 ± 39.23 ml/min/m², respectively. The net tubular reabsorption of fluconazole was 78.32 ± 13.52 ml/min/m². Overall, this cocktail of renal markers was considered to be safe for use in pigs since no adverse effects were observed. Iohexol, PAH and fluconazole were considered suitable renal marker to assess the porcine renal function. Pindolol seems less appropriate due to the high degree of nonrenal clearance in pigs. The values of GFR, ERPF, and anion secretion are within the same range for both human and pig. Regarding the tubular reabsorption of fluconazole, slightly higher values were obtained for pigs. Nevertheless, these results indicate the conventional pig could be an appropriate animal model to study renal drug elimination processes in humans.https://www.frontiersin.org/article/10.3389/fphar.2020.00883/fullpigletrenal functionanimal modeliohexolpara-aminohippuric acidpindolol