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Physiological and pharmacokinetic effects of multilevel caging on Sprague Dawley rats under ketamine-xylazine anesthesia
While the cage refinement is a necessary step towards improving the welfare of research rats, increasing the complexity and surface area of the living space of an animal may have physiological impacts that need to be taken into consideration. In this study, ketamine (80 mg/kg) and xylazine (10 mg/kg...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japanese Association for Laboratory Animal Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111841/ https://www.ncbi.nlm.nih.gov/pubmed/27263962 http://dx.doi.org/10.1538/expanim.16-0026 |
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author | Dodelet-Devillers, Aurore Zullian, Chiara Beaudry, Francis Gourdon, Jim Chevrette, Julie Hélie, Pierre Vachon, Pascal |
author_facet | Dodelet-Devillers, Aurore Zullian, Chiara Beaudry, Francis Gourdon, Jim Chevrette, Julie Hélie, Pierre Vachon, Pascal |
author_sort | Dodelet-Devillers, Aurore |
collection | PubMed |
description | While the cage refinement is a necessary step towards improving the welfare of research rats, increasing the complexity and surface area of the living space of an animal may have physiological impacts that need to be taken into consideration. In this study, ketamine (80 mg/kg) and xylazine (10 mg/kg) caused a short duration anesthesia that was significantly decreased in Sprague-Dawley rats housed in multilevel cages (MLC), compared to rats housed in standard cages (SDC). The withdrawal reflex, the palpebral reflexes and the time-to-sternal all occurred earlier in MLC housed rats, suggesting an effect of housing on the physiology of the rats. In addition, during anesthesia, cardiac frequencies were increased in animals housed in the smaller SDC. Respiratory frequencies, the blood oxygen saturation and rectal temperatures during anesthesia did not vary between conditions during the anesthesia. While xylazine pharmacokinetics were unchanged with caging conditions, the clearance and half-lives of ketamine and its metabolite, norketamine, were altered in the rats housed in MLC. Finally, while no difference was ultimately seen in rat body weights, isolated liver and adrenal gland weights were significantly lighter in rats housed in the MLC. Increasing cage sizes, while having a positive impact on wellbeing in rats, can alter anesthetic drug metabolism and thus modify anesthesia parameters and associated physiological processes. |
format | Online Article Text |
id | pubmed-5111841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Japanese Association for Laboratory Animal Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51118412016-11-17 Physiological and pharmacokinetic effects of multilevel caging on Sprague Dawley rats under ketamine-xylazine anesthesia Dodelet-Devillers, Aurore Zullian, Chiara Beaudry, Francis Gourdon, Jim Chevrette, Julie Hélie, Pierre Vachon, Pascal Exp Anim Original While the cage refinement is a necessary step towards improving the welfare of research rats, increasing the complexity and surface area of the living space of an animal may have physiological impacts that need to be taken into consideration. In this study, ketamine (80 mg/kg) and xylazine (10 mg/kg) caused a short duration anesthesia that was significantly decreased in Sprague-Dawley rats housed in multilevel cages (MLC), compared to rats housed in standard cages (SDC). The withdrawal reflex, the palpebral reflexes and the time-to-sternal all occurred earlier in MLC housed rats, suggesting an effect of housing on the physiology of the rats. In addition, during anesthesia, cardiac frequencies were increased in animals housed in the smaller SDC. Respiratory frequencies, the blood oxygen saturation and rectal temperatures during anesthesia did not vary between conditions during the anesthesia. While xylazine pharmacokinetics were unchanged with caging conditions, the clearance and half-lives of ketamine and its metabolite, norketamine, were altered in the rats housed in MLC. Finally, while no difference was ultimately seen in rat body weights, isolated liver and adrenal gland weights were significantly lighter in rats housed in the MLC. Increasing cage sizes, while having a positive impact on wellbeing in rats, can alter anesthetic drug metabolism and thus modify anesthesia parameters and associated physiological processes. Japanese Association for Laboratory Animal Science 2016-06-03 2016 /pmc/articles/PMC5111841/ /pubmed/27263962 http://dx.doi.org/10.1538/expanim.16-0026 Text en ©2016 Japanese Association for Laboratory Animal Science http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
spellingShingle | Original Dodelet-Devillers, Aurore Zullian, Chiara Beaudry, Francis Gourdon, Jim Chevrette, Julie Hélie, Pierre Vachon, Pascal Physiological and pharmacokinetic effects of multilevel caging on Sprague Dawley rats under ketamine-xylazine anesthesia |
title | Physiological and pharmacokinetic effects of multilevel caging on Sprague
Dawley rats under ketamine-xylazine anesthesia |
title_full | Physiological and pharmacokinetic effects of multilevel caging on Sprague
Dawley rats under ketamine-xylazine anesthesia |
title_fullStr | Physiological and pharmacokinetic effects of multilevel caging on Sprague
Dawley rats under ketamine-xylazine anesthesia |
title_full_unstemmed | Physiological and pharmacokinetic effects of multilevel caging on Sprague
Dawley rats under ketamine-xylazine anesthesia |
title_short | Physiological and pharmacokinetic effects of multilevel caging on Sprague
Dawley rats under ketamine-xylazine anesthesia |
title_sort | physiological and pharmacokinetic effects of multilevel caging on sprague
dawley rats under ketamine-xylazine anesthesia |
topic | Original |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111841/ https://www.ncbi.nlm.nih.gov/pubmed/27263962 http://dx.doi.org/10.1538/expanim.16-0026 |
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