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Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats
SIMPLE SUMMARY: Carbon dioxide and isoflurane are gases with anesthetic properties that are commonly used in laboratory rodents, especially when anesthetic overdose is used for euthanasia procedures. Concerns have been raised with the use of carbon dioxide as a euthanasia agent due to behavioral res...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459795/ https://www.ncbi.nlm.nih.gov/pubmed/32824345 http://dx.doi.org/10.3390/ani10081431 |
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author | Kulkarni, Satyajit Hickman, Debra |
author_facet | Kulkarni, Satyajit Hickman, Debra |
author_sort | Kulkarni, Satyajit |
collection | PubMed |
description | SIMPLE SUMMARY: Carbon dioxide and isoflurane are gases with anesthetic properties that are commonly used in laboratory rodents, especially when anesthetic overdose is used for euthanasia procedures. Concerns have been raised with the use of carbon dioxide as a euthanasia agent due to behavioral responses that indicate potential distress. This study was designed to assess aversive responses in experimentally naïve Sprague–Dawley rats when exposed to isoflurane or carbon dioxide. When placed in the forced exposure apparatus, these naïve rats were more active in the isoflurane and CO(2) treatments compared to the control groups, suggesting that isoflurane and CO(2) are similarly aversive. The results from the aversion-avoidance experiment supported previous work which demonstrated that while CO(2) is more aversive than isoflurane on initial exposure, rats showed increased aversion when the isoflurane exposure was repeated. We also show that learned aversion to isoflurane is sustained for at least 15 days after initial exposure. Given this result, we suggest that CO(2) is superior to isoflurane when euthanizing rodents with prior exposure to isoflurane. Overall, these results confirm previous studies which suggest that care should be taken when considering the serial use of isoflurane as an anesthetic. ABSTRACT: Euthanasia in rodents is an ongoing topic of debate due to concerns regarding the aversive nature of gases with anesthetic properties such as carbon dioxide (CO(2)) and isoflurane. The aim of this study was to expand upon previously published work evaluating the aversiveness of CO(2) by introducing an isoflurane treatment group in parallel. Aversion was tested using a forced exposure setup and an aversion-avoidance setup. In the first part of the study, 12 naïve female Sprague–Dawley rats were exposed during four consecutive days, once to each of four treatments: isoflurane, fox urine, oxygen, and CO(2). In the second part of the study, 24 naïve female Sprague–Dawley rats and 12 rats from the first experiment were exposed to CO(2), isoflurane, or both gases. In the forced exposure study, there were no significant differences between CO(2) and isoflurane treatments except in line crosses. Overall, rats were more active in the isoflurane and CO(2) treatments compared to the control groups, suggesting that isoflurane and CO(2) are similarly aversive. In the aversion-avoidance study, rats previously exposed to isoflurane left the dark chamber significantly earlier compared to naïve rats during exposure to isoflurane. We also show that learned aversion to isoflurane is sustained for at least 15 days after initial exposure. Given this result, we suggest that CO(2) is superior to isoflurane when euthanizing rodents with prior exposure to isoflurane. Overall, these results confirm previous studies which suggest that care should be taken when considering the serial use of isoflurane as an anesthetic. |
format | Online Article Text |
id | pubmed-7459795 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74597952020-09-02 Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats Kulkarni, Satyajit Hickman, Debra Animals (Basel) Article SIMPLE SUMMARY: Carbon dioxide and isoflurane are gases with anesthetic properties that are commonly used in laboratory rodents, especially when anesthetic overdose is used for euthanasia procedures. Concerns have been raised with the use of carbon dioxide as a euthanasia agent due to behavioral responses that indicate potential distress. This study was designed to assess aversive responses in experimentally naïve Sprague–Dawley rats when exposed to isoflurane or carbon dioxide. When placed in the forced exposure apparatus, these naïve rats were more active in the isoflurane and CO(2) treatments compared to the control groups, suggesting that isoflurane and CO(2) are similarly aversive. The results from the aversion-avoidance experiment supported previous work which demonstrated that while CO(2) is more aversive than isoflurane on initial exposure, rats showed increased aversion when the isoflurane exposure was repeated. We also show that learned aversion to isoflurane is sustained for at least 15 days after initial exposure. Given this result, we suggest that CO(2) is superior to isoflurane when euthanizing rodents with prior exposure to isoflurane. Overall, these results confirm previous studies which suggest that care should be taken when considering the serial use of isoflurane as an anesthetic. ABSTRACT: Euthanasia in rodents is an ongoing topic of debate due to concerns regarding the aversive nature of gases with anesthetic properties such as carbon dioxide (CO(2)) and isoflurane. The aim of this study was to expand upon previously published work evaluating the aversiveness of CO(2) by introducing an isoflurane treatment group in parallel. Aversion was tested using a forced exposure setup and an aversion-avoidance setup. In the first part of the study, 12 naïve female Sprague–Dawley rats were exposed during four consecutive days, once to each of four treatments: isoflurane, fox urine, oxygen, and CO(2). In the second part of the study, 24 naïve female Sprague–Dawley rats and 12 rats from the first experiment were exposed to CO(2), isoflurane, or both gases. In the forced exposure study, there were no significant differences between CO(2) and isoflurane treatments except in line crosses. Overall, rats were more active in the isoflurane and CO(2) treatments compared to the control groups, suggesting that isoflurane and CO(2) are similarly aversive. In the aversion-avoidance study, rats previously exposed to isoflurane left the dark chamber significantly earlier compared to naïve rats during exposure to isoflurane. We also show that learned aversion to isoflurane is sustained for at least 15 days after initial exposure. Given this result, we suggest that CO(2) is superior to isoflurane when euthanizing rodents with prior exposure to isoflurane. Overall, these results confirm previous studies which suggest that care should be taken when considering the serial use of isoflurane as an anesthetic. MDPI 2020-08-16 /pmc/articles/PMC7459795/ /pubmed/32824345 http://dx.doi.org/10.3390/ani10081431 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kulkarni, Satyajit Hickman, Debra Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats |
title | Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats |
title_full | Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats |
title_fullStr | Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats |
title_full_unstemmed | Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats |
title_short | Isoflurane and Carbon Dioxide Elicit Similar Behavioral Responses in Rats |
title_sort | isoflurane and carbon dioxide elicit similar behavioral responses in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459795/ https://www.ncbi.nlm.nih.gov/pubmed/32824345 http://dx.doi.org/10.3390/ani10081431 |
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