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Intravenous ketamine for long term anesthesia in rats
Ketamine/xylazine anesthesia has been used primarily for short term procedures in animals, but two prior reports used intravenous ketamine/xylazine for experiments taking many hours. However, there is a discrepancy about the appropriate dose, which is resolved here. Adult Long-Evans rats were used f...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749388/ https://www.ncbi.nlm.nih.gov/pubmed/33367124 http://dx.doi.org/10.1016/j.heliyon.2020.e05686 |
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author | Linsenmeier, Robert A. Beckmann, Lisa Dmitriev, Andrey V. |
author_facet | Linsenmeier, Robert A. Beckmann, Lisa Dmitriev, Andrey V. |
author_sort | Linsenmeier, Robert A. |
collection | PubMed |
description | Ketamine/xylazine anesthesia has been used primarily for short term procedures in animals, but two prior reports used intravenous ketamine/xylazine for experiments taking many hours. However, there is a discrepancy about the appropriate dose, which is resolved here. Adult Long-Evans rats were used for recording from the retina. Doses of Ketamine/xylazine were adjusted to minimize anesthetic in terminal experiments lasting 10 h. An allometric relation was fitted to the resulting data on doses as a function of body weight, and compared to prior work. The allometric relationship between the continuously infused specific dose and weight was: dose = 9.13 (weight)(−1.213) (r(2) = 0.73), where dose is in mg-kg(−1)-hr(−1) and rat weight is in kg. The dose of xylazine was 3.3% of the ketamine dose. No attempt was made to explore different relative doses of xylazine and ketamine. Prior work is consistent with this relationship, showing that the earlier discrepancy resulted from using rats of different sizes. Ketamine at the doses used here still depressed the electroretinogram relative to historical controls using urethane. We conclude that intravenous ketamine dosing in rats should not use the same mg-kg(−1)-hr(−1) dose for all rats, but take into account the strong allometric relationship between dose and rat weight. There is an advantage in using smaller doses in order to prevent unnecessary depression of neural responses. |
format | Online Article Text |
id | pubmed-7749388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-77493882020-12-22 Intravenous ketamine for long term anesthesia in rats Linsenmeier, Robert A. Beckmann, Lisa Dmitriev, Andrey V. Heliyon Research Article Ketamine/xylazine anesthesia has been used primarily for short term procedures in animals, but two prior reports used intravenous ketamine/xylazine for experiments taking many hours. However, there is a discrepancy about the appropriate dose, which is resolved here. Adult Long-Evans rats were used for recording from the retina. Doses of Ketamine/xylazine were adjusted to minimize anesthetic in terminal experiments lasting 10 h. An allometric relation was fitted to the resulting data on doses as a function of body weight, and compared to prior work. The allometric relationship between the continuously infused specific dose and weight was: dose = 9.13 (weight)(−1.213) (r(2) = 0.73), where dose is in mg-kg(−1)-hr(−1) and rat weight is in kg. The dose of xylazine was 3.3% of the ketamine dose. No attempt was made to explore different relative doses of xylazine and ketamine. Prior work is consistent with this relationship, showing that the earlier discrepancy resulted from using rats of different sizes. Ketamine at the doses used here still depressed the electroretinogram relative to historical controls using urethane. We conclude that intravenous ketamine dosing in rats should not use the same mg-kg(−1)-hr(−1) dose for all rats, but take into account the strong allometric relationship between dose and rat weight. There is an advantage in using smaller doses in order to prevent unnecessary depression of neural responses. Elsevier 2020-12-14 /pmc/articles/PMC7749388/ /pubmed/33367124 http://dx.doi.org/10.1016/j.heliyon.2020.e05686 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Article Linsenmeier, Robert A. Beckmann, Lisa Dmitriev, Andrey V. Intravenous ketamine for long term anesthesia in rats |
title | Intravenous ketamine for long term anesthesia in rats |
title_full | Intravenous ketamine for long term anesthesia in rats |
title_fullStr | Intravenous ketamine for long term anesthesia in rats |
title_full_unstemmed | Intravenous ketamine for long term anesthesia in rats |
title_short | Intravenous ketamine for long term anesthesia in rats |
title_sort | intravenous ketamine for long term anesthesia in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7749388/ https://www.ncbi.nlm.nih.gov/pubmed/33367124 http://dx.doi.org/10.1016/j.heliyon.2020.e05686 |
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