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Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques
Rhesus macaques represent an important species for translational and pre-clinical research studies across a multitude of disease and injury models, including aging. Ketamine anesthesia is used in humans and non-human primates but may be associated with adverse effects, including neuromuscular reacti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505584/ https://www.ncbi.nlm.nih.gov/pubmed/32956357 http://dx.doi.org/10.1371/journal.pone.0236430 |
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author | Havton, Leif A. Biscola, Natalia P. Christe, Kari L. Colman, Ricki J. |
author_facet | Havton, Leif A. Biscola, Natalia P. Christe, Kari L. Colman, Ricki J. |
author_sort | Havton, Leif A. |
collection | PubMed |
description | Rhesus macaques represent an important species for translational and pre-clinical research studies across a multitude of disease and injury models, including aging. Ketamine anesthesia is used in humans and non-human primates but may be associated with adverse effects, including neuromuscular reactions. The effects of aging on ketamine adverse effects is not well characterized. Urodynamic recordings and electromyography (EMG) studies were performed in aged (>20 years old) and adult (3.9–14.9 years old) female rhesus macaques under an equal and light plane of sedation by constant rate infusion (CRI) of ketamine. A total of 4 of 41 adult subjects (9.7%) showed clinical signs of ketamine-induced abnormal neuromuscular reactivity, whereas a larger portion of 14 of 26 aged subjects showed similar ketamine-induced neuromuscular reactivity (53.8%; P< 0.001). The ketamine CRI rate was 19.8±0.9 mg/kg/h in adults and lower in aged subjects at 16.5±1.4 mg/kg/h (P<0.05). The ketamine CRI rate was negatively correlated with age (r = -0.30, P<0.05, n = 64). The incidence of ketamine reactivity or CRI rate was not different between aged pre-and post-menopausal females. EMG recordings during neuromuscular reactivity showed coordinated activation of multiple muscles, suggesting a central nervous system (CNS) mechanism for ketamine-associated neuromuscular reactivity. The incidence of ketamine-induced neuromuscular reactivity is age related but not affected by the estrous cycle in female rhesus macaques. A coordinated activation of multiple muscles, innervated by different peripheral nerves, suggests that ketamine-induced neuromuscular reactivity originates in the CNS. |
format | Online Article Text |
id | pubmed-7505584 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-75055842020-09-30 Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques Havton, Leif A. Biscola, Natalia P. Christe, Kari L. Colman, Ricki J. PLoS One Research Article Rhesus macaques represent an important species for translational and pre-clinical research studies across a multitude of disease and injury models, including aging. Ketamine anesthesia is used in humans and non-human primates but may be associated with adverse effects, including neuromuscular reactions. The effects of aging on ketamine adverse effects is not well characterized. Urodynamic recordings and electromyography (EMG) studies were performed in aged (>20 years old) and adult (3.9–14.9 years old) female rhesus macaques under an equal and light plane of sedation by constant rate infusion (CRI) of ketamine. A total of 4 of 41 adult subjects (9.7%) showed clinical signs of ketamine-induced abnormal neuromuscular reactivity, whereas a larger portion of 14 of 26 aged subjects showed similar ketamine-induced neuromuscular reactivity (53.8%; P< 0.001). The ketamine CRI rate was 19.8±0.9 mg/kg/h in adults and lower in aged subjects at 16.5±1.4 mg/kg/h (P<0.05). The ketamine CRI rate was negatively correlated with age (r = -0.30, P<0.05, n = 64). The incidence of ketamine reactivity or CRI rate was not different between aged pre-and post-menopausal females. EMG recordings during neuromuscular reactivity showed coordinated activation of multiple muscles, suggesting a central nervous system (CNS) mechanism for ketamine-associated neuromuscular reactivity. The incidence of ketamine-induced neuromuscular reactivity is age related but not affected by the estrous cycle in female rhesus macaques. A coordinated activation of multiple muscles, innervated by different peripheral nerves, suggests that ketamine-induced neuromuscular reactivity originates in the CNS. Public Library of Science 2020-09-21 /pmc/articles/PMC7505584/ /pubmed/32956357 http://dx.doi.org/10.1371/journal.pone.0236430 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Havton, Leif A. Biscola, Natalia P. Christe, Kari L. Colman, Ricki J. Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
title | Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
title_full | Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
title_fullStr | Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
title_full_unstemmed | Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
title_short | Ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
title_sort | ketamine-induced neuromuscular reactivity is associated with aging in female rhesus macaques |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505584/ https://www.ncbi.nlm.nih.gov/pubmed/32956357 http://dx.doi.org/10.1371/journal.pone.0236430 |
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