Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus)
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.cbpa.2021.110935 http://hdl.handle.net/11449/207487 |
Resumo: | To characterise the effect of two common induction agents, propofol and alfaxalone, on mean arterial blood pressure (MAP) and heart rate (HR), we equipped 19 adult South American rattlesnakes (Crotalus durissus) with an indwelling arterial catheter approximately 24 h prior to recording of baseline resting values. Then, seven snakes received alfaxalone (15 mg kg−1) intravascularly (IV) through the catheter, while groups two and three (both n = 6) received propofol (15 mg kg−1 IV). The first two groups were not handled, while the group 3 was manually restrained for 2 min for a mock injection of 0.2 ml saline into the ventral tail vein. Baseline HR was similar in all groups and handling caused a significant tachycardia (p = 0.031) in group three. When given IV to undisturbed animals, both propofol and alfaxalone induced a significant increase in HR (p = 0.0022 and p = 0.0045, respectively) lasting approximately 30 min, but with values only significantly exceeding baseline for the first 5 min for propofol and the first 10 min with alfaxalone. Handling caused a significant increase in MAP (p = 0.0313). Propofol did not affect MAP (p = 0.1064), while alfaxalone caused a marked hypertension (although only significant at 2 min; p = 0.031). Manual restraint significantly increases both HR and MAP, which may lead to a masking of true cardiovascular effects of anaesthetic agents. |
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Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus)AnaesthesiaBlood pressureCardiovascularDisturbanceHeart rateReptileTo characterise the effect of two common induction agents, propofol and alfaxalone, on mean arterial blood pressure (MAP) and heart rate (HR), we equipped 19 adult South American rattlesnakes (Crotalus durissus) with an indwelling arterial catheter approximately 24 h prior to recording of baseline resting values. Then, seven snakes received alfaxalone (15 mg kg−1) intravascularly (IV) through the catheter, while groups two and three (both n = 6) received propofol (15 mg kg−1 IV). The first two groups were not handled, while the group 3 was manually restrained for 2 min for a mock injection of 0.2 ml saline into the ventral tail vein. Baseline HR was similar in all groups and handling caused a significant tachycardia (p = 0.031) in group three. When given IV to undisturbed animals, both propofol and alfaxalone induced a significant increase in HR (p = 0.0022 and p = 0.0045, respectively) lasting approximately 30 min, but with values only significantly exceeding baseline for the first 5 min for propofol and the first 10 min with alfaxalone. Handling caused a significant increase in MAP (p = 0.0313). Propofol did not affect MAP (p = 0.1064), while alfaxalone caused a marked hypertension (although only significant at 2 min; p = 0.031). Manual restraint significantly increases both HR and MAP, which may lead to a masking of true cardiovascular effects of anaesthetic agents.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Centre for Zoo and Wild Animal Health Copenhagen ZooZoophysiology Department of Biology University of AarhusDepartment of Physiological Sciences UFSCarDepartamento de Zoologia Centro de Aquicultura UNESPDepartamento de Zoologia Centro de Aquicultura UNESPCopenhagen ZooUniversity of AarhusUniversidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (Unesp)Bertelsen, Mads F. [UNESP]Buchanan, Rasmus [UNESP]Jensen, Heidi M. [UNESP]Leite, Cleo A.C. [UNESP]Abe, Augusto S.Wang, Tobias [UNESP]2021-06-25T10:56:03Z2021-06-25T10:56:03Z2021-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.cbpa.2021.110935Comparative Biochemistry and Physiology -Part A : Molecular and Integrative Physiology, v. 256.1531-43321095-6433http://hdl.handle.net/11449/20748710.1016/j.cbpa.2021.1109352-s2.0-85102884032Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengComparative Biochemistry and Physiology -Part A : Molecular and Integrative Physiologyinfo:eu-repo/semantics/openAccess2024-04-09T15:37:12Zoai:repositorio.unesp.br:11449/207487Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-04-09T15:37:12Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
title |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
spellingShingle |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) Bertelsen, Mads F. [UNESP] Anaesthesia Blood pressure Cardiovascular Disturbance Heart rate Reptile |
title_short |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
title_full |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
title_fullStr |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
title_full_unstemmed |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
title_sort |
Pharmacodynamics of propofol and alfaxalone in rattlesnakes (Crotalus durissus) |
author |
Bertelsen, Mads F. [UNESP] |
author_facet |
Bertelsen, Mads F. [UNESP] Buchanan, Rasmus [UNESP] Jensen, Heidi M. [UNESP] Leite, Cleo A.C. [UNESP] Abe, Augusto S. Wang, Tobias [UNESP] |
author_role |
author |
author2 |
Buchanan, Rasmus [UNESP] Jensen, Heidi M. [UNESP] Leite, Cleo A.C. [UNESP] Abe, Augusto S. Wang, Tobias [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Copenhagen Zoo University of Aarhus Universidade Federal de São Carlos (UFSCar) Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Bertelsen, Mads F. [UNESP] Buchanan, Rasmus [UNESP] Jensen, Heidi M. [UNESP] Leite, Cleo A.C. [UNESP] Abe, Augusto S. Wang, Tobias [UNESP] |
dc.subject.por.fl_str_mv |
Anaesthesia Blood pressure Cardiovascular Disturbance Heart rate Reptile |
topic |
Anaesthesia Blood pressure Cardiovascular Disturbance Heart rate Reptile |
description |
To characterise the effect of two common induction agents, propofol and alfaxalone, on mean arterial blood pressure (MAP) and heart rate (HR), we equipped 19 adult South American rattlesnakes (Crotalus durissus) with an indwelling arterial catheter approximately 24 h prior to recording of baseline resting values. Then, seven snakes received alfaxalone (15 mg kg−1) intravascularly (IV) through the catheter, while groups two and three (both n = 6) received propofol (15 mg kg−1 IV). The first two groups were not handled, while the group 3 was manually restrained for 2 min for a mock injection of 0.2 ml saline into the ventral tail vein. Baseline HR was similar in all groups and handling caused a significant tachycardia (p = 0.031) in group three. When given IV to undisturbed animals, both propofol and alfaxalone induced a significant increase in HR (p = 0.0022 and p = 0.0045, respectively) lasting approximately 30 min, but with values only significantly exceeding baseline for the first 5 min for propofol and the first 10 min with alfaxalone. Handling caused a significant increase in MAP (p = 0.0313). Propofol did not affect MAP (p = 0.1064), while alfaxalone caused a marked hypertension (although only significant at 2 min; p = 0.031). Manual restraint significantly increases both HR and MAP, which may lead to a masking of true cardiovascular effects of anaesthetic agents. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-06-25T10:56:03Z 2021-06-25T10:56:03Z 2021-06-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.cbpa.2021.110935 Comparative Biochemistry and Physiology -Part A : Molecular and Integrative Physiology, v. 256. 1531-4332 1095-6433 http://hdl.handle.net/11449/207487 10.1016/j.cbpa.2021.110935 2-s2.0-85102884032 |
url |
http://dx.doi.org/10.1016/j.cbpa.2021.110935 http://hdl.handle.net/11449/207487 |
identifier_str_mv |
Comparative Biochemistry and Physiology -Part A : Molecular and Integrative Physiology, v. 256. 1531-4332 1095-6433 10.1016/j.cbpa.2021.110935 2-s2.0-85102884032 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Comparative Biochemistry and Physiology -Part A : Molecular and Integrative Physiology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1826304389375066112 |