Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor

Detalhes bibliográficos
Autor(a) principal: Wang, Tobias
Data de Publicação: 2001
Outros Autores: Taylor, E. W., Andrade, Denis, Abe, Augusto S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/230918
Resumo: Reptiles, particularly snakes, exhibit large and quantitatively similar increments in metabolic rate during muscular exercise and following a meal, when they are apparently inactive. The cardiovascular responses are similar during these two states, but the underlying autonomic control of the heart remains unknown. We describe both adrenergic and cholinergic tonus on the heart during rest, during enforced activity and during digestion (24-36 h after ingestion of 30 % of their body mass) in the snake Boa constrictor. The snakes were equipped with an arterial catheter for measurements of blood pressure and heart rate, and autonomic tonus was determined following infusion of the β-adrenergic antagonist propranolol (3 mg kg-1) and the muscarinic cholinoceptor antagonist atropine (3 mg kg-1). The mean heart rate of fasting animals at rest was 26.4±1.4 min-1, and this increased to 36.1±1.4 min-1 (means ± S.E.M.; N=8) following double autonomic block (atropine and propranolol). The calculated cholinergic and adrenergic tones were 60.1±9.3 % and 19.8±2.2 %, respectively. Heart rate increased to 61.4±1.5 min-1 during enforced activity, and this response was significantly reduced by propranolol (maximum values of 35.8±1.6 min-1), but unaffected by atropine. The cholinergic and adrenergic tones were 2.6±2.2 and 41.3±1.9 % during activity, respectively. Double autonomic block virtually abolished tachycardia associated with enforced activity (heart rate increased significantly from 36.1±1.4 to 37.6±1.3 min-1), indicating that non-adrenergic, non-cholinergic effectors are not involved in regulating heart rate during activity. Blood pressure also increased during activity. Digestion was accompanied by an increase in heart rate from 25.6±1.3 to 47.7±2.2 min-1 (N=8). In these animals, heart rate decreased to 44.2±2.7 min-1 following propranolol infusion and increased to 53.9±1.8 min-1 after infusion of atropine, resulting in small cholinergic and adrenergic tones (6.0±3.5 and 11.1±1.1 %, respectively). The heart rate of digesting snakes was 47.0±1.0 min-1 after double autonomic blockade, which is significantly higher than the value of 36.1±1.4 min-1 in double-blocked fasting animals at rest. Therefore, it appears that some other factor exerts a positive chronotropic effect during digestion, and we propose that this factor may be a circulating regulatory peptide, possibly liberated from the gastrointestinal system in response to the presence of food.
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spelling Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictorAtropineAutonomic controlBlood pressureBoa constrictorExerciseFeedingHeart ratePropranololReptileSnakeReptiles, particularly snakes, exhibit large and quantitatively similar increments in metabolic rate during muscular exercise and following a meal, when they are apparently inactive. The cardiovascular responses are similar during these two states, but the underlying autonomic control of the heart remains unknown. We describe both adrenergic and cholinergic tonus on the heart during rest, during enforced activity and during digestion (24-36 h after ingestion of 30 % of their body mass) in the snake Boa constrictor. The snakes were equipped with an arterial catheter for measurements of blood pressure and heart rate, and autonomic tonus was determined following infusion of the β-adrenergic antagonist propranolol (3 mg kg-1) and the muscarinic cholinoceptor antagonist atropine (3 mg kg-1). The mean heart rate of fasting animals at rest was 26.4±1.4 min-1, and this increased to 36.1±1.4 min-1 (means ± S.E.M.; N=8) following double autonomic block (atropine and propranolol). The calculated cholinergic and adrenergic tones were 60.1±9.3 % and 19.8±2.2 %, respectively. Heart rate increased to 61.4±1.5 min-1 during enforced activity, and this response was significantly reduced by propranolol (maximum values of 35.8±1.6 min-1), but unaffected by atropine. The cholinergic and adrenergic tones were 2.6±2.2 and 41.3±1.9 % during activity, respectively. Double autonomic block virtually abolished tachycardia associated with enforced activity (heart rate increased significantly from 36.1±1.4 to 37.6±1.3 min-1), indicating that non-adrenergic, non-cholinergic effectors are not involved in regulating heart rate during activity. Blood pressure also increased during activity. Digestion was accompanied by an increase in heart rate from 25.6±1.3 to 47.7±2.2 min-1 (N=8). In these animals, heart rate decreased to 44.2±2.7 min-1 following propranolol infusion and increased to 53.9±1.8 min-1 after infusion of atropine, resulting in small cholinergic and adrenergic tones (6.0±3.5 and 11.1±1.1 %, respectively). The heart rate of digesting snakes was 47.0±1.0 min-1 after double autonomic blockade, which is significantly higher than the value of 36.1±1.4 min-1 in double-blocked fasting animals at rest. Therefore, it appears that some other factor exerts a positive chronotropic effect during digestion, and we propose that this factor may be a circulating regulatory peptide, possibly liberated from the gastrointestinal system in response to the presence of food.Department of Zoology, UNESP Rio ClaroUniversidade Estadual Paulista (UNESP)Wang, TobiasTaylor, E. W.Andrade, DenisAbe, Augusto S.2022-04-29T08:42:45Z2022-04-29T08:42:45Z2001-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article3553-3560Journal of Experimental Biology, v. 204, n. 20, p. 3553-3560, 2001.0022-0949http://hdl.handle.net/11449/2309182-s2.0-0035745826Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Experimental Biologyinfo:eu-repo/semantics/openAccess2022-04-29T08:42:45Zoai:repositorio.unesp.br:11449/230918Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-29T08:42:45Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
title Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
spellingShingle Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
Wang, Tobias
Atropine
Autonomic control
Blood pressure
Boa constrictor
Exercise
Feeding
Heart rate
Propranolol
Reptile
Snake
title_short Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
title_full Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
title_fullStr Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
title_full_unstemmed Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
title_sort Autonomic control of heart rate during forced activity and digestion in the snake Boa constrictor
author Wang, Tobias
author_facet Wang, Tobias
Taylor, E. W.
Andrade, Denis
Abe, Augusto S.
author_role author
author2 Taylor, E. W.
Andrade, Denis
Abe, Augusto S.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Wang, Tobias
Taylor, E. W.
Andrade, Denis
Abe, Augusto S.
dc.subject.por.fl_str_mv Atropine
Autonomic control
Blood pressure
Boa constrictor
Exercise
Feeding
Heart rate
Propranolol
Reptile
Snake
topic Atropine
Autonomic control
Blood pressure
Boa constrictor
Exercise
Feeding
Heart rate
Propranolol
Reptile
Snake
description Reptiles, particularly snakes, exhibit large and quantitatively similar increments in metabolic rate during muscular exercise and following a meal, when they are apparently inactive. The cardiovascular responses are similar during these two states, but the underlying autonomic control of the heart remains unknown. We describe both adrenergic and cholinergic tonus on the heart during rest, during enforced activity and during digestion (24-36 h after ingestion of 30 % of their body mass) in the snake Boa constrictor. The snakes were equipped with an arterial catheter for measurements of blood pressure and heart rate, and autonomic tonus was determined following infusion of the β-adrenergic antagonist propranolol (3 mg kg-1) and the muscarinic cholinoceptor antagonist atropine (3 mg kg-1). The mean heart rate of fasting animals at rest was 26.4±1.4 min-1, and this increased to 36.1±1.4 min-1 (means ± S.E.M.; N=8) following double autonomic block (atropine and propranolol). The calculated cholinergic and adrenergic tones were 60.1±9.3 % and 19.8±2.2 %, respectively. Heart rate increased to 61.4±1.5 min-1 during enforced activity, and this response was significantly reduced by propranolol (maximum values of 35.8±1.6 min-1), but unaffected by atropine. The cholinergic and adrenergic tones were 2.6±2.2 and 41.3±1.9 % during activity, respectively. Double autonomic block virtually abolished tachycardia associated with enforced activity (heart rate increased significantly from 36.1±1.4 to 37.6±1.3 min-1), indicating that non-adrenergic, non-cholinergic effectors are not involved in regulating heart rate during activity. Blood pressure also increased during activity. Digestion was accompanied by an increase in heart rate from 25.6±1.3 to 47.7±2.2 min-1 (N=8). In these animals, heart rate decreased to 44.2±2.7 min-1 following propranolol infusion and increased to 53.9±1.8 min-1 after infusion of atropine, resulting in small cholinergic and adrenergic tones (6.0±3.5 and 11.1±1.1 %, respectively). The heart rate of digesting snakes was 47.0±1.0 min-1 after double autonomic blockade, which is significantly higher than the value of 36.1±1.4 min-1 in double-blocked fasting animals at rest. Therefore, it appears that some other factor exerts a positive chronotropic effect during digestion, and we propose that this factor may be a circulating regulatory peptide, possibly liberated from the gastrointestinal system in response to the presence of food.
publishDate 2001
dc.date.none.fl_str_mv 2001-12-01
2022-04-29T08:42:45Z
2022-04-29T08:42:45Z
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 Journal of Experimental Biology, v. 204, n. 20, p. 3553-3560, 2001.
0022-0949
http://hdl.handle.net/11449/230918
2-s2.0-0035745826
identifier_str_mv Journal of Experimental Biology, v. 204, n. 20, p. 3553-3560, 2001.
0022-0949
2-s2.0-0035745826
url http://hdl.handle.net/11449/230918
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Experimental Biology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 3553-3560
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
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