Length dependence of activation studied in the isovolumic blood-perfused dog heart

Detalhes bibliográficos
Autor(a) principal: Tucci, P. J.F.
Data de Publicação: 1984
Outros Autores: Bregagnollo, E. A., Spadaro, J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1161/01.RES.55.1.59
http://hdl.handle.net/11449/219106
Resumo: In studies utilizing the isolated isovolumic blood-perfused canine heart, left ventricular pressure was measured following a sudden expansion of ventricular volume. An increase in performance occurred in two phases: first, there was an instantaneous rise of developed pressure simultaneous with ventricular distension; in the second phase, developed pressure continued to increase for several minutes until a final steady state was reached. The immediate increase in developed pressure occurred with a prolongation of the time-to-peak pressure, and there was no further change of time-to-peak pressure during the time-dependent increase of developed pressure. In another series of experiments, systolic pressure was elevated without changing resting volume, and mechanical performance changed in a different manner: after an increase in systolic load, there was a modest and transient decrease of developed pressure; thereafter, ventricular pressure recovered only to original values. The influence of different degrees of ventricular expansion, calcium, and verapamil were studied. Under higher ventricular dilations the immediate as well as the slow increase of contraction were heightened and the time to reach half of the slow increase was shortened. When ventricular dilation was induced during an infusion of calcium chloride, higher values for the immediate pressure increase were observed, whereas the time-dependent increase and the time to reach half of the slow increase did not change in comparison with control studies. Verapamil decreased the immediate and the time-dependent enhancement of contraction. The time-dependent increase in developed pressure occurs more slowly with verapamil. These findings in the intact heart are in accord with the hypothesis that myocardial stretch is followed by an increase in intracellular calcium stores, and with the concept that the Frank-Starling mechanism involves an activation of the contractile state.
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spelling Length dependence of activation studied in the isovolumic blood-perfused dog heartIn studies utilizing the isolated isovolumic blood-perfused canine heart, left ventricular pressure was measured following a sudden expansion of ventricular volume. An increase in performance occurred in two phases: first, there was an instantaneous rise of developed pressure simultaneous with ventricular distension; in the second phase, developed pressure continued to increase for several minutes until a final steady state was reached. The immediate increase in developed pressure occurred with a prolongation of the time-to-peak pressure, and there was no further change of time-to-peak pressure during the time-dependent increase of developed pressure. In another series of experiments, systolic pressure was elevated without changing resting volume, and mechanical performance changed in a different manner: after an increase in systolic load, there was a modest and transient decrease of developed pressure; thereafter, ventricular pressure recovered only to original values. The influence of different degrees of ventricular expansion, calcium, and verapamil were studied. Under higher ventricular dilations the immediate as well as the slow increase of contraction were heightened and the time to reach half of the slow increase was shortened. When ventricular dilation was induced during an infusion of calcium chloride, higher values for the immediate pressure increase were observed, whereas the time-dependent increase and the time to reach half of the slow increase did not change in comparison with control studies. Verapamil decreased the immediate and the time-dependent enhancement of contraction. The time-dependent increase in developed pressure occurs more slowly with verapamil. These findings in the intact heart are in accord with the hypothesis that myocardial stretch is followed by an increase in intracellular calcium stores, and with the concept that the Frank-Starling mechanism involves an activation of the contractile state.Department of Medicine, Faculty of Medicine of Botucatu, State University 'Julio de Mesquita Filho', Botucatu, Sao PauloUniversidade Estadual Paulista (UNESP)Tucci, P. J.F.Bregagnollo, E. A.Spadaro, J.2022-04-28T18:53:51Z2022-04-28T18:53:51Z1984-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article59-66http://dx.doi.org/10.1161/01.RES.55.1.59Circulation Research, v. 55, n. 1, p. 59-66, 1984.0009-7330http://hdl.handle.net/11449/21910610.1161/01.RES.55.1.592-s2.0-0021141630Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengCirculation Researchinfo:eu-repo/semantics/openAccess2022-04-28T18:53:51Zoai:repositorio.unesp.br:11449/219106Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-05-23T11:51:09.444887Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Length dependence of activation studied in the isovolumic blood-perfused dog heart
title Length dependence of activation studied in the isovolumic blood-perfused dog heart
spellingShingle Length dependence of activation studied in the isovolumic blood-perfused dog heart
Tucci, P. J.F.
title_short Length dependence of activation studied in the isovolumic blood-perfused dog heart
title_full Length dependence of activation studied in the isovolumic blood-perfused dog heart
title_fullStr Length dependence of activation studied in the isovolumic blood-perfused dog heart
title_full_unstemmed Length dependence of activation studied in the isovolumic blood-perfused dog heart
title_sort Length dependence of activation studied in the isovolumic blood-perfused dog heart
author Tucci, P. J.F.
author_facet Tucci, P. J.F.
Bregagnollo, E. A.
Spadaro, J.
author_role author
author2 Bregagnollo, E. A.
Spadaro, J.
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Tucci, P. J.F.
Bregagnollo, E. A.
Spadaro, J.
description In studies utilizing the isolated isovolumic blood-perfused canine heart, left ventricular pressure was measured following a sudden expansion of ventricular volume. An increase in performance occurred in two phases: first, there was an instantaneous rise of developed pressure simultaneous with ventricular distension; in the second phase, developed pressure continued to increase for several minutes until a final steady state was reached. The immediate increase in developed pressure occurred with a prolongation of the time-to-peak pressure, and there was no further change of time-to-peak pressure during the time-dependent increase of developed pressure. In another series of experiments, systolic pressure was elevated without changing resting volume, and mechanical performance changed in a different manner: after an increase in systolic load, there was a modest and transient decrease of developed pressure; thereafter, ventricular pressure recovered only to original values. The influence of different degrees of ventricular expansion, calcium, and verapamil were studied. Under higher ventricular dilations the immediate as well as the slow increase of contraction were heightened and the time to reach half of the slow increase was shortened. When ventricular dilation was induced during an infusion of calcium chloride, higher values for the immediate pressure increase were observed, whereas the time-dependent increase and the time to reach half of the slow increase did not change in comparison with control studies. Verapamil decreased the immediate and the time-dependent enhancement of contraction. The time-dependent increase in developed pressure occurs more slowly with verapamil. These findings in the intact heart are in accord with the hypothesis that myocardial stretch is followed by an increase in intracellular calcium stores, and with the concept that the Frank-Starling mechanism involves an activation of the contractile state.
publishDate 1984
dc.date.none.fl_str_mv 1984-01-01
2022-04-28T18:53:51Z
2022-04-28T18:53:51Z
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/10.1161/01.RES.55.1.59
Circulation Research, v. 55, n. 1, p. 59-66, 1984.
0009-7330
http://hdl.handle.net/11449/219106
10.1161/01.RES.55.1.59
2-s2.0-0021141630
url http://dx.doi.org/10.1161/01.RES.55.1.59
http://hdl.handle.net/11449/219106
identifier_str_mv Circulation Research, v. 55, n. 1, p. 59-66, 1984.
0009-7330
10.1161/01.RES.55.1.59
2-s2.0-0021141630
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Circulation Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 59-66
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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