Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue

Detalhes bibliográficos
Autor(a) principal: Menani, JoséV. [UNESP]
Data de Publicação: 1988
Outros Autores: Machado, Benedito H., Krieger, Eduardo M., Salgado, Hélio C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/0006-8993(88)90888-8
http://hdl.handle.net/11449/223909
Resumo: We have previously demonstrated a transitory tachycardia during the early phase of one kidney, one clip (1K1C) hypertension in the rat, when the basal heart rate (HR) is measured daily under resting conditions. In the present study, in control rats, marked tachycardia (406 ± 11 vs 320 ± 4 bpm during the control period) was observed on the first day of electrolytic lesion of the anteroventral third ventricle (AV3V) region. The basal HR declined progressively thereafter and was normal 14 days after AV3V lesion. The peak of tachycardia (388 ± 12 bpm) observed 7 days after clipping in sham-lesioned rats did not occur in 1K1C AV3V-lesioned rats (318 ± 5 bpm). However, hypertension was only partially (65%) abolished in the lesioned animals (135 ± 4 vs 160 ± 3 mm Hg in the sham-lesioned 1K1C). Captopril administered per os (30 mg/kg/day) for up to 20 days produced no change in the basal HR of sham-operated rats but abolished the initial tachycardia in 1K1C rats during the development of hypertension. Captopril also delayed the onset of renal hypertension, with mean arterial pressure reaching hypertensive levels only 2 weeks after clipping. These data indicate that integrity of the AV3V region is necessary for the occurrence of tachycardia during the onset of 1K1C hypertension. Since captopril abolished the tachycardia, the activity of converting enzyme seems to be important for the appearance of this phenomenon. © 1988.
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spelling Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissueAngiotensin IIBaroreflexBasal heart rateBlood pressure regulationCaptoprilConverting enzyme inhibitorSympathetic nervous systemWe have previously demonstrated a transitory tachycardia during the early phase of one kidney, one clip (1K1C) hypertension in the rat, when the basal heart rate (HR) is measured daily under resting conditions. In the present study, in control rats, marked tachycardia (406 ± 11 vs 320 ± 4 bpm during the control period) was observed on the first day of electrolytic lesion of the anteroventral third ventricle (AV3V) region. The basal HR declined progressively thereafter and was normal 14 days after AV3V lesion. The peak of tachycardia (388 ± 12 bpm) observed 7 days after clipping in sham-lesioned rats did not occur in 1K1C AV3V-lesioned rats (318 ± 5 bpm). However, hypertension was only partially (65%) abolished in the lesioned animals (135 ± 4 vs 160 ± 3 mm Hg in the sham-lesioned 1K1C). Captopril administered per os (30 mg/kg/day) for up to 20 days produced no change in the basal HR of sham-operated rats but abolished the initial tachycardia in 1K1C rats during the development of hypertension. Captopril also delayed the onset of renal hypertension, with mean arterial pressure reaching hypertensive levels only 2 weeks after clipping. These data indicate that integrity of the AV3V region is necessary for the occurrence of tachycardia during the onset of 1K1C hypertension. Since captopril abolished the tachycardia, the activity of converting enzyme seems to be important for the appearance of this phenomenon. © 1988.Department of Physiology, School of Medicine of Ribeirao Preto, Ribeirao PretoDepartment of Physiology and Pathology, Faculty of Dentistry, UNESP, AraraquaraHeart Institute, University Hosital Medical School, USP, São PauloDepartment of Physiology and Pathology, Faculty of Dentistry, UNESP, AraraquaraUniversidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)Menani, JoséV. [UNESP]Machado, Benedito H.Krieger, Eduardo M.Salgado, Hélio C.2022-04-28T19:53:46Z2022-04-28T19:53:46Z1988-04-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article295-302http://dx.doi.org/10.1016/0006-8993(88)90888-8Brain Research, v. 446, n. 2, p. 295-302, 1988.0006-8993http://hdl.handle.net/11449/22390910.1016/0006-8993(88)90888-82-s2.0-0023898643Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrain Researchinfo:eu-repo/semantics/openAccess2022-04-28T19:53:47Zoai:repositorio.unesp.br:11449/223909Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-28T19:53:47Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
title Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
spellingShingle Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
Menani, JoséV. [UNESP]
Angiotensin II
Baroreflex
Basal heart rate
Blood pressure regulation
Captopril
Converting enzyme inhibitor
Sympathetic nervous system
title_short Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
title_full Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
title_fullStr Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
title_full_unstemmed Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
title_sort Tachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissue
author Menani, JoséV. [UNESP]
author_facet Menani, JoséV. [UNESP]
Machado, Benedito H.
Krieger, Eduardo M.
Salgado, Hélio C.
author_role author
author2 Machado, Benedito H.
Krieger, Eduardo M.
Salgado, Hélio C.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Menani, JoséV. [UNESP]
Machado, Benedito H.
Krieger, Eduardo M.
Salgado, Hélio C.
dc.subject.por.fl_str_mv Angiotensin II
Baroreflex
Basal heart rate
Blood pressure regulation
Captopril
Converting enzyme inhibitor
Sympathetic nervous system
topic Angiotensin II
Baroreflex
Basal heart rate
Blood pressure regulation
Captopril
Converting enzyme inhibitor
Sympathetic nervous system
description We have previously demonstrated a transitory tachycardia during the early phase of one kidney, one clip (1K1C) hypertension in the rat, when the basal heart rate (HR) is measured daily under resting conditions. In the present study, in control rats, marked tachycardia (406 ± 11 vs 320 ± 4 bpm during the control period) was observed on the first day of electrolytic lesion of the anteroventral third ventricle (AV3V) region. The basal HR declined progressively thereafter and was normal 14 days after AV3V lesion. The peak of tachycardia (388 ± 12 bpm) observed 7 days after clipping in sham-lesioned rats did not occur in 1K1C AV3V-lesioned rats (318 ± 5 bpm). However, hypertension was only partially (65%) abolished in the lesioned animals (135 ± 4 vs 160 ± 3 mm Hg in the sham-lesioned 1K1C). Captopril administered per os (30 mg/kg/day) for up to 20 days produced no change in the basal HR of sham-operated rats but abolished the initial tachycardia in 1K1C rats during the development of hypertension. Captopril also delayed the onset of renal hypertension, with mean arterial pressure reaching hypertensive levels only 2 weeks after clipping. These data indicate that integrity of the AV3V region is necessary for the occurrence of tachycardia during the onset of 1K1C hypertension. Since captopril abolished the tachycardia, the activity of converting enzyme seems to be important for the appearance of this phenomenon. © 1988.
publishDate 1988
dc.date.none.fl_str_mv 1988-04-19
2022-04-28T19:53:46Z
2022-04-28T19:53:46Z
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/10.1016/0006-8993(88)90888-8
Brain Research, v. 446, n. 2, p. 295-302, 1988.
0006-8993
http://hdl.handle.net/11449/223909
10.1016/0006-8993(88)90888-8
2-s2.0-0023898643
url http://dx.doi.org/10.1016/0006-8993(88)90888-8
http://hdl.handle.net/11449/223909
identifier_str_mv Brain Research, v. 446, n. 2, p. 295-302, 1988.
0006-8993
10.1016/0006-8993(88)90888-8
2-s2.0-0023898643
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brain Research
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 295-302
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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