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

dc.contributor.authorMenani, JoséV. [UNESP]
dc.contributor.authorMachado, Benedito H.
dc.contributor.authorKrieger, Eduardo M.
dc.contributor.authorSalgado, Hélio C.
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2022-04-28T19:53:46Z
dc.date.available2022-04-28T19:53:46Z
dc.date.issued1988-04-19
dc.description.abstractWe 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.en
dc.description.affiliationDepartment of Physiology, School of Medicine of Ribeirao Preto, Ribeirao Preto
dc.description.affiliationDepartment of Physiology and Pathology, Faculty of Dentistry, UNESP, Araraquara
dc.description.affiliationHeart Institute, University Hosital Medical School, USP, São Paulo
dc.description.affiliationUnespDepartment of Physiology and Pathology, Faculty of Dentistry, UNESP, Araraquara
dc.format.extent295-302
dc.identifierhttp://dx.doi.org/10.1016/0006-8993(88)90888-8
dc.identifier.citationBrain Research, v. 446, n. 2, p. 295-302, 1988.
dc.identifier.doi10.1016/0006-8993(88)90888-8
dc.identifier.issn0006-8993
dc.identifier.scopus2-s2.0-0023898643
dc.identifier.urihttp://hdl.handle.net/11449/223909
dc.language.isoeng
dc.relation.ispartofBrain Research
dc.sourceScopus
dc.subjectAngiotensin II
dc.subjectBaroreflex
dc.subjectBasal heart rate
dc.subjectBlood pressure regulation
dc.subjectCaptopril
dc.subjectConverting enzyme inhibitor
dc.subjectSympathetic nervous system
dc.titleTachycardia during the onset of one-kidney, one-clip renal hypertension: role of the renin-angiotensin system and AV3V tissueen
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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