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Centrally acting antihypertensives change the psychogenic cardiovascular reactivity

dc.contributor.authorMendonça, Michelle M.
dc.contributor.authorCosta, Amanda N.
dc.contributor.authorMoraes, Gean C.A.
dc.contributor.authorMartins, Gustavo M.
dc.contributor.authorAlmeida, Aline F.
dc.contributor.authorRincon, Gabriel C.N.
dc.contributor.authorSiqueira, João P.R.
dc.contributor.authorPadilha, Daniella M.
dc.contributor.authorMoya, Marcela I.
dc.contributor.authorFerreira-Neto, Marcos L.
dc.contributor.authorGomes, Rodrigo Mello
dc.contributor.authorPedrino, Gustavo Rodrigues
dc.contributor.authorFontes, Marco Antônio Peliky
dc.contributor.authorColombari, Eduardo [UNESP]
dc.contributor.authorCrestani, Carlos C. [UNESP]
dc.contributor.authorFajemiroye, James O.
dc.contributor.authorXavier, Carlos Henrique
dc.contributor.institutionFederal University of Goias
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2021-06-25T11:12:32Z
dc.date.available2021-06-25T11:12:32Z
dc.date.issued2021-01-01
dc.description.abstractClonidine (CL) and Rilmenidine (RI) are among the most frequently prescribed centrally acting antihypertensives. Here, we compared CL and RI effects on psychogenic cardiovascular reactivity to sonant, luminous, motosensory, and vibrotactile stimuli during neurogenic hypertension. The femoral artery and vein of Wistar (WT – normotensive) and spontaneously hypertensive rats (SHR) were catheterized before (24 h interval) i.p. injection of vehicle (NaCl 0.9%, control - CT group), CL (10 µg/kg), or RI (10 µg/kg) and acute exposure to luminous (5000 lm), sonant (75 dB sudden tap), motor (180° cage twist), and air-jet (10 L/min – restraint and vibrotactile). Findings showed that: (i) CL or RI reduced the arterial pressure of SHR, without affecting basal heart rate in WT and SHR; (ii) different stimuli evoked pressor and tachycardic responses; (iii) CL and RI reduced pressor response to sound; (iv) CL or RI reduced pressor responses to luminous stimulus without a change in peak tachycardia in SHR; (v) cage twist increased blood pressure in SHR, which was attenuated by CL or RI; (vi) air-jet increased pressure and heart rate; (vii) CL or RI attenuated the pressor responses to air-jet in SHR while RI reduced the chronotropic reactivity in both strains. Altogether, both antihypertensives relieved the psychogenic cardiovascular responses to different stimuli. The RI elicited higher cardioprotective effects through a reduction in air-jet-induced tachycardia.en
dc.description.affiliationInstitute of Biological Sciences Federal University of Goias
dc.description.affiliationSchool of Medicine Federal University of Goias
dc.description.affiliationInstitute of Biomedical Sciences Federal University of Uberlandia
dc.description.affiliationInstitute of Biological Sciences Federal University of Minas Gerais
dc.description.affiliationSchool of Dentistry São Paulo State University (UNESP)
dc.description.affiliationSchool of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.description.affiliationUnespSchool of Dentistry São Paulo State University (UNESP)
dc.description.affiliationUnespSchool of Pharmaceutical Sciences São Paulo State University (UNESP)
dc.identifierhttp://dx.doi.org/10.1111/fcp.12648
dc.identifier.citationFundamental and Clinical Pharmacology.
dc.identifier.doi10.1111/fcp.12648
dc.identifier.issn1472-8206
dc.identifier.issn0767-3981
dc.identifier.scopus2-s2.0-85101770967
dc.identifier.urihttp://hdl.handle.net/11449/208462
dc.language.isoeng
dc.relation.ispartofFundamental and Clinical Pharmacology
dc.sourceScopus
dc.subjectarousal
dc.subjectdefense reactions
dc.subjectheart rate
dc.subjecthypertension
dc.subjectstress
dc.titleCentrally acting antihypertensives change the psychogenic cardiovascular reactivityen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isDepartmentOfPublication.latestForDiscoveryb3ba3d9c-022e-4521-8805-0bcceea7372e
relation.isOrgUnitOfPublicationca4c0298-cd82-48ee-a9c8-c97704bac2b0
relation.isOrgUnitOfPublication.latestForDiscoveryca4c0298-cd82-48ee-a9c8-c97704bac2b0
unesp.author.orcid0000-0001-7375-9999[1]
unesp.author.orcid0000-0002-9695-7100[10]
unesp.author.orcid0000-0002-9012-3287[11]
unesp.author.orcid0000-0003-0488-5400[12]
unesp.author.orcid0000-0003-4525-3565[13]
unesp.author.orcid0000-0002-1395-4036[14]
unesp.author.orcid0000-0002-1942-858X[15]
unesp.author.orcid0000-0001-7440-7581[16]
unesp.author.orcid0000-0003-4006-8213[17]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Odontologia, Araraquarapt
unesp.departmentFisiologia e Patologia - FOARpt

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