Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat

Detalhes bibliográficos
Autor(a) principal: Ruchaya, Prashant J. [UNESP]
Data de Publicação: 2016
Outros Autores: Speretta, Guilherme F. [UNESP], Blanch, Graziela Torres [UNESP], Li, Hongwei, Sumners, Colin, Menani, Jose V. [UNESP], Colombari, Eduardo [UNESP], Colombari, Debora S. A. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.npep.2016.06.006
http://hdl.handle.net/11449/162228
Resumo: The aim of this study was to investigate the physiological effects of increased angiotensin II type 2 receptor (AT2R) expression in the solitary-vagal complex (nucleus of the solitary tract/dorsal motor nucleus of the vagus; NTS/DVM) on baroreflex function in non-anaesthetised normotensive (NT) and spontaneously hypertensive rats (SHR). Ten week old NT Holtzman and SHR were microinjected with either an adeno-associated virus expressing AT2R (AAV2-CBA-AT2R) or enhanced green fluorescent protein (control; AAV2-CBA-eGFP) into the NTS/DVM. Baroreflex and telemetry recordings were performed on four experimental groups: 1) NTeGFP, 2) NTAT2R, 3) SHReGFP and 4) SHRAT2R (n = 4-7/group). Following in-vivo experimental procedures, brains were harvested for gene expression analysis. Impaired bradycardia in SHReGFP was restored in SHR rats over-expressing AT2R in the NTS/DMV. mRNA levels of angiotensin converting enzyme decreased and angiotensin converting enzyme 2 increased in the NTS/DMV of SHRAT2R compared to SHReGFP. Increased levels of pro inflammatory cytokine mRNA levels in the SHReGFP group also decreased in the SHRAT2R group. AT2R overexpression did not elicit any significant change in mean arterial pressure (MAP) in all groups from baseline to 4 weeks post viral transfection. Both SHReGFP and SHRAT2R showed a significant elevation in MAP compared to the NTeGFP and NTAT2R groups. Increased AT2R expression within the NTS/DMV of SHR was effective at improving baroreflex function but not MAP. We propose possible mediators involved in improving baroreflex are in the ANG II/ACE2 axis, suggesting a potential beneficial modulatory effect of AT2R overexpression in the NTS/DMV of neurogenic hypertensive rats. (C) 2016 Elsevier Ltd. All rights reserved.
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spelling Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive ratHypertensionACE2BaroreflexAngiotensin IIAngiotensin receptorNTSThe aim of this study was to investigate the physiological effects of increased angiotensin II type 2 receptor (AT2R) expression in the solitary-vagal complex (nucleus of the solitary tract/dorsal motor nucleus of the vagus; NTS/DVM) on baroreflex function in non-anaesthetised normotensive (NT) and spontaneously hypertensive rats (SHR). Ten week old NT Holtzman and SHR were microinjected with either an adeno-associated virus expressing AT2R (AAV2-CBA-AT2R) or enhanced green fluorescent protein (control; AAV2-CBA-eGFP) into the NTS/DVM. Baroreflex and telemetry recordings were performed on four experimental groups: 1) NTeGFP, 2) NTAT2R, 3) SHReGFP and 4) SHRAT2R (n = 4-7/group). Following in-vivo experimental procedures, brains were harvested for gene expression analysis. Impaired bradycardia in SHReGFP was restored in SHR rats over-expressing AT2R in the NTS/DMV. mRNA levels of angiotensin converting enzyme decreased and angiotensin converting enzyme 2 increased in the NTS/DMV of SHRAT2R compared to SHReGFP. Increased levels of pro inflammatory cytokine mRNA levels in the SHReGFP group also decreased in the SHRAT2R group. AT2R overexpression did not elicit any significant change in mean arterial pressure (MAP) in all groups from baseline to 4 weeks post viral transfection. Both SHReGFP and SHRAT2R showed a significant elevation in MAP compared to the NTeGFP and NTAT2R groups. Increased AT2R expression within the NTS/DMV of SHR was effective at improving baroreflex function but not MAP. We propose possible mediators involved in improving baroreflex are in the ANG II/ACE2 axis, suggesting a potential beneficial modulatory effect of AT2R overexpression in the NTS/DMV of neurogenic hypertensive rats. (C) 2016 Elsevier Ltd. All rights reserved.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)NIHSao Paulo State Univ, Sch Dent, Dept Physiol & Pathol, Araraquara, SP, BrazilSouthern Med Univ, Sch Biotechnol, Guangzhou, Guangdong, Peoples R ChinaUniv Florida, Coll Med, Dept Physiol & Funct Genom, Gainesville, FL USAUniv Florida, Coll Med, McKnight Brain Inst, Gainesville, FL USASao Paulo State Univ, Sch Dent, Dept Physiol & Pathol, Araraquara, SP, BrazilCNPq: 473108/2011-9CNPq: 304918/2011-3FAPESP: 2011/50770-1FAPESP: 2012/23546-6FAPESP: 2013/50121-9CAPES: 2053/2013NIH: HL-076803Churchill LivingstoneUniversidade Estadual Paulista (Unesp)Southern Med UnivUniv FloridaRuchaya, Prashant J. [UNESP]Speretta, Guilherme F. [UNESP]Blanch, Graziela Torres [UNESP]Li, HongweiSumners, ColinMenani, Jose V. [UNESP]Colombari, Eduardo [UNESP]Colombari, Debora S. A. [UNESP]2018-11-26T17:13:47Z2018-11-26T17:13:47Z2016-12-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article29-36application/pdfhttp://dx.doi.org/10.1016/j.npep.2016.06.006Neuropeptides. Edinburgh: Churchill Livingstone, v. 60, p. 29-36, 2016.0143-4179http://hdl.handle.net/11449/16222810.1016/j.npep.2016.06.006WOS:000389398800005WOS000389398800005.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengNeuropeptides1,038info:eu-repo/semantics/openAccess2024-09-27T14:04:58Zoai:repositorio.unesp.br:11449/162228Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:04:58Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
title Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
spellingShingle Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
Ruchaya, Prashant J. [UNESP]
Hypertension
ACE2
Baroreflex
Angiotensin II
Angiotensin receptor
NTS
title_short Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
title_full Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
title_fullStr Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
title_full_unstemmed Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
title_sort Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
author Ruchaya, Prashant J. [UNESP]
author_facet Ruchaya, Prashant J. [UNESP]
Speretta, Guilherme F. [UNESP]
Blanch, Graziela Torres [UNESP]
Li, Hongwei
Sumners, Colin
Menani, Jose V. [UNESP]
Colombari, Eduardo [UNESP]
Colombari, Debora S. A. [UNESP]
author_role author
author2 Speretta, Guilherme F. [UNESP]
Blanch, Graziela Torres [UNESP]
Li, Hongwei
Sumners, Colin
Menani, Jose V. [UNESP]
Colombari, Eduardo [UNESP]
Colombari, Debora S. A. [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Southern Med Univ
Univ Florida
dc.contributor.author.fl_str_mv Ruchaya, Prashant J. [UNESP]
Speretta, Guilherme F. [UNESP]
Blanch, Graziela Torres [UNESP]
Li, Hongwei
Sumners, Colin
Menani, Jose V. [UNESP]
Colombari, Eduardo [UNESP]
Colombari, Debora S. A. [UNESP]
dc.subject.por.fl_str_mv Hypertension
ACE2
Baroreflex
Angiotensin II
Angiotensin receptor
NTS
topic Hypertension
ACE2
Baroreflex
Angiotensin II
Angiotensin receptor
NTS
description The aim of this study was to investigate the physiological effects of increased angiotensin II type 2 receptor (AT2R) expression in the solitary-vagal complex (nucleus of the solitary tract/dorsal motor nucleus of the vagus; NTS/DVM) on baroreflex function in non-anaesthetised normotensive (NT) and spontaneously hypertensive rats (SHR). Ten week old NT Holtzman and SHR were microinjected with either an adeno-associated virus expressing AT2R (AAV2-CBA-AT2R) or enhanced green fluorescent protein (control; AAV2-CBA-eGFP) into the NTS/DVM. Baroreflex and telemetry recordings were performed on four experimental groups: 1) NTeGFP, 2) NTAT2R, 3) SHReGFP and 4) SHRAT2R (n = 4-7/group). Following in-vivo experimental procedures, brains were harvested for gene expression analysis. Impaired bradycardia in SHReGFP was restored in SHR rats over-expressing AT2R in the NTS/DMV. mRNA levels of angiotensin converting enzyme decreased and angiotensin converting enzyme 2 increased in the NTS/DMV of SHRAT2R compared to SHReGFP. Increased levels of pro inflammatory cytokine mRNA levels in the SHReGFP group also decreased in the SHRAT2R group. AT2R overexpression did not elicit any significant change in mean arterial pressure (MAP) in all groups from baseline to 4 weeks post viral transfection. Both SHReGFP and SHRAT2R showed a significant elevation in MAP compared to the NTeGFP and NTAT2R groups. Increased AT2R expression within the NTS/DMV of SHR was effective at improving baroreflex function but not MAP. We propose possible mediators involved in improving baroreflex are in the ANG II/ACE2 axis, suggesting a potential beneficial modulatory effect of AT2R overexpression in the NTS/DMV of neurogenic hypertensive rats. (C) 2016 Elsevier Ltd. All rights reserved.
publishDate 2016
dc.date.none.fl_str_mv 2016-12-01
2018-11-26T17:13:47Z
2018-11-26T17:13:47Z
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/j.npep.2016.06.006
Neuropeptides. Edinburgh: Churchill Livingstone, v. 60, p. 29-36, 2016.
0143-4179
http://hdl.handle.net/11449/162228
10.1016/j.npep.2016.06.006
WOS:000389398800005
WOS000389398800005.pdf
url http://dx.doi.org/10.1016/j.npep.2016.06.006
http://hdl.handle.net/11449/162228
identifier_str_mv Neuropeptides. Edinburgh: Churchill Livingstone, v. 60, p. 29-36, 2016.
0143-4179
10.1016/j.npep.2016.06.006
WOS:000389398800005
WOS000389398800005.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Neuropeptides
1,038
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 29-36
application/pdf
dc.publisher.none.fl_str_mv Churchill Livingstone
publisher.none.fl_str_mv Churchill Livingstone
dc.source.none.fl_str_mv Web of Science
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 repositoriounesp@unesp.br
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