Overexpression of AT2R in the solitary-vagal complex improves baroreflex in the spontaneously hypertensive rat
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , |
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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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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1813546425391251456 |