Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats

Detalhes bibliográficos
Autor(a) principal: Barbosa, Rafaela Moreira [UNESP]
Data de Publicação: 2017
Outros Autores: Speretta, Guilherme F. [UNESP], Martins Dias, Daniel Penteado, Ruchaya, Prashant Jay [UNESP], Li, Hongwei, Menani, Jose Vanderlei [UNESP], Sumners, Colin, 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/10.1093/ajh/hpx001
http://hdl.handle.net/11449/162833
Resumo: BACKGROUND Macrophage migration inhibitory factor (MIF) is an intracellular inhibitory regulator of the actions of angiotensin II in the central nervous system. Renovascular hypertensive 2-kidney, 1-clip (2K1C) rats have an increased activity of the renin-angiotensin system and a decrease in baroreflex function compared to normotensive (NT) rats. In the present study, we tested the effects of MIF overexpression within the nucleus of the solitary tract (NTS), a key brainstem region for cardiovascular regulation, on the development of hypertension, on baroreflex function, and on water and food intake in 2K1C rats. METHODS Holtzman NT rats received a silver clip around the left renal artery to induce 2K1C hypertension. Three weeks later, rats were microinjected in the NTS with AAV2-CBA-MIF, to increase the expression of MIF, or with the control vector AAV2-CBA-enhanced green fluorescent protein. Mean arterial pressure (MAP) and heart rate were recorded by telemetry. Baroreflex function was tested, and water and food intake were also measured. RESULTS Increasing MIF expression in the NTS of 2K1C rats attenuated the development of hypertension, reversed the impairment of baroreflex function, and reduced the increase in water intake. In contrast to 2K1C rats, similar increases in MIF expression in the NTS of NT rats produced no changes in baseline MAP, baroreflex function, or water intake. CONCLUSIONS These results indicate that an increased expression of MIF within the NTS attenuates the development of hypertension and restores the baroreflex function in 2K1C rats.
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spelling Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Ratsangiotensin IIAT1 receptorbaroreflexblood pressurebrainstemhypertension2K1CBACKGROUND Macrophage migration inhibitory factor (MIF) is an intracellular inhibitory regulator of the actions of angiotensin II in the central nervous system. Renovascular hypertensive 2-kidney, 1-clip (2K1C) rats have an increased activity of the renin-angiotensin system and a decrease in baroreflex function compared to normotensive (NT) rats. In the present study, we tested the effects of MIF overexpression within the nucleus of the solitary tract (NTS), a key brainstem region for cardiovascular regulation, on the development of hypertension, on baroreflex function, and on water and food intake in 2K1C rats. METHODS Holtzman NT rats received a silver clip around the left renal artery to induce 2K1C hypertension. Three weeks later, rats were microinjected in the NTS with AAV2-CBA-MIF, to increase the expression of MIF, or with the control vector AAV2-CBA-enhanced green fluorescent protein. Mean arterial pressure (MAP) and heart rate were recorded by telemetry. Baroreflex function was tested, and water and food intake were also measured. RESULTS Increasing MIF expression in the NTS of 2K1C rats attenuated the development of hypertension, reversed the impairment of baroreflex function, and reduced the increase in water intake. In contrast to 2K1C rats, similar increases in MIF expression in the NTS of NT rats produced no changes in baseline MAP, baroreflex function, or water intake. CONCLUSIONS These results indicate that an increased expression of MIF within the NTS attenuates the development of hypertension and restores the baroreflex function in 2K1C rats.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)NIHSao Paulo State Univ, Sch Dent, Dept Physiol & Pathol, Araraquara, SP, BrazilUniv Sao Paulo, Ribeirao Preto Med Sch, Dept Physiol, Ribeirao Preto, SP, BrazilSouthern Med Univ, Sch Biotechnol, Guangzhou, Guangdong, Peoples R ChinaUniv Florida, Coll Med, Dept Physiol & Funct Genom, Gainesville, FL USASao Paulo State Univ, Sch Dent, Dept Physiol & Pathol, Araraquara, SP, BrazilCNPq: 473108/2011-9CNPq: 304918/2011-3FAPESP: 2011/50770-1FAPESP: 2015/23467-7NIH: HL-076803Oxford Univ PressUniversidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Southern Med UnivUniv FloridaBarbosa, Rafaela Moreira [UNESP]Speretta, Guilherme F. [UNESP]Martins Dias, Daniel PenteadoRuchaya, Prashant Jay [UNESP]Li, HongweiMenani, Jose Vanderlei [UNESP]Sumners, ColinColombari, Eduardo [UNESP]Colombari, Debora S. A. [UNESP]2018-11-26T17:33:01Z2018-11-26T17:33:01Z2017-04-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article435-443application/pdfhttp://dx.doi.org/10.1093/ajh/hpx001American Journal Of Hypertension. Oxford: Oxford Univ Press, v. 30, n. 4, p. 435-443, 2017.0895-7061http://hdl.handle.net/11449/16283310.1093/ajh/hpx001WOS:000402054800017WOS000402054800017.pdfWeb of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAmerican Journal Of Hypertension1,322info:eu-repo/semantics/openAccess2023-12-28T06:19:57Zoai:repositorio.unesp.br:11449/162833Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-28T06:19:57Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
title Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
spellingShingle Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
Barbosa, Rafaela Moreira [UNESP]
angiotensin II
AT1 receptor
baroreflex
blood pressure
brainstem
hypertension
2K1C
title_short Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
title_full Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
title_fullStr Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
title_full_unstemmed Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
title_sort Increased Expression of Macrophage Migration Inhibitory Factor in the Nucleus of the Solitary Tract Attenuates Renovascular Hypertension in Rats
author Barbosa, Rafaela Moreira [UNESP]
author_facet Barbosa, Rafaela Moreira [UNESP]
Speretta, Guilherme F. [UNESP]
Martins Dias, Daniel Penteado
Ruchaya, Prashant Jay [UNESP]
Li, Hongwei
Menani, Jose Vanderlei [UNESP]
Sumners, Colin
Colombari, Eduardo [UNESP]
Colombari, Debora S. A. [UNESP]
author_role author
author2 Speretta, Guilherme F. [UNESP]
Martins Dias, Daniel Penteado
Ruchaya, Prashant Jay [UNESP]
Li, Hongwei
Menani, Jose Vanderlei [UNESP]
Sumners, Colin
Colombari, Eduardo [UNESP]
Colombari, Debora S. A. [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
Southern Med Univ
Univ Florida
dc.contributor.author.fl_str_mv Barbosa, Rafaela Moreira [UNESP]
Speretta, Guilherme F. [UNESP]
Martins Dias, Daniel Penteado
Ruchaya, Prashant Jay [UNESP]
Li, Hongwei
Menani, Jose Vanderlei [UNESP]
Sumners, Colin
Colombari, Eduardo [UNESP]
Colombari, Debora S. A. [UNESP]
dc.subject.por.fl_str_mv angiotensin II
AT1 receptor
baroreflex
blood pressure
brainstem
hypertension
2K1C
topic angiotensin II
AT1 receptor
baroreflex
blood pressure
brainstem
hypertension
2K1C
description BACKGROUND Macrophage migration inhibitory factor (MIF) is an intracellular inhibitory regulator of the actions of angiotensin II in the central nervous system. Renovascular hypertensive 2-kidney, 1-clip (2K1C) rats have an increased activity of the renin-angiotensin system and a decrease in baroreflex function compared to normotensive (NT) rats. In the present study, we tested the effects of MIF overexpression within the nucleus of the solitary tract (NTS), a key brainstem region for cardiovascular regulation, on the development of hypertension, on baroreflex function, and on water and food intake in 2K1C rats. METHODS Holtzman NT rats received a silver clip around the left renal artery to induce 2K1C hypertension. Three weeks later, rats were microinjected in the NTS with AAV2-CBA-MIF, to increase the expression of MIF, or with the control vector AAV2-CBA-enhanced green fluorescent protein. Mean arterial pressure (MAP) and heart rate were recorded by telemetry. Baroreflex function was tested, and water and food intake were also measured. RESULTS Increasing MIF expression in the NTS of 2K1C rats attenuated the development of hypertension, reversed the impairment of baroreflex function, and reduced the increase in water intake. In contrast to 2K1C rats, similar increases in MIF expression in the NTS of NT rats produced no changes in baseline MAP, baroreflex function, or water intake. CONCLUSIONS These results indicate that an increased expression of MIF within the NTS attenuates the development of hypertension and restores the baroreflex function in 2K1C rats.
publishDate 2017
dc.date.none.fl_str_mv 2017-04-01
2018-11-26T17:33:01Z
2018-11-26T17:33:01Z
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/10.1093/ajh/hpx001
American Journal Of Hypertension. Oxford: Oxford Univ Press, v. 30, n. 4, p. 435-443, 2017.
0895-7061
http://hdl.handle.net/11449/162833
10.1093/ajh/hpx001
WOS:000402054800017
WOS000402054800017.pdf
url http://dx.doi.org/10.1093/ajh/hpx001
http://hdl.handle.net/11449/162833
identifier_str_mv American Journal Of Hypertension. Oxford: Oxford Univ Press, v. 30, n. 4, p. 435-443, 2017.
0895-7061
10.1093/ajh/hpx001
WOS:000402054800017
WOS000402054800017.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv American Journal Of Hypertension
1,322
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 435-443
application/pdf
dc.publisher.none.fl_str_mv Oxford Univ Press
publisher.none.fl_str_mv Oxford Univ Press
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
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