Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus

Detalhes bibliográficos
Autor(a) principal: Silva, Camila Zambone Cardoso da [UNESP]
Data de Publicação: 2011
Outros Autores: Menani, José Vanderlei [UNESP], Callera, João Carlos [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.brainresbull.2011.09.003
http://hdl.handle.net/11449/14998
Resumo: GABA(A) and GABA(B) receptors activation with agonists muscimol and baclofen, respectively in the lateral parabrachial nucleus (LPBN), induces water and hypertonic NaCl intake in rats. The purpose of this study was to examine the effects of previous injections of losartan (AT(1) angiotensin receptor antagonist) into the LPBN on 0.3 M NaCl and water intake induced by baclofen injected bilaterally in the same area in fluid replete rats and in rats treated with the diuretic furosemide combined with a low dose of the angiotensin-converting enzyme inhibitor captopril injected subcutaneously. Male Wistar rats with stainless steel cannulas implanted bilaterally into the LPBN were used. Bilateral injections of baclofen (0.5 nmol/0.2 mu l, n=6) into the LPBN in fluid replete rats induced 0.3 M NaCl intake (22.4 +/- 6.5 vs. saline: 0.1 +/- 0.1 ml/210 min) and water intake (14.2 +/- 4.0 vs. saline: 0.6 +/- 0.6 ml/210 min) and pre-treatment of the LPBN with losartan (50 mu g/0.2 mu l,l) reduced 0.3 M NaCl intake (7.4 +/- 7.0 ml/210 min) and water intake (2.8 +/- 2.4 ml/210 min) induced by baclofen. In rats treated with furosemide + captopril, pre-treatment with losartan into the LPBN attenuated the increase in 0.3 M NaCl intake (13.3 +/- 3.2 vs. saline + baclofen: 24.3 +/- 3.9 ml/180 min) and water intake (4.8 +/- 2.1 vs. saline + baclofen: 19.5 +/- 6.6 ml/180 min) produced by baclofen. We conclude that baclofen may produce a non-specific blockade of the inhibitory mechanisms of LPBN (deactivation of LPBN inhibitory mechanisms) and this blockade is facilitated by angiotensin II acting on AT(1) receptors in the LPBN, which drives rats to ingest large amounts of water and hypertonic NaCl independent if rats are fluid depleted or normohydrated. (C) 2011 Elsevier B.V. All rights reserved.
id UNSP_d5c8dbbc00a6bdc34c1e58e960a09d6c
oai_identifier_str oai:repositorio.unesp.br:11449/14998
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleusGABA receptorsAngiotensin IILosartanBaclofenSodium appetiteThirstLateral parabrachial nucleusGABA(A) and GABA(B) receptors activation with agonists muscimol and baclofen, respectively in the lateral parabrachial nucleus (LPBN), induces water and hypertonic NaCl intake in rats. The purpose of this study was to examine the effects of previous injections of losartan (AT(1) angiotensin receptor antagonist) into the LPBN on 0.3 M NaCl and water intake induced by baclofen injected bilaterally in the same area in fluid replete rats and in rats treated with the diuretic furosemide combined with a low dose of the angiotensin-converting enzyme inhibitor captopril injected subcutaneously. Male Wistar rats with stainless steel cannulas implanted bilaterally into the LPBN were used. Bilateral injections of baclofen (0.5 nmol/0.2 mu l, n=6) into the LPBN in fluid replete rats induced 0.3 M NaCl intake (22.4 +/- 6.5 vs. saline: 0.1 +/- 0.1 ml/210 min) and water intake (14.2 +/- 4.0 vs. saline: 0.6 +/- 0.6 ml/210 min) and pre-treatment of the LPBN with losartan (50 mu g/0.2 mu l,l) reduced 0.3 M NaCl intake (7.4 +/- 7.0 ml/210 min) and water intake (2.8 +/- 2.4 ml/210 min) induced by baclofen. In rats treated with furosemide + captopril, pre-treatment with losartan into the LPBN attenuated the increase in 0.3 M NaCl intake (13.3 +/- 3.2 vs. saline + baclofen: 24.3 +/- 3.9 ml/180 min) and water intake (4.8 +/- 2.1 vs. saline + baclofen: 19.5 +/- 6.6 ml/180 min) produced by baclofen. We conclude that baclofen may produce a non-specific blockade of the inhibitory mechanisms of LPBN (deactivation of LPBN inhibitory mechanisms) and this blockade is facilitated by angiotensin II acting on AT(1) receptors in the LPBN, which drives rats to ingest large amounts of water and hypertonic NaCl independent if rats are fluid depleted or normohydrated. (C) 2011 Elsevier B.V. All rights reserved.Brazilian publicFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fundação para o Desenvolvimento da UNESP (FUNDUNESP)Univ Estadual Paulista, Sch Dent, Dept Basic Sci, BR-16018805 São Paulo, BrazilUniv Estadual Paulista, Sch Dent, Dept Physiol & Pathol, BR-16018805 São Paulo, BrazilUniv Estadual Paulista, Sch Dent, Dept Basic Sci, BR-16018805 São Paulo, BrazilUniv Estadual Paulista, Sch Dent, Dept Physiol & Pathol, BR-16018805 São Paulo, BrazilFAPESP: 07/56280-0Pergamon-Elsevier B.V. LtdUniversidade Estadual Paulista (Unesp)Silva, Camila Zambone Cardoso da [UNESP]Menani, José Vanderlei [UNESP]Callera, João Carlos [UNESP]2013-09-30T18:29:19Z2014-05-20T13:43:05Z2013-09-30T18:29:19Z2014-05-20T13:43:05Z2011-11-25info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article348-354application/pdfhttp://dx.doi.org/10.1016/j.brainresbull.2011.09.003Brain Research Bulletin. Oxford: Pergamon-Elsevier B.V. Ltd, v. 86, n. 5-6, p. 348-354, 2011.0361-9230http://hdl.handle.net/11449/1499810.1016/j.brainresbull.2011.09.003WOS:000298711300008WOS000298711300008.pdf66564335394938798550526736462685Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrain Research Bulletin3.4401,398info:eu-repo/semantics/openAccess2023-10-04T06:01:46Zoai:repositorio.unesp.br:11449/14998Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-04T06:01:46Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
title Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
spellingShingle Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
Silva, Camila Zambone Cardoso da [UNESP]
GABA receptors
Angiotensin II
Losartan
Baclofen
Sodium appetite
Thirst
Lateral parabrachial nucleus
title_short Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
title_full Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
title_fullStr Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
title_full_unstemmed Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
title_sort Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
author Silva, Camila Zambone Cardoso da [UNESP]
author_facet Silva, Camila Zambone Cardoso da [UNESP]
Menani, José Vanderlei [UNESP]
Callera, João Carlos [UNESP]
author_role author
author2 Menani, José Vanderlei [UNESP]
Callera, João Carlos [UNESP]
author2_role author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Silva, Camila Zambone Cardoso da [UNESP]
Menani, José Vanderlei [UNESP]
Callera, João Carlos [UNESP]
dc.subject.por.fl_str_mv GABA receptors
Angiotensin II
Losartan
Baclofen
Sodium appetite
Thirst
Lateral parabrachial nucleus
topic GABA receptors
Angiotensin II
Losartan
Baclofen
Sodium appetite
Thirst
Lateral parabrachial nucleus
description GABA(A) and GABA(B) receptors activation with agonists muscimol and baclofen, respectively in the lateral parabrachial nucleus (LPBN), induces water and hypertonic NaCl intake in rats. The purpose of this study was to examine the effects of previous injections of losartan (AT(1) angiotensin receptor antagonist) into the LPBN on 0.3 M NaCl and water intake induced by baclofen injected bilaterally in the same area in fluid replete rats and in rats treated with the diuretic furosemide combined with a low dose of the angiotensin-converting enzyme inhibitor captopril injected subcutaneously. Male Wistar rats with stainless steel cannulas implanted bilaterally into the LPBN were used. Bilateral injections of baclofen (0.5 nmol/0.2 mu l, n=6) into the LPBN in fluid replete rats induced 0.3 M NaCl intake (22.4 +/- 6.5 vs. saline: 0.1 +/- 0.1 ml/210 min) and water intake (14.2 +/- 4.0 vs. saline: 0.6 +/- 0.6 ml/210 min) and pre-treatment of the LPBN with losartan (50 mu g/0.2 mu l,l) reduced 0.3 M NaCl intake (7.4 +/- 7.0 ml/210 min) and water intake (2.8 +/- 2.4 ml/210 min) induced by baclofen. In rats treated with furosemide + captopril, pre-treatment with losartan into the LPBN attenuated the increase in 0.3 M NaCl intake (13.3 +/- 3.2 vs. saline + baclofen: 24.3 +/- 3.9 ml/180 min) and water intake (4.8 +/- 2.1 vs. saline + baclofen: 19.5 +/- 6.6 ml/180 min) produced by baclofen. We conclude that baclofen may produce a non-specific blockade of the inhibitory mechanisms of LPBN (deactivation of LPBN inhibitory mechanisms) and this blockade is facilitated by angiotensin II acting on AT(1) receptors in the LPBN, which drives rats to ingest large amounts of water and hypertonic NaCl independent if rats are fluid depleted or normohydrated. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-11-25
2013-09-30T18:29:19Z
2013-09-30T18:29:19Z
2014-05-20T13:43:05Z
2014-05-20T13:43:05Z
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.brainresbull.2011.09.003
Brain Research Bulletin. Oxford: Pergamon-Elsevier B.V. Ltd, v. 86, n. 5-6, p. 348-354, 2011.
0361-9230
http://hdl.handle.net/11449/14998
10.1016/j.brainresbull.2011.09.003
WOS:000298711300008
WOS000298711300008.pdf
6656433539493879
8550526736462685
url http://dx.doi.org/10.1016/j.brainresbull.2011.09.003
http://hdl.handle.net/11449/14998
identifier_str_mv Brain Research Bulletin. Oxford: Pergamon-Elsevier B.V. Ltd, v. 86, n. 5-6, p. 348-354, 2011.
0361-9230
10.1016/j.brainresbull.2011.09.003
WOS:000298711300008
WOS000298711300008.pdf
6656433539493879
8550526736462685
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brain Research Bulletin
3.440
1,398
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 348-354
application/pdf
dc.publisher.none.fl_str_mv Pergamon-Elsevier B.V. Ltd
publisher.none.fl_str_mv Pergamon-Elsevier B.V. Ltd
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
_version_ 1797789283384295424