Natriorexigenic effect of baclofen is reduced by AT(1) receptor blockade in the lateral parabrachial nucleus
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
DOI: | 10.1016/j.brainresbull.2011.09.003 |
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. |
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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/openAccess2024-09-27T14:04:24Zoai:repositorio.unesp.br:11449/14998Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:04:24Repositório 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 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 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 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 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] Silva, Camila Zambone Cardoso da [UNESP] Menani, José Vanderlei [UNESP] Callera, João Carlos [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 |
repositoriounesp@unesp.br |
_version_ |
1822247078160498688 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.brainresbull.2011.09.003 |