Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake

Detalhes bibliográficos
Autor(a) principal: Menezes, Miguel F. [UNESP]
Data de Publicação: 2011
Outros Autores: Barbosa, Silas P. [UNESP], Andrade, Carina A. F. de [UNESP], Menani, José Vanderlei [UNESP], De Paula, Patricia M. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.brainres.2010.11.075
http://hdl.handle.net/11449/16340
Resumo: Purinergic receptors are present in the lateral parabrachial nucleus (LPBN), a pontine structure involved in the control of sodium intake. In the present study, we investigated the effects of alpha,beta-methyleneadenosine 5'-triphosphate (alpha,beta-methylene ATP, selective P2X purinergic agonist) alone or combined with pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid (PPADS, P2X purinergic antagonist) or suramin (non-selective P2 purinergic antagonist) injected into the LPBN on sodium depletion-induced 1.8% NaCl intake. Male Holtzman rats with stainless steel cannulas implanted into the LPBN were used. Sodium depletion was induced by treating rats with the diuretic furosemide (20 mg/kg of body weight) followed by 24 h of sodium-deficient diet. Bilateral injections of alpha,beta-methylene ATP (2.0 and 4.0 nmol/0.2 mu l) into the LPBN increased sodium depletion-induced 1.8% NaCl intake (25.3 +/- 0.8 and 26.5 +/- 0.9 ml/120 min, respectively, vs. saline: 15.2 +/- 1.3 ml/120 min). PPADS (4 nmol/0.2 mu l) alone into the LPBN did not change 1.8% NaCl intake, however, pretreatment with PPADS into the LPBN abolished the effects of alpha,beta-methylene ATP on 1.8% NaCl intake (16.9 +/- 0.9 ml/120 min). Suramin (2.0 nmol/0.2 mu l) alone into the LPBN reduced sodium depletion-induced 1.8% NaCl intake (5.7 +/- 1.9 ml/120 min, vs. saline: 15.5 +/- 1.1 ml/120 min), without changing 2% sucrose intake or 24 h water deprivation-induced water intake. The combination of suramin and alpha,beta-methylene ATP into the LPBN produced no change of 1.8% NaCl intake (15.2 +/- 1.2 ml/120 min). The results suggest that purinergic P2 receptor activation in the LPBN facilitates NaCl intake, probably by restraining LPBN mechanisms that inhibit sodium intake. (C) 2010 Elsevier B.V. All rights reserved.
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spelling Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intakeAdenosine 5 '-triphosphate (ATP)Sodium appetiteSuraminPPADSalpha,beta-Methylene ATPP2 purinergic receptorsPurinergic receptors are present in the lateral parabrachial nucleus (LPBN), a pontine structure involved in the control of sodium intake. In the present study, we investigated the effects of alpha,beta-methyleneadenosine 5'-triphosphate (alpha,beta-methylene ATP, selective P2X purinergic agonist) alone or combined with pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid (PPADS, P2X purinergic antagonist) or suramin (non-selective P2 purinergic antagonist) injected into the LPBN on sodium depletion-induced 1.8% NaCl intake. Male Holtzman rats with stainless steel cannulas implanted into the LPBN were used. Sodium depletion was induced by treating rats with the diuretic furosemide (20 mg/kg of body weight) followed by 24 h of sodium-deficient diet. Bilateral injections of alpha,beta-methylene ATP (2.0 and 4.0 nmol/0.2 mu l) into the LPBN increased sodium depletion-induced 1.8% NaCl intake (25.3 +/- 0.8 and 26.5 +/- 0.9 ml/120 min, respectively, vs. saline: 15.2 +/- 1.3 ml/120 min). PPADS (4 nmol/0.2 mu l) alone into the LPBN did not change 1.8% NaCl intake, however, pretreatment with PPADS into the LPBN abolished the effects of alpha,beta-methylene ATP on 1.8% NaCl intake (16.9 +/- 0.9 ml/120 min). Suramin (2.0 nmol/0.2 mu l) alone into the LPBN reduced sodium depletion-induced 1.8% NaCl intake (5.7 +/- 1.9 ml/120 min, vs. saline: 15.5 +/- 1.1 ml/120 min), without changing 2% sucrose intake or 24 h water deprivation-induced water intake. The combination of suramin and alpha,beta-methylene ATP into the LPBN produced no change of 1.8% NaCl intake (15.2 +/- 1.2 ml/120 min). The results suggest that purinergic P2 receptor activation in the LPBN facilitates NaCl intake, probably by restraining LPBN mechanisms that inhibit sodium intake. (C) 2010 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)São Paulo State Univ, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, BrazilFed Univ Alfenas Unifal MG, Inst Biomed Sci, BR-37130000 Alfenas, MG, BrazilSão Paulo State Univ, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, BrazilFAPESP: 07/50647-0FAPESP: 08/52757-0Elsevier B.V.Universidade Estadual Paulista (Unesp)Universidade Federal de Alfenas (UNIFAL)Menezes, Miguel F. [UNESP]Barbosa, Silas P. [UNESP]Andrade, Carina A. F. de [UNESP]Menani, José Vanderlei [UNESP]De Paula, Patricia M. [UNESP]2014-05-20T13:46:14Z2014-05-20T13:46:14Z2011-02-04info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article49-58application/pdfhttp://dx.doi.org/10.1016/j.brainres.2010.11.075Brain Research. Amsterdam: Elsevier B.V., v. 1372, p. 49-58, 2011.0006-8993http://hdl.handle.net/11449/1634010.1016/j.brainres.2010.11.075WOS:000287293700006WOS000287293700006.pdf1023597870118105Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBrain Research3.1251,404info:eu-repo/semantics/openAccess2024-09-27T14:05:35Zoai:repositorio.unesp.br:11449/16340Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-27T14:05:35Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
title Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
spellingShingle Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
Menezes, Miguel F. [UNESP]
Adenosine 5 '-triphosphate (ATP)
Sodium appetite
Suramin
PPADS
alpha,beta-Methylene ATP
P2 purinergic receptors
title_short Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
title_full Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
title_fullStr Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
title_full_unstemmed Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
title_sort Purinergic mechanisms of lateral parabrachial nucleus facilitate sodium depletion-induced NaCl intake
author Menezes, Miguel F. [UNESP]
author_facet Menezes, Miguel F. [UNESP]
Barbosa, Silas P. [UNESP]
Andrade, Carina A. F. de [UNESP]
Menani, José Vanderlei [UNESP]
De Paula, Patricia M. [UNESP]
author_role author
author2 Barbosa, Silas P. [UNESP]
Andrade, Carina A. F. de [UNESP]
Menani, José Vanderlei [UNESP]
De Paula, Patricia M. [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Federal de Alfenas (UNIFAL)
dc.contributor.author.fl_str_mv Menezes, Miguel F. [UNESP]
Barbosa, Silas P. [UNESP]
Andrade, Carina A. F. de [UNESP]
Menani, José Vanderlei [UNESP]
De Paula, Patricia M. [UNESP]
dc.subject.por.fl_str_mv Adenosine 5 '-triphosphate (ATP)
Sodium appetite
Suramin
PPADS
alpha,beta-Methylene ATP
P2 purinergic receptors
topic Adenosine 5 '-triphosphate (ATP)
Sodium appetite
Suramin
PPADS
alpha,beta-Methylene ATP
P2 purinergic receptors
description Purinergic receptors are present in the lateral parabrachial nucleus (LPBN), a pontine structure involved in the control of sodium intake. In the present study, we investigated the effects of alpha,beta-methyleneadenosine 5'-triphosphate (alpha,beta-methylene ATP, selective P2X purinergic agonist) alone or combined with pyridoxalphosphate-6-azophenyl-2',4'-disulfonic acid (PPADS, P2X purinergic antagonist) or suramin (non-selective P2 purinergic antagonist) injected into the LPBN on sodium depletion-induced 1.8% NaCl intake. Male Holtzman rats with stainless steel cannulas implanted into the LPBN were used. Sodium depletion was induced by treating rats with the diuretic furosemide (20 mg/kg of body weight) followed by 24 h of sodium-deficient diet. Bilateral injections of alpha,beta-methylene ATP (2.0 and 4.0 nmol/0.2 mu l) into the LPBN increased sodium depletion-induced 1.8% NaCl intake (25.3 +/- 0.8 and 26.5 +/- 0.9 ml/120 min, respectively, vs. saline: 15.2 +/- 1.3 ml/120 min). PPADS (4 nmol/0.2 mu l) alone into the LPBN did not change 1.8% NaCl intake, however, pretreatment with PPADS into the LPBN abolished the effects of alpha,beta-methylene ATP on 1.8% NaCl intake (16.9 +/- 0.9 ml/120 min). Suramin (2.0 nmol/0.2 mu l) alone into the LPBN reduced sodium depletion-induced 1.8% NaCl intake (5.7 +/- 1.9 ml/120 min, vs. saline: 15.5 +/- 1.1 ml/120 min), without changing 2% sucrose intake or 24 h water deprivation-induced water intake. The combination of suramin and alpha,beta-methylene ATP into the LPBN produced no change of 1.8% NaCl intake (15.2 +/- 1.2 ml/120 min). The results suggest that purinergic P2 receptor activation in the LPBN facilitates NaCl intake, probably by restraining LPBN mechanisms that inhibit sodium intake. (C) 2010 Elsevier B.V. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-02-04
2014-05-20T13:46:14Z
2014-05-20T13:46:14Z
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.brainres.2010.11.075
Brain Research. Amsterdam: Elsevier B.V., v. 1372, p. 49-58, 2011.
0006-8993
http://hdl.handle.net/11449/16340
10.1016/j.brainres.2010.11.075
WOS:000287293700006
WOS000287293700006.pdf
1023597870118105
url http://dx.doi.org/10.1016/j.brainres.2010.11.075
http://hdl.handle.net/11449/16340
identifier_str_mv Brain Research. Amsterdam: Elsevier B.V., v. 1372, p. 49-58, 2011.
0006-8993
10.1016/j.brainres.2010.11.075
WOS:000287293700006
WOS000287293700006.pdf
1023597870118105
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Brain Research
3.125
1,404
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 49-58
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
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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