Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist

Detalhes bibliográficos
Autor(a) principal: Andrade, Carina A. F. [UNESP]
Data de Publicação: 2011
Outros Autores: Andrade-Franze, Glaucia M. F. [UNESP], De Luca, Laurival A. [UNESP], Johnson, Alan Kim, Menani, José Vanderlei [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.physbeh.2011.07.020
http://hdl.handle.net/11449/16345
Resumo: Bilateral injections of moxonidine, an alpha(2)-adrenoceptor and imidazoline receptor agonist, into the lateral parabrachial nuclei (LPBN) enhance sodium appetite induced by extracellular dehydration. In the present study, we examined whether LPBN moxonidine treatments change taste reactivity to hypertonic NaCl solution administered into the mouth by intra-oral (IO) cannula. Male Holtzman rats prepared with IO and bilateral LPBN cannulas received subcutaneous injections of furosemide (FURO; 10 mg/kg) and captopril (CAP; 5 mg/kg) to induce hypovolemia with mild hypotension and an accompanying salt appetite and thirst before testing the taste reactivity to oral infusions of 0.3 M NaCl (1.0 ml/min). In the first experiment 45 min after subcutaneous injections of FURO + CAP or vehicle, moxonidine was bilaterally injected into the LPBN, and then 15 min later both bodily and oral-facial ingestive and rejection responses to 0.3 M NaCl delivered through the IO cannula were assessed. Both LPBN vehicle and moxonidine treated rats showed increased ingestive and decreased rejection responses to the IO hypertonic solution. The 100.3 M NaCl infusion-evoked ingestive and rejection taste related behaviors were comparable in the LPBN vehicle- vs. the LPBN moxonidine-injected groups. In a second experiment, rats received the same FURO + CAP treatments and LPBN injections. However, beginning 15 min after the LPBN injections, they were given access to water and 0.3 M NaCl and were allowed to consume the fluids for most of the next 60 min with the free access intake being interrupted only for a few minutes at 15,30 and 60 min after the fluids became available. During each of these three brief periods, a taste reactivity test was conducted. on the three taste reactivity tests rats that received LPBN vehicle injections showed progressive declines in ingestive responses and gradual increases in rejection responses. However, in contrast to the LPBN vehicle treated rats, animals receiving bilateral injections of LPBN moxonidine maintained a high number of ingestive responses and a low number of rejection responses throughout the test period even in spite of evidencing substantial water and 0.3 M NaCl consumption during the periods of free access. The results suggest that after alpha(2)-adrenoceptor agonist delivery to the LPBN the acceptance of 0.3 M NaCl is sustained and the negative attributes of the solution are minimized. The maintained positive rewarding qualities of 0.3 M NaCl are likely to account for why LPBN moxonidine treated rats show such a remarkable salt appetite when assayed by the volume of hypertonic 0.3 M NaCl consumed. (C) 2011 Elsevier B.V. All rights reserved.
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spelling Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonistPalatabilityTasteAdrenoceptorsThirstSodium appetiteHindbrainBilateral injections of moxonidine, an alpha(2)-adrenoceptor and imidazoline receptor agonist, into the lateral parabrachial nuclei (LPBN) enhance sodium appetite induced by extracellular dehydration. In the present study, we examined whether LPBN moxonidine treatments change taste reactivity to hypertonic NaCl solution administered into the mouth by intra-oral (IO) cannula. Male Holtzman rats prepared with IO and bilateral LPBN cannulas received subcutaneous injections of furosemide (FURO; 10 mg/kg) and captopril (CAP; 5 mg/kg) to induce hypovolemia with mild hypotension and an accompanying salt appetite and thirst before testing the taste reactivity to oral infusions of 0.3 M NaCl (1.0 ml/min). In the first experiment 45 min after subcutaneous injections of FURO + CAP or vehicle, moxonidine was bilaterally injected into the LPBN, and then 15 min later both bodily and oral-facial ingestive and rejection responses to 0.3 M NaCl delivered through the IO cannula were assessed. Both LPBN vehicle and moxonidine treated rats showed increased ingestive and decreased rejection responses to the IO hypertonic solution. The 100.3 M NaCl infusion-evoked ingestive and rejection taste related behaviors were comparable in the LPBN vehicle- vs. the LPBN moxonidine-injected groups. In a second experiment, rats received the same FURO + CAP treatments and LPBN injections. However, beginning 15 min after the LPBN injections, they were given access to water and 0.3 M NaCl and were allowed to consume the fluids for most of the next 60 min with the free access intake being interrupted only for a few minutes at 15,30 and 60 min after the fluids became available. During each of these three brief periods, a taste reactivity test was conducted. on the three taste reactivity tests rats that received LPBN vehicle injections showed progressive declines in ingestive responses and gradual increases in rejection responses. However, in contrast to the LPBN vehicle treated rats, animals receiving bilateral injections of LPBN moxonidine maintained a high number of ingestive responses and a low number of rejection responses throughout the test period even in spite of evidencing substantial water and 0.3 M NaCl consumption during the periods of free access. The results suggest that after alpha(2)-adrenoceptor agonist delivery to the LPBN the acceptance of 0.3 M NaCl is sustained and the negative attributes of the solution are minimized. The maintained positive rewarding qualities of 0.3 M NaCl are likely to account for why LPBN moxonidine treated rats show such a remarkable salt appetite when assayed by the volume of hypertonic 0.3 M NaCl consumed. (C) 2011 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Univ Fed Alfenas, Dept Physiol, Inst Biomed Sci, Unifal MG, BR-37130000 Alfenas, MG, BrazilUNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, BrazilUniv Iowa, Dept Psychol, Iowa City, IA 52242 USAUniv Iowa, Dept Pharmacol & Hlth, Iowa City, IA 52242 USAUniv Iowa, Dept Human Physiol, Iowa City, IA 52242 USAUniv Iowa, Ctr Cardiovasc, Iowa City, IA 52242 USAUNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 Araraquara, SP, BrazilFAPESP: 07/52343-8FAPEMIG: APQ-00713-09CAPES: 1419-09-9Pergamon-Elsevier B.V. LtdUniversidade Federal de Alfenas (UNIFAL)Universidade Estadual Paulista (Unesp)Univ IowaAndrade, Carina A. F. [UNESP]Andrade-Franze, Glaucia M. F. [UNESP]De Luca, Laurival A. [UNESP]Johnson, Alan KimMenani, José Vanderlei [UNESP]2014-05-20T13:46:15Z2014-05-20T13:46:15Z2011-10-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article702-708application/pdfhttp://dx.doi.org/10.1016/j.physbeh.2011.07.020Physiology & Behavior. Oxford: Pergamon-Elsevier B.V. Ltd, v. 104, n. 5, p. 702-708, 2011.0031-9384http://hdl.handle.net/11449/1634510.1016/j.physbeh.2011.07.020WOS:000296208200008WOS000296208200008.pdf1023597870118105Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPhysiology & Behavior2.5171,088info:eu-repo/semantics/openAccess2023-12-27T06:22:28Zoai:repositorio.unesp.br:11449/16345Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-27T06:22:28Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
title Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
spellingShingle Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
Andrade, Carina A. F. [UNESP]
Palatability
Taste
Adrenoceptors
Thirst
Sodium appetite
Hindbrain
title_short Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
title_full Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
title_fullStr Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
title_full_unstemmed Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
title_sort Changes in taste reactivity to intra-oral hypertonic NaCl after lateral parabrachial injections of an alpha(2)-adrenergic receptor agonist
author Andrade, Carina A. F. [UNESP]
author_facet Andrade, Carina A. F. [UNESP]
Andrade-Franze, Glaucia M. F. [UNESP]
De Luca, Laurival A. [UNESP]
Johnson, Alan Kim
Menani, José Vanderlei [UNESP]
author_role author
author2 Andrade-Franze, Glaucia M. F. [UNESP]
De Luca, Laurival A. [UNESP]
Johnson, Alan Kim
Menani, José Vanderlei [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de Alfenas (UNIFAL)
Universidade Estadual Paulista (Unesp)
Univ Iowa
dc.contributor.author.fl_str_mv Andrade, Carina A. F. [UNESP]
Andrade-Franze, Glaucia M. F. [UNESP]
De Luca, Laurival A. [UNESP]
Johnson, Alan Kim
Menani, José Vanderlei [UNESP]
dc.subject.por.fl_str_mv Palatability
Taste
Adrenoceptors
Thirst
Sodium appetite
Hindbrain
topic Palatability
Taste
Adrenoceptors
Thirst
Sodium appetite
Hindbrain
description Bilateral injections of moxonidine, an alpha(2)-adrenoceptor and imidazoline receptor agonist, into the lateral parabrachial nuclei (LPBN) enhance sodium appetite induced by extracellular dehydration. In the present study, we examined whether LPBN moxonidine treatments change taste reactivity to hypertonic NaCl solution administered into the mouth by intra-oral (IO) cannula. Male Holtzman rats prepared with IO and bilateral LPBN cannulas received subcutaneous injections of furosemide (FURO; 10 mg/kg) and captopril (CAP; 5 mg/kg) to induce hypovolemia with mild hypotension and an accompanying salt appetite and thirst before testing the taste reactivity to oral infusions of 0.3 M NaCl (1.0 ml/min). In the first experiment 45 min after subcutaneous injections of FURO + CAP or vehicle, moxonidine was bilaterally injected into the LPBN, and then 15 min later both bodily and oral-facial ingestive and rejection responses to 0.3 M NaCl delivered through the IO cannula were assessed. Both LPBN vehicle and moxonidine treated rats showed increased ingestive and decreased rejection responses to the IO hypertonic solution. The 100.3 M NaCl infusion-evoked ingestive and rejection taste related behaviors were comparable in the LPBN vehicle- vs. the LPBN moxonidine-injected groups. In a second experiment, rats received the same FURO + CAP treatments and LPBN injections. However, beginning 15 min after the LPBN injections, they were given access to water and 0.3 M NaCl and were allowed to consume the fluids for most of the next 60 min with the free access intake being interrupted only for a few minutes at 15,30 and 60 min after the fluids became available. During each of these three brief periods, a taste reactivity test was conducted. on the three taste reactivity tests rats that received LPBN vehicle injections showed progressive declines in ingestive responses and gradual increases in rejection responses. However, in contrast to the LPBN vehicle treated rats, animals receiving bilateral injections of LPBN moxonidine maintained a high number of ingestive responses and a low number of rejection responses throughout the test period even in spite of evidencing substantial water and 0.3 M NaCl consumption during the periods of free access. The results suggest that after alpha(2)-adrenoceptor agonist delivery to the LPBN the acceptance of 0.3 M NaCl is sustained and the negative attributes of the solution are minimized. The maintained positive rewarding qualities of 0.3 M NaCl are likely to account for why LPBN moxonidine treated rats show such a remarkable salt appetite when assayed by the volume of hypertonic 0.3 M NaCl consumed. (C) 2011 Elsevier B.V. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-10-24
2014-05-20T13:46:15Z
2014-05-20T13:46:15Z
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.physbeh.2011.07.020
Physiology & Behavior. Oxford: Pergamon-Elsevier B.V. Ltd, v. 104, n. 5, p. 702-708, 2011.
0031-9384
http://hdl.handle.net/11449/16345
10.1016/j.physbeh.2011.07.020
WOS:000296208200008
WOS000296208200008.pdf
1023597870118105
url http://dx.doi.org/10.1016/j.physbeh.2011.07.020
http://hdl.handle.net/11449/16345
identifier_str_mv Physiology & Behavior. Oxford: Pergamon-Elsevier B.V. Ltd, v. 104, n. 5, p. 702-708, 2011.
0031-9384
10.1016/j.physbeh.2011.07.020
WOS:000296208200008
WOS000296208200008.pdf
1023597870118105
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Physiology & Behavior
2.517
1,088
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 702-708
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
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