Mineral intake independent from gastric irritation or pica by cell-dehydrated rats

Detalhes bibliográficos
Autor(a) principal: Constancio, Juliana [UNESP]
Data de Publicação: 2011
Outros Autores: Pereira-Derderian, Daniela T. B. [UNESP], Menani, José Vanderlei [UNESP], De Luca, Laurival A. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.physbeh.2011.07.010
http://hdl.handle.net/11449/16344
Resumo: Gavage of 2 M NaCl (IG 2 M NaCl), a procedure to induce cell-dehydration-and water and 015 M NaCl intake in a two-bottle choice test-is also a potential gastric irritant. In this study, we assessed whether mineral intake induced by IG 2 M NaCl is associated with gastric irritation or production of pica in the rat. We first determined the amount of mineral solution (0.15 M NaCl, 0.15 M NaHCO3, 0.01 M KCl and 0.05 mM CaCl2) and water ingested in response to IG 2 M NaCl in a five-bottle test. Then, we used mineral solutions (0.01 M KCl and 0.15 M NaHCO3), whose intakes were significantly increased compared to controls, and water in three-bottle tests to test the gastric irritation hypothesis. The IG 2 M NaCl induced KCl and NaHCO3 intake that was not inhibited by gavage with gastric protectors Al(OH)(3) or NaHCO3. IG 2 M NaCl or gavage of 0.6 N acetic acid induced mild irritation, hyperemia, of the glandular part of the stomach. A gavage of 50% ethanol induced strong irritation seen as pinpoint ulcerations. Neither ethanol nor acetic acid induced any fluid intake. Neither IG 2 M NaCl nor acetic acid induced kaolin intake, a marker of pica in laboratory rats. Ethanol did induce kaolin intake. These results suggest that IG 2 M NaCl induced a mineral fluid intake not selective for sodium and independent from gastric irritation or pica. (C) 2011 Elsevier B.V. All rights reserved.
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spelling Mineral intake independent from gastric irritation or pica by cell-dehydrated ratsDehydrationThirstSodium appetiteMineral lickSelf-medicationGastric mucosaGavage of 2 M NaCl (IG 2 M NaCl), a procedure to induce cell-dehydration-and water and 015 M NaCl intake in a two-bottle choice test-is also a potential gastric irritant. In this study, we assessed whether mineral intake induced by IG 2 M NaCl is associated with gastric irritation or production of pica in the rat. We first determined the amount of mineral solution (0.15 M NaCl, 0.15 M NaHCO3, 0.01 M KCl and 0.05 mM CaCl2) and water ingested in response to IG 2 M NaCl in a five-bottle test. Then, we used mineral solutions (0.01 M KCl and 0.15 M NaHCO3), whose intakes were significantly increased compared to controls, and water in three-bottle tests to test the gastric irritation hypothesis. The IG 2 M NaCl induced KCl and NaHCO3 intake that was not inhibited by gavage with gastric protectors Al(OH)(3) or NaHCO3. IG 2 M NaCl or gavage of 0.6 N acetic acid induced mild irritation, hyperemia, of the glandular part of the stomach. A gavage of 50% ethanol induced strong irritation seen as pinpoint ulcerations. Neither ethanol nor acetic acid induced any fluid intake. Neither IG 2 M NaCl nor acetic acid induced kaolin intake, a marker of pica in laboratory rats. Ethanol did induce kaolin intake. These results suggest that IG 2 M NaCl induced a mineral fluid intake not selective for sodium and independent from gastric irritation or pica. (C) 2011 Elsevier B.V. All rights reserved.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)São Paulo State Univ, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 São Paulo, BrazilSão Paulo State Univ, UNESP, Sch Dent, Dept Physiol & Pathol, BR-14801903 São Paulo, BrazilFAPESP: 06/58829-7Pergamon-Elsevier B.V. LtdUniversidade Estadual Paulista (Unesp)Constancio, Juliana [UNESP]Pereira-Derderian, Daniela T. B. [UNESP]Menani, José Vanderlei [UNESP]De Luca, Laurival A. [UNESP]2014-05-20T13:46:15Z2014-05-20T13:46:15Z2011-10-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article659-665application/pdfhttp://dx.doi.org/10.1016/j.physbeh.2011.07.010Physiology & Behavior. Oxford: Pergamon-Elsevier B.V. Ltd, v. 104, n. 5, p. 659-665, 2011.0031-9384http://hdl.handle.net/11449/1634410.1016/j.physbeh.2011.07.010WOS:000296208200002WOS000296208200002.pdf1023597870118105Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengPhysiology & Behavior2.5171,088info:eu-repo/semantics/openAccess2023-11-05T06:13:09Zoai:repositorio.unesp.br:11449/16344Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:59:46.678197Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
title Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
spellingShingle Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
Constancio, Juliana [UNESP]
Dehydration
Thirst
Sodium appetite
Mineral lick
Self-medication
Gastric mucosa
title_short Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
title_full Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
title_fullStr Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
title_full_unstemmed Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
title_sort Mineral intake independent from gastric irritation or pica by cell-dehydrated rats
author Constancio, Juliana [UNESP]
author_facet Constancio, Juliana [UNESP]
Pereira-Derderian, Daniela T. B. [UNESP]
Menani, José Vanderlei [UNESP]
De Luca, Laurival A. [UNESP]
author_role author
author2 Pereira-Derderian, Daniela T. B. [UNESP]
Menani, José Vanderlei [UNESP]
De Luca, Laurival A. [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Constancio, Juliana [UNESP]
Pereira-Derderian, Daniela T. B. [UNESP]
Menani, José Vanderlei [UNESP]
De Luca, Laurival A. [UNESP]
dc.subject.por.fl_str_mv Dehydration
Thirst
Sodium appetite
Mineral lick
Self-medication
Gastric mucosa
topic Dehydration
Thirst
Sodium appetite
Mineral lick
Self-medication
Gastric mucosa
description Gavage of 2 M NaCl (IG 2 M NaCl), a procedure to induce cell-dehydration-and water and 015 M NaCl intake in a two-bottle choice test-is also a potential gastric irritant. In this study, we assessed whether mineral intake induced by IG 2 M NaCl is associated with gastric irritation or production of pica in the rat. We first determined the amount of mineral solution (0.15 M NaCl, 0.15 M NaHCO3, 0.01 M KCl and 0.05 mM CaCl2) and water ingested in response to IG 2 M NaCl in a five-bottle test. Then, we used mineral solutions (0.01 M KCl and 0.15 M NaHCO3), whose intakes were significantly increased compared to controls, and water in three-bottle tests to test the gastric irritation hypothesis. The IG 2 M NaCl induced KCl and NaHCO3 intake that was not inhibited by gavage with gastric protectors Al(OH)(3) or NaHCO3. IG 2 M NaCl or gavage of 0.6 N acetic acid induced mild irritation, hyperemia, of the glandular part of the stomach. A gavage of 50% ethanol induced strong irritation seen as pinpoint ulcerations. Neither ethanol nor acetic acid induced any fluid intake. Neither IG 2 M NaCl nor acetic acid induced kaolin intake, a marker of pica in laboratory rats. Ethanol did induce kaolin intake. These results suggest that IG 2 M NaCl induced a mineral fluid intake not selective for sodium and independent from gastric irritation or pica. (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.2011.07.010
Physiology & Behavior. Oxford: Pergamon-Elsevier B.V. Ltd, v. 104, n. 5, p. 659-665, 2011.
0031-9384
http://hdl.handle.net/11449/16344
10.1016/j.physbeh.2011.07.010
WOS:000296208200002
WOS000296208200002.pdf
1023597870118105
url http://dx.doi.org/10.1016/j.physbeh.2011.07.010
http://hdl.handle.net/11449/16344
identifier_str_mv Physiology & Behavior. Oxford: Pergamon-Elsevier B.V. Ltd, v. 104, n. 5, p. 659-665, 2011.
0031-9384
10.1016/j.physbeh.2011.07.010
WOS:000296208200002
WOS000296208200002.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 659-665
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)
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