L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
dARK ID: | ark:/48912/001300001bpq7 |
DOI: | 10.1186/1742-2094-10-147 |
Texto Completo: | https://dx.doi.org/10.1186/1742-2094-10-147 https://repositorio.unifesp.br/handle/11600/37075 |
Resumo: | IL-1 beta-induced anorexia may depend on interactions of the cytokine with neuropeptides and neurotransmitters of the central nervous system control of energy balance and serotonin is likely to be one catabolic mediator targeted by IL-1 beta. in the complex interplay involved in feeding modulation, nitric oxide has been ascribed a stimulatory action, which could be of significance in counteracting IL-1 beta effects.The present study aims to explore the participation of the nitric oxide and the serotonin systems on the central mechanisms induced by IL-1 beta and the relevance of their putative interactions to IL-1 beta hypophagia in normal rats. Serotonin levels were determined in microdialysates of the ventromedial hypothalamus after a single intracerebroventricular injection of 10 ng of IL-1 beta, with or without the pre-injection of 20 mu g of the nitric oxide precursor L-arginine. IL-1 beta significantly stimulated hypothalamic serotonin extracellular levels, with a peak variation of 130 +/-37% above baseline. IL-1 beta also reduced the 4-h and the 24-h food intakes (by 23% and 58%, respectively). the IL-1 beta-induced serotonergic activation was abolished by the pre-injection of L-arginine while the hypophagic effect was unaffected.The data showed that one central effect of IL-1 beta is serotonergic stimulation in the ventromedial hypothalamus, an action inhibited by nitric oxide activity. It is suggested that, although serotonin participates in IL-1 beta anorexia, other mechanisms recruited by IL-1 beta in normal rats are able to override the absence of the serotonergic hypophagic influence. |
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Repositório Institucional da UNIFESP |
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L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal ratsBrain microdialysisFood intakeNitric oxideSerotonin ventromedial hypothalamusIL-1 beta-induced anorexia may depend on interactions of the cytokine with neuropeptides and neurotransmitters of the central nervous system control of energy balance and serotonin is likely to be one catabolic mediator targeted by IL-1 beta. in the complex interplay involved in feeding modulation, nitric oxide has been ascribed a stimulatory action, which could be of significance in counteracting IL-1 beta effects.The present study aims to explore the participation of the nitric oxide and the serotonin systems on the central mechanisms induced by IL-1 beta and the relevance of their putative interactions to IL-1 beta hypophagia in normal rats. Serotonin levels were determined in microdialysates of the ventromedial hypothalamus after a single intracerebroventricular injection of 10 ng of IL-1 beta, with or without the pre-injection of 20 mu g of the nitric oxide precursor L-arginine. IL-1 beta significantly stimulated hypothalamic serotonin extracellular levels, with a peak variation of 130 +/-37% above baseline. IL-1 beta also reduced the 4-h and the 24-h food intakes (by 23% and 58%, respectively). the IL-1 beta-induced serotonergic activation was abolished by the pre-injection of L-arginine while the hypophagic effect was unaffected.The data showed that one central effect of IL-1 beta is serotonergic stimulation in the ventromedial hypothalamus, an action inhibited by nitric oxide activity. It is suggested that, although serotonin participates in IL-1 beta anorexia, other mechanisms recruited by IL-1 beta in normal rats are able to override the absence of the serotonergic hypophagic influence.Universidade Federal de São Paulo, Dept Physiol, BR-04023060 São Paulo, BrazilUniversidade Federal de São Paulo, Div Appl Stat, BR-04023060 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Physiol, BR-04023060 São Paulo, BrazilUniversidade Federal de São Paulo, Div Appl Stat, BR-04023060 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Biomed Central LtdUniversidade Federal de São Paulo (UNIFESP)Iuras, Anderson [UNIFESP]Telles, Monica Marques [UNIFESP]Andrade, Iracema Senna de [UNIFESP]Santos, Gianni Mara Silva dos [UNIFESP]Oyama, Lila Missae [UNIFESP]Nascimento, Claudia Maria da Penha Oller do [UNIFESP]Silveira, Vera Lucia Flor [UNIFESP]Ribeiro, Eliane Beraldi [UNIFESP]2016-01-24T14:34:51Z2016-01-24T14:34:51Z2013-12-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion7application/pdfhttps://dx.doi.org/10.1186/1742-2094-10-147Journal of Neuroinflammation. London: Biomed Central Ltd, v. 10, 7 p., 2013.10.1186/1742-2094-10-147WOS000329208000001.pdf1742-2094https://repositorio.unifesp.br/handle/11600/37075WOS:000329208000001ark:/48912/001300001bpq7engJournal of Neuroinflammationinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T16:49:21Zoai:repositorio.unifesp.br/:11600/37075Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-12-11T21:08:08.573503Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
title |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
spellingShingle |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats Iuras, Anderson [UNIFESP] Brain microdialysis Food intake Nitric oxide Serotonin ventromedial hypothalamus Iuras, Anderson [UNIFESP] Brain microdialysis Food intake Nitric oxide Serotonin ventromedial hypothalamus |
title_short |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
title_full |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
title_fullStr |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
title_full_unstemmed |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
title_sort |
L-arginine abolishes the hypothalamic serotonergic activation induced by central interleukin-1 beta administration to normal rats |
author |
Iuras, Anderson [UNIFESP] |
author_facet |
Iuras, Anderson [UNIFESP] Iuras, Anderson [UNIFESP] Telles, Monica Marques [UNIFESP] Andrade, Iracema Senna de [UNIFESP] Santos, Gianni Mara Silva dos [UNIFESP] Oyama, Lila Missae [UNIFESP] Nascimento, Claudia Maria da Penha Oller do [UNIFESP] Silveira, Vera Lucia Flor [UNIFESP] Ribeiro, Eliane Beraldi [UNIFESP] Telles, Monica Marques [UNIFESP] Andrade, Iracema Senna de [UNIFESP] Santos, Gianni Mara Silva dos [UNIFESP] Oyama, Lila Missae [UNIFESP] Nascimento, Claudia Maria da Penha Oller do [UNIFESP] Silveira, Vera Lucia Flor [UNIFESP] Ribeiro, Eliane Beraldi [UNIFESP] |
author_role |
author |
author2 |
Telles, Monica Marques [UNIFESP] Andrade, Iracema Senna de [UNIFESP] Santos, Gianni Mara Silva dos [UNIFESP] Oyama, Lila Missae [UNIFESP] Nascimento, Claudia Maria da Penha Oller do [UNIFESP] Silveira, Vera Lucia Flor [UNIFESP] Ribeiro, Eliane Beraldi [UNIFESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Iuras, Anderson [UNIFESP] Telles, Monica Marques [UNIFESP] Andrade, Iracema Senna de [UNIFESP] Santos, Gianni Mara Silva dos [UNIFESP] Oyama, Lila Missae [UNIFESP] Nascimento, Claudia Maria da Penha Oller do [UNIFESP] Silveira, Vera Lucia Flor [UNIFESP] Ribeiro, Eliane Beraldi [UNIFESP] |
dc.subject.por.fl_str_mv |
Brain microdialysis Food intake Nitric oxide Serotonin ventromedial hypothalamus |
topic |
Brain microdialysis Food intake Nitric oxide Serotonin ventromedial hypothalamus |
description |
IL-1 beta-induced anorexia may depend on interactions of the cytokine with neuropeptides and neurotransmitters of the central nervous system control of energy balance and serotonin is likely to be one catabolic mediator targeted by IL-1 beta. in the complex interplay involved in feeding modulation, nitric oxide has been ascribed a stimulatory action, which could be of significance in counteracting IL-1 beta effects.The present study aims to explore the participation of the nitric oxide and the serotonin systems on the central mechanisms induced by IL-1 beta and the relevance of their putative interactions to IL-1 beta hypophagia in normal rats. Serotonin levels were determined in microdialysates of the ventromedial hypothalamus after a single intracerebroventricular injection of 10 ng of IL-1 beta, with or without the pre-injection of 20 mu g of the nitric oxide precursor L-arginine. IL-1 beta significantly stimulated hypothalamic serotonin extracellular levels, with a peak variation of 130 +/-37% above baseline. IL-1 beta also reduced the 4-h and the 24-h food intakes (by 23% and 58%, respectively). the IL-1 beta-induced serotonergic activation was abolished by the pre-injection of L-arginine while the hypophagic effect was unaffected.The data showed that one central effect of IL-1 beta is serotonergic stimulation in the ventromedial hypothalamus, an action inhibited by nitric oxide activity. It is suggested that, although serotonin participates in IL-1 beta anorexia, other mechanisms recruited by IL-1 beta in normal rats are able to override the absence of the serotonergic hypophagic influence. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-12-07 2016-01-24T14:34:51Z 2016-01-24T14:34:51Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://dx.doi.org/10.1186/1742-2094-10-147 Journal of Neuroinflammation. London: Biomed Central Ltd, v. 10, 7 p., 2013. 10.1186/1742-2094-10-147 WOS000329208000001.pdf 1742-2094 https://repositorio.unifesp.br/handle/11600/37075 WOS:000329208000001 |
dc.identifier.dark.fl_str_mv |
ark:/48912/001300001bpq7 |
url |
https://dx.doi.org/10.1186/1742-2094-10-147 https://repositorio.unifesp.br/handle/11600/37075 |
identifier_str_mv |
Journal of Neuroinflammation. London: Biomed Central Ltd, v. 10, 7 p., 2013. 10.1186/1742-2094-10-147 WOS000329208000001.pdf 1742-2094 WOS:000329208000001 ark:/48912/001300001bpq7 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Neuroinflammation |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
7 application/pdf |
dc.publisher.none.fl_str_mv |
Biomed Central Ltd |
publisher.none.fl_str_mv |
Biomed Central Ltd |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1822219257186877440 |
dc.identifier.doi.none.fl_str_mv |
10.1186/1742-2094-10-147 |