A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Manuel Lima
Data de Publicação: 2008
Outros Autores: Fernandes, Ana Valle, Lamas, Nuno Jorge, Cruz, Andrea, Baltazar, Fátima, Milanezi, Fernanda, Nunes, Rui, Reis, R. M., Pedrosa, Jorge, Castro, António G., Almeida, Armando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/7897
Resumo: Objectives/Hypothesis: To develop and characterize a new model of laryngeal inflammation by analyzing the presence of neurogenic peptides and expression of cyclooxygenases (COX) and cytokines in the mucosa.Study Design: Laryngitis induced by nasogastric intubation (NGI) was evaluated by histopathologic changes of the mucosa, alterations in calcitonin gene related peptide (CGRP) and substance P (SP) neuropeptides in sensory fibers, and COX-1,2, and cytokine (interleukin [IL]-1, IL-6, IL-10, tumor necrosis factor [TNF]-alpha) expression in the laryngeal mucosa.Methods: Rats submitted to NGI for 1 to 5 weeks were compared with controls. Laryngeal sections were immunostained for stereologic analysis of SP and CGRP fiber density and number of mucosal cells expressing COX-2. Alterations in inflammatory mediators were evaluated by quantitative reverse-transcriptase polymerase chain reaction.Results: NGI induced metaplasia of the epithelium and narrowing of the laryngeal lumen because of hypertrophy of laryngeal glandules and edema. An initial decrease in CGRP- and SP-immunoreactive fibers in the laryngeal mucosa (1-3 wk) was reverted with time (5 wk). COX-2 expression in mucosal cells increased progressively, reaching a maximum level at 5 weeks, and was observed in mononuclear immune cells, which is indicative of a chronic inflammatory process. In regard to mRNA expression levels of inflammatory mediators, TNF-alpha was increased during the 5 week NGI, and IL-10 decreased during the 5 weeks,whereas IL-beta, IL-6, and COX-2 increased in the first 1 to 2 weeks and returned to baseline at 5 weeks.Conclusions: This NGI model results in laryngeal chronic inflammation without direct mechanical aggression of the mucosa and may contribute to the study of future therapeutic approaches to this pathology.
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spelling A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profileLaryngeal inflammationNeuropeptidesCyclooxygenase-2CytokinesNasogastric intubationImmunocytochemistryMRNA expressionReverse transcriptase polymerase chain reaction analysisAnimal modelScience & TechnologyObjectives/Hypothesis: To develop and characterize a new model of laryngeal inflammation by analyzing the presence of neurogenic peptides and expression of cyclooxygenases (COX) and cytokines in the mucosa.Study Design: Laryngitis induced by nasogastric intubation (NGI) was evaluated by histopathologic changes of the mucosa, alterations in calcitonin gene related peptide (CGRP) and substance P (SP) neuropeptides in sensory fibers, and COX-1,2, and cytokine (interleukin [IL]-1, IL-6, IL-10, tumor necrosis factor [TNF]-alpha) expression in the laryngeal mucosa.Methods: Rats submitted to NGI for 1 to 5 weeks were compared with controls. Laryngeal sections were immunostained for stereologic analysis of SP and CGRP fiber density and number of mucosal cells expressing COX-2. Alterations in inflammatory mediators were evaluated by quantitative reverse-transcriptase polymerase chain reaction.Results: NGI induced metaplasia of the epithelium and narrowing of the laryngeal lumen because of hypertrophy of laryngeal glandules and edema. An initial decrease in CGRP- and SP-immunoreactive fibers in the laryngeal mucosa (1-3 wk) was reverted with time (5 wk). COX-2 expression in mucosal cells increased progressively, reaching a maximum level at 5 weeks, and was observed in mononuclear immune cells, which is indicative of a chronic inflammatory process. In regard to mRNA expression levels of inflammatory mediators, TNF-alpha was increased during the 5 week NGI, and IL-10 decreased during the 5 weeks,whereas IL-beta, IL-6, and COX-2 increased in the first 1 to 2 weeks and returned to baseline at 5 weeks.Conclusions: This NGI model results in laryngeal chronic inflammation without direct mechanical aggression of the mucosa and may contribute to the study of future therapeutic approaches to this pathology.FEDERFundação para a Ciência e Tecnologia (FCT) - POCTI/NSE/46399/2002Fundação Calouste Gulbenkian - projecto nº 74551Lippincott, Williams & WilkinsUniversidade do MinhoRodrigues, Manuel LimaFernandes, Ana ValleLamas, Nuno JorgeCruz, AndreaBaltazar, FátimaMilanezi, FernandaNunes, RuiReis, R. M.Pedrosa, JorgeCastro, António G.Almeida, Armando2008-012008-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/7897eng"The Laryngoscope". ISSN 0023-852X. 118:1 (Jan. 2008) 78-86.0023-852X10.1097/MLG.0b013e318149240018251032www.laryngoscope.cominfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:20:04Zoai:repositorium.sdum.uminho.pt:1822/7897Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:13:07.713192Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
title A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
spellingShingle A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
Rodrigues, Manuel Lima
Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
Science & Technology
title_short A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
title_full A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
title_fullStr A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
title_full_unstemmed A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
title_sort A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
author Rodrigues, Manuel Lima
author_facet Rodrigues, Manuel Lima
Fernandes, Ana Valle
Lamas, Nuno Jorge
Cruz, Andrea
Baltazar, Fátima
Milanezi, Fernanda
Nunes, Rui
Reis, R. M.
Pedrosa, Jorge
Castro, António G.
Almeida, Armando
author_role author
author2 Fernandes, Ana Valle
Lamas, Nuno Jorge
Cruz, Andrea
Baltazar, Fátima
Milanezi, Fernanda
Nunes, Rui
Reis, R. M.
Pedrosa, Jorge
Castro, António G.
Almeida, Armando
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Rodrigues, Manuel Lima
Fernandes, Ana Valle
Lamas, Nuno Jorge
Cruz, Andrea
Baltazar, Fátima
Milanezi, Fernanda
Nunes, Rui
Reis, R. M.
Pedrosa, Jorge
Castro, António G.
Almeida, Armando
dc.subject.por.fl_str_mv Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
Science & Technology
topic Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
Science & Technology
description Objectives/Hypothesis: To develop and characterize a new model of laryngeal inflammation by analyzing the presence of neurogenic peptides and expression of cyclooxygenases (COX) and cytokines in the mucosa.Study Design: Laryngitis induced by nasogastric intubation (NGI) was evaluated by histopathologic changes of the mucosa, alterations in calcitonin gene related peptide (CGRP) and substance P (SP) neuropeptides in sensory fibers, and COX-1,2, and cytokine (interleukin [IL]-1, IL-6, IL-10, tumor necrosis factor [TNF]-alpha) expression in the laryngeal mucosa.Methods: Rats submitted to NGI for 1 to 5 weeks were compared with controls. Laryngeal sections were immunostained for stereologic analysis of SP and CGRP fiber density and number of mucosal cells expressing COX-2. Alterations in inflammatory mediators were evaluated by quantitative reverse-transcriptase polymerase chain reaction.Results: NGI induced metaplasia of the epithelium and narrowing of the laryngeal lumen because of hypertrophy of laryngeal glandules and edema. An initial decrease in CGRP- and SP-immunoreactive fibers in the laryngeal mucosa (1-3 wk) was reverted with time (5 wk). COX-2 expression in mucosal cells increased progressively, reaching a maximum level at 5 weeks, and was observed in mononuclear immune cells, which is indicative of a chronic inflammatory process. In regard to mRNA expression levels of inflammatory mediators, TNF-alpha was increased during the 5 week NGI, and IL-10 decreased during the 5 weeks,whereas IL-beta, IL-6, and COX-2 increased in the first 1 to 2 weeks and returned to baseline at 5 weeks.Conclusions: This NGI model results in laryngeal chronic inflammation without direct mechanical aggression of the mucosa and may contribute to the study of future therapeutic approaches to this pathology.
publishDate 2008
dc.date.none.fl_str_mv 2008-01
2008-01-01T00:00:00Z
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://hdl.handle.net/1822/7897
url http://hdl.handle.net/1822/7897
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv "The Laryngoscope". ISSN 0023-852X. 118:1 (Jan. 2008) 78-86.
0023-852X
10.1097/MLG.0b013e3181492400
18251032
www.laryngoscope.com
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Lippincott, Williams & Wilkins
publisher.none.fl_str_mv Lippincott, Williams & Wilkins
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
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