A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , , , , , |
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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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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1799132568293998592 |