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

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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.
Autores principais:Rodrigues, Manuel Lima
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
Assunto:Laryngeal inflammation Neuropeptides Cyclooxygenase-2 Cytokines Nasogastric intubation Immunocytochemistry MRNA expression Reverse transcriptase polymerase chain reaction analysis Animal model
Ano:2008
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
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author Rodrigues, Manuel Lima
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
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
contributor_name_str_mv Universidade do Minho
country_str PT
creators_json_txt [{\"Person.name\":\"Rodrigues, Manuel Lima\"},{\"Person.name\":\"Fernandes, Ana Valle\"},{\"Person.name\":\"Lamas, Nuno Jorge\"},{\"Person.name\":\"Cruz, Andrea\"},{\"Person.name\":\"Baltazar, Fátima\"},{\"Person.name\":\"Milanezi, Fernanda\"},{\"Person.name\":\"Nunes, Rui\"},{\"Person.name\":\"Reis, R. M.\"},{\"Person.name\":\"Pedrosa, Jorge\"},{\"Person.name\":\"Castro, António G.\"},{\"Person.name\":\"Almeida, Armando\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Universidade do Minho
datacite.creators.creator.creatorName.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
datacite.date.Accepted.fl_str_mv 2008-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2008-06-03T14:42:22Z
datacite.date.embargoed.fl_str_mv 2008-06-03T14:42:22Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
datacite.titles.title.fl_str_mv A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
dc.contributor.none.fl_str_mv Universidade do Minho
dc.creator.none.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.date.Accepted.fl_str_mv 2008-01-01T00:00:00Z
dc.date.available.fl_str_mv 2008-06-03T14:42:22Z
dc.date.embargoed.fl_str_mv 2008-06-03T14:42:22Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://hdl.handle.net/1822/7897
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Lippincott, Williams & Wilkins
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
dc.title.fl_str_mv A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
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.
dirty 0
eu_rights_str_mv openAccess
format article
fulltext.url.fl_str_mv https://prod-dspace.uminho.pt/bitstreams/45664afb-34f2-4d9f-9d66-3ddf7e99e4b2/download
id rum_ad263c1bcb11e6ba61347203ee05fa4e
identifier.url.fl_str_mv https://hdl.handle.net/1822/7897
instacron_str repositorium
institution Universidade do Minho
instname_str Universidade do Minho
language eng
network_acronym_str rum
network_name_str RepositóriUM - Universidade do Minho
oai_identifier_str oai:repositorium.uminho.pt:1822/7897
organization_str_mv urn:organizationAcronym:repositorium
person_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
publishDate 2008
publisher.none.fl_str_mv Lippincott, Williams & Wilkins
reponame_str RepositóriUM - Universidade do Minho
repository_id_str urn:repositoryAcronym:rum
service_str_mv urn:repositoryAcronym:rum
spelling engLippincott, Williams & WilkinsporObjectives/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.application/pdfengA new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profileRodrigues, Manuel LimaFernandes, Ana ValleLamas, Nuno JorgeCruz, AndreaBaltazar, FátimaMilanezi, FernandaNunes, RuiReis, R. M.Pedrosa, JorgeCastro, António G.Almeida, ArmandoHostingInstitutionOrganizationalUniversidade do Minhoe-mailmailto:repositorium@usdb.uminho.ptrepositorium@usdb.uminho.ptISSNIsPartOf0023-852XDOIIsPartOf10.1097/MLG.0b013e31814924002008-06-03T14:42:22Z2008-012007-06-272008-01-01T00:00:00ZHandlehttps://hdl.handle.net/1822/7897http://purl.org/coar/access_right/c_abf2open accessLaryngeal inflammationNeuropeptidesCyclooxygenase-2CytokinesNasogastric intubationImmunocytochemistryMRNA expressionReverse transcriptase polymerase chain reaction analysisAnimal model1584215 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://prod-dspace.uminho.pt/bitstreams/45664afb-34f2-4d9f-9d66-3ddf7e99e4b2/download
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
status SINGLETON
subject.fl_str_mv Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
title 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_short A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
title_sort A new model of laryngitis: neuropeptide, cyclooxygenase, and cytokine profile
topic Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
topic_facet Laryngeal inflammation
Neuropeptides
Cyclooxygenase-2
Cytokines
Nasogastric intubation
Immunocytochemistry
MRNA expression
Reverse transcriptase polymerase chain reaction analysis
Animal model
url https://hdl.handle.net/1822/7897
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