Acute Lung Injury in Cholinergic-Deficient Mice Supports Anti-Inflammatory Role of α7 Nicotinic Acetylcholine Receptor

dc.contributor.authorPinheiro, Nathalia Montouro [UNIFESP]
dc.contributor.authorBanzato, Rosana
dc.contributor.authorTibério, Iolanda de Fátima Lopes Calvo
dc.contributor.authorPrado, Marco Antônio Máximo
dc.contributor.authorPrado, Vania Ferreira
dc.contributor.authorHamouda, Ayman
dc.contributor.authorPrado, Carla Máximo [UNIFESP]
dc.contributor.authorLatteshttp://lattes.cnpq.br/8960401765088965pt_BR
dc.date.accessioned2021-11-12T17:12:57Z
dc.date.available2021-11-12T17:12:57Z
dc.date.issued2021-07
dc.description.abstractAbstract: (1) Background: The lung cholinergic pathway is important for controlling pulmonary inflammation in acute lung injury, a condition that is characterized by a sudden onset and intense inflammation. This study investigated changes in the expression levels of nicotinic and muscarinic acetylcholine receptors (nAChR and mAChR) in the lung during acute lung injury. (2) Methods: acute lung injury (ALI) was induced in wild-type and cholinergic-deficient (VAChT-KDHOM) mice using intratracheal lipopolysaccharide (LPS) instillation with or without concurrent treatment with nicotinic ligands. Bronchoalveolar lavage fluid was collected to evaluate markers of inflammation, and then the lung was removed and processed for isolation of membrane fraction and determination of acetylcholine receptors level using radioligand binding assays. (3) Results: LPS-induced increase in lung inflammatory markers (e.g., neutrophils and IL-1β) was significantly higher in VAChT-KDHOM than wild-type mice. In contrast, LPS treatment resulted in a significant increase in lung’s α7 nicotinic receptor level in wild-type, but not in VAChT-KDHOM mice. However, treatment with PNU 282987, a selective α7 nicotinic receptor agonist, restored VAChT-KDHOM mice’s ability to increase α7 nicotinic receptor levels in response to LPS-induced acute lung injury and reduced lung inflammation. LPS also increased muscarinic receptors level in VAChT-KDHOM mice, and PNU 282987 treatment reduced this response. (4) Conclusions: Our data indicate that the anti-inflammatory effects of the lung cholinergic system involve an increase in the level of α7 nicotinic receptors. Pharmacological agents that increase the expression or the function of lung α7 nicotinic receptors have potential clinical uses for treating acute lung injury.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)pt
dc.description.sponsorshipThe University of Texas System STARs Funden
dc.description.sponsorshipIDFAPESP: 2018/15738-9pt_BR
dc.description.sponsorshipIDFAPESP: 2019/15665-4pt_BR
dc.description.sponsorshipIDFAPESP: 2020/13480-4pt_BR
dc.description.sponsorshipIDCNPq: 303035/2018-8pt
dc.identifier.doihttps://doi.org/10.3390/ ijms22147552pt_BR
dc.identifier.urihttps://hdl.handle.net/11600/62225
dc.languageporpt_BR
dc.publisherNicola Scichilonept_BR
dc.relation.ispartofInternational Journal of Molecular Sciencespt_BR
dc.rightsinfo:eu-repo/semantics/openAccesspt_BR
dc.subjectNicotinic acetylcholine receptorsen
dc.subjectMuscarinic acetylcholine receptorsen
dc.subjectAcute lung injuryen
dc.subjectPNU 282987en
dc.subjectCholinergic anti-inflammatory pathwayen
dc.titleAcute Lung Injury in Cholinergic-Deficient Mice Supports Anti-Inflammatory Role of α7 Nicotinic Acetylcholine Receptoren
dc.typeinfo:eu-repo/semantics/articlept_BR
unifesp.campusInstituto de Saúde e Sociedade (ISS)pt_BR
unifesp.departamentoBiociênciaspt_BR
unifesp.graduateProgramInterdisciplinar em Ciências da Saúdept_BR
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