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| Campo DC | Valor | Idioma |
|---|---|---|
| dc.contributor.author | Leite, Camila Ferreira | - |
| dc.contributor.author | Marangoni, Fábio André | - |
| dc.contributor.author | Camargo, Enilton Aparecido | - |
| dc.contributor.author | Braga, Angélica de Fátima de Assunção | - |
| dc.contributor.author | Toro, Ivan Felizardo Contrera | - |
| dc.contributor.author | Antunes, Edson | - |
| dc.contributor.author | Landucci, Elen Cristina Tiezem | - |
| dc.contributor.author | Mussi, Ricardo Kalaf | - |
| dc.date.accessioned | 2025-11-10T20:32:56Z | - |
| dc.date.available | 2025-11-10T20:32:56Z | - |
| dc.date.issued | 2013 | - |
| dc.identifier.citation | LEITE, C. F. et al. Simvastatin attenuates neutrophil recruitment in one-lung ventilation model in rats. Acta Cirúrgica Brasileira, São Paulo, v. 28, n. 4, p. 245-250, 2013. Disponível em: https://www.scielo.br/j/acb/a/tKKdFYDKb6kFRx7R3dHCVDK/?lang=en. Acesso em: 10 nov. 2025. | pt_BR |
| dc.identifier.issn | 1678-2674 | - |
| dc.identifier.uri | https://ri.ufs.br/jspui/handle/riufs/23816 | - |
| dc.language | eng | pt_BR |
| dc.publisher | Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia | pt_BR |
| dc.relation.ispartof | Acta Cirúrgica Brasileira | pt_BR |
| dc.subject | Animals models | eng |
| dc.subject | Pulmonary ventilation | eng |
| dc.subject | Simvastatin | eng |
| dc.subject | Thoracic Surgery | eng |
| dc.subject | Inflammation | eng |
| dc.subject | Rats | eng |
| dc.title | Simvastatin attenuates neutrophil recruitment in one-lung ventilation model in rats | pt_BR |
| dc.type | Artigo | pt_BR |
| dc.identifier.license | Creative Commons Atribuição-NãoComercial 4.0 Internacional (CC BY-NC 4.0) | pt_BR |
| dc.description.resumo | PURPOSE: To investigate the anti-inflammatory effects of simvastatin in rats undergoing one-lung ventilation (OLV) followed by lung re-expansion. METHODS: Male Wistar rats (n=30) were submitted to 1-h OLV followed by 1-h lung re-expansion. Treated group received simvastatin (40 mg/kg for 21 days) previous to OLV protocol. Control group received no treatment or surgical/ventilation interventions. Measurements of pulmonary myeloperoxidase (MPO) activity, pulmonary protein extravasation, and serum levels of cytokines and C-reactive protein (CRP) were performed. RESULTS: OLV significantly increased the MPO activity in the collapsed and continuously ventilated lungs (31% and 52% increase, respectively) compared with control (p<0.05). Treatment with simvastatin significantly reduced the MPO activity in the continuously ventilated lung but had no effect on lung edema after OLV. The serum IL-6 and CRP levels were markedly higher in OLV group, but simvastatin treatment failed to affect the production of these inflammatory markers. Serum levels of IL-1β, TNF-α and IL-10 remained below the detection limit in all groups. CONCLUSIONS: In an experimental one-lung ventilation model pre-operative treatment with simvastatin reduces remote neutrophil infiltration in the continuously ventilated lung. Our findings suggest that simvastatin may be of therapeutic value in OLV-induced pulmonary inflammation deserving clinical investigations. | pt_BR |
| dc.description.local | São Paulo | pt_BR |
| Aparece nas coleções: | DFS - Artigos de periódicos | |
Arquivos associados a este item:
| Arquivo | Descrição | Tamanho | Formato | |
|---|---|---|---|---|
| SimvastatinNeutrophilRecruitmentOneLungVentilation.pdf | 346,33 kB | Adobe PDF | ![]() Visualizar/Abrir |
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