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| Autor(es): Mostrar menos - |
Silva, Jacqueline Cavalcante
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Bavestrello, Margherita
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Gazzola, Valerio
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Spinella, Giovanni
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Pane, Bianca
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Grasselli, Elena
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Demori, Ilaria
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Canesi, Laura
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Emionite, Laura
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Cilli, Michele
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Buschiazzo, Ambra
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Sambuceti, Gianmario
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Pitta, Ivan Rocha
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Pitta, Marina Galdino
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Perego, Patrizia
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Palombo, Domenico
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Parra Abdalla, Dulcineia Saes
Número total de Autores: 17
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| Tipo de documento: | Artigo Científico |
| Fonte: | Life Sciences; v. 297, p. 11-pg., 2022-05-15. |
| Resumo | |
Introduction: Ischemia-Reperfusion (I/R) damage is one of the major challenges in cardiothoracic surgeries and in a pathological manner, is identified by exacerbated damage signals resulted from blood supply restriction and subsequent flow restoration and re-oxygenation. I/R damage includes cellular dysfunction and death, impairing tissue and organ function. Inflammation and oxidative stress are known to underlie either ischemia or reper-fusion, leaded by HIF, TNF-alpha, NF-kappa B, IL-6 and ROS formation. However, the available approaches to prevent I/R damage has been unsuccessful so far. As agonists of peroxisome-proliferation activation receptor (PPAR) are described as transcription factors related to anti-inflammatory factors, we proposed to observe the effects of novel dual agonist, GQ-11, in I/R-related damage.& nbsp;Methods: Male, Wistar rats, 60 days age and 305 g body weight average were treated with vehicle, pioglitazone or GQ-11 (20 mg/kg) for 7 consecutive days and were submitted to aorta clamping for 30 min followed by 3 h of reperfusion. F-18-fluorodeoxyglucose (18F-FDG), an analog of glucose associated with inflammation when accu-mulated, was observed in liver and bowel by positron emission tomography (PET). RESULTS: GQ-11 decreased 18F-FDG uptake in liver and bowel when compared to vehicle and pioglitazone. The treatment also modulated inflammatory markers IL-10, TGF-beta, IL-6, IL1-beta, TNF alpha, and CCL-2, besides antioxidant enzymes such as catalase, GPx and SOD.& nbsp;Conclusion: Inflammation and oxidative stress showed to be important processes to be regulated in I/R in order to prevent exacerbated responses that leads to cell/tissue dysfunction and death. PPAR agonists - including GQ-11 -might be promising agents in a strategy to avoid tissue dysfunction and death after cardiothoracic surgeries. (AU) | |
| Processo FAPESP: | 12/51316-5 - Investigação da atividade de biofármacos, agonistas de PPARs e produtos naturais com potencial terapêutico na aterosclerose |
| Beneficiário: | Dulcineia Saes Parra Abdalla |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |
| Processo FAPESP: | 16/16850-1 - Ação de um novo derivado tiazolidínico (GQ-11) no processo de reparo tecidual em modelo experimental de resistência à insulina e isquemia |
| Beneficiário: | Jacqueline Cavalcante Silva |
| Modalidade de apoio: | Bolsas no Exterior - Estágio de Pesquisa - Doutorado |
| Processo FAPESP: | 16/00233-3 - "Ação de um novo derivado tiazolidínico (GQ-11) no processo de reparo tecidual em modelo experimental de resistência a insulina e cirurgia vascular". |
| Beneficiário: | Jacqueline Cavalcante Silva |
| Modalidade de apoio: | Bolsas no Brasil - Doutorado |