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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorLLIMONA, F.-
dc.contributor.authorLIMA-SALGADO, T. M.-
dc.contributor.authorMORETTI, A. L.-
dc.contributor.authorTHEOBALDO, M.-
dc.contributor.authorJUKEMURA, J.-
dc.contributor.authorMACHADO, M. C. C.-
dc.contributor.authorVELASCO, I. T.-
dc.contributor.authorSOUZA, H. P.-
dc.identifier.citationPANCREAS, v.41, n.8, p.1380-1380, 2012-
dc.description.abstractBackground: Differentiate sepsis from the systemic inflammation caused by AP remains a clinical challenge. We hypothesized that transcription coactivator PGC-1>, a regulator of mitochondrial biogenesis and function, would be distinctly expressed during inflammation or infection, being useful to differentiate these two conditions. Methods: Acute pancreatitis(AP) was induced by retrograde injection o,5 ml of 5% sodium taurocholate into the main pancreatic duct.. PGC-1> mRNA.was evaluated by using a quantitayive Real-time PCR Macrophages were obtained by washing the peritoneum with PBS and placed in culture for 2h. and exposed to lipopolysaccharide, zymosan or vehicle. In another set of experiments, macrophages were transfected with antisense against PGC-1> Cecal ligation puncture (CLP) was used to establish a model of infected peritonitis. Results: In AP animals a marked increase in PGC-1> mRNA levels in circulating leukocytes was observed 48h after the surgical procedure, a time when bacteremia is present. Antibiotic treatment abolished PGC-1> up-regulation. Moreover, PGC-1> expression was higher in peritoneal macrophages from animals submitted to a bacterial insult (CLP) than in animals with acute pancreatitis .In macrophages, we could observe that PGC-1> expression is more prominent in the presence of a phagocytic stimulus (zymosan) compared to an aseptic inflammation induce by lipopolysaccharide. Moreover, abolishing PGC-1> expression with antisense impaired zymosan phagocytosis. Conclusion: Together these findings suggest that PGC-1> is differentially expressed during aseptic inflammation and infection and that it is necessary for adequate phagocytosis. These results could be useful in developing new tests for differentiating infection from inflammation in patients with acute pancreatitis.-
dc.titlePGC-1 alpha is a Valuable Tool to Differentiate Inflammation From Infection in Acute Pancreatitis-
dc.rights.holderCopyright LIPPINCOTT WILLIAMS & WILKINS-
dc.description.conferencedateOCTOBER 31 - NOVEMBER 3, 2012-
dc.description.conferencelocalMiami - FL, EUA-
dc.description.conferencenameJoint 43rd Meeting of the American Pancreatic Association and the 17th Meeting of the International Association of Pancreatology-
dc.subject.wosGastroenterology & Hepatology-
dc.type.categorymeeting abstract-
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Comunicações em Eventos - FM/MCG
Departamento de Cirurgia - FM/MCG

Comunicações em Eventos - FM/MCM
Departamento de Clínica Médica - FM/MCM

Comunicações em Eventos - HC/ICHC
Instituto Central - HC/ICHC

Comunicações em Eventos - HC/InCor
Instituto do Coração - HC/InCor

Comunicações em Eventos - LIM/37
LIM/37 - Laboratório de Transplante e Cirurgia de Fígado

Comunicações em Eventos - LIM/51
LIM/51 - Laboratório de Emergências Clínicas

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