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Protection against lethal intra-abdominal sepsis by 1-(3-dimethylaminopropyl)-3-ethylurea.
Ruiz-Perez, Begoña; Cisneros, Ronald L; Matsumoto, Tetsuya; Miller, Robert J; Vasios, George; Calias, Pericles; Onderdonk, Andrew B.
Afiliação
  • Ruiz-Perez B; Channing Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA. bruiz@rics.bwh.harvard.edu.
J Infect Dis ; 188(3): 378-87, 2003 Aug 01.
Article em En | MEDLINE | ID: mdl-12870119
ABSTRACT
Sodium hyaluronate-carboxymethylcellulose (HA/CMC) formulations are gels that effectively reduce postoperative adhesions in both animals and humans, when placed in the peritoneal or pelvic cavities concomitant with surgical manipulation. However, it has been suggested that the use of these products may increase the risk of peritoneal infection after contamination with intestinal contents during surgery. Using the rat intra-abdominal sepsis model, we found that administration of HA/CMC gels before bacterial challenge did not increase mortality but did significantly protect rats against lethal infection. This effect was dose and time dependent. Protection was conferred not by the HA/CMC gels themselves but by 1-(3-dimethylaminopropyl)-3-ethylurea (EDU), a small molecule released from the gel complex under physiologic conditions. Our results suggest that the protective effect exhibited by EDU is related to down-regulation of T cell-dependent responses and suppression of the proinflammatory-cytokine cascade associated with mortality during the early phase of disease.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ureia / Adjuvantes Imunológicos / Sepse / Abscesso Abdominal / Infecções por Escherichia coli / Géis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Infect Dis Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Estados Unidos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ureia / Adjuvantes Imunológicos / Sepse / Abscesso Abdominal / Infecções por Escherichia coli / Géis Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: J Infect Dis Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Estados Unidos