Your browser doesn't support javascript.
loading
Ischemic preconditioning modifies mortality and inflammatory response.
Pinheiro, Daniel Faria de Campos; Fontes, Belchor; Shimazaki, John Kioshi; Heimbecker, Ana Maria Cattani; Jacysyn, Jacqueline de Fátima; Rasslan, Samir; Montero, Edna Frasson de Souza; Utiyama, Edivaldo Massazo.
Affiliation
  • Pinheiro DF; Department of Surgery, Medical School, Universidade de São Paulo, Brazil.
  • Fontes B; Department of Surgery, Medical School, FMUSP, Sao Paulo, SP, Brazil.
  • Shimazaki JK; FMUSP, Brazil.
  • Heimbecker AM; Department of Surgery, FMUSP, Brazil.
  • Jacysyn Jde F; Department of Surgery, FMUSP, Sao Paulo, SP, Brazil.
  • Rasslan S; Department of Surgery, FMUSP, Sao Paulo, SP, Brazil.
  • Montero EF; Department of Surgery, FMUSP, Sao Paulo, SP, Brazil.
  • Utiyama EM; Department of Surgery, FMUSP, Sao Paulo, SP, Brazil.
Acta Cir Bras ; 31(1): 1-7, 2016 Jan.
Article in En | MEDLINE | ID: mdl-26840349
ABSTRACT

PURPOSE:

To evaluate the effect of ischemic preconditioning on mortality, inflammatory mediators and oxidative stress after intestinal ischemia and reperfusion.

METHODS:

Male Wistar rats were allocated according to the period of ischemia with or without ischemic preconditioning which consist on clamping the superior mesenteric artery for 10 minutes followed by reperfusion for 10 minutes before the sustained ischemia period. Mortality was assessed in Phase 1 study, and the CINC-1, CINC-2 and MDA levels in the lungs were analyzed in Phase 2.

RESULTS:

Mortality was lower in the ischemic preconditioning group subjected to 90 minutes of ischemia compared to the group without ischemic preconditioning (I-90 50% and IPC-90 15%, p=0.018), and it was lower in the ischemic preconditioning group as a whole compared to the groups without ischemic preconditioning (IPC-14% and I=30%, p=0.006). Lower levels of MDA, CINC-1, and CINC-2 were observed in the animals that were subjected to ischemic preconditioning compared to the animals that were not (MDA I-45=1.23 nmol/mg protein, and IPC-45=0.62 nmol/mg protein, p=0.0333; CINC-1 I-45=0.82 ng/mL and IPC-45=0.67 ng/mL, p=0.041; CINC-2 I-45=0.52 ng/mL and IPC-45=0.35 ng/mL, p=0.032).

CONCLUSION:

Ischemic preconditioning reduces mortality, inflammatory process and oxidative stress in rats subjected to intestinal ischemia and reperfusion.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reperfusion Injury / Oxidative Stress / Inflammation Mediators / Ischemic Preconditioning / Mesenteric Ischemia Limits: Animals Language: En Journal: Acta Cir Bras Year: 2016 Document type: Article Affiliation country: Publication country: BR / BRASIL / BRASILE / BRAZIL / BRESIL

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reperfusion Injury / Oxidative Stress / Inflammation Mediators / Ischemic Preconditioning / Mesenteric Ischemia Limits: Animals Language: En Journal: Acta Cir Bras Year: 2016 Document type: Article Affiliation country: Publication country: BR / BRASIL / BRASILE / BRAZIL / BRESIL