Proteomics study in ischemic postconditioning after prolonged ischemia for lessening the ischemia/reperfusion injury of intestinal in rats
10.3760/cma.j.issn.1671-0282.2009.07.007
- VernacularTitle:缺血后处理抗大鼠肠缺血-再灌注损伤的蛋白质组学研究
- Author:
Kexuan LIU
;
Yunsheng LI
;
Cai LI
;
Yi LI
;
Dongjiang LIAO
;
Wenqi HUANG
- Publication Type:Journal Article
- Keywords:
Ischemic postconditioning;
Intestinal ischemic/reperfusion injury;
Proteomics;
Aldose reductase;
Aldehyde dehydrogenase
- From:
Chinese Journal of Emergency Medicine
2009;18(7):692-696
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the changes of proteins expressions in intestinal mucosa of rats after is chemic postconditioning (IPo) against intestinal ischemic/reperfusion (Ⅱ/R) injury of intestine in order to elucidate its potential mechanisms of protective role. Methods Sixteen SD rats were randomly divided into Ⅱ/R group and IPo group ( n = 8). Rats of both groups received an episode of ischemic/reperfusion insult to intstine that was made by occlusion of the superior mesenteric artery (SMA) for 60 minutes. Rats of IPo group underwent three additional episodes of clamping SMA on for 30 seconds and off for 30 seconds successively after prolonged reperfusion/reperfusion of intestine. The intestinal mucosa was taken by scratching immediately after reperfusion in both groups, and total proteins were separated by immobilized pH gradient (IPG) based two-dimensional gel electrophoresis (2-DE). The differentially expressed proteins were analyzed using Image Master 2D Elite 5.0 image analysis software, and the proteins were cut out from the gel and then identified using MALDI-TOF-MS. The biological information of these proteins was looked for in the database of these peptide mass finger-printing (PMF) .Results Ten differentially expressed proteins were found, of which 6 were up-regulated and 4 were down-regulated in IPo group. Nine proteins were identified and characterized by their bioelements including aldose reductase and aldehyde dehydrogenase that were related to anti-oxidative stress and inhibition of cell apoptosis. Conclusions The well-reproducible 2-DE profiles of intestinal mucosa in II/R and IPo groups were established. The potentially protective effects of IPo may be attributed to up-regulating protein expressions of aldose reductase and aldehyde dehydrogenase, and thereby suppressing oxidative stress and cell apoptosis.
