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10.12659/MSM.893924

http://scihub22266oqcxt.onion/10.12659/MSM.893924
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C4404748!4404748 !25863938
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suck abstract from ncbi


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pmid25863938
      Med+Sci+Monit 2015 ; 21 (ä): 1057-65
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  • Transduced PEP-1-heme oxygenase-1 fusion protein reduces remote organ injury induced by intestinal ischemia/reperfusion #MMPMID25863938
  • He XH ; Li QW ; Wang YL ; Zhang ZZ ; Ke JJ ; Yan XT ; Chen K
  • Med Sci Monit 2015[Apr]; 21 (ä): 1057-65 PMID25863938 show ga
  • BACKGROUND: A fusion protein composed of heme oxygenase-1 (HO-1) and cell-penetrating peptide PEP-1 has been shown to reduce local intestinal injury after intestinal ischemia/reperfusion (I/R). In this study, we investigated the effects of PEP-1-HO-1 fusion protein on remote organ injury induced by intestinal I/R in rats. MATERIAL AND METHODS: We randomly assigned 24 male Sprague-Dawley rats to 3 groups: Sham, I/R, and I/R plus PEP-1-HO-1 treatment (HO). The model of intestinal I/R was established by occluding the superior mesenteric artery for 45 min followed by 120-min reperfusion. In HO group, PEP-1-HO-1 was administered intravenously 30 min before ischemia, while animals in the Sham and I/R groups received the equal volume of physiological saline. At the end of the experiment, lung, liver, and blood samples were collected and analyzed. RESULTS: Malondialdehyde levels and histological injury scores were increased, and superoxide dismutase activities were decreased in the lung and liver tissues in the I/R group compared with the Sham group (P<0.05). Serum levels of alanine aminotransferase, aspartate aminotransferase, tumor necrosis factor-?, interleukin-6, and lung tissue wet weight to dry weight ratio were increased in the I/R group compared with the Sham group (P<0.05). NF-?B expression in intestinal tissues was significantly higher in the I/R group than in the Sham group. These changes were significantly reversed by treatment with PEP-1-HO-1. CONCLUSIONS: This study demonstrates that administration of PEP-1-HO-1 has a protective role against lung and liver injury after intestinal I/R, attributable to the reduction of released proinflammatory cytokines regulated by NF-?B.
  • |*Transduction, Genetic [MESH]
  • |Alanine Transaminase/blood [MESH]
  • |Animals [MESH]
  • |Aspartate Aminotransferases/blood [MESH]
  • |Heme Oxygenase-1/genetics/*therapeutic use [MESH]
  • |Interleukin-6/blood [MESH]
  • |Intestines/*blood supply/pathology [MESH]
  • |Liver/enzymology/*pathology [MESH]
  • |Lung/enzymology/*pathology [MESH]
  • |Male [MESH]
  • |Malondialdehyde/metabolism [MESH]
  • |NF-kappa B/metabolism [MESH]
  • |Organ Size [MESH]
  • |Rats, Sprague-Dawley [MESH]
  • |Recombinant Fusion Proteins/genetics/*therapeutic use [MESH]
  • |Reperfusion Injury/blood/pathology/*therapy [MESH]
  • |Superoxide Dismutase/metabolism [MESH]


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