Remote ischemic preconditioning attenuates intestinal mucosal damage: insight from a rat model of ischemia-reperfusion injury

J Transl Med. 2019 Apr 29;17(1):136. doi: 10.1186/s12967-019-1885-4.

Abstract

Background: Remote ischemic preconditioning (RIPC) is a phenomenon, whereby repeated, non-lethal episodes of ischemia to an organ or limb exert protection against ischemia-reperfusion (I/R) injury in distant organs. Despite intensive research, there is still an apparent lack of knowledge concerning the RIPC-mediated mechanisms, especially in the intestine. Aim of this study was to evaluate possible protective effects RIPC on intestinal I/R injury.

Methods: Thirty rats were randomly assigned to four groups: I/R; I/R + RIPC; Sham; Sham + RIPC. Animals were anesthetized and the superior mesenteric artery was clamped for 30 min, followed by 60 min of reperfusion. RIPC-treated rats received 3 × 5 min of bilateral hindlimb I/R prior to surgery, sham groups obtained laparotomy without clamping. After I/R injury serum/tissue was analyzed for: Mucosal damage, Caspase-3/7 activity, expression of cell stress proteins, hydrogen peroxide (H2O2) and malondialdehyde (MDA) production, Hypoxia-inducible factor-1α (HIF-1α) protein expression and matrix metalloproteinase (MMP) activity.

Results: Intestinal I/R resulted in increased mucosal injury (P < 0.001) and elevated Caspase-3/7 activity (P < 0.001). RIPC significantly reduced the histological signs of intestinal I/R injury (P < 0.01), but did not affect Caspase-3/7 activity. Proteome profiling suggested a RIPC-mediated regulation of several cell stress proteins after I/R injury: Cytochrome C (+ 157%); Cited-2 (- 39%), ADAMTS1 (+ 74%). Serum concentrations of H2O2 and MDA remained unchanged after RIPC, while the reduced intestinal injury was associated with increased HIF-1α levels. Measurements of MMP activities in serum and intestinal tissue revealed an attenuated gelatinase activity at 130 kDa within the serum samples (P < 0.001) after RIPC, while the activity of MMPs within the intestinal tissue was not affected by I/R injury or RIPC.

Conclusions: RIPC ameliorates intestinal I/R injury in rats. The underlying mechanisms may involve HIF-1α protein expression and a decreased serum activity of a 130 kDa factor with gelatinase activity.

Keywords: Hypoxia-inducible factor-1α; Intestinal ischemia; Ischemia/reperfusion injury; Matrix metalloproteinases; Remote ischemic preconditioning.

MeSH terms

  • Animals
  • Apoptosis
  • Disease Models, Animal
  • Heat-Shock Proteins / metabolism
  • Hydrogen Peroxide / metabolism
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Intestinal Mucosa / enzymology
  • Intestinal Mucosa / pathology*
  • Ischemic Preconditioning*
  • Lipid Peroxidation
  • Male
  • Matrix Metalloproteinases / metabolism
  • Rats, Wistar
  • Reperfusion Injury / enzymology
  • Reperfusion Injury / pathology*
  • Reperfusion Injury / therapy*

Substances

  • Heat-Shock Proteins
  • Hif1a protein, rat
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Hydrogen Peroxide
  • Matrix Metalloproteinases