Which remote ischemic preconditioning protocol is favorable in renal ischemia-reperfusion injury in the rat?

Clin Hemorheol Microcirc. 2020;76(3):439-451. doi: 10.3233/CH-200916.

Abstract

Background: The optimal timing of remote ischemic preconditioning (RIPC) in renal ischemia-reperfusion (I/R) injury is still unclear. We aimed to compare early- and delayed-effect RIPC with hematological, microcirculatory and histomorphological parameters.

Methods: In anesthetized male CrI:WI Control rats (n = 7) laparotomy and femoral artery cannulation were performed. In I/R group (n = 7) additionally a 45-minute unilateral renal ischemia with 120-minute reperfusion was induced. The right hind-limb was strangulated for 3×10 minutes (10-minute intermittent reperfusion) 1 hour (RIPC-1 group, n = 7) or 24 hour (RIPC-24 group, n = 6) prior to the I/R. Hemodynamic, hematological parameters and organs' surface microcirculation were measured.

Results: Control and I/R group had the highest heart rate (p < 0.05 vs base), while the lowest mean arterial pressure (p < 0.05 vs RIPC-1) were found in the RIPC-24 group. The highest microcirculation values were measured in the I/R group (liver: p < 0.05 vs Control). The leukocyte count increased in I/R group (base: p < 0.05 vs Control), also this group's histological score was the highest (p < 0.05 vs Control). The RIPC-24 group had a significantly lower score than the RIPC-1 (p = 0.0025 vs RIPC-1).

Conclusion: Renal I/R caused significant functional and morphological, also in the RIPC groups. According to the histological examination the delayed-effect RIPC method was more effective.

Keywords: Acute kidney injury; histopathology; ischemia-reperfusion; microcirculation; remote ischemic preconditioning.

MeSH terms

  • Animals
  • Hemodynamics / genetics*
  • Ischemic Preconditioning / methods*
  • Kidney / pathology*
  • Male
  • Rats
  • Reperfusion Injury / drug therapy*
  • Reperfusion Injury / pathology