MicroRNA signatures in ischemia-reperfusion injury

Ann Plast Surg. 2012 Dec;69(6):668-71. doi: 10.1097/SAP.0b013e3182742c45.

Abstract

Background: MicroRNAs (miRs) are involved in gene expression and function, but little is known of their function in ischemia-reperfusion injury (IRI), which plays a critical role in flap compromise during microvascular flap surgeries. This article aimed to determine the expression profiles of miRs in rat flap surgeries after IRI.

Methods: Vessel specimens in rat epigastric flap were initially determined for miRs survey after 2 hours of ischemia and 2 hours of reperfusion. Their miR expressions were further quantified after 2 hours of ischemia and subsequent reperfusion for 2 and 24 hours.

Results: Only 3 miRs (miR-21, miR-193-3p, and miR-210) in rat vessels, but not in flap tissues, were significantly up-regulated at 24 hours of reperfusion after 2 hours of ischemia.

Conclusions: Our findings provide insights into deregulated expressions of miRs in flap surgeries after IRI. They might provide a further therapeutic consideration to prevent vascular compromise due to IRI in flap surgeries.

MeSH terms

  • Animals
  • Epigastric Arteries
  • Female
  • Gene Expression
  • Male
  • MicroRNAs / metabolism*
  • Microsurgery / adverse effects
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury / etiology
  • Reperfusion Injury / genetics*
  • Reperfusion Injury / surgery*
  • Stomach / blood supply
  • Stomach / surgery
  • Surgical Flaps / blood supply*
  • Up-Regulation
  • Vascular Surgical Procedures / methods

Substances

  • MIRN210 microRNA, rat
  • MicroRNAs
  • Mirn193 microRNA, rat
  • mirn21 microRNA, rat