The effects of iloprost and alprostadil on ischemia-reperfusion injury in preventing inflammation, tissue degeneration, and apoptosis in rat skeletal muscle

Turk J Med Sci. 2017 Jun 12;47(3):1028-1036. doi: 10.3906/sag-1604-59.

Abstract

Background/aim: The protective effects of prostaglandin (PG) analogs on ischemia-reperfusion (I/R) have been well documented; however, comparative studies are lacking. The aim of the present study was to determine whether iloprost or alprostadil is more effective in preventing muscle I/R injury.

Materials and methods: Thirty-two rats were divided into four groups (n = 8): sham, control, IL (I/R + iloprost), and AL (I/R + alprostadil). I/R was induced by a tourniquet in the hindlimb for 3 h/3 h. The IL and AL groups received iloprost (0.5 ng kg-1 min-1) and alprostadil (0.05 µg kg-1 min-1) during reperfusion, respectively. After 6 h, blood and muscles were collected for analyses.

Results: Serum TNF-α and IL-1β levels were decreased in the IL and AL groups compared with the control group (P < 0.05), whereas IL-6 levels did not change significantly. Tissue malondialdehyde levels were significantly lower in the IL and AL groups (P < 0.05). Tissue catalase levels showed no difference. The histological damage scores and apoptosis scores were both significantly decreased in the IL and AL groups compared with the control group (P< 0.05).

Conclusion: The present study indicated that iloprost and alprostadil attenuated I/R injury in skeletal muscle. However, no comparable difference was evident regarding the efficacies of either PG analog.

Keywords: Ischemia; alprostadil; iloprost; muscle; reperfusion injury; skeletal.

MeSH terms

  • Alprostadil / pharmacology*
  • Animals
  • Apoptosis / drug effects*
  • Female
  • Iloprost / pharmacology*
  • Inflammation / metabolism
  • Inflammation / pathology
  • Inflammation / prevention & control*
  • Interleukin-1beta / blood
  • Muscle, Skeletal / drug effects*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology
  • Oxidoreductases
  • Protective Agents / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury / metabolism*
  • Tumor Necrosis Factor-alpha / blood

Substances

  • Interleukin-1beta
  • Protective Agents
  • Tumor Necrosis Factor-alpha
  • Oxidoreductases
  • Alprostadil
  • Iloprost