Oxygenated perfluorocarbons protect the intestine from the ischemia/reperfusion injury in rabbits

Vasc Endovascular Surg. 2011 Jul;45(5):426-32. doi: 10.1177/1538574411402223. Epub 2011 May 13.

Abstract

Objective: To investigate whether intraluminal administration of oxygenated perfluorocarbons (PFCs) protects the enterocyte from acute ischemia-reperfusion (I/R) injury.

Materials and methods: Twenty rabbits were divided in 4 groups: sham-operated controls (group A), acute I/R (group B), acute I/R plus infusion of oxygenated PFCs 30 minutes before ischemia (group C), and acute I/R plus infusion of oxygenated PFCs 30 minutes before reperfusion (group D). Serum creatine phosphokinase (CPK) and mucosal disaccharidase activity were examined. Intestinal biopsies were obtained for electron microscopy study.

Results: Group B CPK mean values are 3495.2 ± 157.35 and 4855 ± 350.21 U/L. Group C: 2674.6 ± 265.87 and 3231 ± 232.30. Group D: 2382.2 ± 102.90 and 3217.6 ± 185.61 at 120 and 180 minutes (P<.05). At 180 minutes, maltase and sucrose values were 33.63, 51.88, 8.45, and 19.91, and 17.99, 22.87, 6.62, and 14.24 µmol/min per g for groups A, B, C, and D, respectively (P<.05). Histopathology showed the least cellular deterioration in PFC groups.

Conclusion: Oxygenated PFCs protect the enterocyte during bowel I/R.

MeSH terms

  • Analysis of Variance
  • Animals
  • Biopsy
  • Creatine Kinase / blood
  • Cytoprotection
  • Disease Models, Animal
  • Enterocytes / drug effects*
  • Enterocytes / metabolism
  • Enterocytes / pathology
  • Enterocytes / ultrastructure
  • Fluorocarbons / pharmacology*
  • Intestinal Mucosa / metabolism
  • Intestines / blood supply*
  • Intestines / drug effects*
  • Intestines / ultrastructure
  • Linear Models
  • Microscopy, Electron
  • Oxygen / pharmacology*
  • Protective Agents / pharmacology*
  • Rabbits
  • Reperfusion Injury / prevention & control*
  • Sucrase / metabolism
  • Time Factors
  • alpha-Glucosidases / metabolism

Substances

  • Fluorocarbons
  • Protective Agents
  • Creatine Kinase
  • alpha-Glucosidases
  • Sucrase
  • Oxygen