Caffeic acid phenethyl ester alleviates mesenteric ischemia/reperfusion injury

J Invest Surg. 2012 Dec;25(6):354-65. doi: 10.3109/08941939.2012.677968.

Abstract

Purpose: We aimed to investigate the effects of caffeic acid phenethyl ester (CAPE) on intestinal mucosal injury induced by superior mesenteric occlusion.

Methods: This experimental study was conducted on 48 male Wistar-albino rats. The animals were randomly allocated into four groups: (i) Sham-operated group, laparotomy without intestinal ischemia/reperfusion (IR) injury (n = 12); (ii) Sham + CAPE group, identical to group 1 except for CAPE treatment (10 μmol/kg, intravenously) (n = 12); (iii) Intestinal IR group, 60 min of superior mesenteric ischemia followed by 3 hr of reperfusion (n = 12); and (iv) (IR + CAPE)-treated group, 10 μmol/kg injection of CAPE intravenously 30 min before the reperfusion period (n = 12). We evaluated the degree of intestinal mucosal injury on a grading scale, histopathologically, and by measuring oxidative stress markers and antioxidant parameters, biochemically. Intestinal edema was estimated by using wet/dry weight ratios. The plasma proinflammatory cytokine levels were measured. Animal survival was observed up to one week.

Results: Intestinal mucosal injury scores were significantly decreased with CAPE administration (p < .05). CAPE treatment significantly reduced oxidative stress markers in the intestinal tissues (p < .05) and the plasma proinflammatory cytokine levels (p < .05), and significantly increased antioxidant parameters in the intestinal tissues (p < .05). Intestinal edema was significantly alleviated by CAPE treatment (p < .05). The survival rates of CAPE-treated IR animals were significantly higher than IR-subjected rats (p < .05).

Conclusion: This study clearly showed that CAPE treatment significantly alleviated the intestinal mucosal injury caused by superior mesenteric ischemia/reperfusion. Further clinical studies are required to clarify whether CAPE has a useful role in reperfusion injury during particular surgeries in which IR-induced organ injury occurs.

MeSH terms

  • Animals
  • Antioxidants / pharmacology
  • Antioxidants / therapeutic use*
  • Caffeic Acids / pharmacology
  • Caffeic Acids / therapeutic use*
  • Cytokines / blood
  • Glutathione Peroxidase / metabolism
  • Intestine, Small / blood supply*
  • Intestine, Small / drug effects
  • Intestine, Small / metabolism
  • Male
  • Malondialdehyde / metabolism
  • Models, Animal
  • Nitrates / metabolism
  • Oxidative Stress / drug effects
  • Peroxidase / metabolism
  • Phenylethyl Alcohol / analogs & derivatives*
  • Phenylethyl Alcohol / pharmacology
  • Phenylethyl Alcohol / therapeutic use
  • Plant Bark*
  • Plant Extracts / pharmacology
  • Plant Extracts / therapeutic use*
  • Rats
  • Rats, Wistar
  • Regional Blood Flow / drug effects
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / prevention & control*
  • Xanthine Oxidase / metabolism

Substances

  • Antioxidants
  • Caffeic Acids
  • Cytokines
  • Nitrates
  • Plant Extracts
  • Malondialdehyde
  • Peroxidase
  • Glutathione Peroxidase
  • Xanthine Oxidase
  • caffeic acid phenethyl ester
  • Phenylethyl Alcohol