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https://hdl.handle.net/11499/8221
Title: | Caffeic acid phenethyl ester prevents detrimental effects of remote ischemia-reperfusion injury on healing of colonic anastomoses | Authors: | Teke, Z. Bostanci, E.B. Yenisey, C. Kelten, Esra Canan Sacar, M. Simsek, N.G. Düzcan, Süleyman Ender |
Keywords: | Bursting pressures Caffeic acid phenethyl ester Catalase Colonic anastomosis Glutathione Glutathione peroxidase Glutathione reductase Hydroxyproline Ischemia-reperfusion Malondialdehyde Myeloperoxidase Nitric oxide Wound healing Xanthine oxidase antiinflammatory agent antioxidant caffeic acid phenethyl ester hydroxyproline interleukin 1beta interleukin 6 tumor necrosis factor alpha animal experiment animal model antiinflammatory activity antioxidant activity article body weight chemical analysis colon anastomosis controlled study experimental study histopathology in vivo study intestine injury laparotomy male measurement mesenteric ischemia nonhuman oxidative stress priority journal rat reoperation reperfusion injury superior mesenteric artery wound healing Anastomosis, Surgical Animals Anti-Inflammatory Agents, Non-Steroidal Caffeic Acids Colon Cytokines Drug Evaluation, Preclinical Laparotomy Male Mesenteric Artery, Superior Oxidative Stress Phenylethyl Alcohol Random Allocation Rats Rats, Wistar Reperfusion Injury Surgical Wound Dehiscence Wound Healing Xanthine Oxidase |
Abstract: | Purpose: We aimed to investigate whether caffeic acid phenethyl ester (CAPE) prevents detrimental systemic effects of intestinal ischemia-reperfusion (IR) injury on colonic anastomotic wound healing. Methods: This experimental study was conducted on 48 male Wistar albino rats. The rats were randomly allocated into four groups and a left colonic anastomosis was performed in all rats: (i) sham-operated group (n = 12), laparatomy without intestinal IR injury; (ii) sham + CAPE group (n = 12), identical to Group 1 except for CAPE treatment (10 µmol/kg, intravenously); (iii) intestinal IR group (n = 12), 60 min of superior mesenteric ischemia followed by reperfusion; and (iv) IR + CAPE-treated group (n = 12) (10 µmol/kg, intravenously, 30 min before the construction of colonic anastomosis). On the postoperative day 7, the rats were subjected to relaparotomy for in vivo measurement of the colonic anastomotic bursting pressure. A colonic segment including the anastomotic site was resected for histopathological evaluation and biochemical analyses. The plasma proinflammatory cytokine levels were measured. Body weight changes were examined. Results: CAPE treatment significantly increased colonic anastomotic bursting pressures, and colonic anastomotic tissue hydroxyproline contents and antioxidant parameters (p < .05), and significantly decreased oxidative stress markers in colonic anastomotic tissues and plasma proinflammatory cytokine levels (p < .05). Histopathological scores were significantly better due to CAPE administration (p < .05). Conclusions: This study clearly showed that CAPE treatment prevented the delaying effects of remote IR injury on colonic anastomotic wound healing. Further clinical studies are required to determine whether CAPE has a useful role in the enhancement of gastrointestinal anastomotic wound healing during particular surgeries in which IR-induced organ injury occurs. © 2013 Informa Healthcare USA, Inc. | URI: | https://hdl.handle.net/11499/8221 https://doi.org/10.3109/08941939.2012.687434 |
ISSN: | 0894-1939 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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