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https://hdl.handle.net/11499/8466
Title: | Effects of caffeic acid phenethyl ester on anastomotic healing in secondary peritonitis | Authors: | Teke, Z. Bostanci, E.B. Yenisey, C. Kelten, Esra Canan Sacar, S. Simsek, N.G. Düzcan, Süleyman Ender |
Keywords: | Bursting pressures Caffeic acid phenethyl ester Cecal ligation and puncture Colonic anastomosis Glutathione Hydroxyproline Intraperitoneal sepsis Malondialdehyde Myeloperoxidase Superoxide dismutase Wound healing antioxidant biological marker caffeic acid phenethyl ester glutathione hydroxyproline malonaldehyde myeloperoxidase superoxide dismutase animal experiment animal model animal tissue article cecum colon anastomosis controlled study enzyme activity histopathology laparotomy ligation male nonhuman peritonitis priority journal puncture rat treatment outcome wound healing Anastomosis, Surgical Animals Caffeic Acids Colon Disease Models, Animal Male Peritonitis Peroxidase Phenylethyl Alcohol Pressure Rats Rats, Wistar Stress, Mechanical Superoxide Dismutase Wound Healing |
Abstract: | Purpose: We aimed to investigate the effects of caffeic acid phenethyl ester (CAPE) on wound healing in left colonic anastomoses in the presence of intraperitoneal sepsis induced by cecal ligation and puncture (CLP) in a rodent model. Methods: This experimental study was conducted on 48 male Wistar albino rats. The animals were randomly allocated into four groups and a left colonic anastomosis was performed on the day following sham operation or CLP in all rats: (i) sham-operated control group, laparatomy plus cecal mobilization (n 12) (Group 1), (ii) sham CAPE group, identical to Group 1 except for CAPE treatment (10 µmol/kg, intraperitoneally, 30 min before construction of the colonic anastomosis) (n 12) (Group 2), (iii) CLP group, cecal ligation and puncture (n 12) (Group 3), and (iv) CLP CAPE-treated group, 10 µmol/kg, intraperitoneally, 30 min before the construction of colonic anastomosis (n 12) (Group 4). On the postoperative day 7, the animals 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 of hydroxyproline (Hyp) contents, myeloperoxidase (MPO) acivity, malondialdehyde (MDA) levels, reduced glutathione (GSH) levels, and superoxide dismutase (SOD) activity. Body weight changes were examined. Results: CAPE treatment significantly increased colonic anastomotic bursting pressures (p < .05), colonic anastomotic tissue Hyp contents, and enzymatic and nonenzymatic antioxidant markers (p < .05), and significantly decreased oxidative stress parameters in colonic anastomotic tissues (p < .05). Histopathological scores were significantly better by CAPE administration (p < .05). Conclusion: This study clearly showed that CAPE treatment prevented the detrimental effects of intraperitoneal sepsis 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 sepsis-induced organ injury occurs. © 2012 Informa Healthcare USA, Inc. | URI: | https://hdl.handle.net/11499/8466 https://doi.org/10.3109/08941939.2011.646450 |
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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