Please use this identifier to cite or link to this item: 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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