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