Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/8221
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Teke, Z. | - |
dc.contributor.author | Bostanci, E.B. | - |
dc.contributor.author | Yenisey, C. | - |
dc.contributor.author | Kelten, Esra Canan | - |
dc.contributor.author | Sacar, M. | - |
dc.contributor.author | Simsek, N.G. | - |
dc.contributor.author | Düzcan, Süleyman Ender | - |
dc.date.accessioned | 2019-08-16T12:37:15Z | |
dc.date.available | 2019-08-16T12:37:15Z | |
dc.date.issued | 2013 | - |
dc.identifier.issn | 0894-1939 | - |
dc.identifier.uri | https://hdl.handle.net/11499/8221 | - |
dc.identifier.uri | https://doi.org/10.3109/08941939.2012.687434 | - |
dc.description.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. | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | Journal of Investigative Surgery | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Bursting pressures | en_US |
dc.subject | Caffeic acid phenethyl ester | en_US |
dc.subject | Catalase | en_US |
dc.subject | Colonic anastomosis | en_US |
dc.subject | Glutathione | en_US |
dc.subject | Glutathione peroxidase | en_US |
dc.subject | Glutathione reductase | en_US |
dc.subject | Hydroxyproline | en_US |
dc.subject | Ischemia-reperfusion | en_US |
dc.subject | Malondialdehyde | en_US |
dc.subject | Myeloperoxidase | en_US |
dc.subject | Nitric oxide | en_US |
dc.subject | Wound healing | en_US |
dc.subject | Xanthine oxidase | en_US |
dc.subject | antiinflammatory agent | en_US |
dc.subject | antioxidant | en_US |
dc.subject | caffeic acid phenethyl ester | en_US |
dc.subject | hydroxyproline | en_US |
dc.subject | interleukin 1beta | en_US |
dc.subject | interleukin 6 | en_US |
dc.subject | tumor necrosis factor alpha | en_US |
dc.subject | animal experiment | en_US |
dc.subject | animal model | en_US |
dc.subject | antiinflammatory activity | en_US |
dc.subject | antioxidant activity | en_US |
dc.subject | article | en_US |
dc.subject | body weight | en_US |
dc.subject | chemical analysis | en_US |
dc.subject | colon anastomosis | en_US |
dc.subject | controlled study | en_US |
dc.subject | experimental study | en_US |
dc.subject | histopathology | en_US |
dc.subject | in vivo study | en_US |
dc.subject | intestine injury | en_US |
dc.subject | laparotomy | en_US |
dc.subject | male | en_US |
dc.subject | measurement | en_US |
dc.subject | mesenteric ischemia | en_US |
dc.subject | nonhuman | en_US |
dc.subject | oxidative stress | en_US |
dc.subject | priority journal | en_US |
dc.subject | rat | en_US |
dc.subject | reoperation | en_US |
dc.subject | reperfusion injury | en_US |
dc.subject | superior mesenteric artery | en_US |
dc.subject | wound healing | en_US |
dc.subject | Anastomosis, Surgical | en_US |
dc.subject | Animals | en_US |
dc.subject | Anti-Inflammatory Agents, Non-Steroidal | en_US |
dc.subject | Caffeic Acids | en_US |
dc.subject | Colon | en_US |
dc.subject | Cytokines | en_US |
dc.subject | Drug Evaluation, Preclinical | en_US |
dc.subject | Laparotomy | en_US |
dc.subject | Male | en_US |
dc.subject | Mesenteric Artery, Superior | en_US |
dc.subject | Oxidative Stress | en_US |
dc.subject | Phenylethyl Alcohol | en_US |
dc.subject | Random Allocation | en_US |
dc.subject | Rats | en_US |
dc.subject | Rats, Wistar | en_US |
dc.subject | Reperfusion Injury | en_US |
dc.subject | Surgical Wound Dehiscence | en_US |
dc.subject | Wound Healing | en_US |
dc.subject | Xanthine Oxidase | en_US |
dc.title | Caffeic acid phenethyl ester prevents detrimental effects of remote ischemia-reperfusion injury on healing of colonic anastomoses | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 26 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 16 | |
dc.identifier.startpage | 16 | en_US |
dc.identifier.endpage | 29 | en_US |
dc.identifier.doi | 10.3109/08941939.2012.687434 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 22646141 | en_US |
dc.identifier.scopus | 2-s2.0-84873675895 | en_US |
dc.identifier.wos | WOS:000314650400004 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.fulltext | No Fulltext | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
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 |
CORE Recommender
SCOPUSTM
Citations
4
checked on Dec 14, 2024
WEB OF SCIENCETM
Citations
6
checked on Dec 18, 2024
Page view(s)
40
checked on Aug 24, 2024
Google ScholarTM
Check
Altmetric
Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.