Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/27792
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dc.date.accessioned2022-07-07T10:59:07Z-
dc.date.available2022-07-07T10:59:07Z-
dc.date.issued2010-05-28-
dc.identifier.citationDuman, U. vd. (2010). "Anti-inflammatory efficiency of levobupivacaine in an experimental colitis model". World Journal of Gastroenterology, 16(20), 2537-2541.en_US
dc.identifier.issn1007-9327-
dc.identifier.issn2219-2840-
dc.identifier.urihttps://doi.org/10.3748/wjg.v16.i20.2537-
dc.identifier.urihttps://www.wjgnet.com/1007-9327/full/v16/i20/2537.htm-
dc.identifier.urihttp://hdl.handle.net/11452/27792-
dc.description.abstractAIM: To investigate the efficiency of levobupivacaine in treating experimentally induced colitis in rats. METHODS: Colitis was induced by trinitrobenzene sulfonic acid and ethanol in 30 rats under general anesthesia, and 10 rats were used as a sham group. Subsequent to induction of colitis, rats were divided into three groups; budesonide group received 0.1 mg/kg budesonide, levobupivacaine group received 10 mg/kg levobupivacaine and saline group received 1 mL saline solution via rectal route for 7 d. In the sham group, only routine rectal catheterization was performed without use of any material. At the end of 7 d, laparotomy and total colectomy were performed for histopathological examination in all rats and blood samples were drawn for measurement of tumor necrosis factor (TNF)-alpha and interleukin (IL)-6 following cardiac puncture. Macroscopic and microscopic evaluations of the specimens were performed by a pathologist blinded to group assignment of the rats. RESULTS: Weight loss (P = 0.016) and macroscopic examination scores (P = 0.001) were significantly higher in saline group than others. Histopathological scoring was comparable between all colitis groups (P = 0.350). There was no significant difference in TNF-alpha levels and IL-6 levels (P = 0.150). CONCLUSION: The significant improvement in macroscopic scores suggests that levobupivacaine may have topical anti-inflammatory effects in an experimental colitis model; however, this finding was not supported by microscopic findings.en_US
dc.language.isoenen_US
dc.publisherBaishideng Publishing Groupen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAtıf Gayri Ticari Türetilemez 4.0 Uluslararasıtr_TR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectTrinitrobenzene sulfonic aciden_US
dc.subjectColitisen_US
dc.subjectLevobupivacaineen_US
dc.subjectBudesonideen_US
dc.subjectInflammatory-bowel-diseaseen_US
dc.subjectUlcerative-colitisen_US
dc.subjectLocal-anestheticsen_US
dc.subjectLidocaineen_US
dc.subjectRopivacaineen_US
dc.subjectProctitisen_US
dc.subjectTherapyen_US
dc.subjectCellsen_US
dc.subjectGastroenterology & hepatologyen_US
dc.titleAnti-inflammatory efficiency of levobupivacaine in an experimental colitis modelen_US
dc.typeArticleen_US
dc.identifier.wos000278196800012tr_TR
dc.identifier.scopus2-s2.0-77953260704tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Anesteziyoloji ve Reanimasyon Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Patoloji Anabilim Dalı.tr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyokimya Anabilim Dalı.tr_TR
dc.contributor.orcid0000-0002-2593-7196tr_TR
dc.contributor.orcid0000-0002-4946-555Xtr_TR
dc.identifier.startpage2537tr_TR
dc.identifier.endpage2541tr_TR
dc.identifier.volume16tr_TR
dc.identifier.issue20tr_TR
dc.relation.journalWorld Journal of Gastroenterologyen_US
dc.contributor.buuauthorDuman, Uğur-
dc.contributor.buuauthorYılmazlar, Aysun-
dc.contributor.buuauthorÖztürk, Ersin-
dc.contributor.buuauthorAker, Sibel-
dc.contributor.buuauthorSarandöl, Emre-
dc.contributor.buuauthorYılmazlar, Tuncay-
dc.contributor.researcheridABE-1716-2020tr_TR
dc.contributor.researcheridH-5770-2018tr_TR
dc.identifier.pubmed20503454tr_TR
dc.subject.wosGastroenterology & hepatologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid36971700700tr_TR
dc.contributor.scopusid55899579900tr_TR
dc.contributor.scopusid35070171400tr_TR
dc.contributor.scopusid12795285000tr_TR
dc.contributor.scopusid55943324800tr_TR
dc.contributor.scopusid6701800362tr_TR
dc.subject.scopusLidocaine; Postoperative Nausea and Vomiting; Intravenousen_US
dc.subject.emtreeAlcoholen_US
dc.subject.emtreeBudesonideen_US
dc.subject.emtreeInterleukin 6en_US
dc.subject.emtreeLevobupivacaineen_US
dc.subject.emtreeSodium chlorideen_US
dc.subject.emtreeTrinitrobenzenesulfonic aciden_US
dc.subject.emtreeTumor necrosis factor alphaen_US
dc.subject.emtreeAnimal cellen_US
dc.subject.emtreeAnimal experimenten_US
dc.subject.emtreeAnimal modelen_US
dc.subject.emtreeAnimal tissueen_US
dc.subject.emtreeAntiinflammatory activityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBlood samplingen_US
dc.subject.emtreeCatheterizationen_US
dc.subject.emtreeColitisen_US
dc.subject.emtreeColon resectionen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeDrug efficacyen_US
dc.subject.emtreeEnteritisen_US
dc.subject.emtreeHistopathologyen_US
dc.subject.emtreeLaparotomyen_US
dc.subject.emtreeMaleen_US
dc.subject.emtreeNonhumanen_US
dc.subject.emtreeRaten_US
dc.subject.emtreeSingle drug doseen_US
dc.subject.emtreeWeight reductionen_US
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