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dc.contributor.authorEl-Salhy, Magdyen_US
dc.contributor.authorUmezawa, Kazuoen_US
dc.contributor.authorGilja, Odd Helgeen_US
dc.contributor.authorHatlebakk, Jan Gen_US
dc.contributor.authorGundersen, Doris Ireneen_US
dc.contributor.authorHausken, Trygveen_US
dc.date.accessioned2015-05-15T12:59:35Z
dc.date.available2015-05-15T12:59:35Z
dc.date.issued2014-01-30eng
dc.identifier.issn1537-744X
dc.identifier.urihttps://hdl.handle.net/1956/9888
dc.description.abstractAP-1 and NF-κB inhibitors, namely, DTCM-G and DHMEQ, were investigated in male Wistar rats with severe colitis, induced by TNBS. The animals were randomized into 3 groups. The control group received 0.5 mL of 0.5% of the vehicle i.p., the DTCM-G group received 22.5 mg/kg body weight DTCM-G in 0.5% i.p., and the DHMEQ group received 15 mg/kg body weight DHMEQ i.p., all twice daily for 5 days. The body weight losses and mortality rates were significantly higher in the control group than those in DTCM-G-treated and DHMEQ-treated groups. The endoscopic inflammation scores in the control, DTCM-G-treated, and DHMEQ-treated groups were 6.3 ± 0.7, 1.0 ± 0.3, and 0.7 ± 0.3, respectively (P = 0.004 and 0.02, resp.). The inflammation scores as assessed by the macroscopic appearance were 4.3 ± 0.8, 0.7 ± 0.3, and 1.2 ± 0.4 in the control, DTCM-G-treated, and DHMEQ-treated groups, respectively (P = 0.01 and 0.009, resp.). The histopathological inflammation scores were 6.4 ± 0.7, 2.0 ± 1.0, and 2.2 ± 0.6 in the control, DTCM-G-treated, and DHMEQ-treated groups, respectively (P = 0.03 and 0.01, resp.). It was concluded that DTCM-G and DHMEQ exhibit strong anti-inflammatory and anticancer activities with no apparent toxicity, which make them excellent drug candidates for clinical use in inflammatory bowel diseases.en_US
dc.language.isoengeng
dc.publisherHindawieng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/eng
dc.titleAmelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Ratsen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2015-04-08T12:21:36Zen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2014 Magdy El-Salhy et al.
dc.source.articlenumber813804
dc.identifier.doihttps://doi.org/10.1155/2014/813804
dc.identifier.cristin1104572
dc.source.journalScientific World Journal
dc.source.402014
dc.subject.nsiVDP::Medical sciences: 700::Clinical medical sciences: 750::Gastroenterology: 773eng
dc.subject.nsiVDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Gasteroenterologi: 773nob


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