Show simple item record

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


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

Attribution CC BY
Except where otherwise noted, this item's license is described as Attribution CC BY