Cargando…

Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats

AP-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...

Descripción completa

Detalles Bibliográficos
Autores principales: El-Salhy, Magdy, Umezawa, Kazuo, Gilja, Odd Helge, Hatlebakk, Jan G., Gundersen, Doris, Hausken, Trygve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925602/
https://www.ncbi.nlm.nih.gov/pubmed/24616647
http://dx.doi.org/10.1155/2014/813804
_version_ 1782303887353446400
author El-Salhy, Magdy
Umezawa, Kazuo
Gilja, Odd Helge
Hatlebakk, Jan G.
Gundersen, Doris
Hausken, Trygve
author_facet El-Salhy, Magdy
Umezawa, Kazuo
Gilja, Odd Helge
Hatlebakk, Jan G.
Gundersen, Doris
Hausken, Trygve
author_sort El-Salhy, Magdy
collection PubMed
description AP-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.
format Online
Article
Text
id pubmed-3925602
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-39256022014-03-10 Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats El-Salhy, Magdy Umezawa, Kazuo Gilja, Odd Helge Hatlebakk, Jan G. Gundersen, Doris Hausken, Trygve ScientificWorldJournal Research Article AP-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. Hindawi Publishing Corporation 2014-01-30 /pmc/articles/PMC3925602/ /pubmed/24616647 http://dx.doi.org/10.1155/2014/813804 Text en Copyright © 2014 Magdy El-Salhy et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
El-Salhy, Magdy
Umezawa, Kazuo
Gilja, Odd Helge
Hatlebakk, Jan G.
Gundersen, Doris
Hausken, Trygve
Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats
title Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats
title_full Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats
title_fullStr Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats
title_full_unstemmed Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats
title_short Amelioration of Severe TNBS Induced Colitis by Novel AP-1 and NF-κB Inhibitors in Rats
title_sort amelioration of severe tnbs induced colitis by novel ap-1 and nf-κb inhibitors in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925602/
https://www.ncbi.nlm.nih.gov/pubmed/24616647
http://dx.doi.org/10.1155/2014/813804
work_keys_str_mv AT elsalhymagdy ameliorationofseveretnbsinducedcolitisbynovelap1andnfkbinhibitorsinrats
AT umezawakazuo ameliorationofseveretnbsinducedcolitisbynovelap1andnfkbinhibitorsinrats
AT giljaoddhelge ameliorationofseveretnbsinducedcolitisbynovelap1andnfkbinhibitorsinrats
AT hatlebakkjang ameliorationofseveretnbsinducedcolitisbynovelap1andnfkbinhibitorsinrats
AT gundersendoris ameliorationofseveretnbsinducedcolitisbynovelap1andnfkbinhibitorsinrats
AT hauskentrygve ameliorationofseveretnbsinducedcolitisbynovelap1andnfkbinhibitorsinrats