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Dietary phenethylisothiocyanate attenuates bowel inflammation in mice.

Authors :
Dey M
Kuhn P
Ribnicky D
Premkumar V
Reuhl K
Raskin I
Source :
BMC chemical biology [BMC Chem Biol] 2010 Apr 27; Vol. 10, pp. 4. Date of Electronic Publication: 2010 Apr 27.
Publication Year :
2010

Abstract

Background: Phenethylisothiocyanate (PEITC) is produced by Brassica food plants. PEO is a PEITC Essential Oil containing >95% natural PEITC. PEITC is known to produce various health benefits but its effect in alleviation of ulcerative colitis signs is unknown.<br />Results: In two efficacy studies (acute and chronic) oral administration of PEO was effective at remitting acute and chronic signs of ulcerative colitis (UC) in mice. Disease activity, histology and biochemical characteristics were measured in the treated animals and were compared with appropriate controls. PEO treatment significantly improved body weights and stool consistency as well as decreased intestinal bleeding. PEO treatment also reduced mucosal inflammation, depletion of goblet cells and infiltration of inflammatory cells. Attenuation of proinflammatory interleukin1beta production was observed in the colons of PEO-treated animals. Expression analyses were also carried out for immune function related genes, transcription factors and cytokines in lipopolysaccharide-activated mouse macrophage cells. PEO likely affects an intricate network of immune signaling genes including a novel concentration dependent reduction of total cellular Signal Transducer and Activator of Transcription 1 (STAT1) as well as nuclear phosphorylated-STAT1 (activated form of STAT1). A PEO-concentration dependent decrease of mRNA of C-X-C motif ligand 10 (a STAT1 responsive chemokine) and Interleukin 6 were also observed.<br />Conclusions: PEO might be a promising candidate to develop as a treatment for ulcerative colitis patients. The disease attenuation by PEO is likely associated with suppression of activation of STAT1 transcription and inhibition of pro-inflammatory cytokines.

Details

Language :
English
ISSN :
1472-6769
Volume :
10
Database :
MEDLINE
Journal :
BMC chemical biology
Publication Type :
Academic Journal
Accession number :
20423518
Full Text :
https://doi.org/10.1186/1472-6769-10-4