Evidence map›Paper›PMID 20423518›Full record

ArticleBMC chemical biology2010

Dietary phenethylisothiocyanate attenuates bowel inflammation in mice.

Moul Dey, Peter Kuhn, David Ribnicky, Vummidigiridhar Premkumar, Kenneth Reuhl, Ilya Raskin

Open access · hybridAbstract read
In one paragraph

Article in BMC chemical biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Glucosinolate Derivatives: Emerging Anti-Inflammatory Agents.Pharmaceuticals (Basel, Switzerland) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Moul DeyDepartment of Nutrition, Food Science and Hospitality, South Dakota State University, Box 2275A, Brookings, SD 57007, USA. MOUL.DEY@SDSTATE.EDU.
Peter Kuhn
David Ribnicky
Vummidigiridhar Premkumar
Kenneth Reuhl
Ilya Raskin
Rutgers, The State University of New Jersey · USImmunomedics (United States) · USSouth Dakota State University · USUniversity of Cincinnati · US

Funding

An alternate therapy for treatment of IBD and prevention of colon cancerR00AT004245 · NCCIH · SOUTH DAKOTA STATE UNIVERSITY · PI DEY, MOUL · 2010 to 2012
$682k
An alternate therapy for treatment of IBD and prevention of colon cancerK99AT004245 · NCCIH · RUTGERS, THE STATE UNIV OF N.J. · PI DEY, MOUL · 2007 to 2008
$179k
NCCIH NIH HHS K99 AT004245NCCIH NIH HHS R00 AT004245
6 · The paper itself

Abstract

backgroundPhenethylisothiocyanate (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.

resultsIn 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.

conclusionsPEO 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.

Identifiers

PMID20423518
PMCPMC2881005
OpenAlexW2005714706

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.