Evidence map›Paper›PMID 21955242›Full record

ArticleBritish journal of pharmacology2012

Modulation of mouse gastrointestinal motility by allyl isothiocyanate, a constituent of cruciferous vegetables (Brassicaceae): evidence for TRPA1-independent effects.

Raffaele Capasso, Gabriella Aviello, Barbara Romano, Francesca Borrelli, Luciano De Petrocellis, Vincenzo Di Marzo, Angelo A Izzo

Abstract read
In one paragraph

Article in British journal of pharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Functional TRPA1 Channels Regulate CD56International journal of molecular sciences · 2023
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. TRP channels in the skin.British journal of pharmacology · 2014
    Review
  15. TRP channels in lower urinary tract dysfunction.British journal of pharmacology · 2014
    Review
  16. The pharmacology of TRP channels.British journal of pharmacology · 2014
    Article
  17. Review
  18. Review
  19. Article
  20. Article
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

7 authors.

Raffaele CapassoDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.
Gabriella AvielloDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.
Barbara RomanoDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.
Francesca BorrelliDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.
Luciano De PetrocellisDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.
Vincenzo Di MarzoDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.
Angelo A IzzoDepartment of Experimental Pharmacology, Endocannabinoid Research Group, University of Naples Federico II, Naples, ItalyInstitute of Biomolecular Chemistry, Endocannabinoid Research Group, National Research Council, Pozzuoli (NA), Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeAllyl isothiocyanate (AITC, mustard oil), a constituent of many common cruciferous vegetables (Brassicaceae), activates transient receptor potential of ankyrin type-1 (TRPA1) channels, claimed to regulate gastrointestinal contractility. In this study, we have investigated the effect of AITC on intestinal motility. EXPERIMENTAL APPROACH: Effects of AITC were investigated in vivo on upper gastrointestinal transit in mice and in mouse isolated ileum [contractions induced by electrical field stimulation (EFS), acetylcholine and spontaneous contractility]. The contractor activity of AITC was studied in mouse isolated colon. The ability of TRPA1 channel antagonists to block AITC-induced elevation of intracellular Ca(2+) [Ca(2+)](i) was assessed in HEK293 cells transfected with rat TRPA1 channels. KEY

resultsAITC increased [Ca(2+)](i) in HEK293 cells, reduced ileal contractility (acetylcholine-, EFS-induced contractions and spontaneous contractility), but contracted the isolated colon. Gentamicin and camphor (non-selective TRPA1 channel antagonists), HC-030031 and AP18 (selective TRPA1 channel agonists) inhibited AITC-induced effects in HEK293 cells but not in the ileum or colon. AITC-induced contractions were reduced by tetrodotoxin and strongly reduced by nifedipine, cyclopiazonic acid and ryanodine. In vivo, AITC reduced (following i.p. administration) or increased (following intragastric administration) upper gastrointestinal transit in mice These effects were not affected by HC-030031. CONCLUSION AND IMPLICATIONS: AITC, depending, in vitro, on the regions of gut examined and, in vivo, on the route of administration, exerted both stimulatory and inhibitory effects on intestinal motility, which were not sensitive to TRPA1 channel antagonists. The proposition that TRPA1 channels are the primary targets for AITC to induce contraction should be revised.

Indexed as

AnimalsBrassicaceaeColonGastrointestinal MotilityHEK293 CellsHumansIleumIn Vitro TechniquesIsothiocyanatesMaleMiceMice, Inbred ICRMuscle ContractionParasympatholyticsTransient Receptor Potential ChannelsTRPA1 Cation Channelallyl isothiocyanateIsothiocyanatesParasympatholyticsTransient Receptor Potential ChannelsTRPA1 Cation ChannelTrpa1 protein, mouse

Identifiers

PMID21955242
PMCPMC3372844

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.