Evidence map›Paper›PMID 19211797›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2009

TRPA1 regulates gastrointestinal motility through serotonin release from enterochromaffin cells.

Katsura Nozawa, Eri Kawabata-Shoda, Hitoshi Doihara, Ryosuke Kojima, Hidetsugu Okada, Shinobu Mochizuki, Yorikata Sano, Kohei Inamura, Hitoshi Matsushime, Tomonobu Koizumi and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 190 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed, 2 pooled it
7.6field-weighted citation impact, top 2% 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

190 citing papers in PubMed, 2 syntheses or guidelines pooled it, 398 citations in OpenAlex.

  1. Pooled it
  2. Enterochromaffin Cells: Sentinels to Gut Microbiota in Hyperalgesia?Frontiers in cellular and infection microbiology · 2021
    Pooled it
  3. Trial
  4. Effects of heat-treatedFrontiers in nutrition · 2026
    Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. P2X7R+CD8αβiScience · 2026
    Article
  10. Review
  11. Review
  12. Article
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  14. Review
  15. Review
  16. What goes down may come up: regurgitative behaviors and their underlying gut-brain axes-insights from genetic models and related pathologies.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2026
    Review
  17. Article
  18. Incretin hormones and obesity.The Journal of physiology · 2025
    Review
  19. Review
  20. Sensory signals for nausea.Trends in neurosciences · 2025
    Review

130 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 2 countries.

Katsura NozawaDrug Discovery Research, Astellas Pharma Inc., 21 Miyukigaoka, Tsukuba, Ibaraki, 305-8585, Japan. katsura.nozawa@jp.astellas.com
Eri Kawabata-Shoda
Hitoshi Doihara
Ryosuke Kojima
Hidetsugu Okada
Shinobu Mochizuki
Yorikata Sano
Kohei Inamura
Hitoshi Matsushime
Tomonobu Koizumi
Toshihide Yokoyama
Hiroyuki Ito
Astellas Pharma (Japan) · JPUniversity of California, San Francisco · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serotonin (5-hydroxytryptamine; 5-HT) is abundantly present throughout the gastrointestinal tract and stored mostly in enterochromaffin (EC) cells, which are located on the mucosal surface. 5-HT released from EC cells stimulate both intrinsic and extrinsic nerves, which results in various physiological and pathophysiological responses, such as gastrointestinal contractions. EC cells are believed to have the ability to respond to the chemical composition of the luminal contents of the gut; however, the underlying molecular and cellular mechanisms have not been identified. Here, we demonstrate that the transient receptor potential (TRP) cation channel TRPA1, which is activated by pungent compounds or cold temperature, is highly expressed in EC cells. We also found that TRPA1 agonists, including allyl isothiocyanate and cinnamaldehyde, stimulate EC cell functions, such as increasing intracellular Ca(2+) levels and 5-HT release, by using highly concentrated EC cell fractions and a model of EC cell function, the RIN14B cell line. Furthermore, we showed that allyl isothiocyanate promotes the contraction of isolated guinea pig ileum via the 5-HT(3) receptor. Taken together, our results indicate that TRPA1 acts as a sensor molecule for EC cells and may regulate gastrointestinal function.

Indexed as

Gastrointestinal MotilityAnimalsAnkyrinsCalciumCalcium ChannelsCell LineEnterochromaffin CellsGene Expression RegulationGuinea PigsHumansMaleMiceNerve Tissue ProteinsRatsSerotoninTransient Receptor Potential ChannelsAnkyrinsCalciumCalcium ChannelsNerve Tissue ProteinsSerotoninTransient Receptor Potential ChannelsTRPA1 Cation ChannelTRPA1 protein, humanTrpa1 protein, mouseTrpa1 protein, ratTRPC Cation Channels

Identifiers

PMID19211797
PMCPMC2651261
OpenAlexW2156291426

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.