Evidence map›Paper›PMID 21512155›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2011

Colitis decreases mechanosensitive K2P channel expression and function in mouse colon sensory neurons.

Jun-Ho La, G F Gebhart

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.9field-weighted citation impact, top 17% 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

31 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Sex differences in zymosan-induced behavioral visceral hypersensitivity and colorectal afferent sensitization.American journal of physiology. Gastrointestinal and liver physiology · 2024
    Article
  4. Piezo1 in Digestive System Function and Dysfunction.International journal of molecular sciences · 2023
    Review
  5. Efficacy of Supplemental Diet Gels for Preventing Postoperative Weight Loss in Mice (Journal of the American Association for Laboratory Animal Science : JAALAS · 2023
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Visceral pain from colon and rectum: the mechanotransduction and biomechanics.Journal of neural transmission (Vienna, Austria : 1996) · 2020
    Review
  13. Review
  14. Article
  15. Voltage-gated sodium channels: (NaThe Journal of physiology · 2018
    Review
  16. Article
  17. Article
  18. Biomedical physics & engineering express · 2017
    Article
  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

2 authors at 1 institution in 1 country.

Jun-Ho LaCenter for Pain Research, Department of Anesthesiology, University of Pittsburgh, Pennsylvania, USA. laj@upmc.edu
G F Gebhart
University of Pittsburgh · US

Funding

UNIVERSITY OF PITTSBURGH CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE: BPCAUL1RR024153 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$73.9M
MECHANISMS AND MODULATION OF VISCERAL PAINR01NS019912 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GEBHART, GERALD F · 1985 to 2009
$3.7M
NCRR NIH HHS UL1 RR024153NINDS NIH HHS R01 NS 19912
6 · The paper itself

Abstract

TREK-1, TREK-2 and TRAAK are mechanosensitive two-pore domain K(+) (K(2P)) channels thought to be involved in the attenuation of mechanotransduction. Because colon inflammation is associated with colon mechanohypersensitivity, we hypothesized that the role of these channels in colon sensory (dorsal root ganglion, DRG) neurons would be reduced by colon inflammation. Accordingly, we studied the functional expression of mechanosensitive K(2P) channels in colon sensory neurons in both thoracolumbar (TL) and lumbosacral (LS) DRG that represent the splanchnic and pelvic nerve innervations of the colon, respectively. In colon DRG neurons identified by retrograde tracer previously injected into the colon wall, 62% of TL neurons and 83% of LS neurons expressed at least one of three K(2P) channel mRNAs; the proportion of neurons expressing the TREK-1 gene was greater in LS than in TL DRG. In electrophysiological studies, single-channel activities of TREK-1a, TREK-1b, TREK-2, and TRAAK-like channels were detected in cultured colon DRG neuronal membranes. After trinitrobenzene sulfonic acid-induced colon inflammation, we observed significant decreases in the amount of TREK-1 mRNA, in the response of TREK-2-like channels to membrane stretch, and in the whole cell outward current during osmotic stretch in LS colon DRG neurons. These findings document that the majority of DRG neurons innervating the mouse colon express mechanosensitive K(2P) channels and suggest that a decrease in their expression and activities contributes to the increased colon mechanosensitivity that develops in inflammatory bowel conditions.

Indexed as

Mechanotransduction, CellularAnimalsCells, CulturedColitisColonGanglia, SpinalGene ExpressionMaleMembrane PotentialsMiceMice, Inbred C57BLPotassium Channels, Tandem Pore DomainSensory Receptor CellsSplanchnic NervesTrinitrobenzenesulfonic AcidKcnk10 protein, mousepotassium channel protein TREK-1Potassium Channels, Tandem Pore DomainTrinitrobenzenesulfonic Acid

Identifiers

PMID21512155
PMCPMC3129930
OpenAlexW2139527876

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.