Evidence map›Paper›PMID 24101295›Full record

ArticlePflugers Archiv : European journal of physiology2014

Enteric sensory neurons communicate with interstitial cells of Cajal to affect pacemaker activity in the small intestine.

Yong Fang Zhu, Xuan-Yu Wang, Bobbi-Jo Lowie, Sean Parsons, Liz White, Wolfgang Kunze, Andrew Pawelka, Jan D Huizinga

Abstract read
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.0field-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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  3. Article
  4. The enteric nervous system.Physiological reviews · 2023
    Review
  5. Studying Murine Small Bowel Mechanosensing of Luminal Particulates.Journal of visualized experiments : JoVE · 2022
    Article
  6. Review
  7. Telocytes in the human sinoatrial node.Journal of cellular and molecular medicine · 2018
    Article
  8. Article
  9. Slow Wave Activity and Modulations in Mouse Jejunum Myenteric Plexus In Situ.Journal of neurogastroenterology and motility · 2017
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
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

8 authors at 3 institutions in 1 country.

Yong Fang ZhuFarncombe Family Digestive Health Research Institute, Department of Medicine, Faculty of Health Sciences, McMaster University, HSC-3N8, 1200 Main Street West, Hamilton, Ontario, L8N 3Z5, Canada.
Xuan-Yu Wang
Bobbi-Jo Lowie
Sean Parsons
Liz White
Wolfgang Kunze
Andrew Pawelka
Jan D Huizinga
Population Health Research Institute · CAMcMaster University · CASt. Joseph’s Healthcare Hamilton · CA

Funding

Canadian Institutes of Health Research MOP12874
6 · The paper itself

Abstract

Enteric sensory neurons (the AH neurons) play a role in control of gastrointestinal motor activity; AH neuron activation has been proposed to change propulsion into segmentation. We sought to find a mechanism underlying this phenomenon. We formulated the hypothesis that AH neurons increase local ICC-MP (interstitial cells of Cajal associated with the myenteric plexus) pacemaker frequency to disrupt peristalsis and promote absorption. To that end, we sought structural and physiological evidence for communication between ICC-MP and AH neurons. We designed experiments that allowed us to simultaneously activate AH neurons and observe changes in ICC calcium transients that underlie its pacemaker activity. Neurobiotin injection in AH neurons together with ICC immunohistochemistry proved the presence of multiple contacts between AH neuron varicosities and the cell bodies and processes of ICC-MP. Generating action potential activity in AH neurons led to increase in the frequency and amplitude of calcium transients underlying pacemaker activity in ICC. When no rhythmicity was seen, rhythmic calcium transients were evoked in ICC. As a control, we stimulated nitrergic S neurons, which led to reduction in ICC calcium transients. Hence, we report here the first demonstration of communication between AH neurons and ICC. The following hypothesis can now be formulated: AH neuron activation can disrupt peristalsis directed by ICC-MP slow wave activity, through initiation of a local pacemaker by increasing ICC pacemaker frequency through increasing the frequency of ICC calcium transients. Evoking new pacemakers distal to the proximal lead pacemaker will initiate both retrograde and antegrade propulsion causing back and forth movements that may disrupt peristalsis.

Indexed as

Biological ClocksAction PotentialsAnimalsCalcium SignalingGastrointestinal MotilityInterstitial Cells of CajalIntestine, SmallMiceMyenteric PlexusSensory Receptor Cells

Identifiers

PMID24101295
OpenAlexW1990591073

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.