Evidence map›Paper›PMID 20413719›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2010

Critical role of 5-HT1A, 5-HT3, and 5-HT7 receptor subtypes in the initiation, generation, and propagation of the murine colonic migrating motor complex.

Eamonn J Dickson, Dante J Heredia, Terence K Smith

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. 5-HTThe Journal of physiology · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Nutrients · 2023
    Article
  12. Article
  13. 5-HTLaboratory investigation; a journal of technical methods and pathology · 2022
    Article
  14. Review
  15. Article
  16. Article
  17. Monoamines in the enteric nervous system.Histochemistry and cell biology · 2018
    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

3 authors at 1 institution in 1 country.

Eamonn J DicksonDepartment of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, NV 89557, USA.
Dante J Heredia
Terence K Smith
University of Nevada, Reno · US

Funding

Relex Pathways Controlling Intestinal MotilityR01DK045713 · NIDDK · UNIVERSITY OF NEVADA RENO · PI SMITH, TERENCE KEITH · 1999 to 2012
$3.1M
NIDDK NIH HHS R01 DK45713
6 · The paper itself

Abstract

The colonic migrating motor complex (CMMC) is necessary for fecal pellet propulsion in the murine colon. We have previously shown that 5-hydroxytryptamine (5-HT) released from enterochromaffin cells activates 5-HT(3) receptors on the mucosal processes of myenteric Dogiel type II neurons to initiate the events underlying the CMMC. Our aims were to further investigate the roles of 5-HT(1A), 5-HT(3), and 5-HT(7) receptor subtypes in generating and propagating the CMMC using intracellular microelectrodes or tension recordings from the circular muscle (CM) in preparations with and without the mucosa. Spontaneous CMMCs were recorded from the CM in isolated murine colons but not in preparations without the mucosa. In mucosaless preparations, ondansetron (3 microM; 5-HT(3) antagonist) plus hexamethonium (100 microM) completely blocked spontaneous inhibitory junction potentials, depolarized the CM. Ondansetron blocked the preceding hyperpolarization associated with a CMMC. Spontaneous CMMCs and CMMCs evoked by spritzing 5-HT (10 and 100 microM) or nerve stimulation in preparations without the mucosa were blocked by SB 258719 or SB 269970 (1-5 microM; 5-HT(7) antagonists). Both NAN-190 and (S)-WAY100135 (1-5 microM; 5-HT(1A) antagonists) blocked spontaneous CMMCs and neurally evoked CMMCs in preparations without the mucosa. Both NAN-190 and (S)-WAY100135 caused an atropine-sensitive depolarization of the CM. The precursor of 5-HT, 5-hydroxytryptophan (5-HTP) (10 microM), and 5-carboxamidotryptamine (5-CT) (5 microM; 5-HT(1/5/7) agonist) increased the frequency of spontaneous CMMCs. 5-HTP and 5-CT also induced CMMCs in preparations with and without the mucosa, which were blocked by SB 258719. 5-HT(1A), 5-HT(3), and 5-HT(7) receptors, most likely on Dogiel Type II/AH neurons, are important in initiating, generating, and propagating the CMMC. Tonic inhibition of the CM appears to be driven by ongoing activity in descending serotonergic interneurons; by activating 5-HT(7) receptors on AH neurons these interneurons also contribute to the generation of the CMMC.

Indexed as

Muscle ContractionMyoelectric Complex, Migrating5-HydroxytryptophanAnimalsColonElectric StimulationExcitatory Postsynaptic PotentialsInhibitory Postsynaptic PotentialsInterneuronsIntestinal MucosaIn Vitro TechniquesMaleMiceMice, Inbred C57BLMuscle, SmoothMyenteric Plexus5-HydroxytryptophanNicotinic AntagonistsReceptor, Serotonin, 5-HT1AReceptors, SerotoninReceptors, Serotonin, 5-HT3SerotoninSerotonin 5-HT1 Receptor AntagonistsSerotonin 5-HT3 Receptor Antagonistsserotonin 7 receptorSerotonin AntagonistsSerotonin Receptor Agonists

Identifiers

PMID20413719
PMCPMC2904117
OpenAlexW2147928251

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.