Evidence map›Paper›PMID 22961805›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2012

Enhanced excitability of guinea pig inferior mesenteric ganglion neurons during and following recovery from chemical colitis.

David R Linden

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Role of mesenteric component in Crohn's disease: A friend or foe?World journal of gastrointestinal surgery · 2021
    Review
  4. Article
  5. 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

1 author at 1 institution in 1 country.

David R LindenDepartment of Physiology and Biomedical Engineering and Enteric NeuroScience Program, Mayo Clinic College of Medicine, 200 First St. SW, Rochester, MN 55905, USA. Linden.David@mayo.edu
Mayo Clinic · US

Funding

Extrinsic Neural Control of Gastrointestinal Function in the Disordered BowelR01DK076665 · NIDDK · MAYO CLINIC ROCHESTER · PI LINDEN, DAVID R. · 2008 to 2012
$1.5M
NIDDK NIH HHS DK-76665NIDDK NIH HHS R01 DK076665
6 · The paper itself

Abstract

Postganglionic sympathetic neurons in the prevertebral ganglia (PVG) provide ongoing inhibitory tone to the gastrointestinal tract and receive innervation from mechanosensory intestinofugal afferent neurons primarily located in the colon and rectum. This study tests the hypothesis that colitis alters the excitability of PVG neurons. Intracellular recording techniques were used to evaluate changes in the electrical properties of inferior mesenteric ganglion (IMG) neurons in the trinitrobenzene sulfonic acid (TNBS) and acetic acid models of guinea pig colitis. Visceromotor IMG neurons were hyperexcitable 12 and 24 h, but not 6 h, post-TNBS during "acute" inflammation. Hyperexcitability persisted at 6 days post-TNBS during "chronic" inflammation, as well as at 56 days post-TNBS when colitis had resolved. In contrast, there was only a modest decrease in the current required to elicit an action potential at 24 h after acetic acid administration. Vasomotor neurons from inflamed preparations exhibited normal excitability. The excitatory effects of XE-991, a blocker of the channel that contributes to the M-type potassium current, and heteropodatoxin-2, a blocker of the channel that contributes to the A-type potassium current, were unchanged in TNBS-inflamed preparations, suggesting that these currents did not contribute to hyperexcitability. Riluzole, an inhibitor of persistent sodium currents, caused tonic visceromotor neurons to accommodate to sustained current pulses, regardless of the inflammatory state of the preparation, and restored a normal rheobase in neurons from TNBS-inflamed preparations but did not alter the rheobase of control preparations, suggesting that enhanced activity of voltage-gated sodium channels may contribute to colitis-induced hyperexcitability. Collectively, these data indicate that enhanced sympathetic drive as a result of hyperexcitable visceromotor neurons may contribute to small bowel dysfunction during colitis.

Indexed as

Excitatory Postsynaptic PotentialsIntestinesMyenteric PlexusAcetic AcidAction PotentialsAnimalsAnthracenesColitisDisease Models, AnimalElectrophysiologyExcitatory Amino Acid AntagonistsGuinea PigsIndicators and ReagentsReaction TimeRiluzoleTrinitrobenzenesulfonic Acid10,10-bis(4-pyridinylmethyl)-9(10H)-anthracenoneAcetic AcidAnthracenesExcitatory Amino Acid AntagonistsIndicators and ReagentsRiluzoleTrinitrobenzenesulfonic Acid

Identifiers

PMID22961805
PMCPMC3517667
OpenAlexW2126560502

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.