Evidence map›Paper›PMID 22364507›Full record

ArticleNeurogastroenterology and motility2012

Importance of stress receptor-mediated mechanisms in the amygdala on visceral pain perception in an intrinsically anxious rat.

A C Johnson, L Tran, J Schulkin, B Greenwood-Van Meerveld

Open access · greenAbstract read
In one paragraph

Article in Neurogastroenterology and motility, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
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  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Journal of neurogastroenterology and motility · 2018
    Article
  9. Mechanisms of Stress-induced Visceral Pain.Journal of neurogastroenterology and motility · 2018
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. High Times for Painful Blues: The Endocannabinoid System in Pain-Depression Comorbidity.The international journal of neuropsychopharmacology · 2015
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Importance of CRF receptor-mediated mechanisms of the bed nucleus of the stria terminalis in the processing of anxiety and pain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2014
    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

4 authors at 3 institutions in 1 country.

A C JohnsonOklahoma Center for Neuroscience, University of Oklahoma Health Science Center, Oklahoma City, OK, USA.
L Tran
J Schulkin
B Greenwood-Van Meerveld
University of Oklahoma Health Sciences Center · USAmerican Congress of Obstetricians and Gynecologists · USUniversity of Oklahoma Medical Center · US

Funding

Central Molecular Mechanisms of Stress-Induced Visceral HypersensitivityF31DK089871 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI JOHNSON, ANTHONY C · 2010 to 2012
$77k
Central Mechanisms Modulating Visceral SensitivityI01BX002188 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI HOUCHEN, COURTNEY WAYNE · 2013 to 2022
–
NIDDK NIH HHS F31 DK089871
6 · The paper itself

Abstract

backgroundStress worsens abdominal pain experienced by patients with irritable bowel syndrome (IBS), a chronic disorder of unknown origin with comorbid anxiety. Previously, we have demonstrated colonic hypersensitivity in Wistar-Kyoto rats (WKYs), a high-anxiety strain, which models abdominal pain in IBS. In low-anxiety rats, we have demonstrated that the central nucleus of the amygdala (CeA) regulates colonic hypersensitivity and anxiety induced by selective activation of either glucocorticoid receptors (GR) or mineralocorticoid receptors (MR), which is also mediated by the corticotropin releasing factor (CRF) Type-1 receptor. The goal of the present study was to test the hypothesis that the CeA through GR, MR, and/or CRF-1R regulates colonic hypersensitivity in WKYs.

methodsOne series of WKYs had micropellets of a GR antagonist, an MR antagonist or cholesterol (control) stereotaxically implanted onto the CeA. Another series were infused in the CeA with CRF-1R antagonist, or vehicle. Colonic sensitivity was measured as a visceromotor response (VMR) to graded colorectal distension (CRD). KEY

resultsThe exaggerated VMR to graded CRD in WKYs was unaffected by GR or MR antagonism in the CeA. In contrast, direct CeA infusion of CRF-1R antagonist significantly inhibited the VMR to CRD at noxious distension pressures. CONCLUSIONS & INFERENCES: Stress hormones in the CeA regulate colonic hypersensitivity in the rat through strain-dependent parallel pathways. The colonic hypersensitivity in WKYs is mediated by a CRF-1R mechanism in the CeA, independent of GR and MR. These complementary pathways suggest multiple etiologies whereby stress hormones in the CeA may regulate abdominal pain in IBS patients.

Indexed as

AmygdalaAnimalsAnxietyCatheterizationCorticotropin-Releasing HormoneCRF Receptor, Type 1Data Interpretation, StatisticalHyperalgesiaMalePain PerceptionPhysical StimulationRatsRats, Inbred F344Rats, Inbred WKYReceptors, Corticotropin-Releasing HormoneReceptors, GlucocorticoidCorticotropin-Releasing HormoneCRF Receptor, Type 1Receptors, Corticotropin-Releasing HormoneReceptors, GlucocorticoidReceptors, Mineralocorticoid

Identifiers

PMID22364507
PMCPMC3461498
OpenAlexW1527929911

What OpenQuestion holds

Textmetadata
LicenceTDM
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.