Evidence map›Paper›PMID 31996391›Full record

ArticleeNeuro

Identification of a Sacral, Visceral Sensory Transcriptome in Embryonic and Adult Mice.

C J A Smith-Anttila, E A Mason, C A Wells, B J Aronow, P B Osborne, J R Keast

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. A Spinal Circuit for Modular Gating of Organ Somatosensation.bioRxiv : the preprint server for biology · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. The enteric nervous system.Physiological reviews · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. The development of somatosensory neurons: Insights into pain and itch.Current topics in developmental biology · 2021
    Review
  15. Application of Bioinformatics Methods to Identify Key Genes and Functions in Chronic Pelvic Pain.Evidence-based complementary and alternative medicine : eCAM · 2021
    Article
  16. Article
  17. 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

6 authors at 2 institutions in 2 countries.

C J A Smith-AnttilaDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, 3010 Victoria, Australia.
E A MasonDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, 3010 Victoria, Australia.
C A WellsDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, 3010 Victoria, Australia.
B J AronowDepartment of Pediatrics, College of Medicine, University of Cincinnati, Department of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229.
P B OsborneDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, 3010 Victoria, Australia.ORCID 0000-0002-8458-4159
J R KeastDepartment of Anatomy and Neuroscience, University of Melbourne, Parkville, 3010 Victoria, Australia jkeast@unimelb.edu.au.ORCID 0000-0002-4341-3265
The University of Melbourne · AUCincinnati Children's Hospital Medical Center · US

Funding

High resolution mapping of lower urinary tract innervation during developmentU01DK094479 · NIDDK · UNIVERSITY OF MELBOURNE · PI KEAST, JANET R · 2011 to 2015
$891k
Molecular and spatial mapping of bladder nociceptors during development and maturU01DK101029 · NIDDK · UNIVERSITY OF MELBOURNE · PI KEAST, JANET R · 2013 to 2013
$194k
NIDDK NIH HHS U01 DK094479NIDDK NIH HHS U01 DK101029
6 · The paper itself

Abstract

Visceral sensory neurons encode distinct sensations from healthy organs and initiate pain states that are resistant to common analgesics. Transcriptome analysis is transforming our understanding of sensory neuron subtypes but has generally focused on somatic sensory neurons or the total population of neurons in which visceral neurons form the minority. Our aim was to define transcripts specifically expressed by sacral visceral sensory neurons, as a step towards understanding the unique biology of these neurons and potentially leading to identification of new analgesic targets for pelvic visceral pain. Our strategy was to identify genes differentially expressed between sacral dorsal root ganglia (DRG) that include somatic neurons and sacral visceral neurons, and adjacent lumbar DRG that comprise exclusively of somatic sensory neurons. This was performed in adult and E18.5 male and female mice. By developing a method to restrict analyses to nociceptive Trpv1 neurons, a larger group of genes were detected as differentially expressed between spinal levels. We identified many novel genes that had not previously been associated with pelvic visceral sensation or nociception. Limited sex differences were detected across the transcriptome of sensory ganglia, but more were revealed in sacral levels and especially in Trpv1 nociceptive neurons. These data will facilitate development of new tools to modify mature and developing sensory neurons and nociceptive pathways.

Indexed as

Ganglia, SpinalTranscriptomeAnimalsFemaleMaleMiceNociceptionNociceptorsPainSensory Receptor Cellsautonomic regulationnociceptorpelvic painsexual dimorphismurogenitalvisceral pain

Identifiers

PMID31996391
PMCPMC7036621
OpenAlexW3003727619

What OpenQuestion holds

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LicenceCC BY
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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.