Evidence map›Paper›PMID 36751871›Full record

ArticleCephalalgia : an international journal of headache2023

OnabotulinumtoxinA effects on trigeminal nociceptors.

Ashley A Moore, Mariana Nelson, Christopher Wickware, Shinbe Choi, Gene Moon, Emma Xiong, Lily Orta, Amy Brideau-Andersen, Mitchell F Brin, Ron S Broide and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cephalalgia : an international journal of headache, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Observational
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Animal Models of Chronic Migraine: From the Bench to Therapy.Current pain and headache reports · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. 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

12 authors at 3 institutions in 1 country.

Ashley A MooreDepartment of Neurology, Duke University, Durham, NC, USA.
Mariana NelsonAllergan, an AbbVie company, Irvine, CA, USA.
Christopher WickwareDepartment of Neurology, Duke University, Durham, NC, USA.
Shinbe ChoiDepartment of Neurology, Duke University, Durham, NC, USA.
Gene MoonDepartment of Neurology, Duke University, Durham, NC, USA.
Emma XiongDepartment of Neurology, Duke University, Durham, NC, USA.
Lily OrtaDepartment of Neurology, Duke University, Durham, NC, USA.
Amy Brideau-AndersenAllergan, an AbbVie company, Irvine, CA, USA.
Mitchell F BrinAllergan, an AbbVie company, Irvine, CA, USA.ORCID 0000-0002-1989-6076
Ron S BroideAllergan, an AbbVie company, Irvine, CA, USA.
Wolfgang LiedtkeDepartment of Neurology, Duke University, Durham, NC, USA.
Carlene MooreDepartment of Neurology, Duke University, Durham, NC, USA.
Duke University · USAbbVie (United States) · USUniversity of California, Irvine · US

Funding

Molecular and Cellular signaling mechanisms of TRPV4 in non-neuronal cells: a pathophysiological relevance for migraine pain.K01NS121195 · NINDS · DUKE UNIVERSITY · PI Carlene D Moore · 2022 to 2026
$955k
NINDS NIH HHS K01 NS121195
6 · The paper itself

Abstract

backgroundOnabotulinumtoxinA (onabotA) is approved globally for prevention of chronic migraine; however, the classical mechanism of action of onabotA in motor and autonomic neurons cannot fully explain the effectiveness of onabotulinumtoxinA in this sensory neurological disease. We sought to explore the direct effects of onabotulinumtoxinA on mouse trigeminal ganglion sensory neurons using an inflammatory soup-based model of sensitization.

methodsPrimary cultured trigeminal ganglion neurons were pre-treated with inflammatory soup, then treated with onabotulinumtoxinA (2.75 pM). Treated neurons were used to examine transient receptor potential vanilloid subtype 1 and transient receptor potential ankyrin 1 cell-surface expression, calcium influx, and neuropeptide release.

resultsWe found that onabotulinumtoxinA cleaved synaptosomal-associated protein-25 kDa in cultured trigeminal ganglion neurons; synaptosomal-associated protein-25 kDa cleavage was enhanced by inflammatory soup pre-treatment, suggesting greater uptake of toxin under sensitized conditions. OnabotulinumtoxinA also prevented inflammatory soup-mediated increases in TRPV1 and TRPA1 cell-surface expression, without significantly altering TRPV1 or TRPA1 protein expression in unsensitized conditions. We observed similar inhibitory effects of onabotulinumtoxinA on TRP-mediated calcium influx and TRPV1- and TRPA1-mediated release of calcitonin gene-related peptide and prostaglandin 2 under sensitized, but not unsensitized control, conditions.

conclusionsOur data deepen the understanding of the sensory mechanism of action of onabotulinumtoxinA and support the notion that, once endocytosed, the cytosolic light chain of onabotulinumtoxinA cleaves synaptosomal-associated protein-25 kDa to prevent soluble N-ethylmaleimide-sensitive factor attachment protein receptor-mediated processes more generally in motor, autonomic,

Indexed as

Botulinum Toxins, Type ATransient Receptor Potential ChannelsAnimalsCalciumMiceNociceptorsSensory Receptor CellsTrigeminal GanglionTRPA1 Cation ChannelTRPV Cation ChannelsBotulinum Toxins, Type ACalciumTransient Receptor Potential ChannelsTRPA1 Cation ChannelTRPV Cation Channelsbotulinum neurotoxin type Achronic migraineInflammatory souptransient receptor potential ankyrin 1 (TRPA1)transient receptor potential vanilloid subtype 1 (TRPV1)trigeminal ganglion

Identifiers

PMID36751871
PMCPMC10652784
OpenAlexW4319461760

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.