Evidence map›Paper›PMID 26556371›Full record

ReviewToxins2015

Current status and future directions of botulinum neurotoxins for targeting pain processing.

Sabine Pellett, Tony L Yaksh, Roshni Ramachandran

Abstract readReview
In one paragraph

Review in Toxins, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 4 pooled it
–field-weighted citation impact
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

37 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  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.

Sabine PellettDepartment of Bacteriology, University of Wisconsin, 6340 Microbial Sciences Building, 1550 Linden Dr., Madison, WI 53706, USA. sabine.pellett@wisc.edu.
Tony L YakshDepartment of Anesthesiology 0818, University of California, 214 Dickinson St., San Diego, CA 92103, USA. tyaksh@ucsd.edu.
Roshni RamachandranDepartment of Anesthesiology 0818, University of California, 214 Dickinson St., San Diego, CA 92103, USA. roramachandran@ucsd.edu.

Funding

The Pharmacology of Spinal AnalgesicsR01DA002110 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI YAKSH, TONY L. · 1985 to 2014
$3.8M
Construction and Analysis of BoNT derivatives as Pain Specific InhibitorsR21AI113580 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI JOHNSON, ERIC A., PELLETT, SABINE · 2014 to 2015
$437k
NIAID NIH HHS 5R21AI113580-02NIAID NIH HHS R21 AI113580NIDA NIH HHS DA02110NIDA NIH HHS R01 DA002110
6 · The paper itself

Abstract

Current evidence suggests that botulinum neurotoxins (BoNTs) A1 and B1, given locally into peripheral tissues such as skin, muscles, and joints, alter nociceptive processing otherwise initiated by inflammation or nerve injury in animal models and humans. Recent data indicate that such locally delivered BoNTs exert not only local action on sensory afferent terminals but undergo transport to central afferent cell bodies (dorsal root ganglia) and spinal dorsal horn terminals, where they cleave SNAREs and block transmitter release. Increasing evidence supports the possibility of a trans-synaptic movement to alter postsynaptic function in neuronal and possibly non-neuronal (glial) cells. The vast majority of these studies have been conducted on BoNT/A1 and BoNT/B1, the only two pharmaceutically developed variants. However, now over 40 different subtypes of botulinum neurotoxins (BoNTs) have been identified. By combining our existing and rapidly growing understanding of BoNT/A1 and /B1 in altering nociceptive processing with explorations of the specific characteristics of the various toxins from this family, we may be able to discover or design novel, effective, and long-lasting pain therapeutics. This review will focus on our current understanding of the molecular mechanisms whereby BoNTs alter pain processing, and future directions in the development of these agents as pain therapeutics.

Indexed as

AnimalsBotulinum ToxinsHumansInflammationModels, MolecularNeurotoxinsPainPeripheral Nervous System DiseasesBotulinum ToxinsNeurotoxinsBoNTbotulinum neurotoxinglianeurotransmitterpainprimary afferentSNAREsspinal cord

Identifiers

PMID26556371
PMCPMC4663519

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.