Evidence map›Paper›PMID 26134255›Full record

ReviewToxins2015

Botulinum Toxin as a Pain Killer: Players and Actions in Antinociception.

Dong-Wan Kim, Sun-Kyung Lee, Joohong Ahnn

Open access · goldAbstract 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 30 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 4 pooled it
3.1field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 4 syntheses or guidelines pooled it, 54 citations in OpenAlex.

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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 at 1 institution in 1 country.

Dong-Wan KimDepartment of Life Science, School of Natural Science, Hanyang University, Seoul 133-791, Korea. wizardbook@hanmail.net.
Sun-Kyung LeeDepartment of Life Science, School of Natural Science, Hanyang University, Seoul 133-791, Korea. sunkyungl@hanyang.ac.kr.
Joohong AhnnDepartment of Life Science, School of Natural Science, Hanyang University, Seoul 133-791, Korea. joohong@hanyang.ac.kr.
Hanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Botulinum neurotoxins (BoNTs) have been widely used to treat a variety of clinical ailments associated with pain. The inhibitory action of BoNTs on synaptic vesicle fusion blocks the releases of various pain-modulating neurotransmitters, including glutamate, substance P (SP), and calcitonin gene-related peptide (CGRP), as well as the addition of pain-sensing transmembrane receptors such as transient receptor potential (TRP) to neuronal plasma membrane. In addition, growing evidence suggests that the analgesic and anti-inflammatory effects of BoNTs are mediated through various molecular pathways. Recent studies have revealed that the detailed structural bases of BoNTs interact with their cellular receptors and SNAREs. In this review, we discuss the molecular and cellular mechanisms related to the efficacy of BoNTs in alleviating human pain and insights on engineering the toxins to extend therapeutic interventions related to nociception.

Indexed as

AnalgesicsAnimalsAxonal TransportBotulinum ToxinsDisease Models, AnimalGastrointestinal AbsorptionHumansNerve EndingsNeurotransmitter AgentsPainProtein EngineeringTRPV Cation ChannelsAnalgesicsBotulinum ToxinsNeurotransmitter AgentsTRPV1 protein, humanTRPV Cation Channelsbotulinum neurotoxinneuropeptideneurotransmitternociceptionpainTRP

Identifiers

PMID26134255
PMCPMC4516922
OpenAlexW1560534011

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.