Evidence map›Paper›PMID 28161890›Full record

ArticleBritish journal of pharmacology2018

Homology-guided mutational analysis reveals the functional requirements for antinociceptive specificity of collapsin response mediator protein 2-derived peptides.

Aubin Moutal, Wennan Li, Yue Wang, Weina Ju, Shizhen Luo, Song Cai, Liberty François-Moutal, Samantha Perez-Miller, Jackie Hu, Erik T Dustrude and 4 more

Abstract read
In one paragraph

Article in British journal of pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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, 1 synthesis or guideline pooled it, 53 citations in OpenAlex.

  1. Pooled it
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  6. A peptidomimetic modulator of the CaProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Article
  8. Non-SUMOylated CRMP2 decreases NaMolecular brain · 2021
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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

14 authors at 2 institutions in 2 countries.

Aubin MoutalDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.ORCID 0000-0003-4268-1206
Wennan LiDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Yue WangDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Weina JuDepartment of Neurology, The First Hospital of Jilin University, Jilin University, Changchun, Jilin Province, China.
Shizhen LuoDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Song CaiDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Liberty François-MoutalDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Samantha Perez-MillerDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.ORCID 0000-0002-9034-3693
Jackie HuDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Erik T DustrudeDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.ORCID 0000-0002-1753-8603
Todd W VanderahDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.
Vijay GokhaleDepartment of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ, USA.ORCID 0000-0003-2807-4741
May KhannaDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.ORCID 0000-0002-9989-6374
Rajesh KhannaDepartment of Pharmacology, University of Arizona, Tucson, AZ, USA.ORCID 0000-0002-9066-2969
University of Arizona · USJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeN-type voltage-gated calcium (Ca EXPERIMENTAL APPROACH: Truncated as well as homology-guided mutant versions of CBD3 were generated and assessed using depolarization-evoked calcium influx in rat dorsal root ganglion neurons, binding between CRMP2 and Ca KEY

resultsThe first six amino acids within CBD3 accounted for all in vitro activity and antinociception. Spinal administration of a prototypical peptide (TAT-CBD3-L5M) reversed pain behaviours. Homology-guided mutational analyses of these six amino acids identified at least two residues, Ala1 and Arg4, as being critical for antinociception in two pain models. CONCLUSIONS AND IMPLICATIONS: These results identify an antinociceptive scaffold core in CBD3 that can be used for development of low MW mimetics of CBD3. LINKED ARTICLES: This article is part of a themed section on Recent Advances in Targeting Ion Channels to Treat Chronic Pain. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.12/issuetoc.

Indexed as

MutationAnalgesicsAnimalsFemaleGanglia, SpinalIntercellular Signaling Peptides and ProteinsMaleNerve Tissue ProteinsNeuronsPainPeptide FragmentsRatsRats, Sprague-DawleyAnalgesicscollapsin response mediator protein-2Intercellular Signaling Peptides and ProteinsNerve Tissue ProteinsPeptide Fragments

Identifiers

PMID28161890
PMCPMC5980424
OpenAlexW2601020076

What OpenQuestion holds

Textmetadata
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.