Evidence map›Paper›PMID 21829088›Full record

ArticleChannels (Austin, Tex.)

Further insights into the antinociceptive potential of a peptide disrupting the N-type calcium channel-CRMP-2 signaling complex.

Sarah M Wilson, Joel M Brittain, Andrew D Piekarz, Carrie J Ballard, Matthew S Ripsch, Theodore R Cummins, Joyce H Hurley, May Khanna, Nathan M Hammes, Brian C Samuels and 2 more

Open access · goldAbstract read
In one paragraph

Article in Channels (Austin, Tex.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
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

35 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  9. AAV-encoded CaGene therapy · 2019
    Article
  10. Article
  11. Mining the NaBiochemical pharmacology · 2019
    Review
  12. Review
  13. Article
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  15. Article
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  17. Review
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  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

12 authors at 6 institutions in 1 country.

Sarah M WilsonPaul and Carole Stark Neurosciences Research Institute, Department of Pharmacology and Toxicology, Indiana University School of Medicine, Indianapolis, IN, USA.
Joel M Brittain
Andrew D Piekarz
Carrie J Ballard
Matthew S Ripsch
Theodore R Cummins
Joyce H Hurley
May Khanna
Nathan M Hammes
Brian C Samuels
Fletcher A White
Rajesh Khanna
Indiana University · USNeurosciences Institute · USIndianapolis Zoo · USUniversity School · USHypertension Institute · USIndiana University – Purdue University Indianapolis · US

Funding

Chemokine-mediated Modulaton of Opioid-induced PainR01DA026040 · NIDA · LOYOLA UNIVERSITY CHICAGO · PI MARCHESE, ADRIANO, WHITE, FLETCHER A · 2008 to 2012
$1.5M
Mechanisms of Neuropathic Pain in Demylenated NervesR01NS049136 · NINDS · LOYOLA UNIVERSITY CHICAGO · PI WHITE, FLETCHER A · 2006 to 2010
$1.3M
NIDA NIH HHS DA026040-03NIDA NIH HHS R01 DA026040NINDS NIH HHS R01 NS049136
6 · The paper itself

Abstract

The N-type voltage-gated calcium channel (Cav 2.2) has gained immense prominence in the treatment of chronic pain. While decreased channel function is ultimately anti-nociceptive, directly targeting the channel can lead to multiple adverse side effects. Targeting modulators of channel activity may facilitate improved analgesic properties associated with channel block and a broader therapeutic window. A novel interaction between Cav 2.2 and collapsin response mediator protein 2 (CRMP-2) positively regulates channel function by increasing surface trafficking. We recently identified a CRMP-2 peptide (TAT-CBD3), which effectively blocks this interaction, reduces or completely reverses pain behavior in a number of inflammatory and neuropathic models. Importantly, TAT-CBD3 did not produce many of the typical side effects often observed with Cav 2.2 inhibitors. Notably chronic pain mechanisms offer unique challenges as they often encompass a mix of both neuropathic and inflammatory elements, whereby inflammation likely causes damage to the neuron leading to neuropathic pain, and neuronal injury may produce inflammatory reactions. To this end, we sought to further disseminate the ability of TAT-CBD3 to alter behavioral outcomes in two additional rodent pain models. While we observed that TAT-CBD3 reversed mechanical hypersensitivity associated with a model of chronic inflammatory pain due to lysophosphotidylcholine-induced sciatic nerve focal demyelination (LPC), injury to the tibial nerve (TNI) failed to respond to drug treatment. Moreover, a single amino acid mutation within the CBD3 sequence demonstrated amplified Cav 2.2 binding and dramatically increased efficacy in an animal model of migraine. Taken together, TAT-CBD3 potentially represents a novel class of therapeutics targeting channel regulation as opposed to the channel itself.

Indexed as

AnimalsCalcium Channels, N-TypeChronic PainDemyelinating DiseasesDisease Models, AnimalFemaleInflammationIntercellular Signaling Peptides and ProteinsMigraine DisordersNerve Tissue ProteinsPeptidesPoint MutationProtein TransportRatsRats, Sprague-DawleySciatic NeuropathyCacna1b protein, ratCalcium Channels, N-Typecollapsin response mediator protein-2Intercellular Signaling Peptides and ProteinsNerve Tissue ProteinsPeptides

Identifiers

PMID21829088
PMCPMC3265766
OpenAlexW2046786652

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.