Evidence map›Paper›PMID 17145762›Full record

ArticleThe Journal of biological chemistry2007

Molecular basis of Ca(v)2.3 calcium channels in rat nociceptive neurons.

Zhi Fang, Chul-Kyu Park, Hai Ying Li, Hyun Yeong Kim, Seong-Hae Park, Sung Jun Jung, Joong Soo Kim, Arnaud Monteil, Seog Bae Oh, Richard J Miller

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 51 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

10 authors at 4 institutions in 3 countries.

Zhi FangDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Chul-Kyu ParkDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Hai Ying LiDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Hyun Yeong KimDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Seong-Hae ParkDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Sung Jun JungDepartment of Physiology, College of Medicine, Kangwon National University, Chunchon 200-710, Korea.
Joong Soo KimDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea.
Arnaud MonteilDépartement de Physiologie, Institut de Génomique Fonctionnelle, CNRS-UMR 5203 141, Rue de la Cardonille 34396 Montpellier Cedex 5, France, and the.
Seog Bae OhDepartment of Physiology and Program in Molecular and Cellular Neuroscience, School of Dentistry and Dental Research Institute, Seoul National University, Seoul 110-749, Korea. Electronic address: odolbae@snu.ac.kr.
Richard J MillerDepartment of Molecular Pharmacology and Biological Chemistry, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611.
Seoul National University · KRCentre National de la Recherche Scientifique · FRKangwon National University · KRNorthwestern University · US

Funding

CHEMOKINE RECEPTOR FUNCTION IN THE NERVOUS SYSTEMR01DA013141 · NIDA · UNIVERSITY OF CHICAGO · PI MILLER, RICHARD J · 2000 to 2015
$6.0M
NIDA NIH HHS R01 DA013141
6 · The paper itself

Abstract

Ca(v)2.3 calcium channels play an important role in pain transmission in peripheral sensory neurons. Six Ca(v)2.3 isoforms resulting from different combinations of three inserts (inserts I and II in the II-III loop and insert III in the carboxyl-terminal region) have been identified in different mammalian tissues. To date, however, Ca(v)2.3 isoforms unique to primary sensory neurons have not been identified. In this study, we determined Ca(v)2.3 isoforms expressed in the rat trigeminal ganglion neurons. Whole tissue reverse transcription (RT)-PCR analyses revealed that only two isoforms, Ca(v)2.3a and Ca(v)2.3e, are present in TG neurons. Using single cell RT-PCR, we found that Ca(v)2.3e is the major isoform, whereas Ca(v)2.3e expression is highly restricted to small (<16 mum) isolectin B4-negative and tyrosine kinase A-positive neurons. Ca(v)2.3e was also preferentially detected in neurons expressing the nociceptive marker, transient receptor potential vanilloid 1. Single cell RT-PCR following calcium imaging and whole-cell patch clamp recordings provided evidence of an association between an R-type calcium channel component and Ca(v)2.3e expression. Our results suggest that Ca(v)2.3e in sensory neurons may be a potential target for the treatment of pain.

Indexed as

AnimalsBiomarkersCalcium Channels, R-TypeCation Transport ProteinsNeurons, AfferentNociceptorsPainPain ManagementProtein IsoformsRatsReverse Transcriptase Polymerase Chain ReactionTrigeminal GanglionTRPV Cation ChannelsBiomarkersCacna1e protein, ratCalcium Channels, R-TypeCation Transport ProteinsProtein IsoformsTRPV1 receptorTRPV Cation Channels

Identifiers

PMID17145762
PMCPMC2760738
OpenAlexW2038223161

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.