Evidence map›Paper›PMID 24755485›Full record

ArticleNeuroscience2014

N-type calcium current, Cav2.2, is enhanced in small-diameter sensory neurons isolated from Nf1+/- mice.

J-H Duan, K E Hodgdon, C M Hingtgen, G D Nicol

Open access · bronzeAbstract read
In one paragraph

Article in Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
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  5. Role of nerves in neurofibromatosis type 1-related nervous system tumors.Cellular oncology (Dordrecht, Netherlands) · 2022
    Review
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  9. Review
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  15. Article
  16. Review
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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

4 authors at 1 institution in 1 country.

J-H DuanDepartment of Pharmacology & Toxicology, School of Medicine, Indiana University, Indianapolis, IN 46202, USA.
K E HodgdonDepartment of Pharmacology & Toxicology, School of Medicine, Indiana University, Indianapolis, IN 46202, USA.
C M HingtgenDepartment of Pharmacology & Toxicology, School of Medicine, Indiana University, Indianapolis, IN 46202, USA; Department of Neurology, School of Medicine, Indiana University, Indianapolis, IN 46202, USA.
G D NicolDepartment of Pharmacology & Toxicology, School of Medicine, Indiana University, Indianapolis, IN 46202, USA. Electronic address: gnicol@iupui.edu.
Indiana University – Purdue University Indianapolis · US

Funding

Actions of GTPase-Activating Proteins on Sensory NeuronsR01NS051668 · NINDS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI HINGTGEN, CYNTHIA M · 2006 to 2010
$2.4M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR015481 · NCRR · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FIFE, ROSE S · 2001 to 2001
$1.6M
NCRR NIH HHS C06 RR015481NCRR NIH HHS C06 RR015481-01NINDS NIH HHS NS51668NINDS NIH HHS R01 NS051668
6 · The paper itself

Abstract

Major aspects of neuronal function are regulated by Ca(2+) including neurotransmitter release, excitability, developmental plasticity, and gene expression. We reported previously that sensory neurons isolated from a mouse model with a heterozygous mutation of the Nf1 gene (Nf1+/-) exhibited both greater excitability and evoked release of neuropeptides compared to wildtype mice. Furthermore, augmented voltage-dependent sodium currents but not potassium currents contribute to the enhanced excitability. To determine the mechanisms giving rise to the enhanced release of substance P and calcitonin gene-related peptide in the Nf1+/- sensory neurons, the potential differences in the total voltage-dependent calcium current (ICa) as well as the contributions of individual Ca(2+) channel subtypes were assessed. Whole-cell patch-clamp recordings from small-diameter capsaicin-sensitive sensory neurons demonstrated that the average peak ICa densities were not different between the two genotypes. However, by using selective blockers of channel subtypes, the current density of N-type (Cav2.2) ICa was significantly larger in Nf1+/- neurons compared to wildtype neurons. In contrast, there were no significant differences in L-, P/Q- and R-type currents between the two genotypes. Quantitative real-time polymerase chain reaction measurements made from the isolated but intact dorsal root ganglia indicated that N-type (Cav2.2) and P/Q-type (Cav2.1) Ca(2+) channels exhibited the highest mRNA expression levels although there were no significant differences in the levels of mRNA expression between the genotypes. These results suggest that the augmented N-type (Cav2.2) ICa observed in the Nf1+/- sensory neurons does not result from genomic differences but may reflect post-translational or some other non-genomic modifications. Thus, our results demonstrate that sensory neurons from Nf1+/- mice, exhibit increased N-type ICa and likely account for the increased release of substance P and calcitonin gene-related peptide that occurs in Nf1+/- sensory neurons.

Indexed as

AnimalsCalciumCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeCalcium Channels, N-TypeCapsaicinCells, CulturedGanglia, SpinalMice, Inbred C57BLMice, TransgenicNeurofibromin 1Patch-Clamp TechniquesReal-Time Polymerase Chain ReactionRNA, MessengerSensory Receptor CellsCacna1b protein, mouseCACNA1C protein, mouseCalciumCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeCalcium Channels, N-TypeCapsaicinNeurofibromin 1RNA, MessengerSensory System Agentscalcium channelsdorsal root gangliamRNAneurofibromatosisqPCR

Identifiers

PMID24755485
PMCPMC4075288
OpenAlexW2039201511

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.