Evidence map›Paper›PMID 8815914›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1996

Functional diversity of P-type and R-type calcium channels in rat cerebellar neurons.

A Tottene, A Moretti, D Pietrobon

Open access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

58 citing papers in PubMed, 158 citations in OpenAlex.

  1. Mechanisms of initiation of cortical spreading depression.The journal of headache and pain · 2023
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  2. Article
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  4. Diurnal properties of voltage-gated CaThe Journal of physiology · 2020
    Article
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  6. Mutant α-Synuclein Overexpression Induces Stressless Pacemaking in Vagal Motoneurons at Risk in Parkinson's Disease.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  7. Review
  8. The expression pattern of a Cav3-Kv4 complex differentially regulates spike output in cerebellar granule cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  9. Article
  10. Voltage-gated calcium channels.Cold Spring Harbor perspectives in biology · 2011
    Review
  11. Article
  12. CaV2.1 channelopathies.Pflugers Archiv : European journal of physiology · 2010
    Review
  13. Article
  14. Article
  15. Increased expression of golli myelin basic proteins enhances calcium influx into oligodendroglial cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  16. Article
  17. T-type and L-type Ca2+ conductances define and encode the bimodal firing pattern of vestibulocerebellar unipolar brush cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  18. Article
  19. Article
  20. Specific T-type calcium channel isoforms are associated with distinct burst phenotypes in deep cerebellar nuclear neurons.Proceedings of the National Academy of Sciences of the United States of America · 2006
    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

3 authors at 1 institution in 1 country.

A TotteneDepartment of Biomedical Sciences, University of Padova, Italy.
A Moretti
D Pietrobon
University of Padua · IT

Funding

Telethon 720
6 · The paper itself

Abstract

By combining single-channel and whole-cell patch-clamp recordings, we have established the sensitivity to omega-agatoxin IVA and omega-conotoxin MVIIC (SNX-230) of G1, G2, and G3, the three novel non-L-, non-N-type Ca2+ channels characterized previously in rat cerebellar granule cells. G1 channels were blocked irreversibly by both omega-conotoxin MVIIC and low doses of omega-agatoxin IVA (saturation at 50 nM). Thus, according to pharmacological criteria, G1 channels must be classified as P-type Ca2+ channels. Being slowly inactivating during depolarizing pulses and completely inactivated at voltages in which steady-state inactivation of P-type channels in Purkinje cells is negligible, G1 represents a novel P subtype. Neither G2 nor G3 was blocked irreversibly by omega-conotoxin MVIIC, and therefore both are R-type Ca2+ channels. G2 and G3 have some biophysical properties similar to those of low-voltage-activated (LVA) Ca2+ channels (e.g., voltage range for steady-state inactivation, V 1/2 = -90 mV), some properties similar to those of high-voltage-activated (HVA) Ca2+ channels (e.g., high sensitivity to Cd2+ block), and other properties intermediate between those of LVA and HVA Ca2+ channels, with LVA properties prevailing in G2 and HVA properties prevailing in G3. The R-type whole-cell current was inhibited by Ni2+ with a biphasic dose-response curve (IC50: 4 and 153 microM), suggesting that G2 and G3 may have a different sensitivity to Ni2+ block. Our results uncover functional diversity of both native P-type and R-type Ca2+ channels and show that R subtypes with distinct biophysical properties are coexpressed in rat cerebellar granule cells.

Indexed as

omega-ConotoxinsAnimalsCalcium Channel BlockersCalcium ChannelsCells, CulturedCerebellumDose-Response Relationship, DrugPatch-Clamp TechniquesPeptidesRatsRats, WistarTime FactorsCalcium Channel BlockersCalcium Channelsomega-conotoxin-MVIIComega-ConotoxinsPeptides

Identifiers

PMID8815914
PMCPMC6578912
OpenAlexW2140318655

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.