Evidence map›Paper›PMID 25848093›Full record

ReviewMolecular pharmacology2015

Structural Basis for Pharmacology of Voltage-Gated Sodium and Calcium Channels.

William A Catterall, Teresa M Swanson

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular pharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 2 pooled it
10.1field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 2 syntheses or guidelines pooled it, 184 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  5. Review
  6. Article
  7. Article
  8. Article
  9. All Organisms Can Be Anesthetized, but There's No Point?BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  10. Review
  11. Lurcher Mouse as a Model of Cerebellar Syndromes.Cerebellum (London, England) · 2025
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
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29 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

William A CatterallDepartment of Pharmacology, University of Washington, Seattle, Washington wcatt@uw.edu.
Teresa M SwansonDepartment of Pharmacology, University of Washington, Seattle, Washington.
University of Washington · US

Funding

EXPERIMENTAL PATHOLOGY OF CARDIOVASCULAR DISEASET32HL007312 · NHLBI · UNIVERSITY OF WASHINGTON · PI MAJESKY, MARK W., SCHWARTZ, STEPHEN MARK · 1985 to 2019
$11.8M
Structural Basis for Antiarrhythmic Drug ActionR01HL112808 · NHLBI · UNIVERSITY OF WASHINGTON · PI ZHENG, NING · 2012 to 2025
$7.8M
VOLTAGE-SENSITIVE SODIUM CHANNELS IN BRAINR01NS015751 · NINDS · UNIVERSITY OF WASHINGTON · PI CATTERALL, WILLIAM A · 1985 to 2018
$6.0M
Structural Basis for Calcium Selectivity and Drug Block of Cav ChannelsR01HL117896 · NHLBI · UNIVERSITY OF WASHINGTON · PI CATTERALL, WILLIAM A, ZHENG, NING · 2014 to 2017
$1.5M
NHLBI NIH HHS R01 HL112808NHLBI NIH HHS R01-HL112808NHLBI NIH HHS R01 HL117896NHLBI NIH HHS R01-HL117896NHLBI NIH HHS T32 HL007312NINDS NIH HHS R01 NS015751NINDS NIH HHS R01-NS15751
6 · The paper itself

Abstract

Voltage-gated sodium channels initiate action potentials in nerve, muscle, and other electrically excitable cells. Voltage-gated calcium channels are activated by depolarization during action potentials, and calcium influx through them is the key second messenger of electrical signaling, initiating secretion, contraction, neurotransmission, gene transcription, and many other intracellular processes. Drugs that block sodium channels are used in local anesthesia and the treatment of epilepsy, bipolar disorder, chronic pain, and cardiac arrhythmia. Drugs that block calcium channels are used in the treatment of epilepsy, chronic pain, and cardiovascular disorders, including hypertension, angina pectoris, and cardiac arrhythmia. The principal pore-forming subunits of voltage-gated sodium and calcium channels are structurally related and likely to have evolved from ancestral voltage-gated sodium channels that are widely expressed in prokaryotes. Determination of the structure of a bacterial ancestor of voltage-gated sodium and calcium channels at high resolution now provides a three-dimensional view of the binding sites for drugs acting on sodium and calcium channels. In this minireview, we outline the different classes of sodium and calcium channel drugs, review studies that have identified amino acid residues that are required for their binding and therapeutic actions, and illustrate how the analogs of those key amino acid residues may form drug-binding sites in three-dimensional models derived from bacterial channels.

Indexed as

Action PotentialsAnimalsBinding SitesCalcium Channel BlockersCalcium ChannelsHumansMammalsSodium Channel BlockersSodium ChannelsStructural Homology, ProteinCalcium Channel BlockersCalcium ChannelsSodium Channel BlockersSodium Channels

Identifiers

PMID25848093
PMCPMC4468632
OpenAlexW2166637802

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.