Evidence map›Paper›PMID 21084640›Full record

ArticleAmerican journal of physiology. Cell physiology2011

Antagonist action of progesterone at σ-receptors in the modulation of voltage-gated sodium channels.

Molly Johannessen, Dominique Fontanilla, Timur Mavlyutov, Arnold E Ruoho, Meyer B Jackson

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Multi-Target Directed Ligands (MTDLs) Binding the σInternational journal of molecular sciences · 2021
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Synthesis, radiolabelling, and evaluation of [American journal of nuclear medicine and molecular imaging · 2018
    Article
  18. Article
  19. Sigma-1 receptors modulate neonatal NaEuropean biophysics journal : EBJ · 2016
    Article
  20. Neuropharmacology of N,N-dimethyltryptamine.Brain research bulletin · 2016
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Molly JohannessenDepartment of Physiology, University of Wisconsin School of Medicine and Public Health, Madison, WI 53706, USA. mjackson@physiology.wisc.edu
Dominique Fontanilla
Timur Mavlyutov
Arnold E Ruoho
Meyer B Jackson
University of Wisconsin–Madison · US

Funding

MEMBRANE EXCITABILITY AND SECRETION FROM NERVE ENDINGSR37NS030016 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI JACKSON, MEYER B. · 2001 to 2007
$2.2M
Sigma Receptor Structure/Function/K+ Channel ModulationR01MH065503 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI RUOHO, ARNOLD EINO · 2003 to 2007
$1.6M
Linking State Data to Identify Unmet Need for Drug Treatment in Women Aged 15-49R21DA027181 · NIDA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BERNSTEIN, JUDITH APT, KOTELCHUCK, MILTON · 2010 to 2011
$420k
MEMBRANE EXCITABILITY AND SECRETION FROM NERVE ENDINGSR01NS030016 · NINDS · UNIVERSITY OF WISCONSIN MADISON · PI JACKSON, MEYER B. · 1992 to 2000
$159k
NIDA NIH HHS DA027181NIDA NIH HHS R21 DA027181NIMH NIH HHS MH065503NINDS NIH HHS NS30016
6 · The paper itself

Abstract

σ-Receptors are integral membrane proteins that have been implicated in a number of biological functions, many of which involve the modulation of ion channels. A wide range of synthetic ligands activate σ-receptors, but endogenous σ-receptor ligands have proven elusive. One endogenous ligand, dimethyltryptamine (DMT), has been shown to act as a σ-receptor agonist. Progesterone and other steroids bind σ-receptors, but the functional consequences of these interactions are unclear. Here we investigated progesterone binding to σ(1)- and σ(2)-receptors and evaluated its effect on σ-receptor-mediated modulation of voltage-gated Na(+) channels. Progesterone binds both σ-receptor subtypes in liver membranes with comparable affinities and blocks photolabeling of both subtypes in human embryonic kidney 293 cells that stably express the human cardiac Na(+) channel Na(v)1.5. Patch-clamp recording in this cell line tested Na(+) current modulation by the σ-receptor ligands ditolylguanidine, PB28, (+)SKF10047, and DMT. Progesterone inhibited the action of these ligands to varying degrees, and some of these actions were reduced by σ(1)-receptor knockdown with small interfering RNA. Progesterone inhibition of channel modulation by drugs was consistent with stronger antagonism of σ(2)-receptors. By contrast, progesterone inhibition of channel modulation by DMT was consistent with stronger antagonism of σ(1)-receptors. Progesterone binding to σ-receptors blocks σ-receptor-mediated modulation of a voltage-gated ion channel, and this novel membrane action of progesterone may be relevant to changes in brain and cardiovascular function during endocrine transitions.

Indexed as

AnimalsCells, CulturedGuanidinesHEK293 CellsHumansLiverNAV1.5 Voltage-Gated Sodium ChannelN,N-DimethyltryptaminePhenazocinePiperazinesProgesteroneRatsReceptors, sigmaRNA, Small InterferingSigma-1 ReceptorSodium Channels1,3-ditolylguanidineGuanidinesNAV1.5 Voltage-Gated Sodium ChannelN,N-DimethyltryptaminePB28 compoundPhenazocinePiperazinesProgesteroneReceptors, sigmaRNA, Small InterferingSCN5A protein, humanScn5a protein, ratSigma-1 Receptorsigma-2 receptorSK&F 10047Sodium Channels

Identifiers

PMID21084640
PMCPMC3043630
OpenAlexW2090729149

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.