Evidence map›Paper›PMID 1905814›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1991

Heterologously expressed serotonin 1A receptors couple to muscarinic K+ channels in heart.

A Karschin, B Y Ho, C Labarca, O Elroy-Stein, B Moss, N Davidson, H A Lester

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. RGS proteins reconstitute the rapid gating kinetics of gbetagamma-activated inwardly rectifying K+ channels.Proceedings of the National Academy of Sciences of the United States of America · 1997
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Atrial G protein-activated K+ channel: expression cloning and molecular properties.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
  9. Article
  10. Article
  11. Expression of an atrial G-protein-activated potassium channel in Xenopus oocytes.Proceedings of the National Academy of Sciences of the United States of America · 1993
    Article
  12. 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

7 authors at 1 institution in 1 country.

A KarschinDivision of Biology 156-29, California Institute of Technology, Pasadena 91125.
B Y Ho
C Labarca
O Elroy-Stein
B Moss
N Davidson
H A Lester
California Institute of Technology · US

Funding

INTRACELLULAR SECOND MESSENGERS, BIOPHYSICAL STUDIESR01GM029836 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI LESTER, HENRY A. · 1985 to 2002
$1.2M
NIGMS NIH HHS GM10991NIGMS NIH HHS GM29836
6 · The paper itself

Abstract

In cardiac atrial cells, muscarinic acetylcholine receptors activate a K+ current directly via a guanine nucleotide-binding protein (G protein). Serotonin type 1A receptors may activate a similar pathway in hippocampal neurons. To develop a system in which receptor/G protein/K+ channel coupling can be experimentally manipulated, we have used a highly efficient recombinant vaccinia virus vector system to express human serotonin 1A receptors in primary cultures of rat atrial myocytes. The expressed 1A receptors activated the inwardly rectifying K+ conductance that is normally activated by the endogenous muscarinic acetylcholine receptors. Maximal responses to either agonist occluded further activation by the other agonist. The average activation time constants for serotonin were about 5 times slower than for acetylcholine. The data support suggestions that the intracellular signaling pathway from seven-helix receptors to G proteins and directly to ion channels is widespread in excitable cells. After a fraction of the G proteins are activated irreversibly by guanosine 5'-[gamma-thio]triphosphate, subsequent transduction proceeds more efficiently. One possible interpretation is that multiple G-protein molecules are required to activate each channel. Vaccinia virus expression vectors are thus useful for expressing seven-helix receptors in primary cultures of postmitotic cells and have provided a heterologous expression system for the signaling pathway from seven-helix receptors to G proteins and directly to ion channels.

Indexed as

AcetylcholineAnimalsCells, CulturedCloning, MolecularElectric ConductivityGTP-Binding ProteinsIn Vitro TechniquesMembrane PotentialsMyocardiumPotassium ChannelsRatsReceptor AggregationReceptors, MuscarinicReceptors, SerotoninRecombinant ProteinsSerotoninAcetylcholineGTP-Binding ProteinsPotassium ChannelsReceptors, MuscarinicReceptors, SerotoninRecombinant ProteinsSerotonin

Identifiers

PMID1905814
PMCPMC51944
OpenAlexW2128270968

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.