Evidence map›Paper›PMID 12466226›Full record

ArticleBritish journal of pharmacology2002

Antibodies and a cysteine-modifying reagent show correspondence of M current in neurons to KCNQ2 and KCNQ3 K+ channels.

John P Roche, Ruth Westenbroek, Abraham J Sorom, Bertil Hille, Ken Mackie, Mark S Shapiro

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

50 citing papers in PubMed, 77 citations in OpenAlex.

  1. Review
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  3. Activation ofAmerican journal of physiology. Cell physiology · 2021
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  5. A PIPCommunications biology · 2020
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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

6 authors at 2 institutions in 1 country.

John P RocheDepartment of Physiology and Biophysics, University of Washington School of Medicine, Box 356540, Seattle, WA 98195-6540, U.S.A.
Ruth Westenbroek
Abraham J Sorom
Bertil Hille
Ken Mackie
Mark S Shapiro
University of Washington · USThe University of Texas Health Science Center at San Antonio · US

Funding

TRAINING IN THE MOLECULAR PHARMACOLOGY OF ABUSED DRUGST32DA007278 · NIDA · UNIVERSITY OF WASHINGTON · PI Susan Marie Ferguson, Paul E. M. Phillips · 1993 to 2026
$9.8M
Modulation of Neuronal Ion Channels by 2nd MessengersR01NS043394 · NINDS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI SHAPIRO, MARK S · 2002 to 2014
$4.5M
MOLECULAR PROPERTIES OF IONIC PERMEABILITY IN NERVER01NS008174 · NINDS · UNIVERSITY OF WASHINGTON · PI HILLE, BERTIL · 1985 to 2012
$4.3M
Molecular Properties of Ionic Permeability in NerveR37NS008174 · NINDS · UNIVERSITY OF WASHINGTON · PI HILLE, BERTIL · 2013 to 2019
$3.8M
Neuronal cannabinoidsR01DA011322 · NIDA · UNIVERSITY OF WASHINGTON · PI MACKIE, KENNETH · 1998 to 2014
$3.4M
CANNABINOID MODULATION OF NEURONAL FUNCTIONK02DA000286 · NIDA · UNIVERSITY OF WASHINGTON · PI MACKIE, KENNETH P. · 1996 to 2005
$711k
NIDA NIH HHS DA 00286NIDA NIH HHS DA 07278NIDA NIH HHS DA 11322NIDA NIH HHS K02 DA000286NIDA NIH HHS R01 DA011322NIDA NIH HHS T32 DA007278NINDS NIH HHS NS 08174NINDS NIH HHS NS 43394NINDS NIH HHS R01 NS008174NINDS NIH HHS R01 NS043394NINDS NIH HHS R37 NS008174
6 · The paper itself

Abstract

1. KCNQ K(+) channels are thought to underlie the M current of neurons. To probe if the KCNQ2 and KCNQ3 subtypes underlie the M current of rat superior cervical ganglia (SCG) neurons and of hippocampus, we raised specific antibodies against them and also used the cysteine-alkylating agent N-ethylmaleimide (NEM) as an additional probe of subunit composition. 2. Tested on tsA-201 (tsA) cells transfected with cloned KCNQ1-5 subunits, our antibodies showed high affinity and selectivity for the appropriate subtype. The antibodies immunostained SCG neurons and hippocampal sections at levels similar to those for channels expressed in tsA cells, indicating that KCNQ2 and KCNQ3 are present in SCG and hippocampal neurons. Some hippocampal regions contained only KCNQ2 or KCNQ3 subunits, suggesting the presence of M currents produced by channels other than KCNQ2/3 heteromultimers. 3. We found that NEM augmented M currents in SCG neurons and KCNQ2/3 currents in tsA cells via strong voltage-independent and modest voltage-dependent actions. Expression of individual KCNQ subunits in tsA cells revealed voltage-independent augmentation of KCNQ2, but not KCNQ1 nor KCNQ3, currents by NEM indicating that this action on SCG M currents likely localizes to KCNQ2. Much of the voltage-independent action is lost after the C242T mutation in KCNQ2. 4. The correspondence of NEM effects on expressed KCNQ2/3 and SCG M currents, along with the antibody labelling, provide further evidence that KCNQ2 and KCNQ3 subunits strongly contribute to the M current of neurons. The site of NEM action may be important for treatment of diseases caused by under-expression of these channels.

Indexed as

AnimalsAntibodiesCells, CulturedCysteineHumansIndicators and ReagentsKCNQ2 Potassium ChannelKCNQ3 Potassium ChannelMaleMembrane PotentialsNeuronsPotassium ChannelsPotassium Channels, Voltage-GatedRatsRats, Sprague-DawleySuperior Cervical GanglionAntibodiesCysteineIndicators and ReagentsKCNQ2 Potassium ChannelKCNQ2 protein, humanKcnq2 protein, ratKCNQ3 Potassium ChannelKCNQ3 protein, humanKcnq3 protein, ratPotassium ChannelsPotassium Channels, Voltage-Gated

Identifiers

PMID12466226
PMCPMC1573614
OpenAlexW2009560301

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.