Evidence map›Paper›PMID 25585005›Full record

ArticleAnesthesiology2015

Enhanced effects of isoflurane on the long QT syndrome 1-associated A341V mutant.

Ikuomi Mikuni, Carlos G Torres, Tania Bakshi, Akihito Tampo, Brian E Carlson, Martin W Bienengraeber, Wai-Meng Kwok

Open access · bronzeAbstract read
In one paragraph

Article in Anesthesiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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 3 institutions in 3 countries.

Ikuomi MikuniFrom the Department of Anesthesiology and Critical Care Medicine, Asahikawa Medical University, Asahikawa, Japan (I.M.); Pediatric Residency Program, Massachusetts General Hospital for Children, Boston, Massachusetts (C.G.T.); Department of Biological Sciences, GlaxoSmithKline, Collegeville, Pennsylvania (T.B.); Department of Emergency Medicine, Asahikawa Medical University, Asahikawa, Japan (A.T.); Biotechnology and Bioengineering Center and Department of Physiology, Medical College of Wisconsin, Milwaukee, Wisconsin (B.E.C.); and Department of Anesthesiology and Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, Wisconsin (M.W.B., W.-M.K.). Current address: Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan (B.E.C.).
Carlos G Torres
Tania Bakshi
Akihito Tampo
Brian E Carlson
Martin W Bienengraeber
Wai-Meng Kwok
Massachusetts General Hospital · USGlaxoSmithKline (Japan) · JPAsahikawa Medical University · JP

Funding

VOLATILE ANESTHETIC ACTION ON CARDIAC K CHANNELSR01GM067675 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI KWOK, WAI-MENG · 2005 to 2008
$1.0M
NIGMS NIH HHS R01 GM-067675NIGMS NIH HHS R01 GM067675
6 · The paper itself

Abstract

backgroundThe impact of volatile anesthetics on patients with inherited long QT syndrome (LQTS) is not well understood. This is further complicated by the different genotypes underlying LQTS. No studies have reported on the direct effects of volatile anesthetics on specific LQTS-associated mutations. We investigated the effects of isoflurane on a common LQTS type 1 mutation, A341V, with an unusually severe phenotype.

methodsWhole cell potassium currents (IKs) were recorded from HEK293 and HL-1 cells transiently expressing/coexpressing wild-type KCNQ1 (α-subunit), mutant KCNQ1, wild-type KCNE1 (β-subunit), and fusion KCNQ1 + KCNE1. Current was monitored in the absence and presence of clinically relevant concentration of isoflurane (0.54 ± 0.05 mM, 1.14 vol %). Computer simulations determined the resulting impact on the cardiac action potential.

resultsIsoflurane had significantly greater inhibitory effect on A341V + KCNE1 (62.2 ± 3.4%, n = 8) than on wild-type KCNQ1 + KCNE1 (40.7 ± 4.5%; n = 9) in transfected HEK293 cells. Under heterozygous conditions, isoflurane inhibited A341V + KCNQ1 + KCNE1 by 65.2 ± 3.0% (n = 13) and wild-type KCNQ1 + KCNE1 (2:1 ratio) by 32.0 ± 4.5% (n = 11). A341V exerted a dominant negative effect on IKs. Similar differential effects of isoflurane were also observed in experiments using the cardiac HL-1 cells. Mutations of the neighboring F340 residue significantly attenuated the effects of isoflurane, and fusion proteins revealed the modulatory effect of KCNE1. Action potential simulations revealed a stimulation frequency-dependent effect of A341V.

conclusionsThe LQTS-associated A341V mutation rendered the IKs channel more sensitive to the inhibitory effects of isoflurane compared to wild-type IKs in transfected cell lines; F340 is a key residue for anesthetic action.

Indexed as

Action PotentialsAnesthetics, InhalationHEK293 CellsHumansIsofluraneLong QT SyndromeMutationAnesthetics, InhalationIsoflurane

Identifiers

PMID25585005
PMCPMC4366337
OpenAlexW2013370436

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.