Evidence map›Paper›PMID 30074932›Full record

ArticleAnesthesiology2018

Anesthetics Have Different Effects on the Electrocorticographic Spectra of Wild-type and Mitochondrial Mutant Mice.

Charles William Carspecken, Sirisak Chanprasert, Franck Kalume, Margaret M Sedensky, Philip G Morgan

Open access · bronzeAbstract read
In one paragraph

Article in Anesthesiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 48% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

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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

5 authors at 1 institution in 2 countries.

Charles William CarspeckenFrom the Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington (C.W.C., S.C., F.K., M.M.S., P.G.M.) the Department of Anesthesiology and Pain Medicine (C.W.C., M.M.S., P.G.M.) the Division of Medical Genetics, Department of Medicine (S.C.) the Department of Neurological Surgery (F.K.), University of Washington, Seattle, Washington.
Sirisak Chanprasert
Franck Kalume
Margaret M Sedensky
Philip G Morgan
School of the Art Institute of Chicago · US

Funding

Intellectual and Developmental Disabilities Research CenterU54HD083091 · NICHD · UNIVERSITY OF WASHINGTON · PI GURALNICK, MICHAEL J · 2014 to 2019
$7.9M
A mouse model linking anesthetic sensitivity to mitochondrial functionR01GM105696 · NIGMS · SEATTLE CHILDREN'S HOSPITAL · PI SEDENSKY, MARGARET MARY · 2014 to 2021
$4.4M
Physician Postdoctoral Research Training in Perioperative Medicine (PPRTPM)T32GM112596 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Roderic G Eckenhoff, Max Kelz · 2015 to 2026
$3.4M
Mechanisms of epilepsy-related death in Leigh syndromeR01NS102796 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI KALUME, FRANCK K · 2017 to 2021
$2.1M
NICHD NIH HHS U54 HD083091NIGMS NIH HHS R01 GM105696NIGMS NIH HHS T32 GM112596NINDS NIH HHS R01 NS102796
6 · The paper itself

Abstract

what we already know about this topicWHAT THIS ARTICLE TELLS US THAT IS NEW:

background: Knockout of the mitochondrial protein Ndufs4 (Ndufs4[KO]) in mice causes hypersensitivity to volatile anesthetics but resistance to ketamine. The authors hypothesized that electrocorticographic changes underlying the responses of Ndufs4(KO) to volatile anesthetics and to ketamine would be similar in mutant and control mice.

methodsElectrocorticographic recordings at equipotent volatile anesthetic concentrations were compared between genotypes. In separate studies, control and cell type-specific Ndufs4(KO) mice were anesthetized with intraperitoneal ketamine to determine their ED50s.

resultsNdufs4 (KO) did not differ from controls in baseline electrocorticography (N = 5). Compared to baseline, controls exposed to isoflurane (EC50) lost power (expressed as mean baseline [µV/Hz]; mean isoflurane [µV/Hz]) in delta (2.45; 0.50), theta (1.41; 0.16), alpha (0.23; 0.05), beta (0.066; 0.016), and gamma (0.020; 0.005) frequency bands (N = 5). Compared to baseline, at their isoflurane EC50, Ndufs4(KO) maintained power in delta (1.08; 1.38), theta (0.36; 0.26), and alpha (0.09; 0.069) frequency bands but decreased in beta (0.041; 0.023) and gamma (0.020; 0.0068) frequency bands (N = 5). Similar results were seen for both genotypes in halothane. Vesicular glutamate transporter 2 (VGLUT2)-specific Ndufs4(KO) mice were markedly resistant to ketamine (ED50; 125 mg/kg) compared to control mice (ED50; 75 mg/kg; N = 6). At their respective ED95s for ketamine, mutant (N = 5) electrocorticography spectra showed a decrease in power in the beta (0.040; 0.020) and gamma (0.035; 0.015) frequency bands not seen in controls (N = 7).

conclusionsSignificant differences exist between the electrocorticographies of mutant and control mice at equipotent doses for volatile anesthetics and ketamine. The energetic state specifically of excitatory neurons determines the behavioral response to ketamine.

Indexed as

Anesthetics, GeneralAnesthetics, LocalAnimalsElectrocorticographyElectron Transport Complex IFemaleMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMitochondriaMutationAnesthetics, GeneralAnesthetics, LocalElectron Transport Complex INdufs4 protein, mouse

Identifiers

PMID30074932
PMCPMC6148376
OpenAlexW2886906657

What OpenQuestion holds

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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.