Evidence map›Paper›PMID 27378847›Full record

ReviewFrontiers in molecular neuroscience2016

Energy and Potassium Ion Homeostasis during Gamma Oscillations.

Oliver Kann, Jan-Oliver Hollnagel, Shehabeldin Elzoheiry, Justus Schneider

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  11. Neural oscillatory activity serving sensorimotor control is predicted by superoxide-sensitive mitochondrial redox environments.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Article
  13. Microorganisms · 2021
    Article
  14. Mild metabolic stress is sufficient to disturb the formation of pyramidal cell ensembles during gamma oscillations.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    Article
  15. Review
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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

4 authors at 1 institution in 1 country.

Oliver KannInstitute of Physiology and Pathophysiology, University of HeidelbergHeidelberg, Germany; Interdisciplinary Center for Neurosciences (IZN), University of HeidelbergHeidelberg, Germany.
Jan-Oliver HollnagelInstitute of Physiology and Pathophysiology, University of HeidelbergHeidelberg, Germany; Interdisciplinary Center for Neurosciences (IZN), University of HeidelbergHeidelberg, Germany.
Shehabeldin ElzoheiryInstitute of Physiology and Pathophysiology, University of HeidelbergHeidelberg, Germany; Interdisciplinary Center for Neurosciences (IZN), University of HeidelbergHeidelberg, Germany.
Justus SchneiderInstitute of Physiology and Pathophysiology, University of HeidelbergHeidelberg, Germany; Interdisciplinary Center for Neurosciences (IZN), University of HeidelbergHeidelberg, Germany.
Heidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fast neuronal network oscillations in the gamma frequency band (30-100 Hz) occur in various cortex regions, require timed synaptic excitation and inhibition with glutamate and GABA, respectively, and are associated with higher brain functions such as sensory perception, attentional selection and memory formation. However, little is known about energy and ion homeostasis during the gamma oscillation. Recent studies addressed this topic in slices of the rodent hippocampus using cholinergic and glutamatergic receptor models of gamma oscillations (GAM). Methods with high spatial and temporal resolution were applied in vitro, such as electrophysiological recordings of local field potential (LFP) and extracellular potassium concentration ([K(+)]o), live-cell fluorescence imaging of nicotinamide adenine dinucleotide (phosphate) and flavin adenine dinucleotide [NAD(P)H and FAD, respectively] (cellular redox state), and monitoring of the interstitial partial oxygen pressure (pO2) in depth profiles with microsensor electrodes, including mathematical modeling. The main findings are: (i) GAM are associated with high oxygen consumption rate and significant changes in the cellular redox state, indicating rapid adaptations in glycolysis and oxidative phosphorylation; (ii) GAM are accompanied by fluctuating elevations in [K(+)]o of less than 0.5 mmol/L from baseline, likely reflecting effective K(+)-uptake mechanisms of neuron and astrocyte compartments; and (iii) GAM are exquisitely sensitive to metabolic stress induced by lowering oxygen availability or by pharmacological inhibition of the mitochondrial respiratory chain. These findings reflect precise cellular adaptations to maintain adenosine-5'-triphosphate (ATP), ion and neurotransmitter homeostasis and thus neural excitability and synaptic signaling during GAM. Conversely, the exquisite sensitivity of GAM to metabolic stress might significantly contribute the exceptional vulnerability of higher brain functions in brain disease.

Indexed as

cognitionextracellular potassium concentrationGABA-A receptormembrane ion transportmitochondriaNa+/K+-ATPaseneural information processingtissue oxygen tension

Identifiers

PMID27378847
PMCPMC4909733
OpenAlexW2432453090

What OpenQuestion holds

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LicenceCC BY
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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.