Evidence map›Paper›PMID 24702645›Full record

ArticleEpilepsia2014

In vivo ketogenic diet treatment attenuates pathologic sharp waves and high frequency oscillations in in vitro hippocampal slices from epileptic Kv 1.1α knockout mice.

Timothy A Simeone, Kaeli K Samson, Stephanie A Matthews, Kristina A Simeone

Abstract read
In one paragraph

Article in Epilepsia, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
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

33 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Adam, amigo, brain, and K channel.Biophysical reviews · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Changes in lipid profiles of epileptic mouse model.Metabolomics : Official journal of the Metabolomic Society · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review
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.

Timothy A SimeoneDepartment of Pharmacology, School of Medicine, Creighton University, Omaha, Nebraska, U.S.A.
Kaeli K SamsonDepartment of Pharmacology, School of Medicine, Creighton University, Omaha, Nebraska, U.S.A.
Stephanie A MatthewsDepartment of Pharmacology, School of Medicine, Creighton University, Omaha, Nebraska, U.S.A.
Kristina A SimeoneDepartment of Pharmacology, School of Medicine, Creighton University, Omaha, Nebraska, U.S.A.

Funding

Adenosine, Hypocretin and Sleep Disorder Comorbidities Associated with EpilepsyR01NS072179 · NINDS · CREIGHTON UNIVERSITY · PI SIMEONE, KRISTINA A · 2012 to 2016
$1.5M
Replacing an Animal Resource Facility Cage Washer.G20RR024001 · NCRR · CREIGHTON UNIVERSITY · PI DRESCHER, KRISTEN · 2007 to 2007
$638k
NCRR NIH HHS G20 RR024001NCRR NIH HHS G20RR024001NINDS NIH HHS NS072179-02NINDS NIH HHS R01 NS072179
6 · The paper itself

Abstract

The ketogenic diet (KD) is an effective therapy for pediatric refractory epilepsies; however, whether the KD changes the pathologic network oscillations generated by an epileptic brain remains unknown. We have reported that hippocampal CA3 regions of epileptic Kv1.1α knockout (KO) mice generate pathologic sharp waves (SPWs) and high-frequency oscillations (HFOs) that have higher incidence, longer duration, and fast ripples compared to wild-type (WT). Synaptic activity of hyperexcitable KO mossy fibers significantly decreased CA3 principal cell spike-timing reliability, which contributed to this network pathology. In addition, we have demonstrated that the KD reduces seizures by 75% in KO mice. Here, we determined whether 10- to 14-day in vivo KD treatment exerts disease-modifying effects that alter the spontaneous SPW-HFO complexes generated by the hippocampal CA3 region of KO mice in vitro using extracellular multielectrode array recordings. We found that KD treatment significantly attenuated the pathologic features of KO SPWs and ripples and reduced the incidence of fast ripples. The KD also improved spike-timing reliability of KO CA3 principal cells, decreased mossy fiber excitability, increased mossy fiber-CA3 paired-pulse ratios, and reduced coupling of field excitatory postsynaptic potentials and population spikes in the CA3 region. Collectively, these data indicate that KD treatment modulates CA3-generated pathologic oscillations by dampening hyperactive mossy fiber synapses.

Indexed as

Diet, KetogenicElectroencephalographyAnimalsCA3 Region, HippocampalEpilepsyEvoked PotentialsFemaleGene ExpressionHeterozygoteKv1.1 Potassium ChannelMaleMiceMice, Inbred C3HMice, KnockoutMossy Fibers, HippocampalSynapsesKcna1 protein, mouseKv1.1 Potassium ChannelEpilepsyFast rippleHigh-frequency oscillationsKetogenic dietKv1.1Sharp wave

Identifiers

PMID24702645
PMCPMC4031271

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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.