Evidence map›Paper›PMID 36187562›Full record

ArticleNeuropsychiatric disease and treatment2022

Ketogenic Diet Alleviates Hippocampal Neurodegeneration Possibly via ASIC1a and the Mitochondria-Mediated Apoptotic Pathway in a Rat Model of Temporal Lobe Epilepsy.

Qi Qiao, Zhenzhen Qu, Shuang Tian, Huifang Cao, Yange Zhang, Can Sun, Lijing Jia, Weiping Wang

Abstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

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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

12 citing papers in PubMed.

  1. Review
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  11. Research progress on correlations between trace element levels and epilepsy.Frontiers in cell and developmental biology · 2023
    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

8 authors.

Qi QiaoThe Department of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Zhenzhen QuThe Department of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Shuang TianThe Department of Neurology, Shijiazhuang People's Hospital, Shijiazhuang, People's Republic of China.
Huifang CaoThe Department of Rehabilitation, The Second Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Yange ZhangThe Department of Pediatrics, The Second Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Can SunThe Department of Neurology, The Third Hospital of Peking University, Beijing, People's Republic of China.
Lijing Jia *The Department of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.
Weiping Wang *The Department of Neurology, The Second Hospital of Hebei Medical University, Shijiazhuang, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The ketogenic diet (KD) is a proven therapy for refractory epilepsy. Although the anti-seizure properties of this diet are understood to a certain extent, the exploration of its neuroprotective effects and underlying mechanisms is still in its infancy. Tissue acidosis is a common feature of epileptogenic foci. Interestingly, the activation of acid-sensing ion channel 1a (ASIC1a), which mediates Ca Methods: Male Sprague-Dawley rats were fed either the KD or a normal diet for four weeks after undergoing pilocarpine-induced status epilepticus (SE). The effects of KD on epileptogenesis, cognitive impairment and hippocampal neuron injury in the epileptic rats were subsequently evaluated by video electroencephalogram, Morris water maze test and Nissl staining, respectively. The expression of ASIC1a and cleaved caspase-3 in the hippocampus were determined using Western blot analysis during the chronic period following SE. Moreover, the intracellular Ca Results: We found that the KD treatment strongly attenuated the spontaneous recurrent seizures, ameliorated learning and memory impairments and prevented hippocampal neuronal injury and apoptosis. The KD was also shown to inhibit the upregulation of ASIC1a and the ensuing intracellular Ca Conclusion: These findings indicate that the KD suppresses mitochondria-mediated apoptosis possibly by regulating ASIC1a to exert neuroprotective effects. This may provide a mechanistic explanation of the therapeutic effects of KD.

Indexed as

acid-sensing ion channel 1aketogenic dietmitochondrial pathwayneuroprotectiontemporal lobe epilepsy

Identifiers

PMID36187562
PMCPMC9521243

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