Evidence map›Paper›PMID 38935224›Full record

ArticleNeurochemical research2024

Ketogenic Diets Alter the Gut Microbiome, Resulting in Decreased Susceptibility to and Cognitive Impairment in Rats with Pilocarpine-Induced Status Epilepticus.

Bianli Li, Yue Ma, Xuhui Wang, Di Zhao, Ziqin Wang, Guoyang Wang, Chunyi Li, Lin Yang, Hui Ji, Kunmei Liu and 7 more

Abstract read
PubMed Publisher
In one paragraph

Article in Neurochemical research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. The Interplay between the Gut and Ketogenic Diets in Health and Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. 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

17 authors.

Bianli Li *Department of Emergency Medicine, General Hospital of Ningxia Medical University, Yinchuan, 750001, Ningxia, China.
Yue Ma *Shenzhen MicroBT Technology Co., LTD, Yuehai Street, Nanshan District, Shenzhen, 518000, Guangdong, China.
Xuhui Wang *Ningxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Di ZhaoDepartment of Respiratory Medicine, People's Hospital of Ningxia Hui Autonomous Region, 301 Zhengyuan North Road, Yinchuan, 750001, Ningxia, China.
Ziqin WangDepartment of Pathophysiology, Xiangya School of Medicine, Central South University, Changsha, 410008, Hunan, China.
Guoyang WangThird Clinical School of Medicine, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Chunyi LiBasic Medical School, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Lin YangNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Hui JiThird Clinical School of Medicine, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Kunmei LiuNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Qiuyuan ChenNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Yong YangNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Wenqian MaNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China.
Jianbin DuDepartment of Emergency Medicine, General Hospital of Ningxia Medical University, Yinchuan, 750001, Ningxia, China.
Lei MaDepartment of Emergency Medicine, General Hospital of Ningxia Medical University, Yinchuan, 750001, Ningxia, China. 13895306161@163.com.
Lianxiang ZhangNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China. zhlianxiang@163.com.
Yuanyuan QiangNingxia Key Laboratory of Cerebrocranial Diseases, Incubation Base of National Key Laboratory, Ningxia Medical University, 1160 Shengli Street, Yinchuan, 750001, Ningxia, China. qiangyy@nxmu.edu.cn.

Funding

Director Foundation of Ningxia Key Laboratory of Cerebrocranial Diseases LNZR202307Natural Science Foundation of Ningxia Hui Autonomous Region 2022AAC03156
6 · The paper itself

Abstract

A ketogenic diet (KD) is a high-fat, low-carbohydrate, and low-protein diet that exerts antiepileptic effects by attenuating spontaneous recurrent seizures, ameliorating learning and memory impairments, and modulating the gut microbiota composition. However, the role of the gut microbiome in the antiepileptic effects of a KD on temporal lobe epilepsy (TLE) induced by lithium-pilocarpine in adult rats is still unknown. Our study provides evidence demonstrating that a KD effectively mitigates seizure behavior and reduces acute-phase epileptic brain activity and that KD treatment alleviates hippocampal neuronal damage and improves cognitive impairment induced by TLE. We also observed that the beneficial effects of a KD are compromised when the gut microbiota is disrupted through antibiotic administration. Analysis of gut microbiota components via 16S rRNA gene sequencing in fecal samples collected from TLE rats fed either a KD or a normal diet. The Chao1 and ACE indices showed decreased species variety in KD-fed rats compared to TLE rats fed a normal diet. A KD increased the levels of Actinobacteriota, Verrucomicrobiota and Proteobacteria and decreased the level of Bacteroidetes. Interestingly, the abundances of Actinobacteriota and Verrucomicrobiota were positively correlated with learning and memory ability, and the abundance of Proteobacteria was positively correlated with seizure susceptibility. In conclusion, our study revealed the significant antiepileptic and neuroprotective effects of a KD on pilocarpine-induced epilepsy in rats, primarily mediated through the modulation of the gut microbiota. However, whether the gut microbiota mediates the antiseizure effects of a KD still needs to be better elucidated.

Indexed as

Cognitive DysfunctionDiet, KetogenicGastrointestinal MicrobiomePilocarpineRats, Sprague-DawleyStatus EpilepticusAnimalsEpilepsy, Temporal LobeHippocampusMaleRatsPilocarpineCognitive functionGut microbiotaKetogenic dietLithium-pilocarpineStatus epilepticusTemporal lobe epilepsy

Identifiers

What OpenQuestion holds

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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.