Volume 46, Issue 9 e14217
ORIGINAL ARTICLE

Ameliorating effect of ketogenic diet on acute status epilepticus: Insights into biochemical and histological changes in rat hippocampus

Nagwa I. Shehata

Nagwa I. Shehata

Biochemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt

Contribution: Methodology, Supervision, Validation, Visualization, Writing - review & editing

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Mai A. Abdelsamad

Corresponding Author

Mai A. Abdelsamad

Biochemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt

Correspondence

Mai A. Abdelsamad, Biochemistry Department, Faculty of Pharmacy, Cairo University, Kasr el Ainy st., Cairo 11562, Egypt.

Email: [email protected]

Contribution: Data curation, Formal analysis, ​Investigation, Resources, Software, Visualization, Writing - original draft

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Hebat Allah A. Amin

Hebat Allah A. Amin

Pathology Department, Faculty of Medicine, Helwan University, Cairo, Egypt

Contribution: Data curation, ​Investigation, Methodology, Visualization, Writing - review & editing

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Nermin A. H. Sadik

Nermin A. H. Sadik

Biochemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt

Contribution: Methodology, Supervision, Validation, Visualization, Writing - review & editing

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Amira A. Shaheen

Amira A. Shaheen

Biochemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt

Contribution: Conceptualization, Methodology, Project administration, Supervision, Validation, Visualization, Writing - review & editing

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First published: 11 May 2022
Citations: 4

Abstract

This study aimed to evaluate the potential neuroprotective effects of ketogenic diet (KD) against the neuronal disruptions induced by SE in lithium-pilocarpine rat model of status epilepticus (SE). Four groups of female rats include; groups I and III received standard diet and groups II and IV received KD for 3 weeks. Groups I and II were left untreated, while groups III and IV were injected with LiCl (127 mg/kg, i.p.) followed by pilocarpine HCl (10 mg/kg, i.p.) 18–24 h later, repeatedly, till induction of SE. 72 h post-SE, KD effectively ameliorated the balance between excitatory (glutamate) and inhibitory (GABA) neurotransmitters and the oxidative stress indices, increased adenine nucleotides and decreased immunoreactivity of iNOS, TNFα, glial fibrillary acidic protein, and synaptophysin. Thiswas in association with improvement in inflammatory response and neuronal tissue characteristics in hippocampus of SE rats. Histological changes showed preservation of neuronal integrity. These findings highlight the protective effects of KD in the acute phase post-SE via ameliorating biochemical and histological changes involved.

Practical applications

Epilepsy is the fourth most common neurological disorder that requires lifelong treatment. It stigmatizes patients and their families. The use of the ketogenic diet (KD) as a therapy for epilepsy developed from observations that fasting could reduce seizures. From 1920s, the KD was a common epilepsy treatment until it was gradually superseded by anticonvulsant drugs so that by the 1980s it was rarely used. However, there has been a resurgence of interest and usage of the KD for epilepsy since the turn of the century. Despite its long history, the mechanisms by which KD exhibits its anti-seizure action are not fully understood. Our study aims to identify the mechanism of KD which may help further studies to achieve the same benefits with a drug or supplement to overcome its unpalatability and gastrointestinal side effects.

CONFLICT OF INTEREST

The authors declare no competing interests.

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