The link between brain acidosis, breathing and seizures: a novel mechanism of action for the ketogenic diet in a model of infantile spasms

Author:

Choudhary Anamika1234,Mu Chunlong135ORCID,Barrett Karlene T13,Charkhand Behshad1,Williams-Dyjur Christine1,Marks Wendie N135,Shearer Jane35,Rho Jong M6,Scantlebury Morris H1234ORCID

Affiliation:

1. Department of Paediatrics, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

2. Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

3. Alberta Children’s Hospital Research Institute, University of Calgary Alberta, Calgary, Alberta, Canada

4. Hotchkiss Brain Institute, University of Calgary, Calgary, Alberta, Canada

5. Department of Biochemistry & Molecular Biology, Cumming School of Medicine and Faculty of Kinesiology, University of Calgary, Calgary, Alberta, Canada

6. Departments of Neurosciences and Pediatrics, University of California San Diego (UCSD), San Diego, CA, USA

Abstract

Abstract Infantile spasms (IS) syndrome is a catastrophic, epileptic encephalopathy of infancy that is often refractory to current antiepileptic therapies. The ketogenic diet (KD) has emerged as an alternative treatment for patients with medically intractable epilepsy, though the prospective validity and mechanism of action for IS remains largely unexplored. We investigated the KD’s efficacy as well as its mechanism of action in a rodent model of intractable IS. The spasms were induced using the triple-hit paradigm and the animals were then artificially reared and put on either the KD (4:1 fats: carbohydrate + protein) or a control milk diet (CM; 1.7:1). 31Phosphorus magnetic resonance spectroscopy (31P MRS) and head-out plethysmography were examined in conjunction with continuous video-EEG behavioural recordings in lesioned animals and sham-operated controls. The KD resulted in a peripheral ketosis observed both in the blood and urine. The KD led to a robust reduction in the frequency of spasms observed, with approximately a 1.5-fold increase in the rate of survival. Intriguingly, the KD resulted in an intracerebral acidosis as measured with 31P MRS. In addition, the respiratory profile of the lesioned rats on the KD was significantly altered with slower, deeper and longer breathing, resulting in decreased levels of expired CO2. Sodium bicarbonate supplementation, acting as a pH buffer, partially reversed the KD’s protective effects on spasm frequency. There were no differences in the mitochondrial respiratory profiles in the liver and brain frontal cortex measured between the groups, supporting the notion that the effects of the KD on breathing are not entirely due to changes in intermediary metabolism. Together, our results indicate that the KD produces its anticonvulsant effects through changes in respiration leading to intracerebral acidosis. These findings provide a novel understanding of the mechanisms underlying the anti-seizure effects of the KD in IS. Further research is required to determine whether the effects of the KD on breathing and intracerebral acid-base balance are seen in other paediatric models of epilepsy.

Funder

Alberta Innovates Health Solutions

Alberta Children’s Hospital Research Institute for Child and Maternal Health

Branch Out Neurological Foundation (to M.H.S.) and University of Calgary Eyes High Post-Doctoral Fellowship

Publisher

Oxford University Press (OUP)

Subject

General Earth and Planetary Sciences,General Environmental Science

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