Ketogenic diet dampens excitatory neurotransmission by shrinking synaptic vesicle pools

Ketogenic diet (KD) is used for the treatment of drug-resistant childhood epilepsy and has been proposed to improve outcomes in neurodegenerative diseases. However, the mechanisms by which KD alters brain circuitry remain unclear. Here, we investigated the impact of KD on hippocampal function through integrative analysis of gene expression and neurotransmission. We found that KD induces extensive transcriptional reprogramming, including altered expression of numerous synaptic genes. Proteomic and genomic profiling revealed significant changes in histone modifications, particularly at promoters of KD-regulated genes. Electrophysiological recordings showed that KD reduces excitatory synaptic gain and short-term plasticity at CA3-CA1 synapses, dampening the summation of excitatory inputs and enhancing the summation of inhibitory inputs. These functional changes were driven, in part, by a reduction in the readily releasable vesicle pool at excitatory synapses under KD. Together, our findings demonstrate that KD drives transcriptional remodeling of hippocampal circuits, leading to synaptic adaptations that may underlie its anti-epileptic and neuroprotective effects.

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Journal
Cell Reports
Published
2026-02-01
DOI
https://doi.org/10.1016/j.celrep.2026.116945
Primary Topic
Diet and metabolism studies
Type
article
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article

Ketogenic diet dampens excitatory neurotransmission by shrinking synaptic vesicle pools

Francisca N. de Luna Vitorino, Jasmin Sponagel, Vitaly A. Klyachko, Gabor Egervári et al.
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Diet and metabolism studies
article

Ketogenic diet dampens excitatory neurotransmission by shrinking synaptic vesicle pools

Francisca N. de Luna Vitorino, Jasmin Sponagel, Vitaly A. Klyachko, Gabor Egervári, Erica M. Periandri, Layla Foroughi, Michael B Thomsen, Ghazaleh Ashrafi, Anjali Yadav, Pan-Yue Deng, Amelia J Barfield, Benjamin A. Garcia, Renzelle J. Ponce, Marion I. Stunault
article en

Abstract

Ketogenic diet (KD) is used for the treatment of drug-resistant childhood epilepsy and has been proposed to improve outcomes in neurodegenerative diseases. However, the mechanisms by which KD alters brain circuitry remain unclear. Here, we investigated the impact of KD on hippocampal function through integrative analysis of gene expression and neurotransmission. We found that KD induces extensive transcriptional reprogramming, including altered expression of numerous synaptic genes. Proteomic and genomic profiling revealed significant changes in histone modifications, particularly at promoters of KD-regulated genes. Electrophysiological recordings showed that KD reduces excitatory synaptic gain and short-term plasticity at CA3-CA1 synapses, dampening the summation of excitatory inputs and enhancing the summation of inhibitory inputs. These functional changes were driven, in part, by a reduction in the readily releasable vesicle pool at excitatory synapses under KD. Together, our findings demonstrate that KD drives transcriptional remodeling of hippocampal circuits, leading to synaptic adaptations that may underlie its anti-epileptic and neuroprotective effects.

Cell ReportsVol. 45(2)
Washington University in St. Louis (US), Institute of Bioinformatics (IN)
Good health and well-being
Openalex Percentile: Top 60%
Diet and metabolism studies
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