4.4 Article Proceedings Paper

Excitatory/Inhibitory Synaptic Ratios in Polymicrogyria and Down Syndrome Help Explain Epileptogenesis in Malformations

Journal

PEDIATRIC NEUROLOGY
Volume 116, Issue -, Pages 41-54

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.pediatrneurol.2020.11.001

Keywords

Epilepsy; Polymicrogyria; Heterotopia; Holoprosencephaly; Down syndrome; Satellitosis; Synaptic ratios

Funding

  1. Alberta Children's Hospital Research Institute [60-28450, 10013167]

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This study examines how the ratio of excitatory and inhibitory inputs into mature individual cortical neurons affect their epileptic potential, along with structural factors and mitochondrial activity demonstrated through neuropathology. Results show that factors such as polymicrogyria and Down syndrome can influence afferent synaptic ratios, thus impacting epileptogenesis.
Background: The ratio between excitatory (glutamatergic) and inhibitory (GABAergic) inputs into maturing individual cortical neurons influences their epileptic potential. Structural factors during development that alter synaptic inputs can be demonstrated neuropathologically. Increased mitochondrial activity identifies neurons with excessive discharge rates. Methods: This study focuses on the neuropathological examinaion of surgical resections for epilepsy and at autopsy, in fetuses, infants, and children, using immunocytochemical markers, and electron microscopy in selected cases. Polymicrogyria and Down syndrome are highlighted. Results: Factors influencing afferent synaptic ratios include the following: (1) synaptic short-circuitry in fused molecular zones of adjacent gyri (polymicrogyria); (2) impaired development of dendritic spines decreasing excitation (Down syndrome); (3) extracellular keratan sulfate proteoglycan binding to somatic membranes but not dendritic spines may be focally diminished (cerebral atrophy, schizencephaly, lissencephaly, polymicrogyria) or augmented, ensheathing individual axons (holoprosencephaly), or acting as a barrier to axonal passage in the U-fiber layer. If keratan is diminished, glutamate receptors on the neuronal soma enable ectopic axosomatic excitatory synapses to form; (4) dysplastic, megalocytic neurons and balloon cells in mammalian target of rapamycin disorders; (5) satellitosis of glial cells displacing axosomatic synapses; (6) peri-neuronal inflammation (tuberous sclerosis) and heat-shock proteins. Conclusions: Synaptic ratio of excitatory/inhibitory afferents is a major fundamental basis of epileptogenesis at the neuronal level. Neuropathology can demonstrate subcellular changes that help explain either epilepsy or lack of seizures in immature brains. Synaptic ratios in malformations influence postnatal epileptogenesis. Single neurons can be hypermetabolic and potentially epileptogenic. (C) 2020 Elsevier Inc. All rights reserved.

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