Loss of function mutations of SCN1A, the gene coding for the voltage-gated sodium channel NaV1.1, cause different types of epilepsy, whereas gain of function mutations cause sporadic and familial hemiplegic migraine type 3 (FHM-3). However, it is not clear yet how these opposite effects can induce paroxysmal pathological activities involving neuronal networks' hyperexcitability that are specific of epilepsy (seizures) or migraine (cortical spreading depolarization, CSD). To better understand differential mechanisms leading to the initiation of these pathological activities, we used a two-neuron conductance-based model of interconnected GABAergic and pyramidal glutamatergic neurons, in which we incorporated ionic concentration dynamics in both neurons. We modeled FHM-3 mutations by increasing the persistent sodium current in the interneuron and epileptogenic mutations by decreasing the sodium conductance in the interneuron. Therefore, we studied both FHM-3 and epileptogenic mutations within the same framework, modifying only two parameters. In our model, the key effect of gain of function FHM-3 mutations is ion fluxes modification at each action potential (in particular the larger activation of voltage-gated potassium channels induced by the NaV1.1 gain of function), and the resulting CSD-triggering extracellular potassium accumulation, which is not caused only by modifications of firing frequency. Loss of function epileptogenic mutations, on the other hand, increase GABAergic neurons' susceptibility to depolarization block, without major modifications of firing frequency before it. Our modeling results connect qualitatively to experimental data: potassium accumulation in the case of FHM-3 mutations and facilitated depolarization block of the GABAergic neuron in the case of epileptogenic mutations. Both these effects can lead to pyramidal neuron hyperexcitability, inducing in the migraine condition depolarization block of both the GABAergic and the pyramidal neuron. Overall, our findings suggest different mechanisms of network hyperexcitability for migraine and epileptogenic NaV1.1 mutations, implying that the modifications of firing frequency may not be the only relevant pathological mechanism.
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http://dx.doi.org/10.1371/journal.pcbi.1009239 | DOI Listing |
Epilepsia
December 2024
Aix Marseille Univ, INSERM, INS, Inst Neurosci Syst,, Marseille, France.
Periventricular nodular heterotopia (PVNH) is a neuronal migration disorder often associated with drug-resistant epilepsy. The epileptogenic zone network (EZN) in PVNH is generally large, contraindicating surgery. Stereoelectroencephalography (SEEG) can be proposed to map the EZN and perform radiofrequency thermocoagulation (THC) with an efficacy rate of approximately 65%.
View Article and Find Full Text PDFActa Neuropathol Commun
November 2024
Department of Neurosurgery, Xuanwu Hospital, Capital Medical University, Beijing, 100053, China.
Focal cortical dysplasia (FCD) type IIb (FCD IIb) is an epileptogenic malformation of the neocortex that is characterized by cortical dyslamination, dysmorphic neurons (DNs) and balloon cells (BCs). Approximately 30-60% of lesions are associated with brain somatic mutations in the mTOR pathway. Herein, we investigated the transcriptional changes around the DNs and BCs regions in freshly frozen brain samples from three patients with FCD IIb by using spatial transcriptomics.
View Article and Find Full Text PDFZh Nevrol Psikhiatr Im S S Korsakova
November 2024
Pirogov Russian National Research Medical University, Moscow, Russia.
Neurobiol Dis
December 2024
Department of Physiology, Second Faculty of Medicine, Charles University, Prague 15000, Czech Republic; Department of Pharmacology, University of Oxford, Oxford OX1 3QT, UK. Electronic address:
Ictal central apnoea is a feature of focal temporal seizures. It is implicated as a risk factor for sudden unexpected death in epilepsy (SUDEP). Here we study seizure-related apnoeas in two different models of experimental seizures, one chronic and one acute, in adult genetically-unmodified rats, to determine mechanisms of seizure-related apnoeas.
View Article and Find Full Text PDFNeurobiol Dis
December 2024
Reeve-Irvine Research Center, Gillespie Neuroscience Research Facility, 837 Health Sciences Road, University of California at Irvine, Irvine, CA 92697, USA; Department of Anatomy & Neurobiology, University of California at Irvine, Irvine, CA 92697, USA; Department of Neurobiology & Behavior, University of California at Irvine, Irvine, CA 92697, USA; Department of Neurosurgery, University of California at Irvine, Irvine, CA 92697, USA; Center for the Neurobiology of Learning and Memory, University of California at Irvine, Irvine, CA 92697, USA; University of California at Irvine School of Medicine, Irvine, CA, 92697, USA. Electronic address:
Embryonic and early postnatal promotor-driven deletion of the phosphatase and tensin homolog (PTEN) gene results in neuronal hypertrophy, hyperexcitable circuitry and development of spontaneous seizures in adulthood. We previously documented that focal, vector-mediated PTEN deletion in mature granule cells of the adult dentate gyrus triggers dramatic growth of cell bodies, dendrites, and axons, similar to that seen with early postnatal PTEN deletion. Here, we assess the functional consequences of focal, adult PTEN deletion, focusing on its pro-epileptogenic potential.
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