Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy
Open Access
- 26 January 2016
- journal article
- research article
- Published by Oxford University Press (OUP) in Cerebral Cortex
- Vol. 26 (4), 1778-1794
- https://doi.org/10.1093/cercor/bhw002
Abstract
Severe myoclonic epilepsy of infancy (SMEI) is associated with loss of function of the SCN1A gene encoding the NaV1.1 sodium channel isoform. Previous studies in Scn1a−/+ mice during the pre-epileptic period reported selective reduction in interneuron excitability and proposed this as the main pathological mechanism underlying SMEI. Yet, the functional consequences of this interneuronal dysfunction at the circuit level in vivo are unknown. Here, we investigated whether Scn1a−/+ mice showed alterations in cortical network function. We found that various forms of spontaneous network activity were similar in Scn1a−/+ during the pre-epileptic period compared with wild-type (WT) in vivo. Importantly, in brain slices from Scn1a−/+ mice, the excitability of parvalbumin (PV) and somatostatin (SST) interneurons was reduced, epileptiform activity propagated more rapidly, and complex synaptic changes were observed. However, in vivo, optogenetic reduction of firing in PV or SST cells in WT mice modified ongoing network activities, and juxtasomal recordings from identified PV and SST interneurons showed unaffected interneuronal firing during spontaneous cortical dynamics in Scn1a−/+ compared with WT. These results demonstrate that interneuronal hypoexcitability is not observed in Scn1a−/+ mice during spontaneous activities in vivo and suggest that additional mechanisms may contribute to homeostatic rearrangements and the pathogenesis of SMEI.Keywords
Funding Information
- Telethon-Italy
- Istituto Italiano di Tecnologia, European Research Council
- MIUR FIRB (RBAP11X42L)
- Institut du Cerveau et de la Moelle Épinière
- Giovanni Armenise-Harvard Foundation: Career Development Award, European Research Council
- ERC (FP7/2007-2013, 200808)
- Investissements d'Avenir (ANR-10-IAIHU-06)
- ANR Programme Blanc (ANR-13-BSV4-0015-01)
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