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Goirand-Lopez, L.

Publications and source records attributed to Goirand-Lopez, L..

2 recordsLinked to original sources

Kainate receptors are critical for permissivity to sustained, disorganized and network-wide pathological activity in the epileptic dentate gyrus

In temporal lobe epilepsy, the dentate gyrus (DG) undergoes extensive reorganization through recurrent mossy fiber (rMF) sprouting, involving both AMPA and kainate receptors (KARs) at granule cell-to-granule cell (GC-GC) recurrent synapses. While KARs are known to enhance neural excitability, their specific contribution to the dynamics of the epileptogenic GC-GC network remains poorly understood. Here, by building and assessing a DG network model endowed with KARs, we revealed that the slow excitatory postsynaptic potentials (EPSPs) they mediate, in synergy with persistent sodium currents, profoundly reshape epileptogenic dynamics by facilitating the conditions for pathological activity, through two complementary mechanisms. Regarding input processing, KARs extended the window for temporal integration in GCs, favoring the initiation of network aberrant activities in response to more dispersed input patterns. Concerning network interactions, KARs reduced the number of sprouted connections needed for the development of epileptiform discharges. In fact, the extension of the structural and functional parameter region driving epileptiform activity was effective both for their initiation and, critically, their sustained maintenance. Moreover, KARs drove a striking transition in network behaviour, from partially organized collective dynamics to a highly disordered regime. In their presence, massive firing propagated through the DG network, disrupting spatial and temporal spiking patterns. This resulted in increased activity dimensionality and entropy, together with reduced mutual information between neurons. Altogether, our results suggest that KARs are not merely amplifiers of network excitation but critical determinants that fundamentally reshape the dynamical landscape, rendering the sprouted DG network permissive to self-sustaining pathological activity.

neuroscience↗

Distinct subtypes of grey matter heterotopia show subtype-specific morpho-electric neuronal properties and dynamics of epileptiform activity in mice

Grey matter heterotopia (GMH) are neurodevelopmental disorders associated with abnormal cortical function and epilepsy. Subcortical band heterotopia (SBH) and periventricular nodular heterotopia (PVNH) are two well-recognized GMH subtypes in which neurons are misplaced, either forming nodules lining the ventricles in PVNH, or forming bands in the white matter in SBH. Although both PVNH and SBH are commonly associated with epilepsy, it is unclear whether these two GMH subtypes differ in terms of pathological consequences or, on the contrary, share common altered mechanisms. Here, we studied two robust preclinical models of SBH and PVNH, and performed a systematic comparative assessment of the physiological and morphological diversity of heterotopia neurons, as well as the dynamics of epileptiform activity and input connectivity. We uncovered a complex set of altered properties, including both common and distinct physiological and morphological features across heterotopia subtypes, and associated with specific dynamics of epileptiform activity. Taken together, these results suggest that pro-epileptic circuits in GMH are, at least in part, composed of neurons with distinct, subtype-specific, physiological and morphological properties depending on the heterotopia subtype. Our work supports the notion that GMH represent a complex set of disorders, associating both shared and diverging pathological consequences, and contributing to forming epileptogenic networks with specific properties. A deeper understanding of these properties may help to refine current GMH classification schemes by identifying morpho-electric signatures of GMH subtypes, to potentially inform new treatment strategies.

neuroscience↗