
Enhanced responses to somatostatin interneuron activation in developmentally malformed cortex
Author(s) -
Ekanem Nicole B.,
Reed Laura K.,
Weston Nicole,
Jacobs Kimberle M.
Publication year - 2019
Publication title -
epilepsia open
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.247
H-Index - 16
ISSN - 2470-9239
DOI - 10.1002/epi4.12316
Subject(s) - neuroscience , optogenetics , interneuron , disinhibition , excitatory postsynaptic potential , inhibitory postsynaptic potential , somatostatin , biology , channelrhodopsin , cortex (anatomy) , postsynaptic potential , electrophysiology , receptor , biochemistry
Summary Intractable epilepsy is commonly associated with developmental cortical malformations. Using the rodent freeze lesion model, we have sought the underlying circuit abnormalities contributing to the epileptiform activity that occurs in association with the structural pathology of four‐layered microgyria. We showed previously that within the epileptogenic paramicrogyral region ( PMR ) surrounding the malformation, non–fast‐spiking neurons commonly containing somatostatin ( SS t) exhibit alterations, including having a greater maximum firing rate. Here we examined the output of SS t interneurons with optogenetics, using SS t‐Cre mice mated to mice with floxed channelrhodopsin‐2. Voltage clamp recordings from layer V pyramidal neurons in ex vivo slices had significantly enhanced SS t‐evoked inhibitory postsynaptic currents in PMR cortex compared to control. In addition, under conditions of low‐Mg 2+ artificial cerebral spinal fluid (aCSF), light activation of the SS t neurons evoked field potential epileptiform activity in the PMR cortex, but not in control. These data suggest that within the PMR cortex, SS ts have a significantly larger effect on excitatory neurons. Surprisingly, the network effect of this enhanced inhibition is hyperexcitability with propagating epileptiform activity, perhaps due to disinhibition of other interneuron cell types or to enhanced synchrony of excitatory cortical elements. This identification creates a new locus for potential modulation of epileptiform activity associated with cortical malformation.