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Publication : Medial septal GABAergic neurons reduce seizure duration upon optogenetic closed-loop stimulation.

First Author  Hristova K Year  2021
Journal  Brain Volume  144
Issue  5 Pages  1576-1589
PubMed ID  33769452 Mgi Jnum  J:343828
Mgi Id  MGI:6728593 Doi  10.1093/brain/awab042
Citation  Hristova K, et al. (2021) Medial septal GABAergic neurons reduce seizure duration upon optogenetic closed-loop stimulation. Brain 144(5):1576-1589
abstractText  Seizures can emerge from multiple or large foci in temporal lobe epilepsy, complicating focally targeted strategies such as surgical resection or the modulation of the activity of specific hippocampal neuronal populations through genetic or optogenetic techniques. Here, we evaluate a strategy in which optogenetic activation of medial septal GABAergic neurons, which provide extensive projections throughout the hippocampus, is used to control seizures. We utilized the chronic intrahippocampal kainate mouse model of temporal lobe epilepsy, which results in spontaneous seizures and as is often the case in human patients, presents with hippocampal sclerosis. Medial septal GABAergic neuron populations were immunohistochemically labelled and were not reduced in epileptic conditions. Genetic labelling with mRuby of medial septal GABAergic neuron synaptic puncta and imaging across the rostral to caudal extent of the hippocampus, also indicated an unchanged number of putative synapses in epilepsy. Furthermore, optogenetic stimulation of medial septal GABAergic neurons consistently modulated oscillations across multiple hippocampal locations in control and epileptic conditions. Finally, wireless optogenetic stimulation of medial septal GABAergic neurons, upon electrographic detection of spontaneous hippocampal seizures, resulted in reduced seizure durations. We propose medial septal GABAergic neurons as a novel target for optogenetic control of seizures in temporal lobe epilepsy.
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