Excitatory/inhibitory balance and circuit homeostasis in autism spectrum disorders

SB Nelson, V Valakh - Neuron, 2015 - cell.com
Autism spectrum disorders (ASDs) and related neurological disorders are associated with
mutations in many genes affecting the ratio between neuronal excitation and inhibition …

Fast-spiking, parvalbumin+ GABAergic interneurons: From cellular design to microcircuit function

H Hu, J Gan, P Jonas - Science, 2014 - science.org
Background Neuronal networks in the brain include glutamatergic principal neurons and
GABAergic interneurons (GABA, γ-aminobutyric acid). The latter may be a minority cell type …

Viral manipulation of functionally distinct interneurons in mice, non-human primates and humans

D Vormstein-Schneider, JD Lin, KA Pelkey… - Nature …, 2020 - nature.com
Recent success in identifying gene-regulatory elements in the context of recombinant adeno-
associated virus vectors has enabled cell-type-restricted gene expression. However, within …

Microcircuits and their interactions in epilepsy: is the focus out of focus?

JT Paz, JR Huguenard - Nature neuroscience, 2015 - nature.com
Epileptic seizures represent dysfunctional neural networks dominated by excessive and/or
hypersynchronous activity. Recent progress in the field has outlined two concepts regarding …

The GABAA receptor as a therapeutic target for neurodevelopmental disorders

S Braat, RF Kooy - Neuron, 2015 - cell.com
Intellectual disability, autism spectrum disorder, and epilepsy are prime examples of
neurodevelopmental disorders that collectively affect a significant percentage of the world …

[HTML][HTML] Inhibitory control of the excitatory/inhibitory balance in psychiatric disorders

M Selten, H van Bokhoven, NN Kasri - F1000Research, 2018 - ncbi.nlm.nih.gov
Neuronal networks consist of different types of neurons that all play their own role in order to
maintain proper network function. The two main types of neurons segregate in excitatory and …

Impaired excitability of somatostatin-and parvalbumin-expressing cortical interneurons in a mouse model of Dravet syndrome

C Tai, Y Abe, RE Westenbroek… - Proceedings of the …, 2014 - National Acad Sciences
Haploinsufficiency of the voltage-gated sodium channel NaV1. 1 causes Dravet syndrome,
an intractable developmental epilepsy syndrome with seizure onset in the first year of life …

Clemizole and modulators of serotonin signalling suppress seizures in Dravet syndrome

A Griffin, KR Hamling, K Knupp, SG Hong, LP Lee… - Brain, 2017 - academic.oup.com
Dravet syndrome is a catastrophic childhood epilepsy with early-onset seizures, delayed
language and motor development, sleep disturbances, anxiety-like behaviour, severe …

A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients

Y Sun, SP Paşca, T Portmann, C Goold, KA Worringer… - elife, 2016 - elifesciences.org
Dravet Syndrome is an intractable form of childhood epilepsy associated with deleterious
mutations in SCN1A, the gene encoding neuronal sodium channel Nav1. 1. Earlier studies …

Aberrant epilepsy-associated mutant Nav1.6 sodium channel activity can be targeted with cannabidiol

RR Patel, C Barbosa, T Brustovetsky, N Brustovetsky… - Brain, 2016 - academic.oup.com
Mutations in brain isoforms of voltage-gated sodium channels have been identified in
patients with distinct epileptic phenotypes. Clinically, these patients often do not respond …