Abstract
GABA is the main inhibitory neurotransmitter in the vertebrate CNS and it modulates every aspect of brain function. On the molecular level, the action of GABA is mediated by ionotropic (GABAA)1 and metabotropic (GABAB)2 receptors, which are ubiquitously expressed in developing and adult brain. The significance of GABAA receptor-mediated neurotransmission is underscored by the multiple neurological and psychiatric diseases for which alterations in the GABAergic system have been postulated, including epilepsy3–5, Huntington’s disease6, Angelman syndrome7, autism8, 9, anxiety disorders10, bipolar disorders, schizophrenia11–13, and alcohol use disorders14. In particular, GABAA receptors represent a major site of action for clinically important drugs, including benzodiazepines and barbiturates, some general anesthetics such as halothane, etomidate and propofol, as well as ethanol15–18.
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Fritschy, JM., Crestani, F., Rudolph, U., Möhler, H. (2003). GABAA Receptor Subtypes: Memory Function and Neurological Disorders. In: Hensch, T.K., Fagiolini, M. (eds) Excitatory-Inhibitory Balance. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-0039-1_14
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