By controlling spike timing and sculpting neuronal rhythms, inhibitory interneurons play a key role in brain function. GABAergic interneurons are highly diverse. The respective GABAA receptor subtypes, therefore, provide new opportunities not only for understanding GABA-dependent pathophysiologies but also for targeting of selective neuronal circuits by drugs. The pharmacological relevance of GABAA receptor subtypes is increasingly being recognized. A new central nervous system pharmacology is on the horizon. The development of anxiolytic drugs devoid of sedation and of agents that enhance hippocampus-dependent learning and memory has become a novel and highly selective therapeutic opportunity. © 2005 Springer-Verlag Berlin Heidelberg.
CITATION STYLE
Möhler, H., Fritschy, J. M., Vogt, K., Crestani, F., & Rudolph, U. (2005). Pathophysiology and pharmacology of GABAA receptors. Handbook of Experimental Pharmacology, 169, 225–247. https://doi.org/10.1007/3-540-28082-0_9
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