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Biochemical and Molecular Properties of GABAB Receptors

  • Kinya Kuriyama
  • Masaaki Hirouchi
Part of the The Receptors book series (REC)

Abstract

γ-Aminobutyric acid (GABA) is known as one of the major inhibitory neurotransmitters in the brain. GABA receptors are many, and are pharmacologically classified into two major subtypes, GABAA and GABAB. The GABAA receptor is well-characterized pharmacologically. Muscimol and bicuculline, which are, respectively, an agonist and an antagonist for the GABAA receptor, bind selectively to the GABAA. Various central acting drugs, such as benzodiazepines and barbiturates, also have binding sites within the GABAA receptor complex (Doble and Martin, 1992). In addition, the GABAA receptor consists of heterogeneous subunits, and functions as a Cl-channel (Burt and Kamatchi, 1991; see also Chapter 2 of this volume).

Keywords

Adenylate Cyclase Xenopus Oocyte Gaba Receptor Cerebellar Granule Cell Gaba Release 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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© Springer Science+Business Media New York 1997

Authors and Affiliations

  • Kinya Kuriyama
  • Masaaki Hirouchi

There are no affiliations available

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