Gaba A Receptor Article Index for
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Information About

Gaba A Receptor




The GABAA receptor is one of the three Ligand-gated Ion Channel s responsible for mediating the effects of Gamma-AminoButyric Acid ( GABA ), the major inhibitory Neurotransmitter in the human body.


STRUCTURE AND FUNCTION

The receptor is a . Because the chloride ion concentration is high outside the Cell , opening of the channel pore results in an influx of chloride into the cell, thus making it more negative ( Hyperpolarizing it). The GABAA channel opens quickly and thus contributes to the early part of the Inhibitory Postsynaptic Potential (IPSP) (Siegel et al., 1999; Chen et al., 2005).


Subunits

There are numerous subunit Isoform s for the GABAA receptor, which determine the receptor’s agonist affinity, chance of opening, conductance, and other properties (Cossart et al., 2005). There are six types of α subunits, three β's, three γ's, as well as a δ, an ε, a π, a θ, and three ρs (Martin and Dunn, 2002; Sieghart et al., Neurochem Int 1999;34:379–85). Five subunits can combine in different ways to form GABAA channels, but the most common type in the brain has two α's, two β's, and a γ (Martin and Dunn, 2002). The receptor binds two GABA molecules (Siegel et al., 1999; Colquhoun and Sivilotti, 2004), somewhere between an α and a β subunit (Martin and Dunn, 2002).


AGONISTS AND ANTAGONISTS

Other ligands (besides GABA) interact with the GABAA receptor to activate it (agonists), to inhibit its activation (antagonists) or to increase or decrease its response to an agonist (positive and negative allosteric modulators). Such other ligands include Benzodiazepine s (increase pore opening frequency; often the ingredient of sleep pills and anxiety medications), Barbiturate s (increase pore opening duration; used as sedatives), and certain Steroids , called Neuroactive Steroid s.

Among antagonists are picrotoxin (which blocks the channel pore) and bicuculline (which occupies the GABA site and prevents GABA from activating the receptor). The antagonist Flumazenil is used medically to reverse the effects of the benzodiazepines.

A useful property of the many agonists and some antagonists is that they often have a greater interaction with GABAA receptors which contain specific subunits. This allows one to determine which GABAA receptor subunit combinations are prevalent in particular brain areas and provides a clue as to which subunit combintations may be responsible for behavioral effects of drugs acting at GABAA receptors. Among the behavioral effects of such drugs are relief of anxiety (anxiolysis), Muscle relaxation, Sedation , Anticonvulsion , and Anesthesia .


SEE ALSO



REFERENCES

  • Chen K., Lia H.Z., Yea N., Zhanga J., and Wang J.J. 2005. Role of GABAB receptors in GABA and baclofen-induced inhibition of adult rat cerebellar interpositus nucleus neurons in vitro. ''Brain Research Bulletin'', 67(4), 310-318.

  • Colquhoun D. and Sivilotti L.G. 2004. Function and structure in glycine receptors and some of their relatives. ''Trends in Neurosciences'', 27(6), 337-344.

  • Martin I.L., and Dunn S.M.J. 2002. GABA Receptors . Tocris Cookson Ltd.

  • Siegel G.J., Agranoff B.W., Fisher S.K., Albers R.W., and Uhler M.D. 1999. ''Basic Neurochemistry: Molecular, Cellular and Medical Aspects'', Sixth Edition . GABA Receptor Physiology and Pharmacology. American Society for Neurochemistry. Lippincott Williams and Wilkins.



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