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APV (NMDAR antagonist)



 

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APV (2-amino-5-phosphonovaleric acid; AP5, 2-amino-5-phosphonopentanoate) is a selective NMDA receptor (NMDAR) antagonist that competitively inhibits the active site of NMDAR. Its chemical name is R-2-amino-5-phosphonopentanoate.

APV blocks the cellular analog of classical conditioning in the sea slug Aplysia californica, and has similar effects on Aplysia long-term potentiation, since NMDA receptors are required for both. It is sometimes used in conjunction with the calcium chelator BAPTA to determine whether NMDARs are required for a particular cellular process.

APV is generally very fast acting within in vitro preparations, and can block NMDA receptor action at a reasonably small concentration. The active isomer of APV is considered to be the D configuration, although many preparations are available as a racemic mixture of D- and L-isomers. It is useful to isolate the action of other glutamate receptors in the brain, i.e. AMPA and kainate receptors.

APV can block the conversion of a silent synapse to an active one, since this conversion is NMDA receptor-dependent.

APV was developed by Jeff Watkins and Harry Olverman.

References

  • Cellular Analog of Differential Classical Conditioning in Aplysia: Disruption by the NMDA Receptor Antagonist DL-2-Amino-5-Phosphonovalerate

See also

 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "APV_(NMDAR_antagonist)". A list of authors is available in Wikipedia.
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