HOME WEB NEWS IMAGES CLASSIFIEDS YELLOW PAGESPOLLS - SURVEYS WIKI COUNTRIES PHOTOS US UK INDIA
Avoo.com provides meta search results from various sources

Nmda


Google




NMDA
IUPAC name N-methyl-D-aspartic acid
Identifiers
CAS number [6384-92-5]
PubChem 22880
MeSH NMDA
Properties
Molecular formula C5H9N1O4
Molar mass 147.13 D
Boiling point

549.62

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

NMDA (N-methyl-D-aspartic acid) is an amino acid derivative acting as a specific agonist at the NMDA receptor, and therefore mimics the action of the neurotransmitter glutamate on that receptor. In contrast to glutamate, NMDA binds to and regulates the above receptor only, but not other glutamate receptors.

NMDA is a water-soluble synthetic substance that is not normally found in biological tissue. It was first synthesized in the 1960\'s. NMDA is an excitotoxin; this trait has applications in behavioral neuroscience research. The body of work utilizing this technique falls under the term "lesion studies." Researchers apply NMDA to specific regions of an (animal) subject\'s brain or spinal cord and subsequently test for the behavior of interest, such as operant behavior. If the behavior is compromised, it suggests the destroyed tissue was part of a brain region that made an important contribution to the normal expression of that behavior.

Contents

Antagonists

Main article: NMDA receptor antagonist

Examples of antagonists of the NMDA receptor are APV, Amantadine, dextromethorphan, ketamine, phencyclidine (PCP), riluzole, memantine, and kynurenic acid, the only known endogenous antagonist. They are commonly referred to as NMDA receptor antagonists.

Forms

The structural formula of NMDA pictured above is written down as the neutral form. At physiological pH both carboxyl groups are deprotonated.

References

  • Watkins J, Jane D (2006). "The glutamate story". Br J Pharmacol 147 Suppl 1: S100-8. PMID 16402093.

Bibliography

 This neuroscience article is a stub. You can help Wikipedia by expanding it.

This article is licensed under the GNU Free Documentation License. It uses material from Wikipedia


Advertise with Us | Search Marketing | Help | Suggest a Site | Privacy Policy
© 2008 www.avoo.com. All rights reserved.