Quisqualic acid

Quisqualic acid is an agonist of the AMPA, kainate, and group I metabotropic glutamate receptors. It is one of the most potent AMPA receptor agonists known.[1][2][3][4] It causes excitotoxicity and is used in neuroscience to selectively destroy neurons in the brain or spinal cord.[5][6][7] Quisqualic acid occurs naturally in the seeds of Quisqualis species.

Quisqualic acid
Names
IUPAC name
(2S)-2-amino-3-(3,5-dioxo-1,2,4-oxadiazolidin-2-yl)propanoic acid
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.164.809
KEGG
MeSH Quisqualic+Acid
UNII
Properties
C5H7N3O5
Molar mass 189.126 g/mol
Melting point 187 to 188 °C (369 to 370 °F; 460 to 461 K) decomposes
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Research conducted by the USDA Agricultural Research Service, has demonstrated quisqualic acid is also present within the flower petals of zonal geranium (Pelargonium x hortorum) and is responsible for causing rigid paralysis of the Japanese beetle.[8][9] Quisqualic acid is thought to mimic L-glutamic acid, which is a neurotransmitter in the insect neuromuscular junction and mammalian central nervous system.[10]

See also

References

  1. Jin, Rongsheng; Horning, Michelle; Mayer, Mark L.; Gouaux, Eric (December 2002). "Mechanism of Activation and Selectivity in a Ligand-Gated Ion Channel: Structural and Functional Studies of GluR2 and Quisqualate". Biochemistry. 41 (52): 15635–15643. doi:10.1021/bi020583k. PMID 12501192.
  2. Kuang, Donghui; Hampson, David R. (June 2006). "Ion dependence of ligand binding to metabotropic glutamate receptors". Biochemical and Biophysical Research Communications. 345 (1): 1–6. doi:10.1016/j.bbrc.2006.04.064. PMID 16674916.
  3. Zhang, Wei; Robert, Antoine; Vogensen, Stine B.; Howe, James R. (August 2006). "The Relationship between Agonist Potency and AMPA Receptor Kinetics". Biophysical Journal. 91 (4): 1336–1346. Bibcode:2006BpJ....91.1336Z. doi:10.1529/biophysj.106.084426. PMC 1518651. PMID 16731549.
  4. Bigge, Christopher F; Boxer, Peter A; Ortwine, Daniel F (August 1996). "AMPA/Kainate Receptors". Current Pharmaceutical Design. 2 (4): 397–412.
  5. Muir, Janice L.; Page, Keith J.; Sirinathsinghji, D.J.S.; Robbins, Trevor W.; Everitt, Barry J. (November 1993). "Excitotoxic lesions of basal forebrain cholinergic neurons: Effects on learning, memory and attention". Behavioural Brain Research. 57 (2): 123–131. doi:10.1016/0166-4328(93)90128-d. PMID 7509608. S2CID 3994174.
  6. Giovannelli, L.; Casamenti, F.; Pepeu, G. (4 November 1998). "C-fos expression in the rat nucleus basalis upon excitotoxic lesion with quisqualic acid: a study in adult and aged animals". Journal of Neural Transmission. 105 (8–9): 935–948. doi:10.1007/s007020050103. PMID 9869327. S2CID 24942954.
  7. Lee, Jeung Woon; Furmanski, Orion; Castellanos, Daniel A.; Daniels, Linda A.; Hama, Aldric T.; Sagen, Jacqueline (July 2008). "Prolonged nociceptive responses to hind paw formalin injection in rats with a spinal cord injury". Neuroscience Letters. 439 (2): 212–215. doi:10.1016/j.neulet.2008.05.030. PMC 2680189. PMID 18524486.
  8. Geraniums and Begonias: New Research on Old Garden Favorites (the March 2010 issue of Agricultural Research magazine.)
  9. Ranger, Christopher M.; Winter, Rudolph E.; Singh, Ajay P.; Reding, Michael E.; Frantz, Jonathan M.; Locke, James C.; Krause, Charles R. (31 December 2010). "Rare excitatory amino acid from flowers of zonal geranium responsible for paralyzing the Japanese beetle". Proceedings of the National Academy of Sciences. 108 (4): 1217–1221. doi:10.1073/pnas.1013497108. PMC 3029778. PMID 21205899.
  10. Usherwood, P. N. R. (1 January 1994). "Insect Glutamate Receptors". Advances in Insect Physiology. 24: 309–341. doi:10.1016/S0065-2806(08)60086-7. ISBN 9780120242245.
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