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PMID: 9225313 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Desensitization of kainate receptors by kainate, glutamate and diastereomers of 4-methylglutamate.

Neuropharmacology ·Vol. 36 ·No. 6 ·1997-06-00 ·Pages 853-63

Jones KA, Wilding TJ, Huettner JE, Costa AM

Abstract

The potencies of kainate, glutamate and diastereomers of 4-methylglutamate were determined for activation and steady-state desensitization of GluR6 and dorsal root ganglion-type kainate receptors using whole-cell voltage clamp. In HEK293 cells expressing GluR6, all four diastereomers induced desensitizing inward currents at relatively high concentrations (> 50 microM), however, the 2S,4R diastereomer (2S,4R-4MG; SYM 2081) was approximately 100-fold more potent than the other three. The EC50 for receptor activation by 2S,4R-4MG (1.0 microM) was similar to that for kainic acid (1.8 microM), but 2S,4R-4MG was significantly more potent than kainate, glutamate or the other diastereomers of 4-methylglutamate at producing steady-state desensitization of GluR6 receptors. IC50s for desensitization quantified using a fixed concentration of kainate as a test agonist were 7.6, 31 and 667 nM for 2S,4R-4MG, kainate and glutamate, respectively. In addition, 2S,4R-4MG fully desensitized native kainate receptors (of the GluR5 subtype) in dorsal root ganglion neurons with an IC50 of 11 nM, compared to 3.4 microM for glutamate. For GluR6, recovery from desensitization displayed a similar time course for kainate and glutamate (tau = 3-4 s) but was roughly 20-fold slower for 2S,4R-4MG, which suggests that the rate of recovery is not entirely dependent on the affinity of ligand for the desensitized receptor. Following exposure to concanavalin A, application of kainate, glutamate and 2S,4R-4MG evoked very similar maximal currents that showed little or no desensitization. Lectin pretreatment produced a leftward shift in the concentration-response relationship for 2S,4R-4MG with an 11-fold reduction in the EC50; however, no significant change in the EC50 for kainate was observed. The characteristic of 2S,4R-4MG to potently and completely desensitize both recombinant GluR6 receptors and native receptors on dorsal root ganglion neurons suggests that this compound will be useful to study selective blockade of these receptors in the nervous system.

MeSH Terms
Animals Cells, Cultured Ganglia, Spinal/drug effects Glutamates/pharmacology Glutamic Acid/pharmacology In Vitro Techniques Kainic Acid/pharmacology Osmolar Concentration Patch-Clamp Techniques Rats Receptors, Kainic Acid/drug effects Stereoisomerism
Chemicals
Glutamates Receptors, Kainic Acid 4-methylglutamic acid Glutamic Acid Kainic Acid
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Jones K A
Symphony Pharmaceuticals Inc., Malvern, PA 19355, USA. kjones@synapticcomp.com
Wilding T J
Huettner J E
Costa A M
Article Info
Journal
Neuropharmacology
Abbr.
Neuropharmacology
ISSN
0028-3908
Published
1997-06-00
Pages
853-63
Language
English
Region
England
NLM ID
0236217
Subset
IM
Grants
NINDS NIH HHS · R01 NS030888 · United States
NINDS NIH HHS · NS30888 · United States
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