In vitro release and electrophysiological effects in situ of homocysteic acid, an endogenous N-methyl-(D)-aspartic acid agonist, in the mammalian striatum.

Details

Serval ID
serval:BIB_E383318EDFF5
Type
Article: article from journal or magazin.
Collection
Publications
Title
In vitro release and electrophysiological effects in situ of homocysteic acid, an endogenous N-methyl-(D)-aspartic acid agonist, in the mammalian striatum.
Journal
Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Author(s)
Do K.Q., Herrling P.L., Streit P., Turski W.A., Cuenod M.
ISSN
0270-6474 (Print)
ISSN-L
0270-6474
Publication state
Published
Issued date
1986
Peer-reviewed
Oui
Volume
6
Number
8
Pages
2226-2234
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Abstract
A potassium-induced, calcium-dependent release of endogenous homocysteic acid (HCA) from rat striatal slices was demonstrated. A precolumn derivatization high-performance liquid chromatography method was developed that allowed quantitative determination of sulfur-containing amino acids at the picomole level. Intracellular recordings from cat caudate neurons during simultaneous microiontophoretic application of drugs and electrical stimulation of the corticocaudate pathway showed that (L)-HCA evoked a depolarization pattern similar to that induced by N-methyl-(D)-aspartic acid (NMDA), and both these depolarizations could be selectively inhibited by a specific NMDA antagonist, (D)-2-amino-7-phosphonoheptanoic acid [(D)-AP-7]. A selective antagonism of (L)-HCA-induced depolarizations by (D)-AP-7 was confirmed in quantitative experiments with the frog hemisected spinal cord in vitro. Small quantities of iontophoretically applied (L)-HCA, but not of quisqualate, potentiated cortically evoked EPSPs in cat caudate neurons. These observations suggest that (L)-HCA might be a candidate as an NMDA-receptor-preferring endogenous transmitter in the caudate nucleus. One possible function for such transmitter systems could be the enhancement of EPSPs.
Keywords
Animals, Aspartic Acid/metabolism, Calcium/metabolism, Cats, Caudate Nucleus/drug effects, Chromatography, High Pressure Liquid, Corpus Striatum/drug effects, Corpus Striatum/metabolism, Drug Synergism, Electric Stimulation, Electrophysiology, Evoked Potentials, Glutamates/metabolism, Glutamic Acid, Homocysteine/analogs & derivatives, Homocysteine/metabolism, Iontophoresis, Oxadiazoles/pharmacology, Potassium/pharmacology, Quisqualic Acid, Rana temporaria, Rats, Veratrine/pharmacology
Pubmed
Create date
06/03/2014 16:04
Last modification date
20/08/2019 16:07
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