Abstract
1. Depolarization-induced suppression of inhibition (DSI) is a form of synaptic plasticity which involves a retrograde messenger. We have performed experiments in Purkinje cells of rat cerebellar slices to determine the nature of this messenger. 2. DSI is mimicked by 2-(2,3-dicarboxycyclopropyl)-glycine (DCG-IV), a specific agonist of group II metabotropic glutamate receptors (mGluRs). 3. DSI is reduced if transmitter release is inhibited by saturating doses of DCG-IV. 4. Both DSI and DCG-IV-induced inhibition are inhibited by L-2-amino-3-phosphonopropionic acid (L-AP3), a drug which interferes with several subtypes of mGluRs. 5. DSI is reduced if synaptic activity is enhanced by application of forskolin. 6. We propose that glutamate or a glutamate-like substance is the retrograde messenger implicated in DSI, and that the inhibition resulting from presynaptic glutamate binding is mediated by a decrease in the presynaptic concentration of cAMP.
MeSH Terms
2-Amino-5-phosphonovalerate/pharmacology
Alanine/analogs & derivatives,pharmacology
Animals
Benzoates/pharmacology
Colforsin/pharmacology
Cyclopropanes/pharmacology
Electrophysiology
Excitatory Amino Acid Antagonists/pharmacology
Glutamic Acid/physiology
Glycine/analogs & derivatives,pharmacology
Interneurons/chemistry,physiology
Kinetics
Presynaptic Terminals/chemistry,physiology
Purkinje Cells/chemistry,physiology,ultrastructure
Quinoxalines/pharmacology
Rats
Receptors, Metabotropic Glutamate/agonists,antagonists & inhibitors,physiology
Synapses/chemistry,drug effects,physiology
Synaptic Transmission/drug effects,physiology
Tetrodotoxin/pharmacology
Chemicals
Benzoates
Cyclopropanes
Excitatory Amino Acid Antagonists
Quinoxalines
Receptors, Metabotropic Glutamate
2-amino-3-phosphonopropionic acid
2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
alpha-methyl-4-carboxyphenylglycine
2-(2,3-dicarboxycyclopropyl)glycine
Colforsin
Glutamic Acid
Tetrodotoxin
2-Amino-5-phosphonovalerate
Alanine
Glycine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Glitsch M
Arbeitsgruppe Zelluläre Neurobiologie, Max-Planck-Institut für Biophysikalische Chemie, Göttingen, Germany.
Llano I
Marty A
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