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Excitatory Amino Acids
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Excitatory amino acid receptors Transmitter is L-glutamate Formed by GABA-transaminase Inactivated by uptake Receptor classification based on –electrophysiology, binding & cloning Nomenclature - –NMDA, AMPA, kainate, metabotropic
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AMPA receptors Overview –ionotropic receptor –opens channel permeable to Na + /K + –reversal potential ~ 0mV –therefore generates fast EPSP Pharmacology –Agonist = AMPA –Antagonist = CNQX
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Molecular biology –Cloned subunits = GluRA-D –similar to nicotinic receptor subunits H N 2 COOH H N 2 COOH
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– form pentamers? – GluRB bestows AMPA receptor-like properties Function –nicotinic-like –mediates most fast excitatory transmission Molecular biology –Cloned subunits = GluRA-D –similar to nicotinic receptor subunits
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NMDA receptors Overview –ionotropic receptor –opens channel permeable to Na + /K + /Ca 2+ –reversal potential ~ 0mV –therefore generates fast(-ish) EPSP Pharmacology –agonist = NMDA –antagonist = AP5
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Molecular biology –cloned subunits = NR1 & NR2A-D –similar to nicotinic receptor sub-units –form pentamers? –NR1 bestows NMDA receptor-like properties Modulated by –Mg 2+ causes a voltage-dependent channel block
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L-glutamate
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+60 mV Na/K/Ca 2pA 20msec 0 mV Na/K/Ca -60 mV Na/K/Ca Mg 2+
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2pA 20msec +50-50 V (mV) I (pA) Mg 2+ -free Mg 2+ I-V curve
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Molecular biology –cloned subunits = NR1 & NR2A-D –similar to nicotinic receptor sub-units –form pentamers? –NR1 bestows NMDA receptor-like properties Modulated by –Mg 2+ causes a voltage-dependent channel block – glycine is a cofactor
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NMDA 10sec 100pA NMDA + CM CM glycineNMDA + glycine NMDA + glycine + strychnine
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Molecular biology –cloned subunits = NR1 & NR2A-D –similar to nicotinic receptor sub-units –form pentamers? –NR1 bestows NMDA receptor-like properties Modulated by –Mg 2+ causes a voltage-dependent channel block – glycine is a cofactor – ketamine/phencyclidine/MK801 block ion channel
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Function –Ca 2+ “switch” Molecular biology –cloned subunits = NR1 & NR2A-D –similar to nicotinic receptor sub-units –form pentamers? –NR1 bestows NMDA receptor-like properties Modulated by –Mg 2+ causes a voltage-dependent channel block – glycine is a cofactor – ketamine/phencyclidine/MK801 block ion channel
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Kainate receptors Confusion over identification –kainate activates AMPA receptors –part of kainate binding is not displaced by AMPA Molecular Biology –Cloned subunits = KA1-2 & GluR5-7 –form pentamers? –rapidly desensitising (AMPA insensitive) channel Function?
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Metabotropic glutamate receptors Overview –g-protein coupled positively linked to PLC negatively linked to adenylate cyclase or direct to ion channels Molecular biology COOH H N 2
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Metabotropic glutamate receptors – mGluR 1-8 Group I = mGluR 1&5 linked to PLC Group II = mGluR 2&3 linked to adenylate cyclase Group III = mGluR 4&6-8 linked to adenylate cyclase Overview –g-protein coupled positively linked to PLC negatively linked to adenylate cyclase or direct to ion channels Molecular biology
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Pharmacology –most commonly used agonist = (1S,3R) ACPD is selective for Group I and Group II –most commonly used antagonist = MCPG non-selective antagonist? Electrophysiological actions –blocks I AHP –blocks M-current (therefore evokes slow EPSP) –blocks voltage dependent Ca 2+ channels Functions –Neuromodulator - analgous to ACh muscarinic receptors
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Physiological/pathological roles Metabotropic glutamate receptors –probably many, including synaptic plasticity AMPA receptors –mediate most fast EPSPs in the CNS Kainate receptors –anyones guess
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NMDA receptors –Anaesthesia –Learning and memory –Developmental plasticity –Epilepsy –Excitotoxicity (eg stroke)
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Summary Classification of EAA receptors Diversity of actions Similarities with other neurotransmitter systems Factors modulating NMDA receptors Physiological/pathological processes
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