Synaptic activation of mGluR1 generates persistent depression of a fast after-depolarizing potential in CA3 pyramidal neurons

• Published in: The European journal of neuroscience 2011-03, Vol.33 (5), p.879-889
• Main Authors: Brown, Jon T., Booth, Clair A., Randall, Andrew D.
• Format: Article
• Language: English
• Subjects: Action potential; Action Potentials - drug effects; Action Potentials - physiology; alpha -Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid; Animals; Benzoates - pharmacology; burst; Calcium (intracellular); Data processing; Depression; Excitability; Excitatory Amino Acid Antagonists - pharmacology; Firing pattern; gamma -Aminobutyric acid; glutamate receptor; Glutamic acid receptors (metabotropic); Glycine - analogs & derivatives; Glycine - pharmacology; Hippocampus; Hippocampus - cytology; Male; N-Methyl-D-aspartic acid; Nervous system; Neurons; Neurons - cytology; Neurons - drug effects; Neurons - physiology; Patch-Clamp Techniques; plasticity; Pyramidal cells; Rats; Rats, Wistar; Receptors, Metabotropic Glutamate - metabolism; Synapses - drug effects; Synapses - metabolism
• ISSN: 0953-816X; 1460-9568
• DOI: 10.1111/j.1460-9568.2010.07565.x

Burst firing is an important property of hippocampal pyramidal neurons. Group I metabotropic glutamate receptors (mGluRs) produce a multitude of effects on both the synaptic and intrinsic properties of neurons. We investigated whether brief activation of these receptors results in persistent modifications to the intrinsic excitability of rat hippocampal CA3 pyramidal cells (CA3‐PCs). In whole‐cell current‐clamp recordings, current stimuli consisting of filtered, pseudo‐random noise produced action potential firing with a mean frequency of ∼1.5–2 Hz. Analysis of spike intervals revealed that this firing included a substantial component (∼20%) of high‐frequency (∼100 Hz) bursting activity. Activation of group I mGluRs with (S)‐3,5‐dihydroxyphenylglycine [(S)‐DHPG] selectively eliminated the high‐frequency bursts, an effect that persisted > 30 min after (S)‐DHPG washout. The fast after‐depolarizing potential (ADP) of CA3‐PCs is known to be important for generating high‐frequency action potential bursting. This ADP was persistently depressed following a short application of (S)‐DHPG. This effect was blocked by the mGluR1 antagonist, (S)‐(+)‐α‐amino‐4‐carboxy‐2‐methylbenzeneacetic acid (LY367385). In contrast, the depression was resistant to the mGluR5 antagonist 2‐methyl‐6‐(phenylethynyl)pyridine hydrochloride (MPEP) and α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazolepropionic acid (AMPA)/kainate, N‐methyl‐d‐aspartate (NMDA) and γ‐aminobutyric acid (GABA)A antagonists. Unlike other manipulations that generate persistent depression of the ADP in CA3‐PCs, DHPG‐mediated ADP depression was insensitive to the Kv7 channel inhibitor 10,10‐bis(4‐Pyridinylmethyl)‐9(10H)‐anthracenone dihydrochloride (XE991) and strong intracellular Ca2+ buffering by 1,2‐Bis(2‐aminophenoxy)ethane‐N,N,N′,N′‐tetraacetic acid (BAPTA). Synaptic activation of mGluRs in the associational‐commissural pathway also resulted in persistent depression of the ADP in postsynaptic CA3‐PCs, which was blocked by LY367385. These data represent the first evidence that synaptic activation of mGluR1 can modulate the intrinsic excitability properties of hippocampal neurons.