Fast and slow voltage-dependent dynamics of magnesium block in the NMDA receptor: the asymmetric trapping block model
Fast and slow voltage-dependent dynamics of magnesium block in the NMDA receptor: the asymmetric trapping block model
The NMDA receptor (NMDAR) produces a long-lasting component of the glutamatergic EPSC in mammalian central neurons. The current through NMDARs is voltage dependent as a result of block by extracellular magnesium, which has recently been shown to give rise to a complex time dependence, with fast and slow components of responses to changes in membrane potential. Here, we studied the dynamics of block and unblock by measuring voltage step responses in conjunction with fast perfusion of agonist in nucleated patches isolated from rat cortical pyramidal neurons. We found that slow unblock shows a progressive onset during synaptic-like responses to brief pulses of agonist. Repolarizing briefly from +40 to -70 mV revealed that slow unblock is reestablished with a time constant of approximately 5 msec at room temperature. Also, the time course of deactivation, in response to a pulse of agonist, slows twofold over the potential range -30 to +40 mV. An asymmetric "trapping block" model in which the voltage-independent closing rate constant of the blocked channel is approximately three times that of the unblocked channel accounts quantitatively for all of these phenomena and for responses to action potential waveform clamp. This model allows much more accurate prediction of NMDAR current in physiological conditions of magnesium concentration and changing membrane potential than previously possible. It suggests a positive allosteric link between occupation of the NMDAR pore by magnesium and closure of the permeation gate.
magnesium, open-channel block, synaptic integration, nucleated patch, kinetics, rat cortex
6171-6180
Vargas-Caballero, Mariana
de2178ac-77fd-4748-9fe5-109ab8ad93e1
Robinson, Hugh P.C.
9e490d5e-ab13-42f4-bee8-8dc5312bad83
7 July 2004
Vargas-Caballero, Mariana
de2178ac-77fd-4748-9fe5-109ab8ad93e1
Robinson, Hugh P.C.
9e490d5e-ab13-42f4-bee8-8dc5312bad83
Vargas-Caballero, Mariana and Robinson, Hugh P.C.
(2004)
Fast and slow voltage-dependent dynamics of magnesium block in the NMDA receptor: the asymmetric trapping block model.
Journal of Neuroscience, 24 (27), .
(doi:10.1523/JNEUROSCI.1380-04.2004).
(PMID:15240809)
Abstract
The NMDA receptor (NMDAR) produces a long-lasting component of the glutamatergic EPSC in mammalian central neurons. The current through NMDARs is voltage dependent as a result of block by extracellular magnesium, which has recently been shown to give rise to a complex time dependence, with fast and slow components of responses to changes in membrane potential. Here, we studied the dynamics of block and unblock by measuring voltage step responses in conjunction with fast perfusion of agonist in nucleated patches isolated from rat cortical pyramidal neurons. We found that slow unblock shows a progressive onset during synaptic-like responses to brief pulses of agonist. Repolarizing briefly from +40 to -70 mV revealed that slow unblock is reestablished with a time constant of approximately 5 msec at room temperature. Also, the time course of deactivation, in response to a pulse of agonist, slows twofold over the potential range -30 to +40 mV. An asymmetric "trapping block" model in which the voltage-independent closing rate constant of the blocked channel is approximately three times that of the unblocked channel accounts quantitatively for all of these phenomena and for responses to action potential waveform clamp. This model allows much more accurate prediction of NMDAR current in physiological conditions of magnesium concentration and changing membrane potential than previously possible. It suggests a positive allosteric link between occupation of the NMDAR pore by magnesium and closure of the permeation gate.
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Published date: 7 July 2004
Keywords:
magnesium, open-channel block, synaptic integration, nucleated patch, kinetics, rat cortex
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Centre for Biological Sciences
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Local EPrints ID: 348679
URI: http://eprints.soton.ac.uk/id/eprint/348679
PURE UUID: 7573e49e-209b-48a4-9722-258e5d4ca6f1
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Date deposited: 05 Mar 2013 12:00
Last modified: 15 Mar 2024 03:43
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Author:
Hugh P.C. Robinson
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