NR2 subunit-dependence of NMDA receptor channel block by external Mg super(2+)

The vital roles played by NMDA receptors in CNS physiology depend critically on powerful voltage-dependent channel block by external Mg super(2+) (Mg super(2+) sub(o)). NMDA receptor channel block by Mg super(2+) sub(o) depends on receptor subunit composition: NR1/2A receptors (receptors composed of...

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Veröffentlicht in:The Journal of physiology 2005-01, Vol.562 (2), p.319-331
Hauptverfasser: Qian, Anqi, Buller, Amy L, Johnson, Jon W
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Sprache:eng
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Zusammenfassung:The vital roles played by NMDA receptors in CNS physiology depend critically on powerful voltage-dependent channel block by external Mg super(2+) (Mg super(2+) sub(o)). NMDA receptor channel block by Mg super(2+) sub(o) depends on receptor subunit composition: NR1/2A receptors (receptors composed of NR1 and NR2A subunits) and NR1/2B receptors are more strongly inhibited by Mg super(2+) sub(o) than are NR1/2C or NR1/2D receptors. We investigated the effects of Mg super(2+) sub(o) on single-channel and whole-cell currents recorded from recombinant NR1/2D and NR1/2A receptors expressed in HEK293 and 293T cells. The main conclusions are as follows: (1) Voltage-dependent inhibition by Mg super(2+) sub(o) of whole-cell NR1/2D receptor responses was at least 4-fold weaker than inhibition of NR1/2A receptor responses at all voltages tested. (2) Channel block by Mg super(2+) sub(o) reduced the duration of NR1/2D receptor single-channel openings; this reduction was used to estimate the apparent blocking rate of Mg super(2+) sub(o) (k sub(+,app)). The k sub(+,app) for NR1/2D receptors was similar to but moderately slower than the k sub(+,app) obtained from cortical NMDA receptors composed of NR1, NR2A and NR2B subunits at all voltages tested. (3) Mg super(2+) sub(o) blocking events induced an additional component in the closed- duration distribution; this component was used to estimate the apparent unblocking rate of Mg super(2+) sub(o) (k sub(-,app)). The k sub(-,app) for NR1/2D receptors was much faster than the k sub(-,app) for cortical receptors at all voltages tested. The voltage-dependence of the k sub(-,app) of NR1/2D and cortical receptors differed in a manner that suggested that Mg super(2+) sub(o) may permeate NR1/2D receptors more easily than cortical receptors. (4) Mg super(2+) sub(o) inhibits NR1/2D receptors less effectively than cortical receptors chiefly because Mg super(2+) sub(o) unbinds much more rapidly from NR1/2D receptors.
ISSN:0022-3751