NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurones

Amy B. Macdermott, Mark L. Mayer, Gary L. Westbrook, Stephen J. Smith, Jeffery L. Barker

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Abstract

Excitatory amino acids act via receptor subtypes in the mammalian central nervous system (CNS)1-3. The receptor selectively activated by N-methyl-D-aspartic acid (NMDA) has been best characterized using voltage-clamp and single-channel recording; the results suggest that NMDA receptors gate channels that are permeable to Na+, K+ and other monovalent cations4-7. Various experiments suggest that Ca 2+ flux is also associated with the activation of excitatory amino-acid receptors on vertebrate neurones8-11. Whether Ca 2+ enters through voltage-dependent Ca2+ channels or through excitatory amino-acid-activated channels of one or more subtype is unclear. Mg2+ can be used to distinguish NMDA-receptor-activated channels from voltage-dependent Ca2+ channels, because at micromolar concentrations Mg2+ has little effect on voltage-dependent Ca 2+ channels12 while it enters and blocks NMDA receptor channels4,5,7,13,14. Marked differences in the potency of other divalent cations acting as Ca2+ channel blockers compared with their action as NMDA antagonists also distinguish the NMDA channel from voltage-sensitive Ca2+ channels5,7. However, we now directly demonstrate that excitatory amino acids acting at NMDA receptors on spinal cord neurones increase the intracellular Ca2+ activity, measured using the indicator dye arsenazo III, and that this is the result of Ca2+ influx through NMDA receptor channels. Kainic acid (KA), which acts at another subtype of excitatory amino-acid receptor, was much less effective in triggering increases in intracellular free Ca2+.

Original languageEnglish (US)
Pages (from-to)519-522
Number of pages4
JournalNature
Volume321
Issue number6069
DOIs
StatePublished - Dec 1 1986

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