Functional reduction of SK3-mediated currents precedes AMPA-receptor- mediated excitotoxicity in dopaminergic neurons

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Abstract

In primary cultures of mesencephalon small-conductance calcium-activated potassium channels (SK) are expressed in dopaminergic neurons. We characterized SK-mediated currents (I SK) in this system and evaluated their role on homeostasis against excitotoxicity. I SK amplitude was reduced by the glutamatergic agonist AMPA through a reduction in SK channel number in the membrane. Blockade of I SK for 12 h with apamin or NS8593 reduced the number of dopaminergic neurons in a concentration-dependent manner. The effect of apamin was not additive to AMPA toxicity. On the other hand, two I SK agonists, 1-EBIO and CyPPA, caused a significant reduction of spontaneous loss of dopaminergic neurons. 1-EBIO reversed the effects of both AMPA and apamin as well. Thus, I SK influences survival and differentiation of dopaminergic neurons in vitro, and is part of protective homeostatic responses, participating in a rapidly acting negative feedback loop coupling calcium levels, neuron excitability and cellular defenses. This article is part of a Special Issue entitled 'Trends in Neuropharmacology: In Memory of Erminio Costa'.

Original languageEnglish
Pages (from-to)1176-1186
Number of pages11
JournalNeuropharmacology
Volume60
Issue number7-8
DOIs
StatePublished - Jun 2011

Keywords

  • 1-Ebio
  • Apamin
  • CyPPA
  • Dopaminergic
  • Excitotoxicity
  • NS8593 AMPA
  • Neuroprotection
  • SK channels

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