PubMed · 2001 · 33 citations · 0 references
Life SciencesNeurobiologyNeuroscienceElectrophysiologyIon Channel BiophysicsNeurophysiologyIon Channel PhysiologyIon Channel RegulationIon Channel SignalingIon ChannelsMembrane ElectrophysiologyNeurotransmissionCalcium-activated Potassium ChannelsChannelsHek293 Cell ExpressionNitric OxideNitric Oxide BiologyNitric Oxide SignalingPotassium Channel PhysiologyVoltage-dependent Channel Activation
We investigated whether nitric oxide (NO) directly activates the cloned alpha-subunit of large conductance Ca2+-activated K+ (Maxi-K) channels from rat brain (rSlo), expressed either in HEK293 cells or Xenopus oocytes. In inside-out patches, the application of S-nitroso-N-acetylpenicillamine (SNAP), a NO-releasing compound, reversibly activated the channel shifting the voltage dependent activation curve of the macroscopic Maxi-K current to the left by about 15 mV. Pretreatment of the patches with N-ethylmaleimide to alkylate free sulfhydryl groups did not prevent the effect of SNAP, suggesting that NO may directly interact with the channels. These results suggest that Maxi-K channels might be one of the physiological targets of NO in the brain.