Subtypes of K+ channels differentiated by the effect of K+ channel openers upon K+ channel blocker-induced seizures

This publication has 17 references indexed in Scilit:

• Analogies and differences in the mode of action and properties of binding sites (localization and mutual interactions) of two K+ channel toxins, MCD peptide and dendrotoxin I
  Brain Research, 1989
• Ca2+ channel blockers prevent seizures induced by a class of K+ channel inhibitors
  European Journal of Pharmacology, 1989
• Comparison of the effluxes of 42K+ and 86Rb+ elicited by cromakalim (BRL 34915) in tonic and phasic vascular tissue
  Naunyn-Schmiedeberg's Archives of Pharmacology, 1988
• The receptor site for the bee venom mast cell degranulating peptide. Affinity labeling and evidence for a common molecular target for mast cell degranulating peptide and dendrotoxin I, a snake toxin active on potassium channels
  Biochemistry, 1988
• The pharmacology of potassium channels and their therapeutic potential
  Trends in Pharmacological Sciences, 1988
• Mast cell degranulating peptide and dendrotoxin selectively inhibit a fast-activating potassium current and bind to common neuronal proteins
  Neuroscience, 1987
• The brain response to the bee venom peptide MCD. Activation and desentization of a hippocampal target
  Brain Research, 1987
• Effect of the K⁺ efflux stimulating vasodilator BRL 34915 on ⁸⁶Rb⁺ efflux and spontaneous activity in guinea‐pig portal vein
  British Journal of Pharmacology, 1987
• Two potent central convulsant peptides, a bee venom toxin, the MCD peptide, and a snake venom toxin, dendrotoxin I, known to block K+ channels, have interacting receptor sites
  Biochemical and Biophysical Research Communications, 1987
• Identification by cross‐linking of a neuronal acceptor protein for dendrotoxin, a convulsant polypeptide
  FEBS Letters, 1984