Inhibition of Kv2.1 Potassium Channels by MiDCA1, A Pre-Synaptically Active PLA2-Type Toxin from Micrurus dumerilii carinicauda Coral Snake Venom

Toxins (Basel). 2019 Jun 12;11(6):335. doi: 10.3390/toxins11060335.

Abstract

MiDCA1, a phospholipase A2 (PLA2) neurotoxin isolated from Micrurus dumerilii carinicauda coral snake venom, inhibited a major component of voltage-activated potassium (Kv) currents (41 ± 3% inhibition with 1 μM toxin) in mouse cultured dorsal root ganglion (DRG) neurons. In addition, the selective Kv2.1 channel blocker guangxitoxin (GxTx-1E) and MiDCA1 competitively inhibited the outward potassium current in DRG neurons. MiDCA1 (1 µM) reversibly inhibited the Kv2.1 current by 55 ± 8.9% in a Xenopus oocyte heterologous system. The toxin showed selectivity for Kv2.1 channels over all the other Kv channels tested in this study. We propose that Kv2.1 channel blockade by MiDCA1 underlies the toxin's action on acetylcholine release at mammalian neuromuscular junctions.

Keywords: Kv2 selective inhibition; Micrurus dumerilii carinicauda venom; mouse dorsal root ganglion neurons; phospholipase A2 neurotoxin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Coral Snakes*
  • Elapid Venoms / toxicity*
  • Ganglia, Spinal / cytology
  • Ganglia, Spinal / physiology
  • Kv1.2 Potassium Channel / antagonists & inhibitors*
  • Kv1.2 Potassium Channel / genetics
  • Kv1.2 Potassium Channel / physiology
  • Male
  • Mice, Inbred C57BL
  • Neurons / drug effects
  • Neurons / physiology
  • Oocytes / physiology
  • Phospholipases A2
  • Potassium Channel Blockers / toxicity*
  • Xenopus

Substances

  • Elapid Venoms
  • Kv1.2 Potassium Channel
  • Potassium Channel Blockers
  • Phospholipases A2