Palytoxin: membrane mechanisms of action

Toxicon. 2009 Dec 15;54(8):1183-9. doi: 10.1016/j.toxicon.2009.02.030. Epub 2009 Mar 6.

Abstract

Palytoxin is a marine toxin originally isolated from the zoantharians of the genus Palythoa, but now is found in marine organisms ranging from dinoflagellates to fishes. With a MW of 2680, it is one of the largest nonpolymeric natural products ever found. Its complex structure has been elucidated and total synthesis has been achieved. With an LD(50) of 25 ng/kg for rabbits (the most sensitive species), it is one of the most lethal marine toxins. It binds to the Na,K-ATPase specifically with a K(D) of 20 pM. It has a unique action on the Na,K-ATPase, converting the pump into an ion channel and resulting in K(+) efflux, Na(+) influx and membrane depolarization. As a result palytoxin causes a wide spectrum of secondary pharmacological actions. By acting like a key to unlock the internal structure of the Na,K-ATPase, palytoxin holds promise as a useful tool for investigation of the pump molecule.

Publication types

  • Review

MeSH terms

  • Acrylamides / chemical synthesis
  • Acrylamides / chemistry*
  • Acrylamides / metabolism
  • Acrylamides / pharmacology*
  • Animals
  • Cell Membrane / drug effects*
  • Cell Membrane / metabolism
  • Cnidarian Venoms
  • Ion Channels / drug effects
  • Ion Channels / metabolism
  • Marine Toxins / chemical synthesis
  • Marine Toxins / chemistry*
  • Marine Toxins / metabolism
  • Marine Toxins / pharmacology*
  • Sodium-Potassium-Exchanging ATPase / drug effects
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Toxicity Tests, Acute

Substances

  • Acrylamides
  • Cnidarian Venoms
  • Ion Channels
  • Marine Toxins
  • Sodium-Potassium-Exchanging ATPase
  • palytoxin