Neuroprotective and cardioprotective conopeptides: an emerging class of drug leads

Curr Opin Drug Discov Devel. 2009 Mar;12(2):231-9.

Abstract

The peptides in the venoms of predatory marine snails belonging to the genus Conus ('cone snails') have well-established therapeutic applications for the treatment of pain and epilepsy. This review discusses the neuroprotective and cardioprotective potential of four families of Conus peptides (conopeptides), including omega-conotoxins that target voltage-gated Ca2+ channels, conantokins that target NMDA receptors, mu-conotoxins that target voltage-gated Na+ channels, and kappa- and kappaM-conotoxins that target K+ channels. The diversity of Conus peptides that have already been shown to exhibit neuroprotective/cardioprotective activity suggests that marine snail venoms are a potentially rich source of drug leads with diverse mechanisms.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Calcium Channel Blockers / pharmacology
  • Cardiovascular Agents / chemistry
  • Cardiovascular Agents / isolation & purification
  • Cardiovascular Agents / pharmacology*
  • Conotoxins / chemistry
  • Conotoxins / isolation & purification
  • Conotoxins / pharmacology*
  • Drug Discovery*
  • Excitatory Amino Acid Antagonists / pharmacology
  • Humans
  • Neuroprotective Agents / chemistry
  • Neuroprotective Agents / isolation & purification
  • Neuroprotective Agents / pharmacology*
  • Potassium Channel Blockers / pharmacology
  • Receptors, N-Methyl-D-Aspartate / antagonists & inhibitors
  • Sodium Channel Blockers / pharmacology
  • Structure-Activity Relationship
  • omega-Conotoxins / pharmacology

Substances

  • Calcium Channel Blockers
  • Cardiovascular Agents
  • Conotoxins
  • Excitatory Amino Acid Antagonists
  • Neuroprotective Agents
  • Potassium Channel Blockers
  • Receptors, N-Methyl-D-Aspartate
  • Sodium Channel Blockers
  • omega-Conotoxins