A tarantula peptide against pain via ASIC1a channels and opioid mechanisms.

Nat Neurosci

Institut de Pharmacologie Moléculaire et Cellulaire, Centre National de la Recherche Scientifique (CNRS), Institut Paul Hamel, Université de Nice-Sophia-Antipolis, 660 Route des Lucioles 06560 Valbonne, France.

Published: August 2007

AI Article Synopsis

  • Psalmotoxin 1 is a peptide from the South American tarantula that effectively reduces various types of pain in rodents, including thermal and neuropathic pain.
  • It works by blocking a specific ion channel (acid-sensing ion channel 1a), which activates the body's natural pain-relieving system (endogenous enkephalin pathway).
  • The pain-relief effects of Psalmotoxin 1 can be inhibited by certain opioid receptor blockers, and are absent in genetically modified mice lacking the Penk1 gene.

Article Abstract

Psalmotoxin 1, a peptide extracted from the South American tarantula Psalmopoeus cambridgei, has very potent analgesic properties against thermal, mechanical, chemical, inflammatory and neuropathic pain in rodents. It exerts its action by blocking acid-sensing ion channel 1a, and this blockade results in an activation of the endogenous enkephalin pathway. The analgesic properties of the peptide are suppressed by antagonists of the mu and delta-opioid receptors and are lost in Penk1-/- mice.

Download full-text PDF

Source
http://dx.doi.org/10.1038/nn1940DOI Listing

Publication Analysis

Top Keywords

analgesic properties
8
tarantula peptide
4
peptide pain
4
pain asic1a
4
asic1a channels
4
channels opioid
4
opioid mechanisms
4
mechanisms psalmotoxin
4
psalmotoxin peptide
4
peptide extracted
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!