The PAR-1-activating peptide attenuates carrageenan-induced hyperalgesia in rats

Peptides. 2002 Jun;23(6):1181-3. doi: 10.1016/s0196-9781(02)00053-0.

Abstract

We examined if thrombin or a receptor-activating peptide for protease-activated receptor-1 (PAR-1), a thrombin receptor, could modulate nociception at peripheral levels. Intraplantar administration of PAR-1 activators, thrombin or TFLLR-NH(2), but not its inactive control FTLLR-NH(2) or a PAR-2 activator SLIGRL-NH(2), significantly attenuated the hyperalgesia in rats treated with carrageenan, although they had no effect on nociception in naïve rats. The thrombin-PAR-1 system might thus act to attenuate nociception during inflammatory hyperalgesia.

MeSH terms

  • Animals
  • Carrageenan / metabolism*
  • Dose-Response Relationship, Drug
  • Hyperalgesia / metabolism*
  • Male
  • Oligopeptides / metabolism
  • Oligopeptides / pharmacology
  • Oligopeptides / physiology*
  • Pain
  • Rats
  • Rats, Wistar
  • Thrombin / metabolism
  • Time Factors

Substances

  • Oligopeptides
  • PAR-1-activating peptide
  • seryl-leucyl-isoleucyl-glycyl--arginyl-leucinamide
  • Carrageenan
  • Thrombin