Antinociceptive effect of botulinum toxin type a in rat model of carrageenan and capsaicin induced pain

Croat Med J. 2005 Apr;46(2):201-8.

Abstract

Aim: To test antinociceptive properties of botulinum toxin type A (BTX-A) in rats with carrageenan- and capsaicin-induced pain and inflammation.

Methods: Pain was provoked with carrageenan (1%) or capsaicin (0.1%) injection into the plantar surface of the rat paw-pad. The effect of BTX-A 5 U/kg on carrageenan- and capsaicin-induced mechanical and thermal hypersensitivity, as well as the size of carrageenan-induced paw edema were tested 24 hours and 6 days following the toxin injection into the rat paw-pad. In the dose-response experiment, the effect of different doses of BTX-A (2, 3, 3.5, 5, and 7 U/kg) on carrageenan-induced mechanical hypersensitivity was investigated on day 5 after BTX-A application.

Results: Pretreatment with 5 U/kg BTX-A significantly reduced or completely abolished the enhanced sensitivity to mechanical and thermal stimuli provoked by peripheral carrageenan or capsaicin injections. This reduction was significant when BTX-A was applied 6 days before the induction of pain and inflammation, but the toxin was ineffective when applied 24 hours before the challenge. In the dose-response experiment, the lowest effective dose was 3.5 U/kg, but apparently the effect was not dose-dependent. In contrast to the antinociceptive effect, 5 U/kg BTX-A had no effect on the carrageenan-induced paw edema.

Conclusion: The study demonstrated the efficacy of peripherally applied BTX-A pretreatment on the pain component of inflammatory process in experimental animals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Botulinum Toxins, Type A / pharmacology
  • Botulinum Toxins, Type A / therapeutic use*
  • Capsaicin
  • Carrageenan
  • Hindlimb / drug effects
  • Hindlimb / physiopathology
  • Hyperalgesia / chemically induced
  • Hyperalgesia / drug therapy
  • Male
  • Models, Animal
  • Nociceptors / drug effects
  • Pain / chemically induced
  • Pain / drug therapy*
  • Rats
  • Rats, Wistar

Substances

  • Carrageenan
  • Botulinum Toxins, Type A
  • Capsaicin