The effects of alpha,
beta-amyrin, a pentacyclic
triterpene isolated from
Protium heptaphylum was investigated on rat model of
orofacial pain induced by
formalin or
capsaicin. Rats were pretreated with alpha,
beta-amyrin (10, 30, and 100mg/kg, i.p.),
morphine (5mg/kg, s.c.) or vehicle (3%
Tween 80), before
formalin (20 microl, 1.5%) or
capsaicin (20 microl, 1.5 microg) injection into the right vibrissa. In vehicle-treated controls,
formalin induced a biphasic nociceptive face-rubbing behavioral response with an early first phase (0-5 min) and a late second phase (10-20 min) appearance, whereas
capsaicin produced an immediate face-rubbing (grooming) behavior that was maximal
at 10-20 min. Treatment with alpha,
beta-amyrin or
morphine significantly inhibited the face-rubbing response in both test models. While
morphine produced significant antinociception in both phases of
formalin test, alpha,
beta-amyrin inhibited only the second phase response, more prominently at 30 mg/kg, in a
naloxone-sensitive manner. In contrast, alpha,
beta-amyrin produced much greater antinociceptive effect at 100mg/kg in the
capsaicin test, which was also
naloxone-sensitive. These results provide first time evidence to show that alpha,
beta-amyrin attenuates
orofacial pain at least, in part, through a peripheral
opioid mechanism but warrants further detailed study for its utility in painful orofacial pathologies.