Cannabis has been used for thousands of years for the treatment of pain res
ulting from a wide range of disorders. Although clinical evaluations of Can
nabis and its psychoactive constituent THC: have not led to a general conse
nsus regarding their analgesic effectiveness, THC and other synthetic canna
binoid analogs elicit antinociception in a variety of pain tests in laborat
ory animals. These antinociceptive effects are mediated through cannabinoid
receptors in the central nervous system which, in turn, modulate the perce
ption of painful stimuli. The endogenous ligand, arachinodyl-ethanolamine (
anandamide), is also an effective antinociceptive agent in experimental mod
els. The extent to which the endogenous cannabinoid system is involved in t
he modulation of pain is currently unknown. Coadministration of opioids and
THC by the intrathecal route produces an additive antalgic effect. Recent
work indicates that coadministration of opioids and cannabinoids produces a
t least an additive effect. The possibility exists that the analgesic effec
ts can be optimized and untoward effects be minimized if agents from these
two classes of drugs were coadministered for the treatment of painful condi
tions.