This study presents a brief description of the role of opioid peptides
in pain control. an inhibitory effect of beta-endorphin and Met-enkep
halin has been described in the peripheral inflamed tissues; this evid
ence suggests a local action of these peptides during inflammation. In
hibitory pain systems have also been documented either within the spin
al cord and in relation with the descending inhibition from midbrain n
uclei to dorsal horn of the spinal cord, by the efferent conexions loc
alized throughout dorsolateral fascicules to the dorsal horn of the sp
inal cord. Whit this idea in mind, beta-endorphine and related substan
ces participation in analgesia has been analyzed. The involvement of m
u, delta and kappa receptors in pain control is discussed. The evidenc
e suggests that opioid analgesia is due to mu receptor activation, but
delta and kappa receptors may be also activated by their endogeneous
ligands and potentiate analgesia. Enkephalines show high-affinity by d
elta opioid receptors and an indirect involvement in analgesia has bee
n suggested. The role of kappa receptors and dynorphin in analgesia re
mains unclear, even controversial results have been published. On the
other hand, naloxone (an opioid antagonist) exhibits paradoxical effec
ts on pain: high doses induce hyperalgesia and low doses produce analg
esia.