Opioid analgesia, the selective suppression of pain without effects on
other sensations, also distinguishes between different types of pain:
severe, persistent pain is potently inhibited by opioids, but they fa
il to conceal the sensation of a pinprick. The cellular basis for this
specificity was analyzed by means of patch-clamp experiments performe
d on fluorescently labeled nociceptive neurons (nociceptors) that inne
rvate rat tooth pulp. Activation of the mu opioid receptor inhibited c
alcium channels on almost all small nociceptors but had minimal effect
on large nociceptors. Somatostatin had the opposite specificity, pref
erentially inhibiting calcium channels on the large cells. Because per
sistent pain is mediated by slow-conducting, small nociceptors, opioid
s are thus likely to inhibit neurotransmitter release only at those pr
imary synapses specialized for persistent pain.