A selective delta -opioid antagonist, naltrindole, was used to study the ro
le of the delta -opioid receptor in the antinociceptive actions of a synthe
tic NPFF analog, (1DMe)NPYF. I.t. (1DMe)NPYF (5 nmol) produced antinocicept
ion in the rail flick test and(1DMe)NPYF (0.5 nmol) potentiated the antinoc
iceptive effect of i.t. morphine 7.8 nmol. (1DMe)NPYF (5 nmol) had an antih
yperalgesic effect in carrageenan inflammation and it significantly reduced
mechanical allodynia in the spinal nerve ligation model. All these effects
were prevented or significantly reduced by protreatment with naltrindole (
28 nmol) (P < 0.01-0.001). These data suggest that activation of spinal <de
lta>-opioid receptors plays an important rule in mediating the spinal antin
ociceptive effects of (1DMe)NPYF. (C) 2001 Elsevier Science Inc. All rights
reserved.