Fentanyl increases dopamine release in rat nucleus accumbens: Involvement of mesolimbic Mu- and delta-2-opioid receptors

Citation
Y. Yoshida et al., Fentanyl increases dopamine release in rat nucleus accumbens: Involvement of mesolimbic Mu- and delta-2-opioid receptors, NEUROSCIENC, 92(4), 1999, pp. 1357-1365
Citations number
58
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROSCIENCE
ISSN journal
03064522 → ACNP
Volume
92
Issue
4
Year of publication
1999
Pages
1357 - 1365
Database
ISI
SICI code
0306-4522(1999)92:4<1357:FIDRIR>2.0.ZU;2-W
Abstract
The effects of the mu-receptor agonist fentanyl on extracellular levels of dopamine in rat nucleus accumbens were studied in awake animals by in vivo brain microdialysis. Fentanyl dose-dependently increased the levels of dopa mine when given intravenously (mu g/kg) or via a microdialysis probe placed into the ventral tegmental area or the nucleus accumbens (nmol). The effec t of fentanyl given into the nucleus accumbens was blocked by systemic admi nistration of the non-selective opioid receptor antagonist naloxone and by accumbens administration of D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Phe-Thr-NH2 (nmol), a mu-opioid receptor antagonist, and naltrindole (nmol), a non-selective d elta-opioid receptor antagonist, in a dose-dependent manner. The delta(2)-o pioid receptor antagonist, naltriben (nmol), also blocked the effects of fe ntanyl, whereas the delta(1)-opioid receptor antagonist, (E)-7-benzylidenen altrexone (nmol), was ineffective. When marginally effective doses of D-Phe -Cys-Tyr-D-Trp-Orn-Thr-Phe-Thr-NH2 and naltriben were given simultaneously, the effect of fentanyl was nearly fully blocked; the pretreatment itself h ad no effect. Administration of the mu-opioid receptor agonist [D-Ala(2), N -Me-Phe(4),Gly(5)-ol]-enkephalin (nmol), the delta(1)-opioid receptor agoni st [D-Pen(2,5)]-enkephalin (nmol) or the delta(2)-opioid receptor agonist [ D-Ala(2),Glu(5)]-deltorphin (nmol) into the nucleus accumbens enhanced the amount of accumbal dopamine. This study provides evidence that not only act ivation of delta(1)- and delta(2)-opioid receptors, but also activation of mu-opioid receptors in the nucleus accumbens increases the release of accum bal dopamine in freely moving rats. We suggest that the effect of intra-acc umbens administration of fentanyl upon accumbal release of dopamine is eith er due to the simultaneous activation of mu-opioid receptors and delta(2)-o pioid receptors or due to activation of mu-opioid receptors that interact w ith delta(2)-opioid receptors in a complex manner. (C) 1999 IBRO. Published by Elsevier Science Ltd.