μ-opioid receptor-mediated inhibition of the release of radiolabelled noradrenaline and acetylcholine from rat amygdala slices |
| |
Authors: | Abraham L Frankhuijzen Frank P Jansen Anton NM Schoffelmeer Arie H Mulder |
| |
Institution: | Department of Pharmacology, Medical Faculty/Free University, van der Boechorststraat 7, 1081 BT, Amsterdam, The Netherlands |
| |
Abstract: | Presynaptic modulation by opioids of electrically-evoked neurotransmitter release from superfused rat amygdala slices prelabelled with 3H]noradrenaline (NA) and 14C]choline was examined. Both 3H]NA and 14C]acetylcholine release were strongly inhibited by morphine, the mixed δ/μ-receptor agonist
-Ala2,
-Leu5]enkephalin (DADLE) and the highly selective μ-agonist
-Ala2, MePhe4, Gly-ol5]enkephalin (DAMGO), whereas the highly selective δ-agonist
-Pen2,
-Pen5]enkephalin and the κ-agonist bremazocine were without effect. The inhibitory effects were potently antagonized by naloxone but not by the selective δ-receptor antagonist fentanylisothiocyanate. When the selective uptake inhibitor desipramine was used to prevent uptake of 3H]NA into noradrenergic nerve terminals, but sparing the uptake into dopaminergic nerve terminals, the electrically evoked release of tritium was strongly inhibited by bremazocine but not by DADLE or DAMGO.The data indicate, that in the amygdala transmitter release from dopaminergic nerve fibres is inhibited only via activation of κ-receptors, whereas transmitter release from noradrenergic and cholinergic nerve fibers is subjected to inhibition by opioids via activation of μ-receptors only. Regional differences and similarities of modulation of neurotransmitter release by opioids in the rat brain are briefly discussed. |
| |
Keywords: | |
本文献已被 ScienceDirect 等数据库收录! |
|