Członkowski A, Herman Z
Pol J Pharmacol Pharm. 1980 Sep-Oct;32(5):639-41.
The aim of this paper was to study whether prostaglandins (PGs) E1, E2 and F2 alpha affect the binding of specific ligands for dopaminergic or opiate receptors 3H-spiroperidol or 3H-naloxone in the rat striatum. The PGs, even in very high concentrations, did not change 3H-spiroperidol or 3H-naloxone binding to rat striatal membranes in vitro. This indicates that in the striatum of rats PGs do not interact directly with dopaminergic and opiate receptors.
本文的目的是研究前列腺素(PGs)E1、E2和F2α是否会影响大鼠纹状体中多巴胺能或阿片受体特异性配体3H-螺哌啶醇或3H-纳洛酮的结合。即使在非常高的浓度下,PGs在体外也不会改变3H-螺哌啶醇或3H-纳洛酮与大鼠纹状体膜的结合。这表明在大鼠纹状体中,PGs不会直接与多巴胺能和阿片受体相互作用。