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SummaryAn in vivo system has been used to investigate the ability of dopamine agonists and antagonists to alter dopamine… Expand RAT dopamine D2short receptors expressed in CHO cells were characterized by activation of [35S]GTPgammaS binding. There were no… Expand Quinelorane is a BCD partial ergoline with potent dopaminergic effects in vitro and in vivo. Partial ergoline compounds of this… Expand We have previously identified [3H]quinpirole‐labeled dopamine receptors in the molecular layer of cerebellar lobule 10 which have… Expand 3-(2'-[18F]fluoroethyl)spiperone (FESP), a recently developed dopamine D2-receptor binding radiopharmaceutical, was used for… Expand N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline (EEDQ) inactivates a variety of monoamine neurotransmitter receptors. In this… Expand In primary culture of anterior pituitary cells, BAY-K-8644, a calcium channel agonist, stimulated PRL secretion by 83% with EC50… Expand Tail vein injections of [3H]N-propylnorapomorphine ([3H]NPA) in male mice resulted in a dose-related accumulaton of radioactivity… Expand Unanesthetized adult male rats with indwelling right atrial cannulae were used in the majority of experiments. Morphine (MOR, 3.0… Expand : The syntheses and the structural and stereochemical requirements for antagonism of (+)-amphetamine-induced sterotypy are… Expand