Zj. Dong et al., DUAL ACTIONS OF (-)-STEPHOLIDINE ON THE DOPAMINE RECEPTOR-MEDIATED ADENYLATE-CYCLASE ACTIVITY IN RAT CORPUS STRIATUM, Life sciences, 61(4), 1997, pp. 465-472
Citations number
24
Categorie Soggetti
Biology,"Medicine, Research & Experimental","Pharmacology & Pharmacy
(-)-Stepholidine (SPD) is an antagonist of normosensitive dopamine (DA
) receptors, but it exhibits D-1 agonistic action on rotational behavi
our in rats with unilateral 6-hydroxydopamine (6-OHDA) lesions of the
substantia nigra pars compacta (SNC). In the present study, agonistic
and antagonistic effects of SPD on the DA receptor-mediated synaptosom
al adenylate cyclase (AC) activity in rat striatum were investigated.
After blockade of D-2 receptors, SPD augmented AC activity dose-depend
ently. The EC50 value was 41.1 +/- 8.6 mu mol/L. At the concentration
of 10 mu mol/L, SPD increased cAMP formation from a basal level (50.8
+/- 10.3 pmol/mg protein/min) to 133.7 +/- 31.8 pmol/mg protein/min. T
he SPD-induced stimulation of AC activity was almost completely revers
ed by 10 mu mol/L Sch23390. These results indicate that SPD possesses
an agonistic action on the D-1 receptor. Forskolin-stimulated adenylat
e cyclase (FSAC) activity was used as a model to elucidate the effect
of SPD on D-2 receptors. The results indicate that DA inhibited FSAC a
ctivity dose-dependently, while SPD partially restored FSAC activity.
Taken together, these results support the conclusion that SPD has dual
actions on DA receptors that mediate AC activity, i.e., an agonistic
action on D-1 receptors and an antagonistic action on D-2 receptors.