H. Morishita et T. Katsuragi, Existence and pharmacological properties of dopamine D-4 receptors in guinea pig vas deferens, EUR J PHARM, 374(2), 1999, pp. 255-261
This study was carried out to identify subtypes of dopamine D-2-like recept
ors in guinea pig isolated vas deferens. Dopamine had no effect on the musc
le tone in the presence of prazosin, an alpha(1)-adrenoceptor antagonist. H
owever, contractile responses to adenosine triphosphate (ATP). noradrenalin
e and acetylcholine were potentiated in a concentration dependent manner by
dopamine in the presence of prazosin. This potentiation was not inhibited
by raclopride, an antagonist for dopamine D-2 and D-3 receptors. However, t
he potentiation of ATP- and noradrenaline induced contraction was inhibited
by clozapine and 8-methyl-6-(4-methyl-1-piperazinyl)-11 H-pyrido[2-,3-b][
1,4]benzodiazepine (JL-18), dopamine D-4 receptor antagonists. Further, the
potentiation of noradrenaline- and acetylcholine-induced contraction was a
lso inhibited by spiperone. an antagonist for dopamine D-2, D-3 and D-4 rec
eptors. These results suggest that the dopamine D-4 receptor is located on
the postsynaptic site of guinea pig vas deferens and that activation of the
dopamine D-4 receptor enhances contractile responses to agonists without a
ffecting muscle tone. (C) 1999 Elsevier Science B.V. All rights reserved.