Dopamine is known to inhibit aldosterone secretion. In the present stu
dy using whole-cell voltage-clamp technique we found that dopamine, br
omocriptine and quinpirole inhibit low-threshold (T-type) voltage depe
ndent Ca2+ channels. The inhibition was sustained and reversible, and
it was prevented by sulpiride. These findings indicate that the effect
of dopamine was mediated via DA2 receptors.