A, application of a mixture of V1a and V2 (1 μm) agonists significantly increased vasopressin release from the isolated SON in vitro, but did not potentiate subsequent K+-induced release. B, this response was only partially blocked by preapplication of a mixture of Ca2+-channel blockers. C, however, pretreatment with Ca2+-channel blockers blocked the high-K+ evoked response in vasopressin release. Data are means ± s.e.m., t tests, n = 4 per group for each experiment.