Abstract
We evaluatedthe role of Ca 2+-activated K + channels in the regulation of prolactin (PRL) secretion with a perifusion system using acutely dispersed rat anterior pituitary cells. Apamin, which blocks Ca 2+-activated K + channels, induced PRL secretion in a dose-dependent fashion between 1 and 300 nM ( r = 0.99, P < 0.01). Charybdotoxin, another Ca 2+-activated K + channel-blocker, also induced PRL secretion at 20 nM concentration. These were not non-specific toxic effects, since stimulation of PRL secretion by 10 nM thyrotropin-releasing hormone (TRH) was not different before and after applying the channel-blockers. Both 10 μM dopamine and 2 μM nifedipine significantly, but incompletely, depressed PRL secretion induced by 100 nM apamin; 10 μM dopamine completely blocked PRL secretion induced by 20 nM charybdotoxin. Our data indicate that Ca 2+-activated K + channels may play an important role in the regulation of PRL secretion.
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