Abstract

The effects of two K + channel openers, cromakalim and pinacidil, on voltage-dependent and receptor-mediated catecholamine secretion and Ca 2+ mobilization in bovine adrenal chromaffin cells were studied to determine the role of membrane K + channels in the regulation of a Ca 2+-dependent secretory process. Both cromakalim and pinacidil stimulated the efflux of 86Rb (used to monitor K + permeability) from preloaded cells. Cromakalim and pinacidil did not affect the catecholamine secretion induced by excessive depolarization with 56 mM K +, but inhibited that induced by moderate depolarization with 31 mM K + in a concentration-dependent manner (1 μM–100 μM). The 31 mM K +-induced 45Ca 2+ influx and increase in intracellular free Ca 2+ concentration [Ca 2+]i were also inhibited by these agents at similar concentrations to those for inhibition of catecholamine secretion. Cromakalim and pinacidil inhibited catecholamine secretion, 45Ca 2+ influx and increase in (Ca 2+]i induced by stimulation of nicotinic acetylcholine (ACh) receptors with carbamylcholine. Furthermore, both cromakalim and pinacidil inhibited the increase in [Ca 2+]i induced by carbamylcholine in the absence of extracellular Ca 2+, which is thought to be mediated by muscarinic ACh receptors. On the other hand, they did not affect catecholamine secretion induced by Bay-K 8644, Ba 2+, A23187, histamine or bradykinin. These results indicate that the K + channel openers, cromakalim and pinacidil, selectively inhibit catecholamine secretion induced by moderate depolarization or by nicotinic ACh receptor stimulation by inhibiting Ca 2+ influx and increase in [Ca 2+]i. Furthermore, the results suggest that these K + channel openers-sensitive membrane K + channels are involved in the regulation of catecholamine secretion mainly indirectly through effects on the voltage-dependent membrane Ca 2+ channels.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call