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Closure of ATP-regulated K+channels (KATPchannels) plays a central role in glucose-stimulated insulin secretion in beta cells. KATPchannels are also highly expressed in glucagon-producing alpha cells, where their function remains unresolved. Under hypoglycaemic conditions, KATPchannels are open in alpha cells but their activity is low and only ~1% of that in beta cells. Like beta cells, alpha cells respond to hyperglycaemia with KATPchannel closure, membrane depolarisation and stimulation of action potential firing. Yet, hyperglycaemia reciprocally regulates glucagon (inhibition) and insulin secretion (stimulation). Here we discuss how this conundrum can be resolved and how reduced KATPchannel activity, via membrane depolarisation, paradoxically reduces alpha cell Ca2+entry and glucagon exocytosis. Finally, we consider whether the glucagon secretory defects associated with diabetes can be attributed to impaired KATPchannel regulation and discuss the potential for remedial pharmacological intervention using sulfonylureas. © 2014 Springer-Verlag Berlin Heidelberg.

Original publication

DOI

10.1007/s00125-014-3279-8

Type

Journal article

Journal

Diabetologia

Publication Date

01/01/2014

Volume

57

Pages

1749 - 1761