Dual functional role of membrane depolarization/Ca2+ influx in rat pancreatic B-cell - PubMed (original) (raw)
Dual functional role of membrane depolarization/Ca2+ influx in rat pancreatic B-cell
Y Sato et al. Diabetes. 1992 Apr.
Abstract
Transient exposure of rat pancreatic B-cell to 50 mM K+ ([K+50]) makes exocytosis unresponsive to further depolarization, i.e., stimulation with 100 mM K+ or 1 uM glyburide, which closes the ATP-sensitive K+ (K+ATP) channel, simultaneously with [K+50] does not produce any greater insulin secretion compared with [K+50] alone. In sharp contrast, 16.7 mM glucose ([G16.7]) applied simultaneously with [K+50] elicits an insulin response markedly greater than that produced by [K+50] alone, which is not attenuated by 100 uM diazoxide, an inhibitor of K+ATP channel closure. [G16.7]-induced insulin secretion at the basal K+ concn of 4.7 mM was greatly (93%) suppressed by 100 uM diazoxide. Insulin secretion induced by [K+50] plus [G16.7] ([K+50 + G16.7]) was markedly suppressed (70%) by 1 uM nifedipine, a Ca(2+)-channel blocker and was completely abolished by 2 mM 2-cyclohexen-1-one, which reportedly decreases reduced glutathione level and blocks glucokinase. This finding indicates that insulin release induced by [K+50 + G16.7] is not due to leakage produced by toxic stimuli but to activation of exocytosis. When graded concentrations (25 and 50 mM) of K+ were applied simultaneously with [G16.7] in the presence of 100 uM diazoxide, insulin response was clearly dependent on K+ concentration, indicating that the physiological range of membrane depolarization also activates the glucose-responsive effector. Membrane depolarization/Ca2+ influx directly stimulates hormone exocytosis on one hand and activates the K+ATP channel-independent glucose-responsive effector or effectors on the other in the B-cell. The nature of the glucose-responsive effector or effectors remains to be established.
Similar articles
- Glucose regulation of insulin secretion independent of the opening or closure of adenosine triphosphate-sensitive K+ channels in beta cells.
Sato Y, Anello M, Henquin JC. Sato Y, et al. Endocrinology. 1999 May;140(5):2252-7. doi: 10.1210/endo.140.5.6729. Endocrinology. 1999. PMID: 10218978 - Sulfatide controls insulin secretion by modulation of ATP-sensitive K(+)-channel activity and Ca(2+)-dependent exocytosis in rat pancreatic beta-cells.
Buschard K, Høy M, Bokvist K, Olsen HL, Madsbad S, Fredman P, Gromada J. Buschard K, et al. Diabetes. 2002 Aug;51(8):2514-21. doi: 10.2337/diabetes.51.8.2514. Diabetes. 2002. PMID: 12145165 - Evidence that glucose can control insulin release independently from its action on ATP-sensitive K+ channels in mouse B cells.
Gembal M, Gilon P, Henquin JC. Gembal M, et al. J Clin Invest. 1992 Apr;89(4):1288-95. doi: 10.1172/JCI115714. J Clin Invest. 1992. PMID: 1556189 Free PMC article. - Potassium channels of the insulin-secreting B cell.
Petit P, Loubatières-Mariani MM. Petit P, et al. Fundam Clin Pharmacol. 1992;6(3):123-34. doi: 10.1111/j.1472-8206.1992.tb00103.x. Fundam Clin Pharmacol. 1992. PMID: 1628875 Review. - Triggering and amplifying pathways of regulation of insulin secretion by glucose.
Henquin JC. Henquin JC. Diabetes. 2000 Nov;49(11):1751-60. doi: 10.2337/diabetes.49.11.1751. Diabetes. 2000. PMID: 11078440 Review.
Cited by
- Rab27a: a new face in beta cell metabolism-secretion coupling.
Aizawa T, Komatsu M. Aizawa T, et al. J Clin Invest. 2005 Feb;115(2):227-30. doi: 10.1172/JCI24269. J Clin Invest. 2005. PMID: 15690078 Free PMC article. Review. - Glucose stimulation of insulin release in the absence of extracellular Ca2+ and in the absence of any increase in intracellular Ca2+ in rat pancreatic islets.
Komatsu M, Schermerhorn T, Aizawa T, Sharp GW. Komatsu M, et al. Proc Natl Acad Sci U S A. 1995 Nov 7;92(23):10728-32. doi: 10.1073/pnas.92.23.10728. Proc Natl Acad Sci U S A. 1995. PMID: 7479873 Free PMC article. - Alterations of insulin secretion from mouse islets treated with sulphonylureas: perturbations of Ca2+ regulation prevail over changes in insulin content.
Anello M, Gilon P, Henquin JC. Anello M, et al. Br J Pharmacol. 1999 Aug;127(8):1883-91. doi: 10.1038/sj.bjp.0702731. Br J Pharmacol. 1999. PMID: 10482920 Free PMC article. - Tolbutamide stimulation of pancreatic beta-cells involves both cell recruitment and increase in the individual Ca(2+) response.
Jonkers FC, Guiot Y, Rahier J, Henquin JC. Jonkers FC, et al. Br J Pharmacol. 2001 Jun;133(4):575-85. doi: 10.1038/sj.bjp.0704108. Br J Pharmacol. 2001. PMID: 11399675 Free PMC article. - Pancreatic islets from hypothalamic obese rats maintain K+ATP channel-dependent but not -independent pathways on glucose-induced insulin release process.
Grassiolli S, Bonfleur ML, Scomparin DX, de Freitas Mathias PC. Grassiolli S, et al. Endocrine. 2006 Oct;30(2):191-6. doi: 10.1385/endo:30:2:191. Endocrine. 2006. PMID: 17322578
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous