Hellman B, Lenzen S, Sehlin J, Täljedal I B
Diabetologia. 1977 Jan;13(1):49-53. doi: 10.1007/BF00996327.
The uptake of 45Ca2+ by a lanthanum-non-displaceable pool in pancreatic islets was studied; Raising the extracellular D-glucose concentration from 3 to 20 mM stimulated the 45Ca2+ uptake in hand-dissected islets of ob/bo-mice as well as in collagenase-isolated islets of ob/ob or normal mice. The effect was dose-dependent in the range of 0-20 mM D-glucose and was seen throughout a wide range of extracellular calcium concentrations (16 mumol-2.56 mmol of Ca2+ added per litre of medium). The 45Ca2+ uptake was also enhanced by other known insulin secretagogues (D-mannose, L-leucine, tolbutamide) and was uninfluenced by compounds lacking insulin-releasing capacity (3-O-methyl-D-glucose, L-glucose, D-galactose, D-leucine). The stimulatory effect of D-glucose was blocked by inhibitors of glucose-induced insulin release (D-mannoheptulose, diazoxide, L-adrenaline). The results support the view that the lanthanum-nondisplaceable calcium pool is related to the insulin-releasing mechanism, although the exact nature of this relationship is still unclear.
研究了胰岛中镧不可置换池对45Ca2+的摄取;将细胞外D-葡萄糖浓度从3 mM提高到20 mM,可刺激ob/bo小鼠手工分离的胰岛以及ob/ob或正常小鼠胶原酶分离的胰岛对45Ca2+的摄取。在0-20 mM D-葡萄糖范围内,该效应呈剂量依赖性,且在广泛的细胞外钙浓度范围内(每升培养基中添加16 μmol-2.56 mmol的Ca2+)均可观察到。其他已知的胰岛素促分泌剂(D-甘露糖、L-亮氨酸、甲苯磺丁脲)也可增强45Ca2+的摄取,而缺乏胰岛素释放能力的化合物(3-O-甲基-D-葡萄糖、L-葡萄糖、D-半乳糖、D-亮氨酸)对其无影响。葡萄糖诱导的胰岛素释放抑制剂(D-甘露庚酮糖、二氮嗪、L-肾上腺素)可阻断D-葡萄糖的刺激作用。结果支持这样的观点,即镧不可置换钙池与胰岛素释放机制有关,尽管这种关系的确切性质仍不清楚。