Lundquist I, Fanska R, Grodsky G M
Endocrinology. 1976 Nov;99(5):1304-12. doi: 10.1210/endo-99-5-1304.
The interrelationship between calcium ion and glucose on glucagon release was studied in the in vitro perfused pancreas. Spontaneous release during perfusion with glucose-free, calcium-depleted (0.2 mEq/l calcium) medium was completely abolished by ethylene glycol bis (beta-aminoethyl ether)-N,N'-tetraacetic acid (EGTA; 0.2 mM). Glucose added to calcium-depleted perfusate caused only partial inhibition of glucagon release, even at concentrations of 500 mg/dl, and there was no evidence of a paradoxical increase in secretion with time. When calcium was added in a series of steps (in the absence of additional secretagogues) more than half of the increased glucagon released was elicited by the first step (0.5 mEq/l). Release patterns at subsequent steps suggested that higher concentrations of calcium may cause mixed stimulation and inhibition. With 70 mg/dl glucose, calcium-stimulated release was partially suppressed at all calcium concentrations up through 9 mEq/l. With 150 mg/dl glucose, addition of the normally stimulating 0.5 mEq/l calcium caused abrupt and complete inhibition of glucagon secretion, and this persisted at all higher calcium concentrations. Insulin release, when high enough to be detected, did not correlate with the glucose/calcium suppression of glucagon. In other experiments, control results and all insulin secretion patterns were qualitatively similar to those reported by other investigators; however, various attempts to demonstrate a paradoxical increase glucagon secretion by glucose during calcium deprivation were unsuccessful. It is concluded that small amounts of calcium are normally required for glucagon secretion, although at higher concentrations the effects become complex. In addition, glucagon suppression by glucose is calcium-requiring. Thus, changes in glucagon secretion caused by addition or depletion of calcium can depend on the relative amount of glucose in the milieu.
在体外灌注胰腺中研究了钙离子与葡萄糖对胰高血糖素释放的相互关系。在用无葡萄糖、钙缺乏(0.2 mEq/L钙)的培养基灌注期间的自发释放被乙二醇双(β-氨基乙基醚)-N,N'-四乙酸(EGTA;0.2 mM)完全消除。添加到钙缺乏灌注液中的葡萄糖即使在浓度为500 mg/dl时也仅引起胰高血糖素释放的部分抑制,并且没有证据表明随着时间的推移分泌会出现反常增加。当以一系列步骤添加钙(在没有额外促分泌剂的情况下)时,超过一半的增加的胰高血糖素释放是由第一步(0.5 mEq/L)引起的。后续步骤的释放模式表明,更高浓度的钙可能会引起混合的刺激和抑制。对于70 mg/dl葡萄糖,在所有高达9 mEq/L的钙浓度下,钙刺激的释放均被部分抑制。对于150 mg/dl葡萄糖,添加通常具有刺激作用的0.5 mEq/L钙会导致胰高血糖素分泌突然且完全抑制,并且在所有更高的钙浓度下均持续存在。当胰岛素释放量高到足以被检测到时,其与葡萄糖/钙对胰高血糖素的抑制作用无关。在其他实验中,对照结果和所有胰岛素分泌模式在质量上与其他研究者报道的相似;然而,各种试图证明在钙缺乏期间葡萄糖引起胰高血糖素分泌反常增加的尝试均未成功。得出的结论是,正常情况下胰高血糖素分泌需要少量钙,尽管在较高浓度下作用会变得复杂。此外,葡萄糖对胰高血糖素的抑制作用需要钙。因此,钙的添加或缺乏引起的胰高血糖素分泌变化可能取决于环境中葡萄糖的相对含量。