Somers G, Sener A, Devis G, Malaisse W J
Pflugers Arch. 1980 Dec;388(3):249-53. doi: 10.1007/BF00658490.
Replacement of extracellular chloride by the impermeant anion isethionate, increase in extracellular osmotic strength by addition of sucrose, or exposure to the anion transport blocking agent probenecid inhibited insulin release evoked by glucose or alpha-ketoisocaproate in rat isolated islets. The inhibition of insulin release due to Cl- substitution was associated with a modest decrease in glucose oxidation, but no significant change in glucose-stimulated 45Ca net uptake by the islets. In the isolated perfused rat pancreas, the isethionate- or sucrose-induced inhibition of insulin release was a rapid and rapidly reversible phenomenon. Chloride substitution by isethionate inhibited more severely the second than the first phase of the secretory response to glucose, and failed to affect the insulin response to gliclazide. A chemosmotic mechanism for exocytosis, as proposed for epinephrine and parathyroid hormone release, may also be involved in insulin release.
用不易渗透的阴离子羟乙磺酸盐替代细胞外氯离子、添加蔗糖增加细胞外渗透压强度或暴露于阴离子转运阻断剂丙磺舒,均可抑制大鼠分离胰岛中葡萄糖或α-酮异己酸诱发的胰岛素释放。由于氯离子替代导致的胰岛素释放抑制与葡萄糖氧化的适度降低有关,但胰岛对葡萄糖刺激的45Ca净摄取无显著变化。在离体灌注的大鼠胰腺中,羟乙磺酸盐或蔗糖诱导的胰岛素释放抑制是一种快速且可逆的现象。用羟乙磺酸盐替代氯离子对葡萄糖分泌反应的第二阶段的抑制比对第一阶段更严重,且不影响胰岛素对格列齐特的反应。如肾上腺素和甲状旁腺激素释放所提出的那样,一种用于胞吐作用的化学渗透机制也可能参与胰岛素释放。