Rorsman P, Abrahamsson H, Gylfe E, Hellman B
FEBS Lett. 1984 May 7;170(1):196-200. doi: 10.1016/0014-5793(84)81398-8.
The cytosolic Ca2+ activity of mouse pancreatic beta-cells was studied with the intracellular fluorescent indicator quin2 . When the extracellular Ca2+ concentration was 1.20 mM, the basal cytosolic Ca2+ activity was 162 +/- 9 nM. Stimulation with 20 mM glucose increased this Ca2+ activity by 40%. In the presence of only 0.20 mM Ca2+ or after the addition of the voltage-dependent Ca2+ -channel blocker D-600, glucose had an opposite and more prompt effect in reducing cytosolic Ca2+ by about 15%. It is concluded that an early result of glucose exposure is a lowering of the cytosolic Ca2+ activity and that this effect tends to be masked by a subsequent increase of the Ca2+ activity due to influx of Ca2+ through the voltage-dependent Ca2+ channels.
利用细胞内荧光指示剂喹啉-2研究了小鼠胰腺β细胞的胞质Ca2+活性。当细胞外Ca2+浓度为1.20 mM时,基础胞质Ca2+活性为162±9 nM。用20 mM葡萄糖刺激可使该Ca2+活性增加40%。在仅存在0.20 mM Ca2+的情况下或加入电压依赖性Ca2+通道阻滞剂D-600后,葡萄糖对降低胞质Ca2+有相反且更迅速的作用,降低幅度约为15%。得出的结论是,葡萄糖暴露的早期结果是胞质Ca2+活性降低,并且由于Ca2+通过电压依赖性Ca2+通道内流导致的Ca2+活性随后增加,这种作用往往被掩盖。