Grill V
Am J Physiol. 1981 Jan;240(1):E24-31. doi: 10.1152/ajpendo.1981.240.1.E24.
Short-term exposure to glucose increases insulin secretion during subsequent stimulation. This priming effect of glucose was further investigated in the perfused rat pancreas. A 5-min pulse of 27.7 mM glucose enhanced the response to a second pulse of the sugar after a 5- or 30-min period of 3.9 mM glucose. With a 10-min pulse of 27.7 mM glucose, the priming effect tended to persist also after a 60-min but not after a 90-min rest period. The priming effects of glucose were also evaluated from enhancement of stimulation 15 min later with 3-isobutyl-l-methylxanthine (IBMX). A 10-min pulse of 8.3 and 27.7, but not 5.6 mM glucose enhanced IBMX-induced insulin secretion. Cycloheximide did not abolish the priming effect of glucose on IBMX-induced insulin secretion. Conclusions are 1) priming is rapidly induced; 2) it persists longer than the time of induction; 3) threshold concentrations of glucose that induce priming are similar to those that initiate insulin secretions; and 4) mechanisms causing priming may not involve protein synthesis.
短期暴露于葡萄糖会增加后续刺激期间的胰岛素分泌。在灌注的大鼠胰腺中进一步研究了葡萄糖的这种引发效应。27.7 mM葡萄糖的5分钟脉冲增强了在3.9 mM葡萄糖的5分钟或30分钟期间后对第二次糖脉冲的反应。用27.7 mM葡萄糖的10分钟脉冲,引发效应在60分钟后也倾向于持续,但在90分钟的休息期后则不然。葡萄糖的引发效应也通过15分钟后用3-异丁基-1-甲基黄嘌呤(IBMX)增强刺激来评估。8.3和27.7 mM葡萄糖的10分钟脉冲,但不是5.6 mM葡萄糖,增强了IBMX诱导的胰岛素分泌。放线菌酮并没有消除葡萄糖对IBMX诱导的胰岛素分泌的引发效应。结论是:1)引发迅速诱导;2)它持续的时间比诱导时间长;3)诱导引发的葡萄糖阈值浓度与引发胰岛素分泌的浓度相似;4)导致引发的机制可能不涉及蛋白质合成。