Giddings S J, Chirgwin J, Permutt M A
Diabetes. 1982 Jul;31(7):624-9. doi: 10.2337/diab.31.7.624.
The purpose of these studies was to determine whether glucose, the principal regulator of insulin biosynthesis in mammals, controls synthesis through alterations in levels of proinsulin mRNA in whole animals. Rats were starved for 3 days and then either refed or injected with glucose or saline for 24 h. Glucose injection raised plasma glucose levels equivalent to levels seen with refeeding but provided less than 20% of caloric replacement. Pancreatic RNA was extracted and the relative concentration of proinsulin mRNA was determined by blot hybridization with a cloned rat proinsulin cDNA probe. In starved animals proinsulin mRNA levels were 15-20% that of fed controls. Glucose injection produced a specific three- to fourfold increase in proinsulin mRNA levels relative to total pancreatic RNA, within 24 h. The effect was measurable 2 h after glucose injection and appeared largely complete by 12 h. Actinomycin D blocked the glucose-induced increase in proinsulin mRNA. These studies demonstrate effects of changes of plasma glucose on levels of proinsulin mRNA. Their rapidity of onset and large magnitude are comparable to effects of glucose on rates of insulin biosynthesis in isolated islets and suggest that insulin biosynthesis is regulated at least in part by levels of proinsulin mRNA.
这些研究的目的是确定葡萄糖(哺乳动物胰岛素生物合成的主要调节因子)是否通过改变全动物体内胰岛素原mRNA的水平来控制合成。大鼠饥饿3天,然后重新喂食或注射葡萄糖或生理盐水24小时。注射葡萄糖使血浆葡萄糖水平升高至与重新喂食时相当的水平,但提供的热量替代不足20%。提取胰腺RNA,并通过与克隆的大鼠胰岛素原cDNA探针进行印迹杂交来测定胰岛素原mRNA的相对浓度。在饥饿的动物中,胰岛素原mRNA水平是喂食对照组的15%-20%。注射葡萄糖后24小时内,相对于总胰腺RNA,胰岛素原mRNA水平特异性地增加了三到四倍。葡萄糖注射2小时后即可检测到这种效应,到12小时时基本完成。放线菌素D可阻断葡萄糖诱导的胰岛素原mRNA增加。这些研究证明了血浆葡萄糖变化对胰岛素原mRNA水平的影响。其起效速度和幅度与葡萄糖对分离胰岛中胰岛素生物合成速率的影响相当,表明胰岛素生物合成至少部分受胰岛素原mRNA水平的调节。