Orskov L, Schmitz O, Bak J F, Lund S, Kaal A, Nyholm B, Møller N
Department of Medicine C, Aarhus University Hospital, Denmark.
Scand J Clin Lab Invest. 2001;61(5):371-81. doi: 10.1080/003655101316911413.
In healthy subjects, hypoglycaemia induces a profound 80% reduction in skeletal muscle glucose uptake and a similar suppression of glycogen synthase activity. The aim of this study was to examine the efficacy of this counterregulatory mechanism in type 1 diabetic subjects, who are especially prone to hypoglycaemic incidents. Nine type 1 diabetic male subjects were examined twice; during 120 min of hyperinsulinaemic (1.5 mU x kg(-1) x min(-1)) euglycaemia followed by (i) 240 min of graded hypoglycaemia (glucose nadir 2.8 mM) or (ii) 240 min of euglycaemia. At 345-360 min a muscle biopsy was taken and indirect calorimetry was performed at 210-240 and 320-340 min. The sensitivity of glycogen synthase to glucose-6-P was reduced by hypoglycaemia, as shown by an increase in A0.5 for glucose-6-P (at 0.07 mmol/L) from 0.21+/-0.02 to 0.28+/-0.03 mM (p=0.06). Likewise, the fractional velocity for glycogen synthase was reduced by 25%; i.e. from 20.8+/-2.0 to 15.5+/-1.4% (p<0.05). Total glucose disposal was decreased during hypoglycaemia (5.3+/-0.6 vs. 8.3+/-0.7 mg x kg(-1) x min(-1) (euglycaemia), n = 9; p<0.05), primarily due to a reduction of non-oxidative glucose disposal (2.7+/-0.3 vs. 5.1+/-0.6 mg x kg(-1) x min(-1) (euglycaemia), n=7; p<0.05). Forearm arteriovenous glucose differences were decreased by 50% in the hypoglycaemic situation (0.7+/-0.1 vs. 1.4+/-0.3 mmol/L (320-340 min)), and counterregulatory hormonal responses seemed less conspicuous than described in healthy subjects. We conclude that hypoglycaemia induces decrements of forearm glucose uptake and glycogen synthase activity in type 1 diabetic subjects. The study indicates a decreased magnitude of these responses, but this remains to be confirmed.
在健康受试者中,低血糖可导致骨骼肌葡萄糖摄取量大幅降低80%,糖原合酶活性也受到类似程度的抑制。本研究的目的是检验这种反调节机制在1型糖尿病患者中的效果,这类患者尤其容易发生低血糖事件。对9名1型糖尿病男性受试者进行了两次检查:在120分钟的高胰岛素血症(1.5 mU·kg⁻¹·min⁻¹)正常血糖状态后,接着进行(i)240分钟的分级低血糖(血糖最低点为2.8 mM)或(ii)240分钟的正常血糖状态。在345 - 360分钟时进行肌肉活检,并在210 - 240分钟和320 - 340分钟时进行间接测热法。低血糖使糖原合酶对葡萄糖 - 6 - 磷酸的敏感性降低,表现为葡萄糖 - 6 - 磷酸(0.07 mmol/L时)的A0.5从0.21±0.02增加到0.28±0.03 mM(p = 0.06)。同样,糖原合酶的分数速度降低了25%,即从20.8±2.0降至15.5±1.4%(p < 0.05)。低血糖期间总葡萄糖处置量减少(5.3±0.6对8.3±0.7 mg·kg⁻¹·min⁻¹(正常血糖),n = 9;p < 0.05),主要是由于非氧化葡萄糖处置减少(2.7±0.3对5.1±0.6 mg·kg⁻¹·min⁻¹(正常血糖),n = 7;p < 0.05)。低血糖状态下前臂动静脉葡萄糖差值降低了50%(0.7±0.1对1.4±0.3 mmol/L(320 - 340分钟)),且反调节激素反应似乎不如在健康受试者中描述的那么明显。我们得出结论,低血糖会导致1型糖尿病患者前臂葡萄糖摄取和糖原合酶活性降低。该研究表明这些反应的程度有所降低,但仍有待证实。