Lei Hongxia, Gruetter Rolf
Department of Radiology, University of Minnesota, Minneapolis, Minnesota, USA.
J Neurochem. 2006 Oct;99(1):260-8. doi: 10.1111/j.1471-4159.2006.04115.x.
While chronic hypoglycaemia has been reported to increase unidirectional glucose transport across the blood-brain barrier (BBB) and to increase GLUT1 expression at the endothelium, the effect on steady-state brain d-glucose and brain glycogen content is currently unknown. Brain glucose and glycogen concentrations were directly measured in vivo using localized 13C magnetic resonance spectroscopy (MRS) following 12-14 days of hypoglycaemia. Brain glucose content was significantly increased by 48%, which is consistent with an increase in the maximal glucose transport rate, Tmax, by 58% compared with the sham-treated animals. The localized 13C NMR measurements of brain glucose were directly validated by comparison with biochemically determined brain glucose content after rapid focused microwave fixation (1.4 s at 4 kW). Both in vivo MRS and biochemical measurements implied that brain glycogen content was not affected by chronic hypoglycaemia, consistent with brain glucose being a major factor controlling brain glycogen content. We conclude that the increased glucose transporter expression in chronic hypoglycaemia leads to increased brain glucose content at a given level of glycaemia. Such increased brain glucose concentrations can result in a lowered glycaemic threshold of counter-regulation observed in chronic hypoglycaemia.
虽然据报道慢性低血糖会增加葡萄糖跨血脑屏障(BBB)的单向转运,并增加内皮细胞中GLUT1的表达,但目前尚不清楚其对稳态脑葡萄糖和脑糖原含量的影响。在低血糖12 - 14天后,使用局部13C磁共振波谱(MRS)在体内直接测量脑葡萄糖和糖原浓度。脑葡萄糖含量显著增加了48%,这与最大葡萄糖转运速率Tmax相比假手术处理动物增加了58%一致。通过与快速聚焦微波固定(4 kW下1.4秒)后生化测定的脑葡萄糖含量进行比较,直接验证了局部13C NMR对脑葡萄糖的测量。体内MRS和生化测量均表明,慢性低血糖不影响脑糖原含量,这与脑葡萄糖是控制脑糖原含量的主要因素一致。我们得出结论,慢性低血糖中葡萄糖转运体表达增加导致在给定血糖水平下脑葡萄糖含量增加。这种脑葡萄糖浓度升高可能导致慢性低血糖中观察到的反调节血糖阈值降低。