Knudsen G M, Hasselbalch S G, Hertz M M, Paulson O B
Neurobiology Research Unit, Department of Neurology, University Hospital Rigshospitalet, Copenhagen, Denmark.
Eur J Clin Invest. 1999 Aug;29(8):687-91. doi: 10.1046/j.1365-2362.1999.00528.x.
This study re-evaluates previously published data on blood-brain barrier transfer coefficients in humans exposed to high insulin levels.
In this study of seven volunteers, global blood-brain barrier permeability to glucose and phenylalanine was measured by means of the intracarotid double-indicator method before, during, and after an insulin-glucose clamp. Data were reanalyzed by means of a mathematical model that takes capillary heterogeneity and labelled glucose backflux from the brain into account.
The permeability-surface area product (PS) for glucose transport from the blood into the brain, PS1, was 0.145 (0.102-0.211) (median and quartiles), 0.146 (0.113-0.259), and 0.157 (0.133-0.181) ml g-1 min-1 before, during, and after insulin challenge, respectively. In six of the subjects, PS for transport from brain to blood over the brain glucose distribution volume, PS2/Ve decreased under hyperinsulinemia, from a baseline value of 6.56 (3.0-14.9) to 3.86 (1.41-5.32), and restored to a value of 3.8 (2.8-12.1) min-1 after insulin challenge. This decrease in PS2/Ve is probably due to an increase in the brain glucose distribution volume induced by an insulin induced increased intracellular glucose uptake during the experiment. For phenylalanine (n = 5), PS1 was unchanged before, during, and after insulin challenge. In hyperinsulinemia, PS3/Ve for phenylalanine decreased in all subjects.
We conclude that acutely elevated high plasma insulin levels in humans does not alter the brain uptake of glucose or phenylalanine from the blood. It seems, however, that high plasma insulin levels induce an increase in the movement of D-glucose and L-phenylalanine from the brain interstitial fluid into the intracellular compartment.
本研究重新评估了先前发表的关于暴露于高胰岛素水平的人体血脑屏障转运系数的数据。
在这项针对7名志愿者的研究中,通过颈内双指示剂法在胰岛素 - 葡萄糖钳夹试验前、试验期间和试验后测量了血脑屏障对葡萄糖和苯丙氨酸的整体通透性。数据通过一个考虑了毛细血管异质性和标记葡萄糖从脑内回流的数学模型进行重新分析。
从血液到脑内的葡萄糖转运的通透表面积乘积(PS),即PS1,在胰岛素激发前、激发期间和激发后分别为0.145(0.102 - 0.211)(中位数和四分位数)、0.146(0.113 - 0.259)和0.157(0.133 - 0.181)ml g⁻¹ min⁻¹。在6名受试者中,在高胰岛素血症下,通过脑葡萄糖分布容积从脑到血液的转运的PS,即PS2/Ve,从基线值6.56(3.0 - 14.9)降至3.86(1.41 - 5.32),在胰岛素激发后恢复到3.8(2.8 - 12.1)min⁻¹。PS2/Ve的这种降低可能是由于实验期间胰岛素诱导的细胞内葡萄糖摄取增加导致脑葡萄糖分布容积增加所致。对于苯丙氨酸(n = 5),PS1在胰岛素激发前、激发期间和激发后均无变化。在高胰岛素血症下,所有受试者中苯丙氨酸的PS3/Ve均降低。
我们得出结论,人体血浆胰岛素水平急性升高不会改变脑从血液中摄取葡萄糖或苯丙氨酸的情况。然而,似乎高血浆胰岛素水平会导致D - 葡萄糖和L - 苯丙氨酸从脑间质液向细胞内室的转运增加。