St-Denis J F, Comte B, Nguyen D K, Seidman E, Paradis K, Lévy E, van de Werve G
Department of Nutrition, Hôpital Sainte-Justine, Quebec, Canada.
J Clin Endocrinol Metab. 1994 Oct;79(4):955-9. doi: 10.1210/jcem.79.4.7962304.
Rapid kinetics of glucose-6-phosphate (G6P) uptake and hydrolysis as well as of orthophosphate uptake were investigated in microsomes prepared from normal and glycogen storage disease type 1a (GSD 1a) human livers using a fast sampling, rapid filtration apparatus and were compared to those of rat liver microsomes. As shown before with rat microsomes, the production of [U-14C]glucose from 0.2 mmol/L [U-14C]G6P by untreated normal human microsomes was characterized by a burst in activity during the first seconds of incubation, followed by a slower linear rate. The initial velocity of the burst was equal to the rate of glucose production in detergent-treated microsomes. In untreated and detergent-treated GSD 1a microsomes, no glucose-6-phosphatase activity was observed. When untreated normal human or rat microsomes were incubated in the presence of 0.2 mmol/L [U-14C]G6P, an accumulation of [U-14C]glucose was observed, whereas no radioactive compound (G6P and/or glucose) was taken up by GSD 1a microsomes. Orthophosphate uptake was, however, detectable in both GSD 1a and normal untreated vesicles. These results do not support a rate-limiting transport of G6P in untreated normal human microsomes and further show that in this case of GSD 1a, no distinct G6P transport activity is present.
利用快速采样、快速过滤装置,对从正常人和1a型糖原贮积病(GSD 1a)患者肝脏制备的微粒体中葡萄糖-6-磷酸(G6P)摄取与水解以及正磷酸盐摄取的快速动力学进行了研究,并与大鼠肝脏微粒体进行了比较。如之前在大鼠微粒体中所显示的,未经处理的正常人微粒体由0.2 mmol/L [U-14C]G6P产生[U-14C]葡萄糖的过程,其特征是在孵育的最初几秒内活性出现爆发,随后是较慢的线性速率。爆发的初始速度等于经去污剂处理的微粒体中葡萄糖产生的速率。在未经处理和经去污剂处理的GSD 1a微粒体中,未观察到葡萄糖-6-磷酸酶活性。当未经处理的正常人或大鼠微粒体在0.2 mmol/L [U-14C]G6P存在下孵育时,观察到[U-14C]葡萄糖的积累,而GSD 1a微粒体未摄取放射性化合物(G6P和/或葡萄糖)。然而,在GSD 1a和正常未处理的囊泡中均检测到正磷酸盐摄取。这些结果不支持未经处理的正常人微粒体中G6P存在限速转运,并且进一步表明在这种GSD 1a情况下,不存在明显的G6P转运活性。