Audus K L, Borchardt R T
J Neurochem. 1986 Aug;47(2):484-8. doi: 10.1111/j.1471-4159.1986.tb04527.x.
The large neutral amino acid (LNAA) transport system, or L (leucine) system, in primary cultures of bovine brain microvessel endothelial cell monolayers has been characterized. The transendothelial transport of leucine in this in vitro blood-brain barrier (BBB) model was determined to be bidirectional and time, temperature, and concentration dependent. Leucine transport was saturable, and the apparent Km and Vmax were determined to be 0.18 mM and 6.3 nmol/mg/min, respectively. Transendothelial transport of leucine was resistant to inhibition by ouabain and sodium azide. Other LNAAs, including the centrally acting drugs alpha-methyl-3,4-dihydroxyphenylalanine (alpha-methyldopa), L-3,4-dihydroxyphenylalanine (L-DOPA), alpha-methyltyrosine, and baclofen, inhibited leucine transport. The leucine carrier system was also found to be stereospecific. Sucrose, used as a diffusion marker, moved across the monolayers slowly, and its concentration was not significant for at least 30 min.
已对牛脑微血管内皮细胞单层原代培养物中的大中性氨基酸(LNAA)转运系统,即L(亮氨酸)系统进行了表征。在这个体外血脑屏障(BBB)模型中,亮氨酸的跨内皮转运被确定为双向的,且依赖于时间、温度和浓度。亮氨酸转运是可饱和的,表观Km和Vmax分别被确定为0.18 mM和6.3 nmol/mg/min。亮氨酸的跨内皮转运对哇巴因和叠氮化钠的抑制具有抗性。其他LNAA,包括中枢作用药物α-甲基-3,4-二羟基苯丙氨酸(α-甲基多巴)、L-3,4-二羟基苯丙氨酸(L-DOPA)、α-甲基酪氨酸和巴氯芬,均抑制亮氨酸转运。还发现亮氨酸载体系统具有立体特异性。用作扩散标志物的蔗糖缓慢穿过单层细胞,其浓度在至少30分钟内无显著变化。