Lefauconnier J M, Hauw J J
Rev Neurol (Paris). 1984;140(1):3-13.
In the first part of this review, the morphological characteristics of the interfaces between blood and some compartments of the central nervous system have been described. The blood-brain barrier (BBB) is situated between the blood and the brain extracellular space (ECS) at the endothelial cells of brain capillaries joined by tight junctions. The blood-cerebrospinal fluid (CSF) barrier is mainly situated at the epithelium of the choroid plexuses. In this second part, the general mechanisms and methods of study of the transport of low molecular weight substances across the BBB are reviewed. In addition water and solute transports across the interfaces are described. The third part will deal with the transport of metabolic substrates and of drugs, with the barrier to neurotransmitters and with the physiological alterations of the permeability of the blood-brain barrier. Blood-brain transport is transcellular. According to the nature of the transported molecule it can be either by diffusion through the membranes (lipophilic molecules) or carrier-mediated (hydrophilic molecules such as metabolic substrates). In vivo methods of study have first been experimental. The recent use of short-lived positron-emitting radioisotopes should extent their use to clinical studies. In vitro measurement of transport on isolated capillaries or choroid plexuses give additional information. Water exchange between plasma and the brain is rapid. However, the permeability of the brain capillaries for water is lower than that of other capillaries and of most membranes, but more similar to that of lipid bilayers and of most tight epithelia. The permeability for water of the choroid plexuses which secrete CSF is much higher than that of brain capillaries. CSF and ECS electrolyte composition is under strict homeostatic regulation, leaving it independent of fluctuations in plasma composition. This constant composition is the consequence of the low permeability of brain capillaries to electrolytes as well as that of the presence of a sodium potassium dependent ATPase on the abluminal membrane of capillaries and the apical membrane of choroid plexuses. This enzyme contributes to the extrusion of potassium from the CSF and ECS and allows a large gradient of potassium to be created between ECS and plasma. A low level of potassium in CSF and ECS is in fact needed for normal nerve conduction.
在本综述的第一部分,已描述了血液与中枢神经系统某些腔室之间界面的形态学特征。血脑屏障(BBB)位于血液与脑细胞外间隙(ECS)之间,处于由紧密连接相连的脑毛细血管内皮细胞处。血脑脊液(CSF)屏障主要位于脉络丛上皮。在第二部分中,综述了低分子量物质跨血脑屏障转运的一般机制和研究方法。此外,还描述了水和溶质跨这些界面的转运。第三部分将涉及代谢底物和药物的转运、神经递质屏障以及血脑屏障通透性的生理改变。血脑转运是跨细胞的。根据被转运分子的性质,它可以是通过膜扩散(亲脂性分子)或载体介导(亲水性分子如代谢底物)。体内研究方法最初是实验性的。最近对短寿命正电子发射放射性同位素的使用应能将其应用扩展到临床研究。对分离的毛细血管或脉络丛上转运的体外测量可提供更多信息。血浆与脑之间的水交换很快。然而,脑毛细血管对水的通透性低于其他毛细血管和大多数膜,但更类似于脂质双分子层和大多数紧密上皮。分泌脑脊液的脉络丛对水的通透性远高于脑毛细血管。脑脊液和细胞外间隙的电解质组成受到严格的稳态调节,使其不受血浆组成波动的影响。这种恒定的组成是脑毛细血管对电解质低通透性以及毛细血管基底外侧膜和脉络丛顶膜上存在钠钾依赖性ATP酶的结果。这种酶有助于从脑脊液和细胞外间隙排出钾,并使细胞外间隙与血浆之间形成较大的钾梯度。实际上,脑脊液和细胞外间隙中低水平的钾对于正常神经传导是必需的。