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血脑屏障的渗透性开放:原理、机制及治疗应用

Osmotic opening of the blood-brain barrier: principles, mechanism, and therapeutic applications.

作者信息

Rapoport S I

机构信息

Section on Brain Physiology and Metabolism, National Institute on Aging, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Cell Mol Neurobiol. 2000 Apr;20(2):217-30. doi: 10.1023/a:1007049806660.

Abstract
  1. Osmotic opening of the blood-brain barrier by intracarotid infusion of a hypertonic arabinose or mannitol solution is mediated by vasodilatation and shrinkage of cerebrovascular endothelial cells, with widening of the interendothelial tight junctions to an estimated radius of 200 A. The effect may be facilitated by calcium-mediated contraction of the endothelial cytoskeleton. 2. The marked increase in apparent blood-brain barrier permeability to intravascular substances (10-fold for small molecules) following the osmotic procedure is due to both increased diffusion and bulk fluid flow across the tight junctions. The permeability effect is largely reversed within 10 min. 3. In experimental animals, the osmotic method has been used to grant wide access to the brain of water-soluble drugs, peptides, antibodies, boron compounds for neutron capture therapy, and viral vectors for gene therapy. The method also has been used together with anticancer drugs to treat patients with metastatic or primary brain tumors, with some success and minimal morbidity.
摘要
  1. 通过颈内动脉输注高渗阿拉伯糖或甘露醇溶液使血脑屏障发生渗透性开放,是由脑血管内皮细胞的血管舒张和收缩介导的,内皮细胞间紧密连接增宽至估计半径为200埃。钙介导的内皮细胞骨架收缩可能会促进这种效应。2. 渗透性处理后,血管内物质的血脑屏障表观通透性显著增加(小分子增加10倍),这是由于跨紧密连接的扩散增加和大量液体流动所致。通透性效应在10分钟内基本逆转。3. 在实验动物中,渗透法已被用于使水溶性药物、肽、抗体、用于中子俘获治疗的硼化合物以及用于基因治疗的病毒载体广泛进入脑内。该方法也已与抗癌药物一起用于治疗转移性或原发性脑肿瘤患者,取得了一些成功且发病率极低。

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