Brown Rachel C, Egleton Richard D, Davis Thomas P
Department of Pharmacology, The University of Arizona, College of Medicine, PO Box 24-5050, 1501 N. Campbell Ave., Tucson, AZ 85724, USA.
Brain Res. 2004 Jul 16;1014(1-2):221-7. doi: 10.1016/j.brainres.2004.04.034.
Clinically, infusion of hyperosmolar solutions is used to enhance chemotherapeutic drug penetration of the blood-brain barrier (BBB) in patients with malignant brain tumors or metastases. We examined the effect of hyperosmolar BBB disruption on brain permeability of three compounds, 86Rb+, a marker for K+ permeability and transport, [14C]sucrose and Evans blue albumin, using a rat in situ perfusion model. 86Rb+ and [14C]sucrose had increased permeability 20 min after BBB disruption with 1.6 M mannitol. There was no change in Evans blue albumin permeability. Only [14C]sucrose showed regional variation in permeability after mannitol-induced BBB disruption, with the cortex and midbrain having higher sucrose permeability then either the cerebellum or brainstem. These data suggest that the clinical efficacy of hyperosmolar disruption therapy in conjunction with chemotherapeutic agents, of a similar molecular weight to sucrose, may be affected by the location of the tumor within the brain.
临床上,输注高渗溶液用于增强患有恶性脑肿瘤或脑转移瘤患者血脑屏障(BBB)对化疗药物的通透性。我们使用大鼠原位灌注模型,研究了高渗性血脑屏障破坏对三种化合物(86Rb+,一种钾离子通透性和转运的标志物、[14C]蔗糖和伊文思蓝白蛋白)脑通透性的影响。用1.6M甘露醇破坏血脑屏障20分钟后,86Rb+和[14C]蔗糖的通透性增加。伊文思蓝白蛋白的通透性没有变化。在甘露醇诱导血脑屏障破坏后,只有[14C]蔗糖的通透性表现出区域差异,皮质和中脑的蔗糖通透性高于小脑或脑干。这些数据表明,与蔗糖分子量相似的化疗药物联合高渗破坏疗法的临床疗效可能受肿瘤在脑内位置的影响。