Selective increase in blood-tumor barrier permeability by calcium antagonists in transplanted rat brain tumors.

K Matsukado, T Nomura, K Ikezaki, M Fukui
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引用次数: 12

Abstract

To clarify the altered response of calcium antagonists on pathological vessels, we investigated the effect of intracarotid infusion of nifedipine on the blood-brain barrier (BBB) permeability using a rat glioma model. Animals were treated with 0, 0.1, 1, 5, and 10 micrograms/kg/min of intracarotid continuous infusion of nifedipine. 2% Evans blue (EB, 2 ml/kg) was injected intravenously immediately after nifedipine infusion. BBB and blood-tumor barrier (BTB) permeability were evaluated by direct visual and histological observation. During the entire experiment, systemic parameters such as arterial blood pressure and blood analysis were not changed significantly. There was a dose-dependent increase of EB permeability selectively in the tumor tissue without affecting the normal brain. These results indicate that tumor vessels may show an altered response to calcium antagonists. Intracarotid administration of calcium antagonists contribute to a selective enhancement of drug delivery to malignant brain tumors without affecting the normal brain.

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钙拮抗剂选择性增加移植大鼠脑肿瘤血肿瘤屏障通透性。
为了阐明钙拮抗剂对病变血管的改变反应,我们使用大鼠胶质瘤模型研究了颈动脉内输注硝苯地平对血脑屏障(BBB)通透性的影响。分别给予0、0.1、1、5、10微克/kg/min的硝苯地平颈动脉内连续输注。硝苯地平输注后立即静脉注射2%埃文斯蓝(EB, 2ml /kg)。观察血脑屏障(BBB)和血肿瘤屏障(BTB)通透性。在整个实验过程中,动脉血压、血液分析等系统参数无明显变化。在不影响正常脑的情况下,肿瘤组织中选择性EB通透性呈剂量依赖性增加。这些结果表明肿瘤血管可能对钙拮抗剂表现出改变的反应。在颈动脉内施用钙拮抗剂有助于选择性地增强对恶性脑肿瘤的药物递送,而不影响正常的大脑。
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