Functional characteristics of tumor vessels: selective increase in tumor blood flow.

M Suzuki, K Hori, S Saito, S Tanda, I Abe, H Sato, H Sato
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Abstract

This experiment was carried out to elucidate how tumor microcirculation differs from that of normal tissues. Pressure-flow relationship was examined in normal rat tissues, uninvolved tissues in tumor-bearing rats, transplanted AH109A solid tumors, and primary tumors induced by 3-methylcholanthrene. Tumor blood flow was measured by the hydrogen clearance technique. The blood pressure was elevated by continuous iv infusion of angiotensin II. Elevation of blood pressure produced a several-fold increase in tumor blood flow without increasing blood flow in normal tissue and uninvolved tissue in tumor-bearing rats. The increase was selective to tumor tissues as long as the mean arterial blood pressure remained under about 150 mmHg. The lower the resting tumor blood flow, the greater the increase in the flow was at induced hypertension. There were no significant differences in the resting blood flow and in the rate of flow change at induced hypertension between the intramuscularly transplanted tumor, the intrahepatically transplanted tumor, and the sc transplanted tumor. These results indicate that the delivery of systemically administered anticancer drugs could be selectively enhanced in tumor tissues by induced hypertension.

肿瘤血管功能特点:肿瘤血流选择性增加。
本实验旨在阐明肿瘤微循环与正常组织微循环的差异。在正常大鼠组织、荷瘤大鼠未受累组织、移植的AH109A实体瘤和3-甲基胆蒽诱导的原发肿瘤中检测压流关系。采用氢清除技术测量肿瘤血流量。持续静脉输注血管紧张素II使血压升高。血压升高可使荷瘤大鼠正常组织和未受累组织的血流量增加数倍。只要平均动脉血压保持在150毫米汞柱以下,这种增加对肿瘤组织是选择性的。静息肿瘤血流量越低,诱导高血压的血流量增加越大。静息血流量和诱导高血压时血流变化率在肌内移植瘤、肝内移植瘤和sc移植瘤之间无显著差异。这些结果表明,通过诱导高血压,系统给药的抗癌药物可以选择性地增强肿瘤组织的递送。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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