Hori K, Suzuki M, Tanda S, Saito S, Shinozaki M, Zhang Q H
Department of Experimental Oncology, Tohoku University, Sendai.
Jpn J Cancer Res. 1991 Nov;82(11):1309-16. doi: 10.1111/j.1349-7006.1991.tb01797.x.
To elucidate the significance of angiotensin II (AII)-induced hypertension chemotherapy, changes of tissue blood flow both in normal subcutis and in tumors (AH109A, LY80) were measured with the hydrogen gas clearance method. A newly-developed anesthetic machine was used to keep the animals' condition constant. Tissue blood flow in normal subcutis and tumors always fluctuated with time under normotension. The nature and the rate of fluctuation in tumor blood flow were almost identical in two different types of tumors. However, the fluctuation of blood flow in tumor and that in normal subcutis were almost always inversely related when blood flows in these different tissues were measured simultaneously, i.e., when tissue blood flow in normal subcutis decreased, tumor blood flow increased, and vice versa. The findings supported the idea that the connection mode between the tumor vascular bed and normal vascular bed is a parallel circuit. Vascular resistance in the normal vascular bed under AII-induced hypertension seemed to be greater than that under normotension, because the AII-increased tumor blood flow always exceeded the maximum tumor blood flow under normotension. Due to the fluctuations of tumor blood flow, no-flow or low-flow areas, resistant to delivery of anti-cancer drugs, moved sporadically within the tumor under the normotensive condition. However, good conditions for drug delivery to tumor tissue were induced by AII-induced hypertension.
为阐明血管紧张素II(AII)诱导的高血压化疗的意义,采用氢气清除法测量正常皮下组织和肿瘤(AH109A、LY80)中的组织血流量。使用新开发的麻醉机使动物状态保持恒定。在正常血压下,正常皮下组织和肿瘤中的组织血流量总是随时间波动。两种不同类型肿瘤中肿瘤血流量的波动性质和速率几乎相同。然而,当同时测量这些不同组织中的血流量时,肿瘤中的血流量波动与正常皮下组织中的血流量波动几乎总是呈负相关,即当正常皮下组织中的组织血流量减少时,肿瘤血流量增加,反之亦然。这些发现支持了肿瘤血管床与正常血管床之间的连接方式是并联回路的观点。AII诱导的高血压下正常血管床的血管阻力似乎大于正常血压下的血管阻力,因为AII增加的肿瘤血流量总是超过正常血压下的最大肿瘤血流量。由于肿瘤血流量的波动,在正常血压条件下,对抗癌药物输送有抗性的无血流或低血流区域在肿瘤内零星移动。然而,AII诱导的高血压为肿瘤组织的药物输送创造了良好条件。