Hasegawa T, Song C W
University of Minnesota Medical School, Department of Therapeutic Radiology, Minneapolis 55455.
Int J Radiat Oncol Biol Phys. 1991 May;20(5):1001-7. doi: 10.1016/0360-3016(91)90197-c.
The effects of hydralazine on the blood flow in various normal tissues and R3230 Ac adenocarcinomas grown in different sites in rats were studied. Tumors were induced in the kidney, liver, and flank (s.c.) by injection of small pieces of tumors. Tumors were also induced in small intestine, cecum, and mesentery by intraperitoneal injection of finely minced tumor tissue. The blood flow and cardiac output were measured by radioactive microsphere method. An intra-arterial injection of hydralazine at 2.5-10.0 mg/kg significantly reduced the blood flow in most normal tissues, whereas it markedly increased the blood flow in muscle. The blood flow in the brain and testes remained unchanged. The blood flow in the tumors varied depending on the tumor site and was markedly smaller than the blood flow in the host normal tissues in which the tumors grew. The blood flow in tumors decreased significantly upon injection of hydralazine except in the tumors grown in the liver, where the blood flow remained unchanged. The hydralazine injection slightly increased cardiac output and markedly decreased blood pressure. It appeared that the decreases in blood flow by hydralazine in the tumors and most normal tissues were caused mainly by diversion of blood to muscle, resulting in a marked increase in the muscle blood flow without a similar concomitant increase in cardiac output. The results obtained in the present study indicate that hydralazine may be useful for improving the efficacy of hyperthermia or for enhancing the toxicity of hypoxic cell specific bioreductive drugs in treating the tumors grown in skeletal muscle. However, the significant decline in blood flow in most normal tissues may pose potential problems in the use of hydralazine to enhance the effect of hyperthermia or bioreductive drugs on tumors grown in normal tissues other than muscle.
研究了肼屈嗪对大鼠不同部位正常组织及生长于不同部位的R3230 Ac腺癌血流的影响。通过注射小块肿瘤组织在大鼠肾脏、肝脏和胁腹(皮下)诱导肿瘤。也通过腹腔注射精细切碎的肿瘤组织在小肠、盲肠和肠系膜诱导肿瘤。采用放射性微球法测量血流和心输出量。动脉内注射2.5 - 10.0 mg/kg的肼屈嗪可显著降低大多数正常组织的血流,而显著增加肌肉的血流。脑和睾丸的血流保持不变。肿瘤的血流因肿瘤部位而异,且明显小于肿瘤生长部位的宿主正常组织的血流。注射肼屈嗪后,除生长于肝脏的肿瘤血流保持不变外,其他肿瘤的血流均显著降低。注射肼屈嗪使心输出量略有增加,血压显著降低。似乎肼屈嗪使肿瘤和大多数正常组织血流降低主要是由于血液分流至肌肉,导致肌肉血流显著增加而心输出量无类似的相应增加。本研究获得的结果表明,肼屈嗪可能有助于提高热疗效果或增强缺氧细胞特异性生物还原药物在治疗骨骼肌中生长的肿瘤时的毒性。然而,大多数正常组织血流的显著下降可能在使用肼屈嗪增强热疗或生物还原药物对生长于肌肉以外正常组织中的肿瘤的作用时带来潜在问题。