Chaplin D J, Acker B
Int J Radiat Oncol Biol Phys. 1987 Apr;13(4):579-85. doi: 10.1016/0360-3016(87)90075-7.
The effect of the vasodilator hydralazine on both the tumor and systemic toxicity of RSU-1069 has been evaluated in C57B1 mice bearing Lewis lung tumors. The results obtained indicate that both hydralazine and RSU-1069 are cytotoxic to the Lewis lung tumor on their own. However, administration of hydralazine (5 mg/kg PO) at times up to either 3 hr before or 3 hr after RSU-1069 (0.1 mg/g IP) results in a level of cell killing greater than expected from additive effects. This potentiation by hydralazine was observed with doses of RSU-1069 from 0.01 to 0.1 mg/g. The results obtained using excision assays were confirmed using in situ growth delay as the endpoint. Growth delay (+/- s.e.m.) values for tumors to double in volume of 1.5 (+/- 1.2), 2.0 (+/- 1.3) and 6.0 (+/- 0.9) were obtained for hydralazine (5 mg/kg PO) alone, RSU-1069 (0.1 mg/g IP) alone and for hydralazine administered at the same time as RSU-1069 respectively. In contrast to the potentiating effect of hydralazine on the tumor cytotoxicity of RSU-1069, it had no significant effect on the systemic toxicity of RSU-1069 as measured by LD50/30d. No detailed studies to examine the mechanism responsible for the potentiation of tumor cytotoxicity have been performed in the present study. However, the results obtained would be consistent with previous reports that vasodilators such as hydralazine can selectively reduce tumor blood flow and thus oxygenation. Such reduced tumor oxygenation would increase the cytotoxic effects of RSU-1069 which is known to be more toxic to cells at reduced oxygen levels.
在携带Lewis肺癌的C57B1小鼠中,评估了血管扩张剂肼屈嗪对RSU - 1069的肿瘤毒性和全身毒性的影响。所得结果表明,肼屈嗪和RSU - 1069自身对Lewis肺癌均具有细胞毒性。然而,在RSU - 1069(0.1mg/g腹腔注射)前3小时或后3小时内的任何时间给予肼屈嗪(5mg/kg口服),所导致的细胞杀伤水平高于相加效应预期的水平。在RSU - 1069剂量为0.01至0.1mg/g时,均观察到肼屈嗪的这种增效作用。使用切除试验获得的结果,以原位生长延迟作为终点进行了确认。单独使用肼屈嗪(5mg/kg口服)、单独使用RSU - 1069(0.1mg/g腹腔注射)以及与RSU - 1069同时给予肼屈嗪时,肿瘤体积加倍的生长延迟(±标准误)值分别为1.5(±1.2)、2.0(±1.3)和6.0(±0.9)。与肼屈嗪对RSU - 1069肿瘤细胞毒性的增效作用相反,通过LD50/30d测量发现,它对RSU - 1069的全身毒性没有显著影响。在本研究中,尚未进行详细研究以探究导致肿瘤细胞毒性增强的机制。然而,所得结果与先前的报道一致,即诸如肼屈嗪之类的血管扩张剂可选择性地减少肿瘤血流,从而减少肿瘤氧合。这种肿瘤氧合的降低会增加RSU -