Horsman M R, Sampson L E, Chaplin D J, Overgaard J
Danish Cancer Society, Department of Experimental Clinical Oncology, Aarhus C, Denmark.
Int J Hyperthermia. 1996 Nov-Dec;12(6):779-89. doi: 10.3109/02656739609027684.
The in vivo interaction between flavone acetic acid (FAA) and hyperthermia was studied in a C3H mammary carcinoma grown in the feet of female CDF1 mice and in normal foot skin. FAA was intraperitoneally injected prior to local tissue heating in restrained non-anaesthetized animals. Alone, FAA at doses of 100 mg/kg and above, inhibited tumour growth in a dose-dependent fashion. FAA also enhanced the tumour response to heat, the effect being dependent on both the time interval between the two modalities and the FAA dose, the greatest effect occurring when FAA doses of > or = 150 mg/kg preceeded heat by 3-48 h. These effects of FAA correlated with the drug's ability to decrease tumour blood perfusion measured using the RbCl extraction procedure. Injecting 150 mg/kg FAA 3 h before heating (42.7 degrees C) resulted in a 2.2-fold increase in tumour heat damage, but had little effect on the response of normal foot skin in non-tumour-bearing mice. However, this treatment gave a 2.0-fold increase in normal tissue damage when the skin experiments were repeated in tumour-bearing animals. These effects in skin occurred in the absence of any blood perfusion changes, but appeared to be associated with FAA-induced TNF-alpha production.
在雌性CDF1小鼠足部生长的C3H乳腺癌及正常足部皮肤中,研究了黄酮醋酸(FAA)与热疗的体内相互作用。在未麻醉的受限动物局部组织加热前,腹腔注射FAA。单独使用时,100mg/kg及以上剂量的FAA以剂量依赖性方式抑制肿瘤生长。FAA还增强了肿瘤对热的反应,这种效应取决于两种治疗方式之间的时间间隔和FAA剂量,当FAA剂量≥150mg/kg且在加热前3 - 48小时时,效果最为显著。FAA的这些效应与该药物降低肿瘤血流灌注的能力相关,肿瘤血流灌注通过RbCl提取法测量。在加热(42.7℃)前3小时注射150mg/kg FAA,导致肿瘤热损伤增加2.2倍,但对未患肿瘤小鼠的正常足部皮肤反应影响不大。然而,当在患肿瘤动物中重复皮肤实验时,这种治疗使正常组织损伤增加了2.0倍。皮肤中的这些效应在没有任何血流灌注变化的情况下发生,但似乎与FAA诱导的TNF-α产生有关。