Walton M I, Bleehen N M, Workman P
MRC Clinical Oncology and Radiotherapeutics Unit, Cambridge, UK.
Cancer Chemother Pharmacol. 1989;24(3):172-6. doi: 10.1007/BF00300238.
We investigated the effects of a range of temperatures (33 degrees-44 degrees C) on the stability and kinetics of C3H mouse liver microsomal misonidazole (MISO) O-demethylase in vitro. Microsomal O-demethylase activity was stable for 60 min at 37 degrees C and for 30 min at 41 degrees C but was steadily inactivated with longer incubation times. Inactivation at 44 degrees and 47 degrees C was exponential, with half-lives of 41 and 11 min, respectively. MISO O-demethylation followed Michaelis-Menten kinetics from 33 degrees to 44 degrees C. The apparent Vmax for desmethylmisonidazole (Ro 05-9963) formation was decreased by 32% (from 2.14 to 1.47 nmol min-1 mg-1 protein) with a 4 degrees decrease from 37 degrees to 33 degrees C. An increase of 4 degrees from 37 degrees to 41 degrees C enhanced the Vmax by 47%, but there was only an additional 9% increase for a further 3 degrees rise to 44 degrees C. Apparent Km values were unaltered at about 1.6 mM. These results show that elevated temperatures in the clinically relevant hyperthermia range (41 degrees-44 degrees C) can enhance a model mixed-function oxidase reaction in vitro. Such effects may be important for the metabolism, activity and toxicity of anticancer drugs combined with hyperthermia in vivo.
我们在体外研究了一系列温度(33摄氏度至44摄氏度)对C3H小鼠肝脏微粒体米索硝唑(MISO)O-脱甲基酶稳定性和动力学的影响。微粒体O-脱甲基酶活性在37摄氏度下60分钟内稳定,在41摄氏度下30分钟内稳定,但随着孵育时间延长会逐渐失活。在44摄氏度和47摄氏度下的失活呈指数形式,半衰期分别为41分钟和11分钟。在33摄氏度至44摄氏度范围内,MISO的O-脱甲基反应遵循米氏动力学。从37摄氏度降至33摄氏度,随着温度降低4摄氏度,去甲基米索硝唑(Ro 05-9963)形成的表观Vmax降低了32%(从2.14降至1.47 nmol min-1 mg-1蛋白)。从37摄氏度升至41摄氏度,温度升高4摄氏度,Vmax提高了47%,但再升高3摄氏度至44摄氏度时,仅额外增加了9%。表观Km值在约1.6 mM时未改变。这些结果表明,临床相关热疗范围内(41摄氏度至44摄氏度)的高温可在体外增强模型混合功能氧化酶反应。这种影响对于体内联合热疗的抗癌药物的代谢、活性和毒性可能很重要。