Ekelund S, Nygren P, Larsson R
Division of Clinical Pharmacology, Akademiska Hospital, Uppsala University, Sweden.
Anticancer Drugs. 1998 Jul;9(6):531-8.
Microphysiometry is a non-invasive, physiological method where measurement of metabolic activity can be made on living human tumor cells. Indirect measurement of the extracellular acidification is measured over a pH-sensitive silicon membrane. In this study microphysiometry was employed for the study of cytotoxic agents used in therapy of cancer. Standard cytotoxic drugs with different postulated mechanisms of action were investigated using cell lines as well as primary cultures of patient tumor cells. Each investigated cytotoxic drug induced a characteristic pattern of metabolic activity. From these patterns, key features, like stimulation and inhibition of acidification, the time point when the response curves of the drugs fall below the control curve, and the maximum inhibition of acidification at 20 h, could be quantified. Most of the investigated drugs showed some initial stimulation of acidification rate during the experiments. For drugs producing a reduced metabolic rate at 20 h a concentration-response relationship was observed. The drug effects measured at 20 h were irreversible and correlated reasonably well with parallel measurements of membrane integrity using a standard cytotoxicity test. The results demonstrate the feasibility of 'on-line' measurements of metabolic activity using this approach and also revealed an unexpected variety of drug response profiles.
微生理测量法是一种非侵入性的生理学方法,可用于对活的人类肿瘤细胞进行代谢活性测量。通过对pH敏感的硅膜间接测量细胞外酸化情况。在本研究中,微生理测量法被用于研究癌症治疗中使用的细胞毒性药物。使用细胞系以及患者肿瘤细胞的原代培养物,对具有不同假定作用机制的标准细胞毒性药物进行了研究。每种被研究的细胞毒性药物都诱导出一种特征性的代谢活性模式。从这些模式中,可以量化一些关键特征,如酸化的刺激和抑制、药物反应曲线低于对照曲线的时间点以及20小时时酸化的最大抑制程度。在实验过程中,大多数被研究的药物都表现出对酸化速率的一些初始刺激。对于在20小时时产生代谢率降低的药物,观察到了浓度-反应关系。在20小时时测量的药物效应是不可逆的,并且与使用标准细胞毒性试验对膜完整性进行的平行测量结果具有合理的相关性。结果证明了使用这种方法“在线”测量代谢活性的可行性,同时也揭示了意想不到的多种药物反应谱。