A rapid method for the evaluation of compounds with mitochondria-protective properties

被引:49
作者
Nuydens, R
Novalbos, J
Dispersyn, G
Weber, C
Borgers, M
Geerts, H
机构
[1] Janssen Res Fdn, Dept Cell Physiol, B-2340 Beerse, Belgium
[2] Maastricht Univ, Dept Mol Cell Biol & Genet, Maastricht, Netherlands
[3] Univ Antwerp, Dept Biochem, B-2020 Antwerp, Belgium
[4] Univ Autonoma Madrid, Fac Med, Dept Pharmacol & Therapeut, Princesa Hosp,Dept Clin Pharmacol, Madrid, Spain
[5] Janssen Res Fdn, Preclin Dev, D-4040 Neuss, Germany
关键词
fluorescence; microplate; mitochondrial membrane potential; neurons; toxicity;
D O I
10.1016/S0165-0270(99)00107-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondrial dysfunction has been implicated in a number of neurodegenerative diseases, such as ischemia and Parkinson's disease. We present here a method that allows the rapid quantification of interventions, aimed at inhibiting the effect of mitochondrial membrane potential uncouplers, based on the ratioing properties of the fluorescent probe 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolcarbocyanine iodide (JC-1), by using currently available 96-well fluorescent plate readers. A method is presented for evaluation of cross-talk between the two excitation/emission channels. Further characterization of the probe shows that the effect of plasma membrane potential changes on JC-I fluorescence ratio are negligible, but that the signal is very sensitive to pH. One of the most exciting applications is the possibility to perform end-point measurements, thanks to the ratioing properties of the probe. The system is tested in different culture types with different mitochondrial uncouplers. As an example of a quantitative evaluation, we show that flunarizine is able to inhibit, dose-dependently, FCCP mediated JC-l signal increase. The procedure is simple and allows for the fast screening of mitochondria-protective compounds (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 159
页数:7
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