Interference of calmidazolium with measurement of mitochondrial membrane potential using the tetraphenylphosphonium electrode or the fluorescent probe rhodamine 123

被引:27
作者
Saris, NEL
Teplova, VV
Dinokova, IV
Azarashvily, TS
机构
[1] Univ Helsinki, Viikki Bioctr 1, Dept Appl Chem & Microbiol, FIN-00014 Helsinki, Finland
[2] Russian Acad Sci, Inst Theoret & Expt Biophys, RU-142292 Pushchino, Moscow Region, Russia
关键词
calmidazolium; fluorescent probes; membrane potential; mitochondria; rhodamine; tetraphenylphosphonium;
D O I
10.1016/j.ab.2004.02.045
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Calmidazolium (CMZ) is a positively charged, hydrophobic compound used as a calmodulin antagonist. It may cause unspecific effects in mitochondria, e.g., a decrease in membrane potential (DeltaPsi), swelling, and uncoupling. Several groups have advised against use of CMZ in studying signal transduction in mitochondria. We report here that it interferes with measurement of DeltaPsi in rat liver mitochondria (RLM) when using the tetraphenyl phosphonium (TPP+) electrode. We also found that CMZ reduces the signal, indicating an apparent drop in DeltaPsi. CMZ itself gave a signal with the TPP+ electrode in the absence of RLM. At high concentrations, > 10 muM, it also reduced the fluorescence quenching of the probe rhodamine 123. This may be due to an interference with mitochondrial uptake and binding of this positively charged probe or to an uncoupling effect. It is concluded that CMZ and similar positively charged calmodulin antagonists such as trifluoperazine may be used in mitochondria if these interferences are controlled and calibration is carried out under the experimental conditions used. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:109 / 112
页数:4
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