A fast kinetic method for assessing mitochondrial membrane potential in isolated hepatocytes with rhodamine 123 and flow cytometry

Rhodamine 123(Rh123) is widely used as a flow cytometric probe for mitochondrial membrane potential (MMP) in metabolic, pharmacologic, and toxicological studies. However, the use of relatively high concentrations of Rh123 (up to 10 μg/ml) and prolonged incubation times (up to 1 h), including washing sops, may be inconvenient for certain applications in which labile cells are used or which demand rapid or repeated analysis. In this, paper we describe a rapid kinetic assay of MMP in isolated rat hepatocytes, based upon the quantitation of the initial rate of Rh123 uptake by living cells, selected by their scattering properties. The results indicate that at an appropriate dye‐to‐cell ratio (in our experiments, 50 μg Rh123/ml for 250,000–300,000 cells/ml), the initial rate of Rh123 uptake is a highly reproducible and sensitive parameter for estimation of MMP, as demonstrated by the effects of substrates and inhibitors of the glycolytic pathway and mitochondrial respiration. Because of its simplicity, rapidity (about 5 min) and metabolic implications, this assay would be also suitable for the routine evaluation of metabolic state of cell suspensions, as a complementary test to the standard dualstaining tests of viability. Other possible applications in screening pharmacologic and toxicological analysis are discussed. © 1994 Wiley‐Liss, Inc.