Vol. 293, Issue 2, 480-486, May 2000

Inhibition of Glutamate-Induced Mitochondrial Depolarization by Tamoxifen in Cultured Neurons¹

Kari R. Hoyt² , Beth Ann McLaughlin, Donald S. Higgins, Jr. and Ian J. Reynolds³

Departments of Pharmacology (K.R.H, I.J.R.) and Neurobiology (B.A.M.), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania; and Department of Neurology (D.S.H.), The Ohio State University College of Medicine, Columbus, Ohio

In central neurons, glutamate receptor activation causes massive calcium influx and induces a mitochondrial depolarization, which is partially blocked by cyclosporin A, suggesting a possible activation of the mitochondrial permeability transition pore (PTP) as a mechanism. It has been recently reported that tamoxifen (an antiestrogen chemotherapeutic agent) blocks the PTP in isolated liver mitochondria, similar to cyclosporin A. In this study, we tested whether tamoxifen inhibits the mitochondrial depolarization induced by glutamate receptor activation in intact cultured neurons loaded with the fluorescent dye 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolylcarbocyanine iodide. This dye reports disruptions in mitochondrial membrane potential, which can be caused by PTP activation. We found that glutamate (100 µM for 10 min) causes a robust mitochondrial depolarization that is partially inhibited by tamoxifen. The maximum inhibitory concentration of tamoxifen was 0.3 µM, with concentrations higher and lower than 0.3 µM being less effective. However, although tamoxifen (0.3 µM) blocked glutamate-induced mitochondrial depolarization, it did not inhibit glutamate-induced neuronal death, in contrast to the PTP inhibitor cyclosporin A. A relatively high concentration of tamoxifen (100 µM) caused mitochondrial depolarization itself and was neurotoxic. These data suggest that tamoxifen may be an inhibitor of the PTP in intact neurons. However, the lack of specificity of most PTP inhibitors, and the difficulty in measuring PTP in intact cells, preclude definite conclusions about the role of PTP in excitotoxic injury.