Mitochondrial Membrane Potential and Glutamate Excitotoxicity in Cultured Cerebellar Granule Cells

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Fig. 3.
Fig. 3.

Fluorescence of individual granule cell somata equilibrated with 50 nm TMRM+ in response to mitochondrial inhibition; curve fitting with the cell simulation. Ai–Ci, Granule cells were equilibrated with 50 nm TMRM+. Where indicated, 3 μm antimycin A (A), 5 μg/ml oligomycin (O), 2 μm rotenone (R), or 50 mm KCl (K) was added. The incubation medium contained 1.2 mm MgCl2. Each trace is from a single representative soma. Aii–Cii, Values for Δψm (thin line) and Δψp(thick line) were obtained by curve fitting for the cell simulation. Aiii–Ciii, Cell simulation; total fluorescence (thin line) and mitochondrial component of fluorescence (thick line) are shown. The following parameters were used: matrix volume = 1% of cytoplasm; quench threshold = 50 μm; rate constant for plasma membrane equilibration = 0.003/sec (TMRM+).

  1. The Journal of Neuroscience vol. 20 no. 19 7208-7219
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