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. Author manuscript; available in PMC: 2010 Aug 16.
Published in final edited form as: Mitochondrion. 2008 May 4;8(3):262–272. doi: 10.1016/j.mito.2008.04.005

Fig. 3.

Fig. 3

Uptake and release of mitochondrial Ca2+. Ca2+ movement across the inner mitochondrial membrane was followed spectrophotometrically with Arsenazo III as indicator. Seven-months old normotensive genetic control (WKY) and spontaneously hypertensive (SHR) rats were compared. Mitochondria (0.3 mg/ml) were energized with 10 mM succinate (▲ succ) in the presence of rotenone (not shown). Thereafter, 80 nmol of Ca2+ was added for several times which is indicated with arrows. Once net uptake was completed, 0.5 mM EGTA was added to sequester Ca2+. The graph inside the circle shows a zoom corresponding to a more detailed view of the first portion of the plots. Five separate experiments were carried out in duplicates. A representative trace is shown.