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. Author manuscript; available in PMC: 2017 Dec 1.
Published in final edited form as: Biochim Biophys Acta. 2016 Aug 4;1866(2):151–162. doi: 10.1016/j.bbcan.2016.08.001

Figure 4. Lonidamine (LND) inhibits oxidation of glutamate, 2-oxoglutarate and succinate by uncoupled rat heart and liver mitochondria less potently than pyruvate transport.

Figure 4

Rates of oxidation by isolated rat liver A) or heart B) mitochondria at 30°C were measured using an oxygen electrode as described under the methods section of Nancolas et al. (50). Data are expressed as the percentage of rates in the absence of LND to allow better comparison between the different substrates and the lines drawn were fitted by FigSys using a Bezier Spline function. For heart mitochondria, data are presented for a single representative experiment with absolute rates of pyruvate + malate, glutamate + malate, 2-oxoglutarate + malate and succinate + rotenone oxidation in the absence of LND of 84, 83, 67 and 212 nmol O2 per mg protein per min, respectively. For liver mitochondria A), mean data (± S.E.M.) are presented for 3 separate mitochondrial preparations. The absolute rates of glutamate + malate and succinate (+ rotenone) oxidation in the absence of LND were 67.9 ± 3.0 and 109 ± 7.8 nmol O2 per mg protein per min, respectively. This research was originally published in Biochem J (50).