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Lang et al

However, by using stable isotope labeling in isolated perfused mouse hearts, recent models on the mechanism and origin of ischemic succinate accumulation proposed that succinate primarily derives from the existing TCA cycle metabolite pool and canonical TCA cycle activity, with only a minor contribution to ischemic succinate of mitochondrial complex II reversal (reducing fumarate to succinate) and aminotransferase anaplerosis 55 (originating fumarate from aspartate)

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RhoA knockdown cells were selected using 2 g/ml puromycin

They can be converted into each other through multiple enzymes

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