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. Author manuscript; available in PMC: 2007 Sep 21.
Published in final edited form as: Diabetes. 2007 Mar;56(3):786–794. doi: 10.2337/db06-0187

Figure 1. Substrate utilization by cardiac mitochondria.

Figure 1

Pyruvate enters the Krebs cycle by pyruvate dehydrogenase (PDH), producing acetyl-CoA (Ac-CoA). Octanoyl-carnitine undergoes β-oxidation and produces acetyl-CoA, NADH and FADH2. Malate enters mitochondria through oxoglutarate/malate carrier (OMC) and produces mainly NADH by mitochondrial malate dehydrogenase (mMDH), while glycerol-3 phosphate (G3P) produces FADH2 by the mitochondrial glycerol-phosphate dehydrogenase (mGDH). Succinate produces mainly FADH2 that enters the respiratory chain through complex-II. NADH is reoxidized in the respiratory chain at complex-I and FADH2 at complex-II.