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. Author manuscript; available in PMC: 2019 Jul 27.
Published in final edited form as: Biosens Bioelectron. 2019 Mar 11;133:39–47. doi: 10.1016/j.bios.2019.02.069

Fig. 4.

Fig. 4.

Sources of OCR and ECAR and metabolite flux in developing embryos. Oxygen (O2) is consumed by respiring mitochondria in cells to support oxidative metabolism of multiple substrates. Hydrogen ions (H+) are exported from cells with lactate but can also be generated from CO2 in the aqueous G-MOPS buffer or co-transported into cells along with pyruvate or lactate. The six carbons of glucose can be released as CO2 during oxidative metabolism, as two lactate molecules following glycolysis, or utilized in the biosynthetic pentose phosphate pathway (PPP) and one-carbon metabolism (1CM) pathway.