Skip to main content
. 2014 Aug 3;11(3):529–544. doi: 10.1007/s11306-014-0716-0

Fig. 2.

Fig. 2

Fructose oxidation and fructose-derived glutamate synthesis via TCA cycle. Adipocytes were exposed to 0.1, 0.5, 1, 2.5, 5, 7.5 or 10 mM fructose in a medium containing a baseline amount of 5 mM glucose from the initiation of differentiation for 8 days (differentiating adipocytes) or 16 days (differentiated adipocytes). 10 % of fructose was supplied as [U-13C6]-fructose for a period of 48 h before harvest. Fructose oxidation was measured in differentiating adipocytes (a) and differentiated adipocytes (b) by the change Δ in the 13CO2 released in the extracellular medium measured as a ratio of 13C/12C (replacement of 12C by 13C) in extracellular bi-carbonate. 13C Δ is a measure of the ratio of stable isotopes 13C:12C, reported in parts per thousand (per mil,  ‰). Extracellular release of [13C]-glutamate in differentiating adipocytes (c) and differentiated adipocytes (d) is expressed as a percentage of total glutamate released