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. 2013 Oct 30;34(1):153–160. doi: 10.1038/jcbfm.2013.184

Table 3. Glucose metabolism via glycolysis in extracts of the hippocampal formation from CD1 mice fed a control, 35% trioctanoin, or 35% triheptanoin diets.

nmol/g tissue Control n=11 35% Trioctanoin n=10 35% Triheptanoin n=9
Glucose 1860±218 2090±255 2170±286
Glucose 6-phosphate 36.3±10.0 59.3±10.1a 14.7±1.6b
Fructose 6-phosphate 32.7±10.1 49.1±9.4a 10.1±1.2b
Fructose 1,6-biphosphate 105±11.6 62±4.5c 84±8.9
Dihydroxyacetone phosphate 0.50±0.1 0.16±0.02a 0.39±0.09
2-and 3-phosphoglycerate 21.8±3.8 11.5±1.1a 26.9±12.1
Phosphoenolpyruvate 13.5±1.5 11.3±2.5 8.3±1.9
Lactate 3400±371 3150±346 2860±330
Acetyl-CoA 1.4±0.08 1.3±0.1 1.3±0.1
β-hydroxybutyrate 92±10.1 153±7.6a 160±21.4d

Metabolite levels were quantified in polar metabolite extracts from hippocampal tissue from CD1 mice fed a standard, or 35% trioctanoin or triheptanoin diet for three weeks using liquid chromatography tandem mass spectrometry and enzymatic assays. Values represent mean±s.e.m.

a

indicates P<0.05 and between trioctanoin and control groups.

b

indicates that P<0.05 between triheptanoin and trioctanoin treatments.

c

indicates P<0.01 between trioctanoin and control.

d

indicates P<0.05 between triheptanoin and control-fed mice.