Phosphoglucose isomerase fluxes in the intact liver cell have been est
imated from the extent of release of tritium on C-2 of glucose-6P, or
the extent of incorporation of tritium onto C-2 of glucose-6P from tri
tiated water. Phosphomannose isomerase fluxes have been estimated from
the THO formation from [1T]galactose in excess of that formed in the
glucose-6P dehydrogenase reaction, estimated using (14)CO2 production
from [1-C-14]galactose. Liver phosphoglucose isomerase fluxes during g
luconeogenesis from lactate in hepatocytes, or in fasted humans in viv
o, range from about 10 to 14 times the net rate of glucose production.
However, the reverse phosphoglucose isomerase flux, during gluconeoge
nesis from 10 mM fructose in hepatocytes, is less than the net rate of
gluconeogenesis. Reversible phosphomannose isomerase fluxes during gl
uconeogenesis from lactate or dihydroxyacetone in vitro are somewhat l
ower than net gluconeogenic fluxes, but this contribution to THO produ
ction from sugars tritiated on C-1 can not be neglected.