Diabetes, Vol 39, Issue 1 22-30, Copyright © 1990 by American Diabetes Association
Effect of hyperinsulinemia and hyperglycemia on intracellular glucose and fat metabolism in healthy subjects
AW Thorburn, B Gumbiner, G Brechtel and RR Henry
Department of Medicine, University of California, San Diego.
Hyperinsulinemia and hyperglycemia per se both stimulate glucose uptake and
the disposal of glucose by oxidative (Gox) and nonoxidative (Nox)
metabolism. However, the intracellular metabolic fate of glucose may not be
the same when glucose uptake is stimulated predominantly by either of these
mechanisms due to different effects on fat oxidation (Fox). To address this
issue, 11 healthy subjects each had four glucose-clamp studies performed in
combination with indirect calorimetry to compare Gox, Nox, and Fox at two
different rates of glucose uptake (approximately 7 and 10 mg.kg-1 fat-free
mass [FFM].min-1) matched at each level by either hyperglycemia or
hyperinsulinemia. When glucose uptake was matched at the lower rate (7
mg.kg-1 FFM.min-1), there was less suppression of both FFA (33 vs. 43%, P
less than 0.05) and Fox (73 vs. 90%, P less than 0.05) and less stimulation
of incremental (above basal) Gox (1.95 vs. 2.49 mg.kg-1 FFM.min-1, P less
than 0.025) at low insulin (72 pM) and hyperglycemia (21.8 mM) compared
with high insulin (280 pM) and euglycemia (5.1 mM). Matching glucose uptake
at the higher rates (10 mg.kg-1 FFM.min-1) required greater than 300 pM of
insulin (309 and 632 pM) in both studies and resulted in maximal
suppression of FFA (49 vs. 46%, NS) and Fox (both greater than 90%, NS) and
similar incremental Gox (2.89 vs. 2.73 mg.kg-1 FFM.min-1, NS) whether at
hyperglycemia (15.7 mM) or euglycemia (5.2 mM). Therefore, both
hyperinsulinemia and hyperglycemia stimulate glucose uptake and increase
intracellular glucose availability, but insulin also regulates Gox by
suppression of FFA and Fox. However, when FFA and Fox are maximally
suppressed, the rate of glucose uptake, rather than the prevailing insulin
level, determines the distribution of intracellular glucose metabolism.