Dose-dependent effect of insulin on plasma free fatty acid turnover and oxidation in humans

R. C. Bonadonna, L. C. Groop, K. Zych, M. Shank, R. A. DeFronzo

Research output: Contribution to journalArticlepeer-review

139 Scopus citations

Abstract

Methodology for measuring plasma free fatty acid (FFA) turnover/oxidation with [1-14C]palmitate was tested in normal subjects. In study 1, two different approaches (720-min tracer infusion without prime vs. 150-min infusion with NaH14CO3 prime) to achieve steady-state conditions of 14CO2 yielded equivalent rates of plasma FFA turnover/oxidation. In study 2, during staircase NaH14CO3 infusion, calculated rates of 14CO2 appearance agreed closely with NaH14CO3 infusion rates. In study 3, 300-min euglycemic insulin clamp documented that full biological effect of insulin on plasma FFA turnover/oxidation was established within 60-120 min. In study 4, plasma insulin concentration was raised to 14 ± 2, 23 ± 2, 38 ± 2, 72 ± 5, and 215 ± 10 μU/ml. A dose-dependent insulin suppression of plasma FFA turnover/oxidation was observed. Plasma FFA concentration correlated positively with plasma FFA turnover/oxidation in basal and insulinized states. Total lipid oxidation (indirect calorimetry) was significantly higher than plasma FFA oxidation in the basal state, suggesting that intracellular lipid stores contributed to whole body lipid oxidation. Hepatic glucose production and total glucose disposal showed the expected dose-dependent suppression and stimulation, respectively, by insulin. In conclusion, insulin regulation of plasma FFA turnover/oxidation is maximally manifest at low physiological plasma insulin concentrations, and in the basal state a significant contribution to whole body lipid oxidation originates from lipid pool(s) that are different from plasma FFA.

Original languageEnglish (US)
Pages (from-to)E736-E750
JournalAmerican Journal of Physiology - Endocrinology and Metabolism
Volume259
Issue number5 22-5
DOIs
StatePublished - 1990

Keywords

  • Glucose metabolism
  • Lipid metabolism
  • Substrate oxidation

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Physiology
  • Physiology (medical)

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