Skeletal muscle is a major site of lactate uptake and release during hyperinsulinemia

Agostino Consoli, Nurjhan Nurjahan, John E. Gerich, Lawrence J. Mandarino

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    31 Scopus citations

    Abstract

    During conditions of increased glucose disposal, plasma lactate concentrations increase due to an increase in plasma lactate appearance. The tissue sites of the elevated lactate production are controversial. Although skeletal muscle would be a logical source of this lactate, studies using the limb net balance technique have failed to demonstrate a major change in net lactate output when plasma glucose disposal is increased. Because the limb balance technique underestimates production of a substrate when the limb not only produces but also consumes that substrate, we infused 3-14C-lactate basally and during a hyperinsulinemic euglycemic clamp in seven normal volunteers to determine plasma lactate appearance, forearm lactate fractional extraction, and forearm lactate uptake and release. After 3 hours of hyperinsulinemia, glucose and lactate turnovers increased from basal values of 11.8 ± 0.13 and 12.2 ± 0.59 to 32.6 ± 3.4 and 16.5 ± 1.07 μmol/(min · kg), accompanied by an increase in plasma lactate from 0.88 ± 0.07 to 1.16 ± 0.09 mmol/L (P < .05). Forearm lactate extraction increased from 27% ± 2% to 38% ± 2% (P < .001), resulting in an increase in forearm lactate uptake from 0.65 ± 0.09 to 1.18 ± 0.08 μmol/(min · 100 mL tissue) (P < .001). Although forearm lactate net output decreased during hyperinsulinemia, forearm lactate production increased from 1.04 ± 0.12 basally to 1.69 ± 0.13 μmol/(min · 100 mL). When forearm data was extrapolated to whole body, muscle could account for 41% ± 4% of systemic lactate appearance basally and 45% ± 4% during hyperinsulinemia. These results demonstrate that skeletal muscle is a major tissue for both the production and utilization of lactate in humans basally and during hyperinsulinemia, when glucose disposal is increased.

    Original languageEnglish (US)
    Pages (from-to)176-179
    Number of pages4
    JournalMetabolism
    Volume41
    Issue number2
    DOIs
    StatePublished - Feb 1992

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    ASJC Scopus subject areas

    • Endocrinology, Diabetes and Metabolism
    • Endocrinology

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