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1 Department of Endocrinology and Metabolism M, Aarhus University Hospital, 8000 Aarhus, Denmark; 2 Department of Medicine, University of Virginia, and National Science Foundation Center for Biological Timing, Charlottesville, Virginia 22908; and 3 Department of Medicine, The University of Edinburgh, Edinburgh EH4 2XU, Scotland, United Kingdom
Detection of insulin secretory bursts in
peripheral blood is hampered by hepatic insulin extraction, dilution in
the systemic insulin pool, and time-delayed damping of secretory burst
amplitude. Previous studies in dogs in vivo and other experiments in
vitro have shown that ~70% of all insulin is released within
distinct insulin secretory bursts. To establish a method for detection and quantification of pulsatile insulin release in humans on the basis
of peripheral insulin concentration measurements, we used a
high-sensitivity, -specificity, and -precision insulin enzyme-linked immunosorbent assay (ELISA) and optimized an established deconvolution methodology to quantify the frequency, mass, and amplitude of insulin
secretory bursts as well as to estimate the relative contribution of
pulsatile insulin release to overall insulin secretion. By use of
minutely sampled serum insulin concentrations measured by a highly
sensitive insulin ELISA, and insulin kinetics of 2.8 min (first
half-life), 5.0 min (second half-life), and a fractional slow component
of 0.28, the deconvolved insulin secretion rates in 20 healthy subjects
during glucose infusion (4.5 mg · kg
1 · min
1)
could be resolved into a series (4.7 ± 0.1 min/pulse) of
approximately symmetric insulin secretory bursts with a mean mass of 87 ± 12 pmol · l
1 · pulse
1
and a mean amplitude (maximal release rate) of 35 ± 4.7 pmol · l
1 · min
1.
The relative contribution of pulsatile to overall insulin secretion was
75 ± 1.6% (range 59-85%). We conclude that in vivo insulin secretion in humans during nominal glucose stimulation consists of a
series of punctuated insulin secretory bursts accounting for
75% of
total insulin secretion.
oscillations; glucose; C-peptide; amplitude
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