Tb. Price et al., HUMAN MUSCLE GLYCOGEN RESYNTHESIS AFTER EXERCISE - INSULIN-DEPENDENT AND INSULIN-INDEPENDENT PHASES, Journal of applied physiology, 76(1), 1994, pp. 104-111
To study the effects of glycogen depletion and insulin concentration o
n glycogen synthesis, gastrocnemius glycogen was measured with C-13-nu
clear magnetic resonance at 4.7 T after exercise. Subjects performed s
ingle-leg toe raises to deplete gastrocnemius glycogen to 75, 50, or 2
5% of resting concentration (protocol I). Insulin dependence of glycog
en synthesis was assessed after depletion to 25% with (protocol II) an
d without (protocol III) infusion of somatostatin to inhibit insulin s
ecretion. After depletion to 75 and 50%, glycogen resynthesis rates we
re similar (2.4 +/- 0.7 and 2.8 +/- 0.6 mM/h, respectively). When glyc
ogen was depleted to 25% (<30 mM), the resynthesis rate was significan
tly higher (P < 0.02) at 33 +/- 7 mM/h, and it declined to 3.5 +/- 0.9
mM/h at >35 mM glycogen. At <35 mM glycogen, synthesis was not affect
ed by low insulin (24 +/- 4 mM/h, protocol II vs. 19 +/- 3 mM/h, proto
col III), whereas at >35 mM glycogen, synthesis ceased without insulin
(-0.07 +/- 0.19 mM/h, protocol In. After depletion to 25% (protocol I
II), plasma lactate transiently increased (0.81 mM at rest, 1.82 mM 0
h after exercise, and 0.76 mM 2 h after exercise), whereas other plasm
a constituents did not significantly change. We conclude that after de
pletion to <30 mM initial glycogen resynthesis is insulin independent
and glycogen dependent, which suggests local control.