J. Ihlemann et al., Effect of stimulation frequency on contraction-induced glucose transport in rat skeletal muscle, AM J P-ENDO, 279(4), 2000, pp. E862-E867
Citations number
23
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
Previous studies have indicated that frequency of stimulation is a major de
terminant of glucose transport in contracting muscle. We have now studied w
hether this is so also when total force development or metabolic rate is ke
pt constant. Incubated soleus muscles were electrically stimulated to perfo
rm repeated tetanic contractions at four different frequencies (0.25, 0.5,
1, and 2 Hz) for 10 min. Resting length was adjusted to achieve identical t
otal force development or metabolic rate (glycogen depletion and lactate ac
cumulation). Overall, at constant total force development, glucose transpor
t (2-deoxyglucose uptake) increased with stimulation frequency (P < 0.05; b
asal: 25 +/- 2, 0.25 Hz: 50 +/- 4, 0.5 Hz: 50 +/- 3, 1 Hz: 81 +/- 5, 2 Hz:
79 +/- 3 nmol.g(-1).5 min(-1)). However, glucose transport was identical (P
. 0.05) at the two lower (0.25 and 0.5 Hz) as well as at the two higher (1
and 2 Hz) frequencies. Glycogen decreased (P, 0.05; basal: 19 +/- 1, 0.25 H
z: 13 +/- 1, 0.5 Hz: 12 +/- 2, 1 Hz: 7 +/- 1, 2 Hz: 7 +/- 1 mmol/kg) and 5'
-AMP-activated protein kinase (AMPK) activity increased (P, 0.05; basal: 1.
7 +/- 0.4, 0.25 Hz: 32.4 +/- 7.0, 0.5 Hz: 36.5 +/- 2.1, 1 Hz: 63.4 +/- 8.0,
2 Hz: 67.0 +/- 13.4 pmol.mg(-1).min(-1)) when glucose transport increased.
Experiments with constant metabolic rate were carried out in soleus, flexo
r digitorum brevis, and epitrochlearis muscles. In all muscles, glucose tra
nsport was identical at 0.5 and 2 Hz (P. 0.05); also, AMPK activity did not
increase with stimulation frequency. In conclusion, muscle glucose transpo
rt increases with stimulation frequency but only in the face of energy depl
etion and increase in AMPK activity. This indicates that contraction-induce
d glucose transport is elicited by metabolic demands rather than by events
occurring early during the excitation-contraction coupling.