Effect of diffusion distance on measurement of rat skeletal muscle glucose transport in vitro

E. J. HENRIKSEN, J. O. HOLLOSZY

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61 Scopus citations

Abstract

The relationships between muscle size, diffusion distance, and glucose uptake were studied using the Type II b epitrochlearis (13 ± 1 mg intact), Type I soleus (25± 1 mg), and mixed Type II a/II b extensor digitorum longus (25 ± 1 mg) from 60–70 g rats. Using intact muscles, the relative rates of 3‐O‐methyl‐glucose uptake in response to 2 mUml‐1 insulin were soleus = epitrochlearis > extensor digitorum longus, a finding inconsistent with the fibre‐type compositions and the relative GLUT‐4 protein levels (soleus > extensor digitorum longus > epitrochlearis). To test whether these results were influenced by substrate diffusion limitations in the tubular muscles, soleus and extensor digitorum longus were split longitudinally from tendon to tendon into strips of comparable size (13 ± 1 mg) to the epitrochlearis. Insulin‐stimulated rates of 3‐O‐methyl‐glucose uptake were significantly enhanced in the split soleus (+120%) and split extensor digitorum longus (+200%), but not in the epitrochlearis, with the relative rates being soleus > extensor digitorum longus > epitrochlearis. Diffusion distances of the split soleus and extensor digitorum longus, as reflected by [14C]mannitol space equilibration time, were markedly enhanced (by at least 50%) relative to the intact muscles, and were comparable to that of the epitrochlearis. These results indicate that when muscles of different size and/or shape are used for in vitro measurement of glucose transport, the muscle preparations used must have similar diffusion distances for physiologically meaningful comparisons to be made.

Original languageEnglish (US)
Pages (from-to)381-386
Number of pages6
JournalActa Physiologica Scandinavica
Volume143
Issue number4
DOIs
StatePublished - Dec 1991

Keywords

  • Epitrochlearis
  • extensor digitorum longus
  • extracellular space
  • muscle strips
  • soleus

ASJC Scopus subject areas

  • Physiology

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