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. 1988 Jun 15;252(3):733–737. doi: 10.1042/bj2520733

Glucose-induced insulin resistance of skeletal-muscle glucose transport and uptake.

E A Richter 1, B F Hansen 1, S A Hansen 1
PMCID: PMC1149209  PMID: 3421919

Abstract

The ability of glucose and insulin to modify insulin-stimulated glucose transport and uptake was investigated in perfused skeletal muscle. Here we report that perfusion of isolated rat hindlimbs for 5 h with 12 mM-glucose and 20,000 microunits of insulin/ml leads to marked, rapidly developing, impairment of insulin action on muscle glucose transport and uptake. Thus maximal insulin-stimulated glucose uptake at 12 mM-glucose decreased from 34.8 +/- 1.9 to 11.5 +/- 1.1 mumol/h per g (mean +/- S.E.M., n = 10) during 5 h perfusion. This decrease in glucose uptake was accompanied by a similar change in muscle glucose transport as measured by uptake of 3-O-[14C]-methylglucose. Simultaneously, muscle glycogen stores increased to 2-3.5 times initial values, depending on fibre type. Perfusion for 5 h in the presence of glucose but in the absence of insulin decreased subsequent insulin action on glucose uptake by 80% of the effect of glucose with insulin, but without an increase in muscle glycogen concentration. Perfusion for 5 h with insulin but without glucose, and with subsequent addition of glucose back to the perfusate, revealed glucose uptake and transport similar to initial values obtained in the presence of glucose and insulin. The data indicate that exposure to a moderately increased glucose concentration (12 mM) leads to rapidly developing resistance of skeletal-muscle glucose transport and uptake to maximal insulin stimulation. The effect of glucose is enhanced by simultaneous insulin exposure, whereas exposure for 5 h to insulin itself does not cause measurable resistance to maximal insulin stimulation.

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Selected References

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  1. Armstrong R. B., Phelps R. O. Muscle fiber type composition of the rat hindlimb. Am J Anat. 1984 Nov;171(3):259–272. doi: 10.1002/aja.1001710303. [DOI] [PubMed] [Google Scholar]
  2. Brahm J. Kinetics of glucose transport in human erythrocytes. J Physiol. 1983 Jun;339:339–354. doi: 10.1113/jphysiol.1983.sp014720. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Czech M. P., Richardson D. K., Becker S. G., Walters C. G., Gitomer W., Heinrich J. Insulin response in skeletal muscle and fat cells of the genetically obese Zucker rat. Metabolism. 1978 Dec;27(12 Suppl 2):1967–1981. doi: 10.1016/s0026-0495(78)80013-4. [DOI] [PubMed] [Google Scholar]
  4. DeFronzo R. A., Gunnarsson R., Björkman O., Olsson M., Wahren J. Effects of insulin on peripheral and splanchnic glucose metabolism in noninsulin-dependent (type II) diabetes mellitus. J Clin Invest. 1985 Jul;76(1):149–155. doi: 10.1172/JCI111938. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Foley J. E., Kashiwagi A., Verso M. A., Reaven G., Andrews J. Improvement in in vitro insulin action after one month of insulin therapy in obese noninsulin-dependent diabetics. Measurements of glucose transport and metabolism, insulin binding, and lipolysis in isolated adipocytes. J Clin Invest. 1983 Dec;72(6):1901–1909. doi: 10.1172/JCI111153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Garvey W. T., Olefsky J. M., Marshall S. Insulin induces progressive insulin resistance in cultured rat adipocytes. Sequential effects at receptor and multiple postreceptor sites. Diabetes. 1986 Mar;35(3):258–267. doi: 10.2337/diab.35.3.258. [DOI] [PubMed] [Google Scholar]
  7. Garvey W. T., Olefsky J. M., Matthaei S., Marshall S. Glucose and insulin co-regulate the glucose transport system in primary cultured adipocytes. A new mechanism of insulin resistance. J Biol Chem. 1987 Jan 5;262(1):189–197. [PubMed] [Google Scholar]
  8. Haspel H. C., Wilk E. W., Birnbaum M. J., Cushman S. W., Rosen O. M. Glucose deprivation and hexose transporter polypeptides of murine fibroblasts. J Biol Chem. 1986 May 25;261(15):6778–6789. [PubMed] [Google Scholar]
  9. James D. E., Burleigh K. M., Chisholm D. J., Kraegen E. W. In vivo dose response curves of insulin action in heart: anomalous effects at high insulin doses. J Mol Cell Cardiol. 1985 Oct;17(10):981–985. doi: 10.1016/s0022-2828(85)80078-x. [DOI] [PubMed] [Google Scholar]
  10. James D. E., Burleigh K. M., Kraegen E. W. Time dependence of insulin action in muscle and adipose tissue in the rat in vivo. An increasing response in adipose tissue with time. Diabetes. 1985 Oct;34(10):1049–1054. doi: 10.2337/diab.34.10.1049. [DOI] [PubMed] [Google Scholar]
  11. Kolterman O. G., Insel J., Saekow M., Olefsky J. M. Mechanisms of insulin resistance in human obesity: evidence for receptor and postreceptor defects. J Clin Invest. 1980 Jun;65(6):1272–1284. doi: 10.1172/JCI109790. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Richter E. A., Ploug T., Galbo H. Increased muscle glucose uptake after exercise. No need for insulin during exercise. Diabetes. 1985 Oct;34(10):1041–1048. doi: 10.2337/diab.34.10.1041. [DOI] [PubMed] [Google Scholar]
  13. Rizza R. A., Mandarino L. J., Genest J., Baker B. A., Gerich J. E. Production of insulin resistance by hyperinsulinaemia in man. Diabetologia. 1985 Feb;28(2):70–75. doi: 10.1007/BF00279918. [DOI] [PubMed] [Google Scholar]
  14. Rossetti L., Smith D., Shulman G. I., Papachristou D., DeFronzo R. A. Correction of hyperglycemia with phlorizin normalizes tissue sensitivity to insulin in diabetic rats. J Clin Invest. 1987 May;79(5):1510–1515. doi: 10.1172/JCI112981. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ruderman N. B., Houghton C. R., Hems R. Evaluation of the isolated perfused rat hindquarter for the study of muscle metabolism. Biochem J. 1971 Sep;124(3):639–651. doi: 10.1042/bj1240639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Sasson S., Edelson D., Cerasi E. In vitro autoregulation of glucose utilization in rat soleus muscle. Diabetes. 1987 Sep;36(9):1041–1046. doi: 10.2337/diab.36.9.1041. [DOI] [PubMed] [Google Scholar]
  17. Scarlett J. A., Kolterman O. G., Ciaraldi T. P., Kao M., Olefsky J. M. Insulin treatment reverses the postreceptor defect in adipocyte 3-O-methylglucose transport in type II diabetes mellitus. J Clin Endocrinol Metab. 1983 Jun;56(6):1195–1201. doi: 10.1210/jcem-56-6-1195. [DOI] [PubMed] [Google Scholar]
  18. Spriet L. L., Matsos C. G., Peters S. J., Heigenhauser G. J., Jones N. L. Effects of acidosis on rat muscle metabolism and performance during heavy exercise. Am J Physiol. 1985 Mar;248(3 Pt 1):C337–C347. doi: 10.1152/ajpcell.1985.248.3.C337. [DOI] [PubMed] [Google Scholar]
  19. Wajngot A., Roovete A., Vranić M., Luft R., Efendić S. Insulin resistance and decreased insulin response to glucose in lean type 2 diabetics. Proc Natl Acad Sci U S A. 1982 Jul;79(14):4432–4436. doi: 10.1073/pnas.79.14.4432. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Wardzala L. J., Hirshman M., Pofcher E., Horton E. D., Mead P. M., Cushman S. W., Horton E. S. Regulation of glucose utilization in adipose cells and muscle after long-term experimental hyperinsulinemia in rats. J Clin Invest. 1985 Aug;76(2):460–469. doi: 10.1172/JCI111994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Yki-Järvinen H., Helve E., Koivisto V. A. Hyperglycemia decreases glucose uptake in type I diabetes. Diabetes. 1987 Aug;36(8):892–896. doi: 10.2337/diab.36.8.892. [DOI] [PubMed] [Google Scholar]
  22. Young D. A., Uhl J. J., Cartee G. D., Holloszy J. O. Activation of glucose transport in muscle by prolonged exposure to insulin. Effects of glucose and insulin concentrations. J Biol Chem. 1986 Dec 5;261(34):16049–16053. [PubMed] [Google Scholar]
  23. van Putten J. P., Krans H. M. Glucose as a regulator of insulin-sensitive hexose uptake in 3T3 adipocytes. J Biol Chem. 1985 Jul 5;260(13):7996–8001. [PubMed] [Google Scholar]

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