Regulation of the GLUT4/muscle-fat glucose transporter mRNA in adipose tissue of insulin-deficient diabetic rats
Previous studies have documented that streptozotocin-induced insulin deficiency results in a marked decrease in adipose tissue GLUT4 glucose transporter mRNA levels (Sivitz, W.I., DeSautel, S.L., Kayano, T., Bell, G.I., and Pessin, J.E. (1989) Nature 340, 72-74). In this study, nuclear run-on analys...
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Veröffentlicht in: | The Journal of biological chemistry 1993-01, Vol.268 (1), p.640-644 |
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Zusammenfassung: | Previous studies have documented that streptozotocin-induced insulin deficiency results in a marked decrease in adipose tissue
GLUT4 glucose transporter mRNA levels (Sivitz, W.I., DeSautel, S.L., Kayano, T., Bell, G.I., and Pessin, J.E. (1989) Nature
340, 72-74). In this study, nuclear run-on analysis performed on diabetic and insulin-treated diabetic rats demonstrated that
the decrease in GLUT4 mRNA occurs via a diabetes-induced decrease in GLUT4 transcription rate. The decrease in GLUT4 mRNA
levels could be prevented by treatment of the diabetic animals with the adenosine receptor agonist phenylisopropyl-adenosine
(PIA). Under these conditions, PIA completely blocked the elevation of intracellular cAMP levels associated with insulin deficiency.
Surprisingly, isolation of primary rat adipocytes from control animals resulted in a rapid decrease (approximately 20-fold)
in GLUT4 mRNA levels by 24 h with a concomitant increase (approximately 70-fold) in GLUT1 mRNA levels. This rapid loss of
GLUT4 expression did not correlate with changes in adipocyte cAMP levels and was not prevented by treatment of the cells with
either insulin and/or PIA. These data demonstrate that the decrease in GLUT4 transcription induced by insulin deficiency in
vivo predominantly results from an increase in intracellular cAMP levels. In contrast, although GLUT4 transcription also decreases
in adipocytes when removed from their normal physiological environment, this occurs independent of changes in cAMP levels. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1016/S0021-9258(18)54199-5 |