Mandarino L J, Printz R L, Cusi K A, Kinchington P, O'Doherty R M, Osawa H, Sewell C, Consoli A, Granner D K, DeFronzo R A
Department of Medicine, University of Texas Health Science Center, San Antonio 78284, USA.
Am J Physiol. 1995 Oct;269(4 Pt 1):E701-8. doi: 10.1152/ajpendo.1995.269.4.E701.
Insulin regulates the activity of key enzymes of glucose metabolism in skeletal muscle by altering transcription or translation or by producing activity-altering modifications of preexisting enzyme molecules. Because of the small size of percutaneous muscle biopsies, these phenomena have been difficult to study in humans. This study was performed to determine how physiological hyperinsulinemia regulates the activities of hexokinase (HK), glycogen synthase (GS), and GLUT-4 in human skeletal muscle in vivo. We determined mRNA abundance, protein content, and activities for these proteins in muscle biopsies before and after a hyperinsulinemic clamp in normal subjects. HK I, HK II, GS, and GLUT-4 were expressed in muscle. HK II accounted for 80% of total HK activity and was increased by insulin from a basal value of 2.11 +/- 0.26 to 3.35 +/- 0.47 pmol.min-1.mg protein-1 (P < 0.05); HK I activity was unaffected. Insulin increased GS activity from 3.85 +/- 0.82 to 6.06 +/- 0.49 nmol.min-1.mg-1 (P < 0.01). HK II mRNA was increased 3.3 +/- 1.3-fold (P < 0.05) by insulin infusion. HK I, GS, and GLUT-4 mRNA and protein were unaffected. Because insulin infusion increased HK II but not GS mRNA, we conclude that HK II and GS may be regulated by insulin by different mechanisms in human skeletal muscle.
胰岛素通过改变转录或翻译,或通过对已存在的酶分子进行改变活性的修饰,来调节骨骼肌中葡萄糖代谢关键酶的活性。由于经皮肌肉活检样本量小,这些现象在人体中一直难以研究。本研究旨在确定生理性高胰岛素血症如何在体内调节人骨骼肌中己糖激酶(HK)、糖原合酶(GS)和葡萄糖转运蛋白4(GLUT-4)的活性。我们测定了正常受试者在高胰岛素钳夹前后肌肉活检中这些蛋白质的mRNA丰度、蛋白质含量和活性。HK I、HK II、GS和GLUT-4在肌肉中均有表达。HK II占总HK活性的80%,胰岛素使其从基础值2.11±0.26增加到3.35±0.47 pmol·min⁻¹·mg蛋白⁻¹(P<0.05);HK I活性未受影响。胰岛素使GS活性从3.85±0.82增加到6.06±0.49 nmol·min⁻¹·mg⁻¹(P<0.01)。胰岛素输注使HK II mRNA增加3.3±1.3倍(P<0.05)。HK I、GS和GLUT-4的mRNA和蛋白质未受影响。由于胰岛素输注增加了HK II但未增加GS mRNA,我们得出结论,在人骨骼肌中,HK II和GS可能受胰岛素的不同机制调节。