Baron A D, Zhu J S, Zhu J H, Weldon H, Maianu L, Garvey W T
Department of Medicine, Indiana University School of Medicine, Indianapolis 46202, USA.
J Clin Invest. 1995 Dec;96(6):2792-801. doi: 10.1172/JCI118349.
Glucosamine (Glmn), a product of glucose metabolism via the hexosamine pathway, causes insulin resistance in isolated adipocytes by impairing insulin-induced GLUT 4 glucose transporter translocation to the plasma membrane. We hypothesized that Glmn causes insulin resistance in vivo by a similar mechanism in skeletal muscle. We performed euglycemic hyperinsulinemic clamps (12 mU/kg/min + 3H-3-glucose) in awake male Sprague-Dawley rats with and without Glmn infusion at rates ranging from 0.1 to 6.5 mg/kg/min. After 4h of euglycemic clamping, hindquarter muscles were quick-frozen and homogenized, and membranes were subfractionated by differential centrifugation and separated on a discontinuous sucrose gradient (25, 30, and 35% sucrose). Membrane proteins were solubilized and immunoblotted for GLUT 4. With Glmn, glucose uptake (GU) was maximally reduced by 33 +/- 1%, P < 0.001. The apparent Glmn dose to reduce maximal GU by 50% was 0.1 mg/kg/min or 1/70th the rate of GU on a molar basis. Control galactosamine and mannosamine infusions had no effect on GU. Relative to baseline, insulin caused a 2.6-fold increase in GLUT 4 in the 25% membrane fraction (f), P < 0.01, and a 40% reduction in the 35%f, P < 0.05, but had no effect on GLUT 4 in the 30% f, P= NS. Addition of Glmn to insulin caused a 41% reduction of GLUT 4 in the 25%f, P < 0.05, a 29% fall in the 30%f, and prevented the reduction of GLUT 4 in the 35% f. The 30%f membranes were subjected to a second separation with a 27 and 30% sucrose gradient. Insulin mobilized GLUT 4 away from the 30%f, P < 0.05, but not the 27% f. In contrast, Glmn reduced GLUT 4 in the 27%f, P < 0.05, but not the 30%f. Thus Glmn appears to alter translocation of an insulin-insensitive GLUT 4 pool. Coinfusion of Glmn did not alter enrichment of the sarcolemmal markers 5'-nucleotidase, Na+/K+ATPase, and phospholemman in either 25, 30, or 35% f. Thus Glmn completely blocked movement of Glut 4 induced by insulin. Glmn is a potent inducer of insulin resistance in vivo by causing (at least in part) a defect intrinsic to GLUT 4 translocation and/or trafficking. These data support a potential role for Glmn to cause glucose-induced insulin resistance (glucose toxicity).
氨基葡萄糖(Glmn)是葡萄糖经己糖胺途径代谢的产物,通过损害胰岛素诱导的GLUT 4葡萄糖转运体向质膜的转位,在分离的脂肪细胞中引起胰岛素抵抗。我们推测,Glmn在体内通过类似机制在骨骼肌中引起胰岛素抵抗。我们对清醒的雄性Sprague-Dawley大鼠进行了正常血糖高胰岛素钳夹试验(12 mU/kg/min + 3H-3-葡萄糖),钳夹过程中分别以0.1至6.5 mg/kg/min的速率输注或不输注Glmn。在正常血糖钳夹4小时后,将后肢肌肉速冻并匀浆,通过差速离心对膜进行亚分级,并在不连续蔗糖梯度(25%、30%和35%蔗糖)上进行分离。将膜蛋白溶解并进行GLUT 4免疫印迹分析。输注Glmn后,葡萄糖摄取(GU)最大降低了33±1%,P<0.001。使最大GU降低50%的Glmn表观剂量为0.1 mg/kg/min,按摩尔计算是GU速率的1/70。对照半乳糖胺和甘露糖胺输注对GU无影响。相对于基线,胰岛素使25%膜组分(f)中的GLUT 4增加了2.6倍,P<0.01,使35%f中的GLUT 4减少了40%,P<0.05,但对30%f中的GLUT 4无影响,P=无显著性差异。在胰岛素中加入Glmn导致25%f中的GLUT 4减少41%,P<0.05,30%f中的GLUT 4减少29%,并阻止了35%f中GLUT 4的减少。对30%f的膜用27%和30%蔗糖梯度进行第二次分离。胰岛素使GLUT 4从30%f中移出,P<0.05,但未使GLUT 4从27%f中移出。相反,Glmn使27%f中的GLUT 4减少,P<0.05,但未使30%f中的GLUT 4减少。因此,Glmn似乎改变了胰岛素不敏感的GLUT 4池的转位。同时输注Glmn并未改变25%、30%或35%f中肌膜标志物5'-核苷酸酶、Na+/K+ATP酶和磷膜蛋白的富集。因此,Glmn完全阻断了胰岛素诱导的Glut 4的移动。Glmn是体内胰岛素抵抗的强效诱导剂,其作用机制是(至少部分)导致GLUT 4转位和/或运输内在缺陷。这些数据支持了Glmn导致葡萄糖诱导的胰岛素抵抗(葡萄糖毒性)的潜在作用。