Ueyama A, Sato T, Yoshida H, Magata K, Koga N
Third Tokushima Institute of New Drug Research, Otsuka Pharmaceutical Co. Ltd., Kagasuno Kawauchi-cho, Tokushima, Japan.
Biol Signals Recept. 2000 Sep-Oct;9(5):267-74. doi: 10.1159/000014649.
We investigated a nonradioisotope method for the evaluation of glucose uptake activity using enzymatic measurement of 2-deoxyglucose 6-phosphate (2DG6P) content in isolated rat soleus muscle in vitro and in vivo. The 2DG6P content in isolated rat soleus muscle after incubation with 2-deoxyglucose (2DG) was increased in a dose-dependent manner by insulin (ED(50) = 0.6 mU/ml), the maximum response being about 5 times that of the basal content in vitro. This increment was completely abolished by wortmannin (100 nM), with no effect on basal 2DG6P content. An insulin-mimetic compound, vanadium, also increased 2DG6P content in a dose-dependent manner. In isolated soleus muscle of Zucker fa/fa rats, well known as an insulin-resistant model, insulin did not increase 2DG6P content. The 2DG6P content in rat soleus muscle increased after 2DG (3 mmol/kg) injection in vivo, and conversely, the 2DG concentration in plasma was decreased in a dose-dependent manner by insulin (ED(50) = 0.11 U/kg). The maximum response of the accumulation of 2DG6P in soleus muscle was about 4 times that of the basal content. This method could be useful for evaluating glucose uptake (transport plus phosphorylation) activity in soleus muscle in vitro and in vivo without using radioactive materials.
我们研究了一种非放射性同位素方法,该方法通过酶促测量体外和体内分离的大鼠比目鱼肌中6-磷酸-2-脱氧葡萄糖(2DG6P)的含量来评估葡萄糖摄取活性。用2-脱氧葡萄糖(2DG)孵育后,分离的大鼠比目鱼肌中的2DG6P含量在胰岛素作用下呈剂量依赖性增加(半数有效剂量(ED(50))=0.6 mU/ml),最大反应约为体外基础含量的5倍。渥曼青霉素(100 nM)可完全消除这种增加,而对基础2DG6P含量无影响。一种胰岛素模拟化合物钒也以剂量依赖性方式增加2DG6P含量。在作为胰岛素抵抗模型而广为人知的Zucker fa/fa大鼠的分离比目鱼肌中,胰岛素并未增加2DG6P含量。在体内注射2DG(3 mmol/kg)后,大鼠比目鱼肌中的2DG6P含量增加,相反,胰岛素以剂量依赖性方式降低血浆中的2DG浓度(ED(50)=0.11 U/kg)。比目鱼肌中2DG6P积累的最大反应约为基础含量的4倍。该方法可用于在不使用放射性物质的情况下评估体外和体内比目鱼肌中的葡萄糖摄取(转运加磷酸化)活性。