体外和体内2-脱氧葡萄糖- 6-磷酸酶法测定大鼠骨骼肌葡萄糖摄取活性的非放射性同位素测定。

A Ueyama, T Sato, H Yoshida, K Magata, N Koga
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引用次数: 20

摘要

我们研究了一种非放射性同位素方法,通过酶促测量离体大鼠比目鱼肌中2-脱氧葡萄糖6-磷酸(2DG6P)含量来评估葡萄糖摄取活性。2-脱氧葡萄糖(2DG)培养后,胰岛素可使离体大鼠比目鱼肌中2DG6P含量呈剂量依赖性增加(ED(50) = 0.6 mU/ml),最大反应量约为体外基础含量的5倍。wortmannin (100 nM)完全消除了这种增加,对基础2DG6P含量没有影响。一种类似胰岛素的化合物钒也以剂量依赖性的方式增加2DG6P的含量。在被称为胰岛素抵抗模型的Zucker fa/fa大鼠离体比目鱼肌中,胰岛素没有增加2DG6P的含量。体内注射2DG (3 mmol/kg)后,大鼠比目鱼肌中2DG6P含量升高,而胰岛素则使血浆中2DG浓度呈剂量依赖性降低(ED(50) = 0.11 U/kg)。2DG6P在比目鱼肌积累的最大反应约为基础含量的4倍。该方法可用于体外和体内评估比目鱼肌的葡萄糖摄取(运输和磷酸化)活性,而无需使用放射性物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nonradioisotope assay of glucose uptake activity in rat skeletal muscle using enzymatic measurement of 2-deoxyglucose 6-phosphate in vitro and in vivo.

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.

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