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苯胂化氧对基础状态及胰岛素刺激下大鼠脂肪细胞中D-葡萄糖立体特异性摄取的作用。

The action of phenylarsine oxide on the stereospecific uptake of D-glucose in basal and insulin-stimulated rat adipocytes.

作者信息

Douen A G, Jones M N

机构信息

Department of Biochemistry and Molecular Biology, School of Biological Sciences, University of Manchester, U.K.

出版信息

Biochim Biophys Acta. 1988 Jan 18;968(1):109-18. doi: 10.1016/0167-4889(88)90050-x.

Abstract

Phenylarsine oxide (PAO) has been used to inhibit the stereospecific uptake of D-glucose in basal and insulin-stimulated rat adipocytes. The inhibition is dose dependent and is partially reversed by dithiothreitol. The results are consistent with a direct interaction between the glucose transporter and PAO. By manipulating the sequence of exposure of cells to PAO and insulin it is possible to differentiate between the effects of PAO on transport into cells with receptor-rich and transporter-rich plasma membranes. PAO rapidly inhibits transport in insulin-stimulated adipocytes but at low concentrations inhibition is transient and recovery of stereospecific uptake takes place after approx. 20 min. The results can be interpreted in terms of the recruitment mechanism of insulin stimulation of transport and demonstrate that a relatively large intracellular pool of transporters exists after insulin stimulation. It also follows that sulphydryl groups probably play a critical role in the mechanism of glucose uptake.

摘要

苯胂化氧(PAO)已被用于抑制基础状态和胰岛素刺激状态下大鼠脂肪细胞对D-葡萄糖的立体特异性摄取。这种抑制作用呈剂量依赖性,并且可被二硫苏糖醇部分逆转。这些结果与葡萄糖转运体和PAO之间的直接相互作用一致。通过操控细胞接触PAO和胰岛素的顺序,可以区分PAO对葡萄糖转运进入富含受体和富含转运体的质膜的细胞的影响。PAO能迅速抑制胰岛素刺激的脂肪细胞中的葡萄糖转运,但在低浓度时,抑制作用是短暂的,大约20分钟后立体特异性摄取恢复。这些结果可以根据胰岛素刺激转运的募集机制来解释,并表明胰岛素刺激后存在相对大量的细胞内转运体池。由此还可推断,巯基可能在葡萄糖摄取机制中起关键作用。

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