Douen A G, Jones M N
Division of Cell Biology, Hospital for Sick Children, Toronto, Ontario, Canada.
Biofactors. 1990 Jul;2(3):153-61.
The actions of phenylarsine oxide (PAO) on hormone receptors and transport processes are reviewed with particular reference to the mechanism of insulin-stimulated sugar transport. It is suggested that as well as reaction with vicinal -SH groups, vicinal -SH/-OH and -SH/-CO2H groups should also be considered as potential reaction sites for PAO. The relatively high levels of these vicinal combinations of groups in many hormone receptors makes them particularly susceptible to reaction with PAO. In the case of insulin-stimulated sugar transport PAO does not inhibit insulin binding to its receptor at low concentrations but may react directly with the glucose transporters in some cells. A hypothesis is proposed suggesting that PAO may react specifically with one transporter isoform (GLUT-4) which is found almost exclusively in rat adipocytes, skeletal muscle and heart tissue (i.e. insulin responsive tissue) whereas in insulin unresponsive cells such as erythrocytes the GLUT-1 isoform is the predominant transporter which is not inhibited by PAO.
本文综述了苯胂化氧(PAO)对激素受体和转运过程的作用,特别提及了胰岛素刺激的糖转运机制。研究表明,除了与相邻的巯基反应外,相邻的巯基/羟基和巯基/羧基也应被视为PAO的潜在反应位点。许多激素受体中这些相邻基团组合的相对高含量使其特别容易与PAO发生反应。就胰岛素刺激的糖转运而言,低浓度时PAO并不抑制胰岛素与其受体的结合,但可能在某些细胞中直接与葡萄糖转运体发生反应。本文提出了一个假说,认为PAO可能与一种几乎仅在大鼠脂肪细胞、骨骼肌和心脏组织(即胰岛素反应性组织)中发现的转运体异构体(GLUT-4)发生特异性反应,而在诸如红细胞等胰岛素无反应性细胞中,GLUT-1异构体是主要的转运体,不受PAO抑制。