Caron M, Cherqui G, Wicek D, Melin B, Reynet C, Capeau J, Picard J
Laboratoire de Biochimie, INSERM U 181, Faculté de Médecine Saint Antoine, Paris, France.
Biosci Rep. 1990 Feb;10(1):23-9. doi: 10.1007/BF01116847.
Phenylarsine oxide (PhAsO), a dithiol reagent that blocks insulin stimulation of glucose transport in 3T3 L1 cells, also altered insulin stimulation of intracellular glucose metabolism in Zajdela Hepatoma cultured cells. PhAsO (2 microM) similarly inhibited the insulin-induced glycogen and lipid syntheses without modifying the basal level of these processes, cell viability or the ATP content. Prior incubation of the cells with PhAsO did not prevent insulin binding to the cells, or activation of the receptor tyrosine kinase, while it minimally (16%) altered receptor internalization. These results indicate that cellular dithiols located at a post-receptor step are involved in the transduction of the insulin signal to intracellular glucose metabolism.
苯胂氧化物(PhAsO)是一种二硫醇试剂,可阻断胰岛素对3T3 L1细胞葡萄糖转运的刺激作用,它也改变了扎伊德氏肝癌培养细胞中胰岛素对细胞内葡萄糖代谢的刺激作用。PhAsO(2微摩尔)同样抑制胰岛素诱导的糖原和脂质合成,而不改变这些过程的基础水平、细胞活力或ATP含量。细胞先用PhAsO孵育并不妨碍胰岛素与细胞结合或受体酪氨酸激酶的激活,而它对受体内化的影响最小(16%)。这些结果表明,位于受体后步骤的细胞二硫醇参与胰岛素信号向细胞内葡萄糖代谢的转导。