Shimizu Y, Shimazu T
Department of Medical Biochemistry, Ehime University, School of Medicine, Japan.
Biochem Biophys Res Commun. 1994 Jul 29;202(2):660-5. doi: 10.1006/bbrc.1994.1981.
The effects of wortmannin, a selective inhibitor of phosphatidylinositol (PI) 3-kinase, on increases in glucose transport activity induced by insulin and norepinephrine (NE) have been studied in primary culture of brown adipocytes. Both insulin and NE produced 2- to 3-fold increase in 2-deoxy-D-[3H]glucose (2-DG) transport into cultured brown adipocytes. The effect of insulin was dependent upon translocation of the muscle/adipocyte glucose transporter (GLUT4) from microsome to plasma membranes. In contrast, NE did not affect the subcellular distribution of GLUT4. When wortmannin was added to the medium before stimulation with insulin, the increase in glucose transport and translocation of GLUT4 were completely abolished. On the other hand, NE-induced increase in glucose transport was resistant to wortmannin. These results indicate that PI 3-kinase plays a critical role on insulin-induced translocation of GLUT4, but that this pathway is not involved in the increase in glucose transport by NE in brown adipocytes.
在棕色脂肪细胞的原代培养中,研究了磷脂酰肌醇(PI)3激酶的选择性抑制剂渥曼青霉素对胰岛素和去甲肾上腺素(NE)诱导的葡萄糖转运活性增加的影响。胰岛素和NE均可使培养的棕色脂肪细胞对2-脱氧-D-[3H]葡萄糖(2-DG)的转运增加2至3倍。胰岛素的作用取决于肌肉/脂肪细胞葡萄糖转运体(GLUT4)从微粒体向质膜的转位。相反,NE不影响GLUT4的亚细胞分布。在用胰岛素刺激之前向培养基中加入渥曼青霉素时,葡萄糖转运的增加和GLUT4的转位被完全消除。另一方面,NE诱导的葡萄糖转运增加对渥曼青霉素具有抗性。这些结果表明,PI 3激酶在胰岛素诱导的GLUT4转位中起关键作用,但该途径不参与棕色脂肪细胞中NE引起的葡萄糖转运增加。