Wilcox R A, Nahorski S R, Sawyer D A, Liu C, Potter B V
Department of Pharmacology and Therapeutics, University of Leicester, United Kingdom.
Carbohydr Res. 1992 Oct 9;234:237-46. doi: 10.1016/0008-6215(92)85051-z.
The functional significance of the 2- and 3-hydroxyl groups of 1 D-myo-inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] was probed by using Ins(1,4,5)P3 analogues variously modified at positions 2 and 3 or elsewhere. The intrinsic activities of these compounds were compared to that of Ins(1,4,5)P3, using the calcium-mobilising receptor of the 1321N1 human astrocytoma cell line. The ligand-binding affinities were also determined using membrane preparations from rat cerebellum and bovine adrenal cortex. The results show that HO-2 and HO-3 of Ins(1,4,5)P3 have a relatively insignificant role in receptor binding and calcium release. However, the possibility of a regulatory role for the 3-position of Ins(1,4,5)P3 in these processes is proposed.
通过使用在2位和3位或其他位置进行了不同修饰的1 D-肌醇1,4,5-三磷酸[Ins(1,4,5)P3]类似物,探究了Ins(1,4,5)P3的2-羟基和3-羟基的功能意义。利用1321N1人星形细胞瘤细胞系的钙动员受体,将这些化合物的内在活性与Ins(1,4,5)P3的内在活性进行了比较。还使用大鼠小脑和牛肾上腺皮质的膜制剂测定了配体结合亲和力。结果表明,Ins(1,4,5)P3的2-羟基和3-羟基在受体结合和钙释放中作用相对较小。然而,有人提出Ins(1,4,5)P3的3位在这些过程中具有调节作用的可能性。