Huisamen B, Lochner A
Department of Medical Physiology and Biochemistry, Faculty of Medicine, University of Stellenbosch, Tygerberg; Republic of South Africa.
Mol Cell Biochem. 1996;157(1-2):229-32. doi: 10.1007/BF00227903.
Since 1983, when it was discovered that inositol 1,4,5-trisphosphate can act as second messenger to release Ca2+ from the endoplasmic reticulum, widespread research has focused on the phosphatidylinositol signalling transduction pathway and the host of inositolphosphates formed intracellularly after stimulation therof. Although the polyphosphates, inositoltetrakisphosphate (InsP4) and inositolhexakisphosphate (InsP6), have received their share of attention, a definite physiological role has not been ascribed to them as yet. Different binding proteins for these two polyphosphates have been demonstrated, especially in brain tissue, indicating their possible importance in the cell. InsP6 is known as one of nature's most powerful antioxidants and has already been demonstrated to possess the abilities to be of use in the industry as well as in the medical profession. As its natural actions are poorly understood and its possible side-effects have not been widely investigated, basic research regarding its cellular and subcellular activities is urgently called for.
自1983年发现肌醇1,4,5-三磷酸可作为第二信使从内质网释放Ca2+以来,广泛的研究集中在磷脂酰肌醇信号转导途径以及刺激后细胞内形成的一系列肌醇磷酸。尽管多磷酸肌醇四磷酸(InsP4)和肌醇六磷酸(InsP6)已受到一定关注,但尚未确定它们的明确生理作用。已经证明了这两种多磷酸肌醇的不同结合蛋白,特别是在脑组织中,表明它们在细胞中可能具有重要性。InsP6是自然界中最强大的抗氧化剂之一,并且已经证明它具有在工业以及医学领域中使用的能力。由于对其天然作用了解甚少,并且其可能的副作用尚未得到广泛研究,因此迫切需要对其细胞和亚细胞活性进行基础研究。