Vision Research Center and Department of Ophthalmology, School of Medicine, University of Missouri, 2411 Holmes Street, Kansas City, MO 64108, USA.
Molecules. 2010 Mar 3;15(3):1168-95. doi: 10.3390/molecules15031168.
Both acute and chronic degenerative diseases of the nervous system reduce the viability and function of neurons through changes in intracellular calcium signaling. In particular, pathological increases in the intracellular calcium concentration promote such pathogenesis. Disease involvement of numerous regulators of intracellular calcium signaling located on the plasma membrane and intracellular organelles has been documented. Diverse groups of chemical compounds targeting ion channels, G-protein coupled receptors, pumps and enzymes have been identified as potential neuroprotectants. The present review summarizes the discovery, mechanisms and biological activity of neuroprotective molecules targeting proteins that control intracellular calcium signaling to preserve or restore structure and function of the nervous system. Disease relevance, clinical applications and new technologies for the identification of such molecules are being discussed.
神经系统的急性和慢性退行性疾病通过细胞内钙信号的变化降低神经元的活力和功能。特别是,细胞内钙浓度的病理性增加促进了这种发病机制。已经记录了位于质膜和细胞内细胞器上的许多细胞内钙信号转导调节剂的疾病涉及。已经确定了针对离子通道、G 蛋白偶联受体、泵和酶的各种化学化合物作为潜在的神经保护剂。本综述总结了针对控制细胞内钙信号的蛋白质的神经保护分子的发现、机制和生物学活性,以维持或恢复神经系统的结构和功能。讨论了这些分子的疾病相关性、临床应用和新的鉴定技术。