Kubo Takekazu, Yamashita Toshihide
Department of Neurobiology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Recent Pat CNS Drug Discov. 2007 Nov;2(3):173-9. doi: 10.2174/157488907782411738.
Injured axons in the adult central nervous system (CNS) exhibit almost no regeneration. Several myelin-associated proteins such as myelin-associated glycoprotein (MAG), Nogo, and oligodendrocyte-myelin glycoprotein (OMgp) have been identified as inhibitors of CNS axonal regeneration in the CNS. Recently, repulsive guidance molecule (RGM) was identified as a potential myelin-derived neurite outgrowth inhibitor in vitro and in vivo. These axonal growth inhibitors transmit inhibitory signals through common intracellular molecules such as RhoA and its effector Rho kinases (ROCK). The effects of these axonal growth inhibitors are blocked by inhibition of the Rho-ROCK pathway in vitro. Injuries to the adult CNS induce the activation of the Rho-ROCK pathway, and the inhibition of this pathway promotes axonal regeneration and functional recovery in the injured CNS. Therefore, the Rho-ROCK pathway is a promising target for drug development for the treatment of human CNS injuries such as spinal cord injuries. This review also discusses recent patents and future developments which are useful in the treatment of human CNS injuries.
成体中枢神经系统(CNS)中受损的轴突几乎没有再生能力。几种髓磷脂相关蛋白,如髓磷脂相关糖蛋白(MAG)、Nogo和少突胶质细胞髓磷脂糖蛋白(OMgp),已被确定为中枢神经系统中中枢神经系统轴突再生的抑制剂。最近,排斥导向分子(RGM)在体外和体内被确定为一种潜在的髓磷脂源性神经突生长抑制剂。这些轴突生长抑制剂通过常见的细胞内分子如RhoA及其效应物Rho激酶(ROCK)传递抑制信号。在体外,这些轴突生长抑制剂的作用可通过抑制Rho-ROCK途径来阻断。成体中枢神经系统损伤会诱导Rho-ROCK途径的激活,而抑制该途径可促进受损中枢神经系统的轴突再生和功能恢复。因此,Rho-ROCK途径是开发治疗人类中枢神经系统损伤(如脊髓损伤)药物的一个有前景的靶点。本文还讨论了近期在治疗人类中枢神经系统损伤方面有用的专利和未来发展。