Department of Neurology and Neurological Sciences, Stanford University, 300 Pasteur Drive, Stanford, California 94305, USA.
Nat Rev Drug Discov. 2013 Jul;12(7):507-25. doi: 10.1038/nrd4024.
Neurotrophins and their receptors modulate multiple signalling pathways to regulate neuronal survival and to maintain axonal and dendritic networks and synaptic plasticity. Neurotrophins have potential for the treatment of neurological diseases. However, their therapeutic application has been limited owing to their poor plasma stability, restricted nervous system penetration and, importantly, the pleiotropic actions that derive from their concomitant binding to multiple receptors. One strategy to overcome these limitations is to target individual neurotrophin receptors — such as tropomyosin receptor kinase A (TRKA), TRKB, TRKC, the p75 neurotrophin receptor or sortilin — with small-molecule ligands. Such small molecules might also modulate various aspects of these signalling pathways in ways that are distinct from the programmes triggered by native neurotrophins. By departing from conventional neurotrophin signalling, these ligands might provide novel therapeutic options for a broad range of neurological indications.
神经营养因子及其受体调节多种信号通路,以调节神经元存活,并维持轴突和树突网络以及突触可塑性。神经营养因子具有治疗神经疾病的潜力。然而,由于它们在血浆中的稳定性差、对神经系统的穿透性有限,以及重要的是它们与多种受体同时结合所产生的多效性作用,它们的治疗应用受到了限制。克服这些限制的一种策略是用小分子配体靶向个别神经营养因子受体,如原肌球蛋白受体激酶 A(TRKA)、TRKB、TRKC、p75 神经营养因子受体或分选蛋白。这些小分子还可能以不同于天然神经营养因子触发的方案的方式调节这些信号通路的各个方面。通过脱离传统的神经营养因子信号,这些配体可能为广泛的神经适应症提供新的治疗选择。