Choy Fong Chan, Klarić Thomas S, Koblar Simon A, Lewis Martin D
School of Biological Sciences, The University of Adelaide, Adelaide, SA 5005, Australia.
School of Medicine, The University of Adelaide, Adelaide, SA 5005, Australia.
Int J Mol Sci. 2015 Dec 4;16(12):29011-28. doi: 10.3390/ijms161226144.
Stroke is one of the leading causes of death and adult disability in the world. Although many molecules have been documented to have a neuroprotective effect, the majority of these molecules failed to improve the neurological outcomes for patients with brain ischemia. It has been proposed that neuroprotection alone may, in fact, not be adequate for improving the prognosis of ischemic stroke. Neuroprotectants that can regulate other processes which occur in the brain during ischemia could potentially be targets for the development of effective therapeutic interventions in stroke. Neuronal Per-Arnt-Sim domain protein 4 (Npas4) is an activity-dependent transcription factor whose expression is induced in various brain insults, including cerebral ischemia. It has been shown that Npas4 plays an important role in protecting neurons against many types of neurodegenerative insult. Recently, it was demonstrated that Npas4 indeed has a neuroprotective role in ischemic stroke and that Npas4 might be involved in modulating the cell death pathway and inflammatory response. In this review, we summarize the current knowledge of the roles that Npas4 may play in neuroinflammation and ischemia. Understanding how ischemic lesion size in stroke may be reduced through modulation of Npas4-dependent apoptotic and inflammatory pathways could lead to the development of new stroke therapies.
中风是全球主要的死亡原因之一,也是成年人残疾的主要原因。尽管已有许多分子被证明具有神经保护作用,但这些分子中的大多数未能改善脑缺血患者的神经功能结局。有人提出,仅靠神经保护可能实际上不足以改善缺血性中风的预后。能够调节脑缺血期间大脑中发生的其他过程的神经保护剂可能是开发中风有效治疗干预措施的潜在靶点。神经元芳香烃受体核转运蛋白4(Npas4)是一种活性依赖性转录因子,其表达在包括脑缺血在内的各种脑损伤中被诱导。研究表明,Npas4在保护神经元免受多种类型的神经退行性损伤中起重要作用。最近,有研究表明Npas4在缺血性中风中确实具有神经保护作用,并且Npas4可能参与调节细胞死亡途径和炎症反应。在这篇综述中,我们总结了目前关于Npas4在神经炎症和缺血中可能发挥的作用的认识。了解如何通过调节Npas4依赖的凋亡和炎症途径来减少中风中的缺血性损伤大小,可能会导致新的中风治疗方法的开发。