Wurzelmann Mary, Romeika Jennifer, Sun Dong
Department of Neurosurgery, School of Medicine, Virginia Commonwealth University, Richmond, VA, USA.
Neural Regen Res. 2017 Jan;12(1):7-12. doi: 10.4103/1673-5374.198964.
Traumatic brain injury (TBI) is a major health problem worldwide. Following primary mechanical insults, a cascade of secondary injuries often leads to further neural tissue loss. Thus far there is no cure to rescue the damaged neural tissue. Current therapeutic strategies primarily target the secondary injuries focusing on neuroprotection and neuroregeneration. The neurotrophin brain-derived neurotrophic factor (BDNF) has significant effect in both aspects, promoting neuronal survival, synaptic plasticity and neurogenesis. Recently, the flavonoid 7,8-dihydroxyflavone (7,8-DHF), a small TrkB agonist that mimics BDNF function, has shown similar effects as BDNF in promoting neuronal survival and regeneration following TBI. Compared to BDNF, 7,8-DHF has a longer half-life and much smaller molecular size, capable of penetrating the blood-brain barrier, which makes it possible for non-invasive clinical application. In this review, we summarize functions of the BDNF/TrkB signaling pathway and studies examining the potential of BDNF and 7,8-DHF as a therapy for TBI.
创伤性脑损伤(TBI)是全球范围内的一个主要健康问题。在原发性机械性损伤之后,一系列继发性损伤常常导致进一步的神经组织损失。到目前为止,尚无治愈方法来挽救受损的神经组织。当前的治疗策略主要针对继发性损伤,侧重于神经保护和神经再生。神经营养因子脑源性神经营养因子(BDNF)在这两个方面都有显著作用,可促进神经元存活、突触可塑性和神经发生。最近,类黄酮7,8-二羟基黄酮(7,8-DHF),一种模拟BDNF功能的小分子TrkB激动剂,在TBI后促进神经元存活和再生方面显示出与BDNF相似的作用。与BDNF相比,7,8-DHF具有更长的半衰期和小得多的分子大小,能够穿透血脑屏障,这使得其无创临床应用成为可能。在本综述中,我们总结了BDNF/TrkB信号通路的功能以及研究BDNF和7,8-DHF作为TBI治疗方法的潜力。