Medical University of South Carolina, 173 Ashley Ave, Charleston, SC 29424, USA.
College of Charleston, 66 George Street, Charleston, SC 29424, USA.
Neural Plast. 2022 Mar 2;2022:3889300. doi: 10.1155/2022/3889300. eCollection 2022.
Ischemic stroke and traumatic brain injury (TBI) are among the leading causes of death and disability worldwide with impairments ranging from mild to severe. Many therapies are aimed at improving functional and cognitive recovery by targeting neural repair but have encountered issues involving efficacy and drug delivery. As a result, therapeutic options for patients are sparse. Neurotrophic factors are one of the key mediators of neural plasticity and functional recovery. Neurotrophic factors such as brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF) serve as potential therapeutic options to increase neural repair and recovery as they promote neuroprotection and regeneration. BDNF and NGF have demonstrated the ability to improve functional recovery in preclinical and to a lesser extent clinical studies. Direct and indirect methods to increase levels of neurotrophic factors in animal models have been successful in improving postinjury outcome measures. However, the translation of these studies into clinical trials has been limited. Preclinical experiments have largely failed to result in significant impacts in clinical research. This review will focus on the administration of these neurotrophic factors in preclinical and clinical stroke and TBI and the challenges in translating these therapies from the bench to the clinic.
缺血性中风和创伤性脑损伤 (TBI) 是全球范围内导致死亡和残疾的主要原因之一,其损伤程度从轻到重不等。许多治疗方法旨在通过靶向神经修复来改善功能和认知恢复,但在疗效和药物输送方面遇到了问题。因此,患者的治疗选择很少。神经营养因子是神经可塑性和功能恢复的关键介质之一。神经营养因子,如脑源性神经营养因子 (BDNF) 和神经生长因子 (NGF),作为潜在的治疗选择,可以通过促进神经保护和再生来增加神经修复和恢复。BDNF 和 NGF 已被证明能够改善临床前和在较小程度上的临床研究中的功能恢复。在动物模型中增加神经营养因子水平的直接和间接方法已成功改善损伤后结果测量。然而,将这些研究转化为临床试验受到了限制。临床前实验在很大程度上未能在临床研究中产生重大影响。这篇综述将重点介绍这些神经营养因子在临床前和临床中风和 TBI 中的应用,以及将这些治疗方法从实验室转化为临床的挑战。