Department of Pharmaceutical Sciences, Texas Tech University Health Sciences Center, Amarillo, TX 79106, USA.
Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Int J Mol Sci. 2020 Apr 14;21(8):2721. doi: 10.3390/ijms21082721.
Traumatic brain injury (TBI) is among the most pressing global health issues and prevalent causes of cerebrovascular and neurological disorders all over the world. In addition to the brain injury, TBI may also alter the systemic immune response. Thus, TBI patients become vulnerable to infections, have worse neurological outcomes, and exhibit a higher rate of mortality and morbidity. It is well established that brain injury leads to impairments of the blood-brain barrier (BBB) integrity and function, contributing to the loss of neural tissue and affecting the response to neuroprotective drugs. Thus, stabilization/protection of the BBB after TBI could be a promising strategy to limit neuronal inflammation, secondary brain damage, and acute neurodegeneration. Herein, we present a review highlighting the significant post-traumatic effects of TBI on the cerebrovascular system. These include the loss of BBB integrity and selective permeability, impact on BBB transport mechanisms, post-traumatic cerebral edema formation, and significant pathophysiological factors that may further exacerbate post-traumatic BBB dysfunctions. Furthermore, we discuss the post-traumatic impacts of chronic smoking, which has been recently shown to act as a premorbid condition that impairs post-TBI recovery. Indeed, understanding the underlying molecular mechanisms associated with TBI damage is essential to better understand the pathogenesis and progression of post-traumatic secondary brain injury and the development of targeted treatments to improve outcomes and speed up the recovery process. Therapies aimed at restoring/protecting the BBB may reduce the post-traumatic burden of TBI by minimizing the impairment of brain homeostasis and help to restore an optimal microenvironment to support neuronal repair.
创伤性脑损伤(TBI)是全球最紧迫的健康问题之一,也是全世界脑血管和神经紊乱的主要原因。除了脑损伤,TBI 还可能改变全身免疫反应。因此,TBI 患者容易感染,神经预后较差,死亡率和发病率更高。众所周知,脑损伤导致血脑屏障(BBB)完整性和功能受损,导致神经组织丧失,并影响神经保护药物的反应。因此,TBI 后 BBB 的稳定/保护可能是限制神经元炎症、继发性脑损伤和急性神经退行性变的有前途的策略。在此,我们综述了 TBI 对脑血管系统的重要创伤后影响。这些影响包括 BBB 完整性和选择性通透性的丧失、对 BBB 转运机制的影响、创伤后脑水肿的形成以及可能进一步加重创伤后 BBB 功能障碍的重要病理生理因素。此外,我们还讨论了慢性吸烟的创伤后影响,最近的研究表明,慢性吸烟是一种发病前的状况,会损害 TBI 后的恢复。事实上,了解与 TBI 损伤相关的潜在分子机制对于更好地理解创伤后继发性脑损伤的发病机制和进展以及开发靶向治疗以改善预后和加速恢复过程至关重要。旨在恢复/保护 BBB 的治疗方法可以通过最小化对脑内稳态的损害来减轻 TBI 的创伤后负担,并有助于恢复支持神经元修复的最佳微环境。