首页> 外文期刊>American Journal of Physiology >Traumatic brain injury-induced autoregulatory dysfunction and spreading depression-related neurovascular uncoupling: Pathomechanisms, perspectives, and therapeutic implications
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Traumatic brain injury-induced autoregulatory dysfunction and spreading depression-related neurovascular uncoupling: Pathomechanisms, perspectives, and therapeutic implications

机译:创伤性脑损伤诱导的自身调节功能障碍和传播抑郁相关的神经血管解偶联:土地机制,观点和治疗意义

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摘要

Traumatic brain injury (TBI) is a major health problem worldwide. In addition to its high mortality (35-40%), survivors are left with cognitive, behavioral, and communicative disabilities. While little can be done to reverse initial primary brain damage caused by trauma, the secondary injury of cerebral tissue due to cerebro-microvascular alterations and dysregulation of cerebral blood flow (CBF) is potentially preventable. This review focuses on functional, cellular, and molecular changes of autoregulatory function of CBF (with special focus on cerebrovascular myogenic response) that occur in cerebral circulation after TBI and explores the links between autoregulatory dysfunction, impaired myogenic response, microvascular impairment, and the development of secondary brain damage. We further provide a synthesized translational view of molecular and cellular mechanisms involved in cortical spreading depolarization-related neurovascular dysfunction, which could be targeted for the prevention or amelioration of TBI-induced secondary brain damage.
机译:创伤性脑损伤(TBI)是全世界的主要健康问题。除了其高死亡率(35-40%),幸存者留下了认知,行为和交际障碍。虽然较少可以逆转由创伤引起的初始初级脑损伤,但由于脑血流和脑血流(CBF)的脑组织的二次损伤潜在可预防。本综述重点介绍CBF(特别关注脑血管型脑血管源自遗传反应)的功能,细胞和分子变化,在TBI后发生,并探讨了自身疗失血功能障碍,肌原遗传学反应受损,微血管障碍和发展之间的联系继发性脑损伤。我们进一步提供了涉及皮质扩散相关的神经血管功能障碍的分子和细胞机制的合成平移观点,该功能障碍可用于预防或改善TBI诱导的继发性脑损伤。

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