AI Article Synopsis

  • Subarachnoid hemorrhage (SAH) is a critical neurological condition with high risks of serious complications and death, primarily due to early brain injury (EBI) and delayed cerebral ischemia (DCI) linked to thrombin’s role in secondary damage.
  • Thrombin also disrupts cerebrospinal fluid (CSF) circulation, leading to various complications such as cerebral edema, hydrocephalus, cognitive issues, and depressive symptoms following an SAH event.
  • This review emphasizes thrombin's impact on the glymphatic-meningeal lymphatic system and discusses current treatment strategies aimed at reducing brain injury and improving recovery outcomes after SAH.

Article Abstract

Subarachnoid hemorrhage (SAH) is a severe neurological condition characterized by high morbidity and mortality. The unfavorable prognosis of SAH is closely associated with early brain injury (EBI) and delayed cerebral ischemia (DCI), wherein thrombin plays a role as part of the secondary injury components following hemorrhage in these two pathological processes. Additionally, thrombin contributes to disruptions in the circulation of cerebrospinal fluid (CSF), thereby giving rise to a spectrum of sequelae following SAH, including cerebral edema, hydrocephalus, cognitive impairments, and depressive symptoms. This review aims to provide a comprehensive understanding of the pathological role of thrombin in EBI, DCI, and CSF circulation following SAH, with a specific focus on its impact on the glymphatic-meningeal lymphatic system-a crucial mechanism for waste clearance and neurohomeostatic regulation. Additionally, this review offers an overview of current pharmacological interventions and treatment modalities targeting pathogenic mechanisms, aiming to mitigate brain injury and promote neurological recovery post-SAH.

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Source
http://dx.doi.org/10.1016/j.expneurol.2024.115036DOI Listing

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