4.6 Article

The impairment of intramural periarterial drainage in brain after subarachnoid hemorrhage

Journal

ACTA NEUROPATHOLOGICA COMMUNICATIONS
Volume 10, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s40478-022-01492-8

Keywords

Intramural periarterial drainage; Subarachnoid hemorrhage; Matrix metalloproteinase 9; Collagen type IV; Interstitial fluid; Cerebrospinal fluid

Categories

Funding

  1. Key Program of Beijing Natural Science Foundation
  2. National Natural Science Foundation of China [Z200025]
  3. Platform Construction Project of Peking University Health Science Center [81873818, 82171635]
  4. [BMU2021ZC011]

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This study found that Interstitial Periarterial Drainage (IPAD) system is impaired after subarachnoid hemorrhage (SAH), leading to the expansion of perivascular spaces and decreased clearance rate of interstitial fluid (ISF) in the brain. These findings are important for understanding the pathogenesis of cerebral amyloid angiopathy (CAA) and potential long-term complications following SAH.
Interstitial fluid (ISF) from brain drains along the basement membranes of capillaries and arteries as Intramural Periarterial Drainage (IPAD); failure of IPAD results in cerebral amyloid angiopathy (CAA). In this study, we test the hypothesis that IPAD fails after subarachnoid haemorrhage (SAH). The rat SAH model was established using endovascular perforation method. Fluorescence dyes with various molecular weights were injected into cisterna magna of rats, and the pattern of IPAD after SAH was detected using immunofluorescence staining, two-photon fluorescent microscope, transmission electron microscope and magnetic resonance imaging tracking techniques. Our results showed that fluorescence dyes entered the brain along a periarterial compartment and were cleared from brain along the basement membranes of the capillaries, with different patterns based on individual molecular weights. After SAH, there was significant impairment in the IPAD system: marked expansion of perivascular spaces, and ISF clearance rate was significantly decreased, associated with the apoptosis of endothelial cells, activation of astrocytes, over-expression of matrix metalloproteinase 9 and loss of collagen type IV. In conclusion, experimental SAH leads to a failure of IPAD, clinically significant for long term complications such as CAA, following SAH.

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