The Effect of Fibulin-5 on Hydrocephalus After Subarachnoid Hemorrhage in Mice

Int J Mol Sci. 2025 Aug 26;26(17):8259. doi: 10.3390/ijms26178259.

Abstract

Chronic hydrocephalus following aneurysmal subarachnoid hemorrhage (SAH) is a complication that can lead to deterioration in neurological status and cognitive impairment. Our recent clinical study reported that a high concentration of plasma fibulin-5 (FBLN5), a matricellular protein, was associated with the occurrence of chronic hydrocephalus after SAH. This study aimed to investigate whether and how FBLN5 was associated with hydrocephalus during acute to later phases of SAH in mice. C57BL/6 male mice underwent sham or filament perforation SAH modeling, and vehicle or two dosages (0.01 and 0.1 μg) of short or long recombinant FBLN5 (rFBLN5) were randomly administrated by an intracerebroventricular injection. Neurobehavioral tests, measurements of the degree of ventricular enlargement, Western blotting, and immunohistochemical staining were performed to evaluate hydrocephalus 24 and 48 h after SAH. After SAH, ventricular dilatation did not occur at 24 h but developed at 48 h, and both doses of long rFBLN5 with an arginine-glycine-aspartic acid domain suppressed ventricular dilatation at 48 h after SAH. Long rFBLN5 also decreased phosphorylated p38 in the brain parenchyma and prevented post-SAH increases in perivascular macrophages, as well as microglia activation in the brain parenchyma at 48 h after SAH. Although further research is required to clarify the detailed mechanism, this study demonstrated for the first time that exogenous administration of FBLN5 may have a protective effect against ventricular dilatation after experimental SAH.

Keywords: extracellular matrix protein; fibulin; hydrocephalus; perivascular macrophage; subarachnoid hemorrhage.

MeSH terms

  • Animals
  • Brain / drug effects
  • Brain / metabolism
  • Brain / pathology
  • Disease Models, Animal
  • Extracellular Matrix Proteins* / administration & dosage
  • Extracellular Matrix Proteins* / metabolism
  • Extracellular Matrix Proteins* / pharmacology
  • Hydrocephalus* / drug therapy
  • Hydrocephalus* / etiology
  • Hydrocephalus* / metabolism
  • Hydrocephalus* / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Recombinant Proteins / pharmacology
  • Subarachnoid Hemorrhage* / complications
  • Subarachnoid Hemorrhage* / drug therapy
  • Subarachnoid Hemorrhage* / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Extracellular Matrix Proteins
  • Recombinant Proteins
  • p38 Mitogen-Activated Protein Kinases

Grants and funding