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  1. Anuriti Aojula1,
  2. Hannah Botfield1,
  3. James Patterson McAllister2,
  4. Ana Maria Gonzalez1,
  5. Osama Abdullah3,
  6. Ann Logan1,
  7. Alexandra Sinclair1
  1. 1 University of Birmingham
  2. 2 Washington University
  3. 3 University of Utah


Background The use of diffusion tensor imaging (DTI) to examine Decorin's ability to prevent cerebral cytopathology in communicating hydrocephalus is yet to be fully investigated. Hence, this study aimed to determine whether Decorin treatment influences alterations in DTI parameters and cytopathology in an experimental model of the disease.

Method Accordingly, communicating hydrocephalus was induced by injecting Kaolin into the basal cisterns in 3-week old rats followed immediately by 14 days of continuous intraventricular delivery of either human recombinant Decorin (n=5) or vehicle (n=6). At 14-days post-kaolin, just prior to sacrifice, DTI was conducted. Myelin integrity (myelin basic protein), gliosis (glial fibrillary acidic protein, GFAP) and aquaporin-4 levels were evaluated by immunohistochemistry in the same seven cerebral structures analysed by DTI.

Results Decorin significantly decreased myelin damage in the caudal internal capsule and prevented caudal periventricular white matter oedema and astrogliosis. Furthermore, Decorin treatment prevented an increase in caudal periventricular white matter mean diffusivity (p=0.032) as well as caudal corpus callosum axial diffusivity (p=0.004) and radial diffusivity (p=0.034). Furthermore, DTI parameters correlated primarily with periventricular white matter GFAP and aquaporin-4 levels.

Conclusion Overall, these findings suggest that Decorin has the therapeutic potential to reduce white matter cytopathology in communicating hydrocephalus.

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