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Enhanced interstitial fluid drainage in the hippocampus of spontaneously hypertensive rats

Authors :
Bedussi, B.
Naessens, D.M.
Vos, J. de
Olde Engberink, R.
Wilhelmus, M.M.
Richard, E.
Hove, M. Ten
Vanbavel, E.
Bakker, E.N.T.P.
Bedussi, B.
Naessens, D.M.
Vos, J. de
Olde Engberink, R.
Wilhelmus, M.M.
Richard, E.
Hove, M. Ten
Vanbavel, E.
Bakker, E.N.T.P.
Source :
Scientific Reports; 2045-2322; 7; 744; ~Scientific Reports~~~~~2045-2322~~7~~744
Publication Year :
2017

Abstract

Contains fulltext : 175949.pdf (publisher's version ) (Open Access)<br />Hypertension is associated with cognitive decline and various forms of dementia, including Alzheimer's disease. In animal models of hypertension, many of Alzheimer's disease characteristics are recapitulated, including brain atrophy, cognitive decline, amyloid beta accumulation and blood brain barrier dysfunction. Removal of amyloid beta and other waste products depends in part on clearance via the brain interstitial fluid (ISF). Here we studied the impact of hypertension on ISF drainage, using spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto rats (WKY). At 8 months, high (500 kD) and low (3 kD) fluorescent molecular weight tracers released passively into the hippocampus showed a drastically enhanced spreading in SHR. Tracer spreading was inhomogeneous, with accumulation at ISF-CSF borders, around arteries, and towards the stratum lacunosum moleculare. These locations stained positively for the astrocyte marker GFAP, and aquaporin 4. Despite enhanced dispersion, clearance of tracers was not affected in SHR. In conclusion, these data indicate enhanced bulk flow of ISF in the hippocampus of hypertensive rats. ISF drains along astrocytes towards the cerebrospinal fluid compartment, which leads to sieving of high molecular weight solutes. Sieving may lead to a local increase in the concentration of waste products and potentially promotes the aggregation of amyloid beta.

Details

Database :
OAIster
Journal :
Scientific Reports; 2045-2322; 7; 744; ~Scientific Reports~~~~~2045-2322~~7~~744
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284019490
Document Type :
Electronic Resource