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Annals of Neurology· 2014Q1

Impairment of paravascular clearance pathways in the aging brain

Benjamin T. Kress, Jeffrey J. Iliff, Maosheng Xia, Minghuan Wang et al.

Short summary

Aging in mice significantly impairs the brain's waste removal system, reducing the clearance of amyloid-beta by 40% in old mice compared to young ones.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Aging mice show a 40% impairment in clearing injected amyloid-beta from brain tissue.
  • Reduced pulsatility of intracortical arterioles (27% reduction) accompanies age-related clearance decline.
  • Widespread loss of perivascular AQP4 polarization was observed in older mice.
  • CSF-ISF exchange efficiency dramatically declines with advancing age.

AI-generated from the title and abstract; the full text is not read.

Abstract

OBJECTIVE: In the brain, protein waste removal is partly performed by paravascular pathways that facilitate convective exchange of water and soluble contents between cerebrospinal fluid (CSF) and interstitial fluid (ISF). Several lines of evidence suggest that bulk flow drainage via the glymphatic system is driven by cerebrovascular pulsation, and is dependent on astroglial water channels that line paravascular CSF pathways. The objective of this study was to evaluate whether the efficiency of CSF-ISF exchange and interstitial solute clearance is impaired in the aging brain. METHODS: CSF-ISF exchange was evaluated by in vivo and ex vivo fluorescence microscopy and interstitial solute clearance was evaluated by radiotracer clearance assays in young (2-3 months), middle-aged (10-12 months), and old (18-20 months) wild-type mice. The relationship between age-related changes in the expression of the astrocytic water channel aquaporin-4 (AQP4) and changes in glymphatic pathway function was evaluated by immunofluorescence. RESULTS: Advancing age was associated with a dramatic decline in the efficiency of exchange between the subarachnoid CSF and the brain parenchyma. Relative to the young, clearance of intraparenchymally injected amyloid-β was impaired by 40% in the old mice. A 27% reduction in the vessel wall pulsatility of intracortical arterioles and widespread loss of perivascular AQP4 polarization along the penetrating arteries accompanied the decline in CSF-ISF exchange. INTERPRETATION: We propose that impaired glymphatic clearance contributes to cognitive decline among the elderly and may represent a novel therapeutic target for the treatment of neurodegenerative diseases associated with accumulation of misfolded protein aggregates.

The authors' abstract, as published at the source. Annals of Neurology, 2014 · DOI ↗

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Field: Cellular and Molecular Neuroscience

Cellular and Molecular NeuroscienceNeuroscience