Cerebral Amyloid Angiopathy: Amyloid Beta Accumulates in Putative Interstitial Fluid Drainage Pathways in Alzheimer's Disease

Am J Pathol. 1998 Sep;153(3):725-33. doi: 10.1016/s0002-9440(10)65616-7.

Abstract

Cerebral amyloid angiopathy in Alzheimer's disease is characterized by deposition of amyloid beta (Abeta) in cortical and leptomeningeal vessel walls. Although it has been suggested that Abeta is derived from vascular smooth muscle, deposition of Abeta is not seen in larger cerebral vessel walls nor in extracranial vessels. In the present study, we examine evidence for the hypothesis that Abeta is deposited in periarterial interstitial fluid drainage pathways of the brain in Alzheimer's disease and that this contributes significantly to cerebral amyloid angiopathy. There is firm evidence in animals for drainage of interstitial fluid from the brain to cervical lymph nodes along periarterial spaces; similar periarterial channels exist in humans. Biochemical study of 6 brains without Alzheimer's disease revealed a pool of soluble Abeta in the cortex. Histology and immunocytochemistry of 17 brains with Alzheimer's disease showed that Abeta accumulates five times more frequently around arteries than around veins, with selective involvement of smaller arteries. Initial deposits of Abeta occur at the periphery of arteries at the site of the putative interstitial fluid drainage pathways. These observations support the hypothesis that Abeta is deposited in periarterial interstitial fluid drainage pathways of the brain and contributes significantly to cerebral amyloid angiopathy in Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / metabolism*
  • Alzheimer Disease / pathology
  • Amyloid beta-Peptides / metabolism*
  • Cerebral Arteries / metabolism*
  • Cerebral Arteries / pathology
  • Cerebral Cortex / blood supply*
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Extracellular Space / metabolism*
  • Humans
  • Immunohistochemistry
  • Lymphatic System / metabolism*
  • Lymphatic System / pathology
  • Lymphatic System / ultrastructure
  • Meninges / blood supply
  • Meninges / metabolism
  • Meninges / pathology
  • Plaque, Amyloid / metabolism
  • Plaque, Amyloid / pathology
  • Plaque, Amyloid / ultrastructure
  • Veins / metabolism
  • Veins / pathology

Substances

  • Amyloid beta-Peptides