Susceptibility to capillary plugging can predict brain region specific vessel loss with aging

J Cereb Blood Flow Metab. 2020 Dec;40(12):2475-2490. doi: 10.1177/0271678X19895245. Epub 2020 Jan 5.

Abstract

Vessel loss in the aging brain is commonly reported, yet important questions remain concerning whether there are regional vulnerabilities and what mechanisms could account for these regional differences, if they exist. Here we imaged and quantified vessel length, tortuosity and width in 15 brain regions in young adult and aged mice. Our data indicate that vessel loss was most pronounced in white matter followed by cortical, then subcortical grey matter regions, while some regions (visual cortex, amygdala, thalamus) showed no decline with aging. Regions supplied by the anterior cerebral artery were more vulnerable to loss than those supplied by middle or posterior cerebral arteries. Vessel width and tortuosity generally increased with age but neither reliably predicted regional vessel loss. Since capillaries are naturally prone to plugging and prolonged obstructions often lead to vessel pruning, we hypothesized that regional susceptibilities to plugging could help predict vessel loss. By mapping the distribution of microsphere-induced capillary obstructions, we discovered that regions with a higher density of persistent obstructions were more likely to show vessel loss with aging and vice versa. These findings indicate that age-related vessel loss is region specific and can be explained, at least partially, by regional susceptibilities to capillary plugging.

Keywords: Microcirculation; aging; capillary rarefaction; cerebral blood flow; vascular dementia; white matter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / physiology
  • Animals
  • Brain / blood supply*
  • Brain / pathology
  • Brain Ischemia / pathology*
  • Brain Ischemia / physiopathology
  • Capillaries / growth & development
  • Capillaries / pathology*
  • Capillaries / physiopathology
  • Cerebral Cortex / blood supply
  • Cerebral Cortex / pathology*
  • Cerebral Cortex / physiopathology
  • Cerebrovascular Circulation / physiology
  • Dementia, Vascular / etiology
  • Dementia, Vascular / pathology*
  • Dementia, Vascular / physiopathology
  • Female
  • Gray Matter / blood supply
  • Gray Matter / pathology
  • Gray Matter / physiopathology
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Microvascular Rarefaction / physiopathology*
  • Predictive Value of Tests
  • White Matter / blood supply
  • White Matter / pathology
  • White Matter / physiopathology

Grants and funding