4.7 Article

Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection

Journal

AGING CELL
Volume 14, Issue 3, Pages 400-408

Publisher

WILEY-BLACKWELL
DOI: 10.1111/acel.12315

Keywords

arteriole; dementia; microbleed; NADPH oxidase; oxidative stress; cognitive impairment

Funding

  1. American Heart Association
  2. National Center for Complementary and Alternative Medicine [R01-AT006526]
  3. National Institute on Aging [R01-AG038747, R01-NS056218, 1R01AG047879-01]
  4. Ellison Medical Foundation
  5. Hungarian National Science Research Fund (OTKA) [K 108444]
  6. grant: Developing Competitiveness of Universities in the South Transdanubian Region, 'Identification of new biomarkers' [SROP-4.2.2.A-11/1/KONV-2012-0017]
  7. grant: Developing Competitiveness of Universities in the South Transdanubian Region, 'Complex examination of neuropeptide' [SROP-4.2.2.A-11/1/KONV-2012-0024]
  8. Arkansas Claude Pepper Older Americans Independence Center at University of Arkansas Medical Center [P30 AG028718]

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Recent studies demonstrate that aging exacerbates hypertension-induced cognitive decline, but the specific age-related mechanisms remain elusive. Cerebral microhemorrhages (CMHs) are associated with rupture of small intracerebral vessels and are thought to progressively impair neuronal function. To determine whether aging exacerbates hypertension-induced CMHs young (3months) and aged (24months) mice were treated with angiotensin II plus L-NAME. We found that the same level of hypertension leads to significantly earlier onset and increased incidence of CMHs in aged mice than in young mice, as shown by neurological examination, gait analysis, and histological assessment of CMHs in serial brain sections. Hypertension-induced cerebrovascular oxidative stress and redox-sensitive activation of matrix metalloproteinases (MMPs) were increased in aging. Treatment of aged mice with resveratrol significantly attenuated hypertension-induced oxidative stress, inhibited vascular MMP activation, significantly delayed the onset, and reduced the incidence of CMHs. Collectively, aging promotes CMHs in mice likely by exacerbating hypertension-induced oxidative stress and MMP activation. Therapeutic strategies that reduce microvascular oxidative stress and MMP activation may be useful for the prevention of CMHs, protecting neurocognitive function in high-risk elderly patients.

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