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

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...

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Autores principales: Toth, Peter, Tarantini, Stefano, Springo, Zsolt, Tucsek, Zsuzsanna, Gautam, Tripti, Giles, Cory B, Wren, Jonathan D, Koller, Akos, Sonntag, William E, Csiszar, Anna, Ungvari, Zoltan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406669/
https://www.ncbi.nlm.nih.gov/pubmed/25677910
http://dx.doi.org/10.1111/acel.12315
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author Toth, Peter
Tarantini, Stefano
Springo, Zsolt
Tucsek, Zsuzsanna
Gautam, Tripti
Giles, Cory B
Wren, Jonathan D
Koller, Akos
Sonntag, William E
Csiszar, Anna
Ungvari, Zoltan
author_facet Toth, Peter
Tarantini, Stefano
Springo, Zsolt
Tucsek, Zsuzsanna
Gautam, Tripti
Giles, Cory B
Wren, Jonathan D
Koller, Akos
Sonntag, William E
Csiszar, Anna
Ungvari, Zoltan
author_sort Toth, Peter
collection PubMed
description 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 (3 months) and aged (24 months) 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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spelling pubmed-44066692015-06-01 Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection Toth, Peter Tarantini, Stefano Springo, Zsolt Tucsek, Zsuzsanna Gautam, Tripti Giles, Cory B Wren, Jonathan D Koller, Akos Sonntag, William E Csiszar, Anna Ungvari, Zoltan Aging Cell Original Articles 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 (3 months) and aged (24 months) 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. BlackWell Publishing Ltd 2015-06 2015-02-09 /pmc/articles/PMC4406669/ /pubmed/25677910 http://dx.doi.org/10.1111/acel.12315 Text en © 2015 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Toth, Peter
Tarantini, Stefano
Springo, Zsolt
Tucsek, Zsuzsanna
Gautam, Tripti
Giles, Cory B
Wren, Jonathan D
Koller, Akos
Sonntag, William E
Csiszar, Anna
Ungvari, Zoltan
Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
title Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
title_full Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
title_fullStr Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
title_full_unstemmed Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
title_short Aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
title_sort aging exacerbates hypertension-induced cerebral microhemorrhages in mice: role of resveratrol treatment in vasoprotection
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4406669/
https://www.ncbi.nlm.nih.gov/pubmed/25677910
http://dx.doi.org/10.1111/acel.12315
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