Cargando…

Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation

Aging is a major risk factor for cognitive impairment. Aerobic exercise benefits brain function and may promote cognitive health in older adults. However, underlying biological mechanisms across cerebral gray and white matter are poorly understood. Selective vulnerability of the white matter to smal...

Descripción completa

Detalles Bibliográficos
Autores principales: Shin, Paul, Pian, Qi, Ishikawa, Hidehiro, Hamanaka, Gen, Mandeville, Emiri T, Guo, Shuzhen, Fu, Buyin, Alfadhel, Mohammed, Allu, Srinivasa Rao, Şencan-Eğilmez, Ikbal, Li, Baoqiang, Ran, Chongzhao, Vinogradov, Sergei A, Ayata, Cenk, Lo, Eng, Arai, Ken, Devor, Anna, Sakadžić, Sava
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319437/
https://www.ncbi.nlm.nih.gov/pubmed/37402178
http://dx.doi.org/10.7554/eLife.86329
_version_ 1785068251517026304
author Shin, Paul
Pian, Qi
Ishikawa, Hidehiro
Hamanaka, Gen
Mandeville, Emiri T
Guo, Shuzhen
Fu, Buyin
Alfadhel, Mohammed
Allu, Srinivasa Rao
Şencan-Eğilmez, Ikbal
Li, Baoqiang
Ran, Chongzhao
Vinogradov, Sergei A
Ayata, Cenk
Lo, Eng
Arai, Ken
Devor, Anna
Sakadžić, Sava
author_facet Shin, Paul
Pian, Qi
Ishikawa, Hidehiro
Hamanaka, Gen
Mandeville, Emiri T
Guo, Shuzhen
Fu, Buyin
Alfadhel, Mohammed
Allu, Srinivasa Rao
Şencan-Eğilmez, Ikbal
Li, Baoqiang
Ran, Chongzhao
Vinogradov, Sergei A
Ayata, Cenk
Lo, Eng
Arai, Ken
Devor, Anna
Sakadžić, Sava
author_sort Shin, Paul
collection PubMed
description Aging is a major risk factor for cognitive impairment. Aerobic exercise benefits brain function and may promote cognitive health in older adults. However, underlying biological mechanisms across cerebral gray and white matter are poorly understood. Selective vulnerability of the white matter to small vessel disease and a link between white matter health and cognitive function suggests a potential role for responses in deep cerebral microcirculation. Here, we tested whether aerobic exercise modulates cerebral microcirculatory changes induced by aging. To this end, we carried out a comprehensive quantitative examination of changes in cerebral microvascular physiology in cortical gray and subcortical white matter in mice (3–6 vs. 19–21 months old), and asked whether and how exercise may rescue age-induced deficits. In the sedentary group, aging caused a more severe decline in cerebral microvascular perfusion and oxygenation in deep (infragranular) cortical layers and subcortical white matter compared with superficial (supragranular) cortical layers. Five months of voluntary aerobic exercise partly renormalized microvascular perfusion and oxygenation in aged mice in a depth-dependent manner, and brought these spatial distributions closer to those of young adult sedentary mice. These microcirculatory effects were accompanied by an improvement in cognitive function. Our work demonstrates the selective vulnerability of the deep cortex and subcortical white matter to aging-induced decline in microcirculation, as well as the responsiveness of these regions to aerobic exercise.
format Online
Article
Text
id pubmed-10319437
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-103194372023-07-05 Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation Shin, Paul Pian, Qi Ishikawa, Hidehiro Hamanaka, Gen Mandeville, Emiri T Guo, Shuzhen Fu, Buyin Alfadhel, Mohammed Allu, Srinivasa Rao Şencan-Eğilmez, Ikbal Li, Baoqiang Ran, Chongzhao Vinogradov, Sergei A Ayata, Cenk Lo, Eng Arai, Ken Devor, Anna Sakadžić, Sava eLife Neuroscience Aging is a major risk factor for cognitive impairment. Aerobic exercise benefits brain function and may promote cognitive health in older adults. However, underlying biological mechanisms across cerebral gray and white matter are poorly understood. Selective vulnerability of the white matter to small vessel disease and a link between white matter health and cognitive function suggests a potential role for responses in deep cerebral microcirculation. Here, we tested whether aerobic exercise modulates cerebral microcirculatory changes induced by aging. To this end, we carried out a comprehensive quantitative examination of changes in cerebral microvascular physiology in cortical gray and subcortical white matter in mice (3–6 vs. 19–21 months old), and asked whether and how exercise may rescue age-induced deficits. In the sedentary group, aging caused a more severe decline in cerebral microvascular perfusion and oxygenation in deep (infragranular) cortical layers and subcortical white matter compared with superficial (supragranular) cortical layers. Five months of voluntary aerobic exercise partly renormalized microvascular perfusion and oxygenation in aged mice in a depth-dependent manner, and brought these spatial distributions closer to those of young adult sedentary mice. These microcirculatory effects were accompanied by an improvement in cognitive function. Our work demonstrates the selective vulnerability of the deep cortex and subcortical white matter to aging-induced decline in microcirculation, as well as the responsiveness of these regions to aerobic exercise. eLife Sciences Publications, Ltd 2023-07-04 /pmc/articles/PMC10319437/ /pubmed/37402178 http://dx.doi.org/10.7554/eLife.86329 Text en © 2023, Shin et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Shin, Paul
Pian, Qi
Ishikawa, Hidehiro
Hamanaka, Gen
Mandeville, Emiri T
Guo, Shuzhen
Fu, Buyin
Alfadhel, Mohammed
Allu, Srinivasa Rao
Şencan-Eğilmez, Ikbal
Li, Baoqiang
Ran, Chongzhao
Vinogradov, Sergei A
Ayata, Cenk
Lo, Eng
Arai, Ken
Devor, Anna
Sakadžić, Sava
Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
title Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
title_full Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
title_fullStr Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
title_full_unstemmed Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
title_short Aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
title_sort aerobic exercise reverses aging-induced depth-dependent decline in cerebral microcirculation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10319437/
https://www.ncbi.nlm.nih.gov/pubmed/37402178
http://dx.doi.org/10.7554/eLife.86329
work_keys_str_mv AT shinpaul aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT pianqi aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT ishikawahidehiro aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT hamanakagen aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT mandevilleemirit aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT guoshuzhen aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT fubuyin aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT alfadhelmohammed aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT allusrinivasarao aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT sencanegilmezikbal aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT libaoqiang aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT ranchongzhao aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT vinogradovsergeia aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT ayatacenk aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT loeng aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT araiken aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT devoranna aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation
AT sakadzicsava aerobicexercisereversesaginginduceddepthdependentdeclineincerebralmicrocirculation