Compromised microvascular oxygen delivery increases brain tissue vulnerability with age
Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO 2 with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake a...
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Published in | Scientific reports Vol. 8; no. 1; pp. 8219 - 17 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Nature Publishing Group UK
29.05.2018
Nature Publishing Group |
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Abstract | Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO
2
with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake aged mice, we demonstrate decreased arteriolar and tissue pO
2
with age. These changes are exacerbated after middle-age. We further uncovered evidence of the presence of hypoxic micro-pockets in the cortex of awake old mice. Our data suggests that from young to middle-age, a well-regulated capillary oxygen supply maintains the oxygen availability in cerebral tissue, despite decreased tissue pO
2
next to arterioles. After middle-age, due to decreased hematocrit, reduced capillary density and higher capillary transit time heterogeneity, the capillary network fails to compensate for larger decreases in arterial pO
2
. The substantial decrease in brain tissue pO
2
, and the presence of hypoxic micro-pockets after middle-age are of significant importance, as these factors may be related to cognitive decline in elderly people. |
---|---|
AbstractList | Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO
2
with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake aged mice, we demonstrate decreased arteriolar and tissue pO
2
with age. These changes are exacerbated after middle-age. We further uncovered evidence of the presence of hypoxic micro-pockets in the cortex of awake old mice. Our data suggests that from young to middle-age, a well-regulated capillary oxygen supply maintains the oxygen availability in cerebral tissue, despite decreased tissue pO
2
next to arterioles. After middle-age, due to decreased hematocrit, reduced capillary density and higher capillary transit time heterogeneity, the capillary network fails to compensate for larger decreases in arterial pO
2
. The substantial decrease in brain tissue pO
2
, and the presence of hypoxic micro-pockets after middle-age are of significant importance, as these factors may be related to cognitive decline in elderly people. Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO2 with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake aged mice, we demonstrate decreased arteriolar and tissue pO2 with age. These changes are exacerbated after middle-age. We further uncovered evidence of the presence of hypoxic micro-pockets in the cortex of awake old mice. Our data suggests that from young to middle-age, a well-regulated capillary oxygen supply maintains the oxygen availability in cerebral tissue, despite decreased tissue pO2 next to arterioles. After middle-age, due to decreased hematocrit, reduced capillary density and higher capillary transit time heterogeneity, the capillary network fails to compensate for larger decreases in arterial pO2. The substantial decrease in brain tissue pO2, and the presence of hypoxic micro-pockets after middle-age are of significant importance, as these factors may be related to cognitive decline in elderly people.Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO2 with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake aged mice, we demonstrate decreased arteriolar and tissue pO2 with age. These changes are exacerbated after middle-age. We further uncovered evidence of the presence of hypoxic micro-pockets in the cortex of awake old mice. Our data suggests that from young to middle-age, a well-regulated capillary oxygen supply maintains the oxygen availability in cerebral tissue, despite decreased tissue pO2 next to arterioles. After middle-age, due to decreased hematocrit, reduced capillary density and higher capillary transit time heterogeneity, the capillary network fails to compensate for larger decreases in arterial pO2. The substantial decrease in brain tissue pO2, and the presence of hypoxic micro-pockets after middle-age are of significant importance, as these factors may be related to cognitive decline in elderly people. Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO2 with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake aged mice, we demonstrate decreased arteriolar and tissue pO2 with age. These changes are exacerbated after middle-age. We further uncovered evidence of the presence of hypoxic micro-pockets in the cortex of awake old mice. Our data suggests that from young to middle-age, a well-regulated capillary oxygen supply maintains the oxygen availability in cerebral tissue, despite decreased tissue pO2 next to arterioles. After middle-age, due to decreased hematocrit, reduced capillary density and higher capillary transit time heterogeneity, the capillary network fails to compensate for larger decreases in arterial pO2. The substantial decrease in brain tissue pO2, and the presence of hypoxic micro-pockets after middle-age are of significant importance, as these factors may be related to cognitive decline in elderly people. Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO with age. Using a detailed investigation of the age-related changes in cerebral tissue oxygenation in the barrel cortex of healthy, awake aged mice, we demonstrate decreased arteriolar and tissue pO with age. These changes are exacerbated after middle-age. We further uncovered evidence of the presence of hypoxic micro-pockets in the cortex of awake old mice. Our data suggests that from young to middle-age, a well-regulated capillary oxygen supply maintains the oxygen availability in cerebral tissue, despite decreased tissue pO next to arterioles. After middle-age, due to decreased hematocrit, reduced capillary density and higher capillary transit time heterogeneity, the capillary network fails to compensate for larger decreases in arterial pO . The substantial decrease in brain tissue pO , and the presence of hypoxic micro-pockets after middle-age are of significant importance, as these factors may be related to cognitive decline in elderly people. |
ArticleNumber | 8219 |
Author | Kakkar, Ashok Moeini, Mohammad Damseh, Rafat Lesage, Frédéric Lu, Xuecong Bélanger, Samuel Avti, Pramod K. Picard, Frédéric Boas, David |
Author_xml | – sequence: 1 givenname: Mohammad surname: Moeini fullname: Moeini, Mohammad organization: Biomedical Engineering Institute, École Polytechnique de Montréal, Research Center of Montreal Heart Institute, Department of Chemistry, McGill University – sequence: 2 givenname: Xuecong surname: Lu fullname: Lu, Xuecong organization: Biomedical Engineering Institute, École Polytechnique de Montréal, Research Center of Montreal Heart Institute – sequence: 3 givenname: Pramod K. surname: Avti fullname: Avti, Pramod K. organization: Biomedical Engineering Institute, École Polytechnique de Montréal, Research Center of Montreal Heart Institute, Department of Biophysics, Postgraduate Institute of Medical Education and Research – sequence: 4 givenname: Rafat surname: Damseh fullname: Damseh, Rafat organization: Biomedical Engineering Institute, École Polytechnique de Montréal – sequence: 5 givenname: Samuel surname: Bélanger fullname: Bélanger, Samuel organization: Biomedical Engineering Institute, École Polytechnique de Montréal, Research Center of Montreal Heart Institute – sequence: 6 givenname: Frédéric surname: Picard fullname: Picard, Frédéric organization: Centre de Recherche de l’Institut Universitaire de Cardiologie et Pneumologie de Québec (IUCPQ) – sequence: 7 givenname: David surname: Boas fullname: Boas, David organization: Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Biomedical Engineering Department, College of Engineering, Boston University – sequence: 8 givenname: Ashok surname: Kakkar fullname: Kakkar, Ashok organization: Department of Chemistry, McGill University – sequence: 9 givenname: Frédéric surname: Lesage fullname: Lesage, Frédéric email: frederic.lesage@polymtl.ca organization: Biomedical Engineering Institute, École Polytechnique de Montréal, Research Center of Montreal Heart Institute |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29844478$$D View this record in MEDLINE/PubMed |
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Snippet | Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO... Despite the possible role of impaired cerebral tissue oxygenation in age-related cognition decline, much is still unknown about the changes in brain tissue pO2... |
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Title | Compromised microvascular oxygen delivery increases brain tissue vulnerability with age |
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