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VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s Disease Mice
Vascular dysfunction plays a critical role in the development of Alzheimer’s disease. Cerebral blood flow reductions of 10% to 25% present early in disease pathogenesis. Vascular Endothelial Growth Factor-A (VEGF-A) drives angiogenesis, which typically addresses blood flow reductions and global hypo...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298729/ https://www.ncbi.nlm.nih.gov/pubmed/35873789 http://dx.doi.org/10.1177/26331055221109254 |
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author | Ali, Muhammad Bracko, Oliver |
author_facet | Ali, Muhammad Bracko, Oliver |
author_sort | Ali, Muhammad |
collection | PubMed |
description | Vascular dysfunction plays a critical role in the development of Alzheimer’s disease. Cerebral blood flow reductions of 10% to 25% present early in disease pathogenesis. Vascular Endothelial Growth Factor-A (VEGF-A) drives angiogenesis, which typically addresses blood flow reductions and global hypoxia. However, recent evidence suggests aberrant VEGF-A signaling in Alzheimer’s disease may undermine its physiological angiogenic function. Instead of improving cerebral blood flow, VEGF-A contributes to brain capillary stalls and blood flow reductions, likely accelerating cognitive decline. In this commentary, we explore the evidence for pathological VEGF signaling in Alzheimer’s disease, and discuss its implications for disease therapy. |
format | Online Article Text |
id | pubmed-9298729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-92987292022-07-21 VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s Disease Mice Ali, Muhammad Bracko, Oliver Neurosci Insights Commentary Vascular dysfunction plays a critical role in the development of Alzheimer’s disease. Cerebral blood flow reductions of 10% to 25% present early in disease pathogenesis. Vascular Endothelial Growth Factor-A (VEGF-A) drives angiogenesis, which typically addresses blood flow reductions and global hypoxia. However, recent evidence suggests aberrant VEGF-A signaling in Alzheimer’s disease may undermine its physiological angiogenic function. Instead of improving cerebral blood flow, VEGF-A contributes to brain capillary stalls and blood flow reductions, likely accelerating cognitive decline. In this commentary, we explore the evidence for pathological VEGF signaling in Alzheimer’s disease, and discuss its implications for disease therapy. SAGE Publications 2022-07-04 /pmc/articles/PMC9298729/ /pubmed/35873789 http://dx.doi.org/10.1177/26331055221109254 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Commentary Ali, Muhammad Bracko, Oliver VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s Disease Mice |
title | VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s
Disease Mice |
title_full | VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s
Disease Mice |
title_fullStr | VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s
Disease Mice |
title_full_unstemmed | VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s
Disease Mice |
title_short | VEGF Paradoxically Reduces Cerebral Blood Flow in Alzheimer’s
Disease Mice |
title_sort | vegf paradoxically reduces cerebral blood flow in alzheimer’s
disease mice |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9298729/ https://www.ncbi.nlm.nih.gov/pubmed/35873789 http://dx.doi.org/10.1177/26331055221109254 |
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