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Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions
The brain, demanding constant level of cholesterol, precisely controls its synthesis and homeostasis. The brain cholesterol pool is almost completely separated from the rest of the body by the functional blood-brain barrier (BBB). Only a part of cholesterol pool can be exchanged with the blood circu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504126/ https://www.ncbi.nlm.nih.gov/pubmed/28432486 http://dx.doi.org/10.1007/s11011-017-0015-3 |
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author | Czuba, Ewelina Steliga, Aleksandra Lietzau, Grażyna Kowiański, Przemysław |
author_facet | Czuba, Ewelina Steliga, Aleksandra Lietzau, Grażyna Kowiański, Przemysław |
author_sort | Czuba, Ewelina |
collection | PubMed |
description | The brain, demanding constant level of cholesterol, precisely controls its synthesis and homeostasis. The brain cholesterol pool is almost completely separated from the rest of the body by the functional blood-brain barrier (BBB). Only a part of cholesterol pool can be exchanged with the blood circulation in the form of the oxysterol metabolites such, as 27-hydroxycholesterol (27-OHC) and 24S–hydroxycholesterol (24S–OHC). Not only neurons but also blood vessels and neuroglia, constituting neurovascular unit (NVU), are crucial for the brain cholesterol metabolism and undergo precise regulation by numerous modulators, metabolites and signal molecules. In physiological conditions maintaining the optimal cholesterol concentration is important for the energetic metabolism, composition of cell membranes and myelination. However, a growing body of evidence indicates the consequences of the cholesterol homeostasis dysregulation in several pathophysiological processes. There is a causal relationship between hypercholesterolemia and 1) development of type 2 diabetes due to long-term high-fat diet consumption, 2) significance of the oxidative stress consequences for cerebral amyloid angiopathy and neurodegenerative diseases, 3) insulin resistance on progression of the neurodegenerative brain diseases. In this review, we summarize the current state of knowledge concerning the cholesterol influence upon functioning of the NVU under physiological and pathological conditions. |
format | Online Article Text |
id | pubmed-5504126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-55041262017-07-25 Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions Czuba, Ewelina Steliga, Aleksandra Lietzau, Grażyna Kowiański, Przemysław Metab Brain Dis Review Article The brain, demanding constant level of cholesterol, precisely controls its synthesis and homeostasis. The brain cholesterol pool is almost completely separated from the rest of the body by the functional blood-brain barrier (BBB). Only a part of cholesterol pool can be exchanged with the blood circulation in the form of the oxysterol metabolites such, as 27-hydroxycholesterol (27-OHC) and 24S–hydroxycholesterol (24S–OHC). Not only neurons but also blood vessels and neuroglia, constituting neurovascular unit (NVU), are crucial for the brain cholesterol metabolism and undergo precise regulation by numerous modulators, metabolites and signal molecules. In physiological conditions maintaining the optimal cholesterol concentration is important for the energetic metabolism, composition of cell membranes and myelination. However, a growing body of evidence indicates the consequences of the cholesterol homeostasis dysregulation in several pathophysiological processes. There is a causal relationship between hypercholesterolemia and 1) development of type 2 diabetes due to long-term high-fat diet consumption, 2) significance of the oxidative stress consequences for cerebral amyloid angiopathy and neurodegenerative diseases, 3) insulin resistance on progression of the neurodegenerative brain diseases. In this review, we summarize the current state of knowledge concerning the cholesterol influence upon functioning of the NVU under physiological and pathological conditions. Springer US 2017-04-21 2017 /pmc/articles/PMC5504126/ /pubmed/28432486 http://dx.doi.org/10.1007/s11011-017-0015-3 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Review Article Czuba, Ewelina Steliga, Aleksandra Lietzau, Grażyna Kowiański, Przemysław Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
title | Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
title_full | Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
title_fullStr | Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
title_full_unstemmed | Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
title_short | Cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
title_sort | cholesterol as a modifying agent of the neurovascular unit structure and function under physiological and pathological conditions |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5504126/ https://www.ncbi.nlm.nih.gov/pubmed/28432486 http://dx.doi.org/10.1007/s11011-017-0015-3 |
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