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Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke
Neurovascular units (NVUs) are basic functional units in the central nervous system and include neurons, astrocytes and vascular compartments. Ischemic stroke triggers not only neuronal damage, but also dissonance of intercellular crosstalk within the NVU. Stroke is sexually dimorphic, but the sex-a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012443/ https://www.ncbi.nlm.nih.gov/pubmed/35431804 http://dx.doi.org/10.3389/fnmol.2022.860959 |
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author | Tang, Tianchi Hu, Libin Liu, Yang Fu, Xiongjie Li, Jianru Yan, Feng Cao, Shenglong Chen, Gao |
author_facet | Tang, Tianchi Hu, Libin Liu, Yang Fu, Xiongjie Li, Jianru Yan, Feng Cao, Shenglong Chen, Gao |
author_sort | Tang, Tianchi |
collection | PubMed |
description | Neurovascular units (NVUs) are basic functional units in the central nervous system and include neurons, astrocytes and vascular compartments. Ischemic stroke triggers not only neuronal damage, but also dissonance of intercellular crosstalk within the NVU. Stroke is sexually dimorphic, but the sex-associated differences involved in stroke-induced neurovascular dysfunction are studied in a limited extend. Preclinical studies have found that in rodent models of stroke, females have less neuronal loss, stronger repairing potential of astrocytes and more stable vascular conjunction; these properties are highly related to the cerebroprotective effects of female hormones. However, in humans, these research findings may be applicable only to premenopausal stroke patients. Women who have had a stroke usually have poorer outcomes compared to men, and because stoke is age-related, hormone replacement therapy for postmenopausal women may exacerbate stroke symptoms, which contradicts the findings of most preclinical studies. This stark contrast between clinical and laboratory findings suggests that understanding of neurovascular differences between the sexes is limited. Actually, apart from gonadal hormones, differences in neuroinflammation as well as genetics and epigenetics promote the sexual dimorphism of NVU functions. In this review, we summarize the confirmed sex-associated differences in NVUs during ischemic stroke and the possible contributing mechanisms. We also describe the gap between clinical and preclinical studies in terms of sexual dimorphism. |
format | Online Article Text |
id | pubmed-9012443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90124432022-04-16 Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke Tang, Tianchi Hu, Libin Liu, Yang Fu, Xiongjie Li, Jianru Yan, Feng Cao, Shenglong Chen, Gao Front Mol Neurosci Neuroscience Neurovascular units (NVUs) are basic functional units in the central nervous system and include neurons, astrocytes and vascular compartments. Ischemic stroke triggers not only neuronal damage, but also dissonance of intercellular crosstalk within the NVU. Stroke is sexually dimorphic, but the sex-associated differences involved in stroke-induced neurovascular dysfunction are studied in a limited extend. Preclinical studies have found that in rodent models of stroke, females have less neuronal loss, stronger repairing potential of astrocytes and more stable vascular conjunction; these properties are highly related to the cerebroprotective effects of female hormones. However, in humans, these research findings may be applicable only to premenopausal stroke patients. Women who have had a stroke usually have poorer outcomes compared to men, and because stoke is age-related, hormone replacement therapy for postmenopausal women may exacerbate stroke symptoms, which contradicts the findings of most preclinical studies. This stark contrast between clinical and laboratory findings suggests that understanding of neurovascular differences between the sexes is limited. Actually, apart from gonadal hormones, differences in neuroinflammation as well as genetics and epigenetics promote the sexual dimorphism of NVU functions. In this review, we summarize the confirmed sex-associated differences in NVUs during ischemic stroke and the possible contributing mechanisms. We also describe the gap between clinical and preclinical studies in terms of sexual dimorphism. Frontiers Media S.A. 2022-04-01 /pmc/articles/PMC9012443/ /pubmed/35431804 http://dx.doi.org/10.3389/fnmol.2022.860959 Text en Copyright © 2022 Tang, Hu, Liu, Fu, Li, Yan, Cao and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Tang, Tianchi Hu, Libin Liu, Yang Fu, Xiongjie Li, Jianru Yan, Feng Cao, Shenglong Chen, Gao Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke |
title | Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke |
title_full | Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke |
title_fullStr | Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke |
title_full_unstemmed | Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke |
title_short | Sex-Associated Differences in Neurovascular Dysfunction During Ischemic Stroke |
title_sort | sex-associated differences in neurovascular dysfunction during ischemic stroke |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012443/ https://www.ncbi.nlm.nih.gov/pubmed/35431804 http://dx.doi.org/10.3389/fnmol.2022.860959 |
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