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Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model

BACKGROUND: Age-related changes in the cerebrovasculature, including blood–brain barrier (BBB) disruption and vascular dementia, are emerging as potential risks for many neurodegenerative diseases. Therefore, the endothelial cells that constitute the cerebrovasculature may play key roles in preventi...

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Autores principales: Kim, Hyejeong, Noh, Minyoung, Zhang, Haiying, Kim, Yeomyeong, Park, Songyi, Park, Jeongeun, Kwon, Young-Guen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9893613/
https://www.ncbi.nlm.nih.gov/pubmed/36726154
http://dx.doi.org/10.1186/s12987-023-00410-x
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author Kim, Hyejeong
Noh, Minyoung
Zhang, Haiying
Kim, Yeomyeong
Park, Songyi
Park, Jeongeun
Kwon, Young-Guen
author_facet Kim, Hyejeong
Noh, Minyoung
Zhang, Haiying
Kim, Yeomyeong
Park, Songyi
Park, Jeongeun
Kwon, Young-Guen
author_sort Kim, Hyejeong
collection PubMed
description BACKGROUND: Age-related changes in the cerebrovasculature, including blood–brain barrier (BBB) disruption and vascular dementia, are emerging as potential risks for many neurodegenerative diseases. Therefore, the endothelial cells that constitute the cerebrovasculature may play key roles in preventing brain injury. Our previous study showed that CU06-1004, an endothelial cell dysfunction blocker, prevented vascular leakage, enhanced vascular integrity in ischemic reperfusion injury, and promoted the normalization of tumor vasculature. Here, we evaluated the effects of CU06-1004 on age-related cerebrovascular functional decline in the aged mouse brain. RESULTS: In this study, we investigated the protective effects of CU06-1004 against oxidative stress–induced damage in human brain microvascular endothelial cells (HBMECs). HBMECs were treated with hydrogen peroxide (H(2)O(2)) to establish an oxidative stress–induced model of cellular injury. Compared with H(2)O(2) treatment alone, pretreatment of HBMECs with CU06-1004 considerably reduced oxidative stress–induced cytotoxicity, reactive oxygen species generation, senescence-associated β-galactosidase activity, senescence marker expression, and the expression levels of inflammatory proteins. Based on the observed cytoprotective effects of CU06-1004 in HBMECs, we examined whether CU06-1004 displayed protective effects against cerebrovascular aging in mice. Long-term administration of CU06-1004 alleviated age-associated cerebral microvascular rarefaction and cerebrovascular senescence in the aged mouse brain. CU06-1004 supplementation also reduced the extravasation of plasma IgG by improving BBB integrity in the aged mouse brain, associated with reductions in neuronal injury. A series of behavioral tests also revealed improved motor and cognitive functions in aged mice that received long-term CU06-1004 administration. CONCLUSIONS: These findings suggest that CU06-1004 may represent a promising therapeutic approach for delaying age-related cerebrovascular impairment and improving cognitive function in old age. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00410-x.
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spelling pubmed-98936132023-02-03 Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model Kim, Hyejeong Noh, Minyoung Zhang, Haiying Kim, Yeomyeong Park, Songyi Park, Jeongeun Kwon, Young-Guen Fluids Barriers CNS Research BACKGROUND: Age-related changes in the cerebrovasculature, including blood–brain barrier (BBB) disruption and vascular dementia, are emerging as potential risks for many neurodegenerative diseases. Therefore, the endothelial cells that constitute the cerebrovasculature may play key roles in preventing brain injury. Our previous study showed that CU06-1004, an endothelial cell dysfunction blocker, prevented vascular leakage, enhanced vascular integrity in ischemic reperfusion injury, and promoted the normalization of tumor vasculature. Here, we evaluated the effects of CU06-1004 on age-related cerebrovascular functional decline in the aged mouse brain. RESULTS: In this study, we investigated the protective effects of CU06-1004 against oxidative stress–induced damage in human brain microvascular endothelial cells (HBMECs). HBMECs were treated with hydrogen peroxide (H(2)O(2)) to establish an oxidative stress–induced model of cellular injury. Compared with H(2)O(2) treatment alone, pretreatment of HBMECs with CU06-1004 considerably reduced oxidative stress–induced cytotoxicity, reactive oxygen species generation, senescence-associated β-galactosidase activity, senescence marker expression, and the expression levels of inflammatory proteins. Based on the observed cytoprotective effects of CU06-1004 in HBMECs, we examined whether CU06-1004 displayed protective effects against cerebrovascular aging in mice. Long-term administration of CU06-1004 alleviated age-associated cerebral microvascular rarefaction and cerebrovascular senescence in the aged mouse brain. CU06-1004 supplementation also reduced the extravasation of plasma IgG by improving BBB integrity in the aged mouse brain, associated with reductions in neuronal injury. A series of behavioral tests also revealed improved motor and cognitive functions in aged mice that received long-term CU06-1004 administration. CONCLUSIONS: These findings suggest that CU06-1004 may represent a promising therapeutic approach for delaying age-related cerebrovascular impairment and improving cognitive function in old age. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00410-x. BioMed Central 2023-02-01 /pmc/articles/PMC9893613/ /pubmed/36726154 http://dx.doi.org/10.1186/s12987-023-00410-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kim, Hyejeong
Noh, Minyoung
Zhang, Haiying
Kim, Yeomyeong
Park, Songyi
Park, Jeongeun
Kwon, Young-Guen
Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model
title Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model
title_full Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model
title_fullStr Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model
title_full_unstemmed Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model
title_short Long-term administration of CU06-1004 ameliorates cerebrovascular aging and BBB injury in aging mouse model
title_sort long-term administration of cu06-1004 ameliorates cerebrovascular aging and bbb injury in aging mouse model
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9893613/
https://www.ncbi.nlm.nih.gov/pubmed/36726154
http://dx.doi.org/10.1186/s12987-023-00410-x
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