Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease
The aim was to study the molecular mechanisms of the violation of the structural and functional integrity ofthe blood-brain barrier in chronic neurodegeneration of the Alzheimer’s type associated with the development of cerebral angiopathy.Materials and methods. The transgenic model of Alzheimer’s d...
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Language: | English |
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Siberian State Medical University (Tomsk)
2021-01-01
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Series: | Бюллетень сибирской медицины |
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Online Access: | https://bulletin.ssmu.ru/jour/article/view/4149 |
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author | Ya. V. Gorina Yu. K. Komleva E. D. Osipova A. V. Morgun N. A. Malinovskaya O. L. Lopatina A. B. Salmina |
author_facet | Ya. V. Gorina Yu. K. Komleva E. D. Osipova A. V. Morgun N. A. Malinovskaya O. L. Lopatina A. B. Salmina |
author_sort | Ya. V. Gorina |
collection | DOAJ |
description | The aim was to study the molecular mechanisms of the violation of the structural and functional integrity ofthe blood-brain barrier in chronic neurodegeneration of the Alzheimer’s type associated with the development of cerebral angiopathy.Materials and methods. The transgenic model of Alzheimer’s disease is the B6SLJ-Tg line mice (APPSwFlLon,PSEN1 * M146L * L286V) 6799Vas group which includes 9 months aged males. The control group included C57BL / 6 x SJL mice, males aged 9 months.Results. The total length of the vessels in the area of the dentate gyrus is 2.5 times greater in transgenic animal models of Alzheimer’s disease than in animals of the control group (p < 0.01). The average diameter of blood vessels in all areas of the hippocampus is smaller compared with the control (p < 0.05). Transgenic modeling of neurodegeneration in the CA2 zone of the hippocampus increases the relative area of tissue with increased permeability of blood-brain barrier (BBB) (17.80 [9.15; 36.75]) compared to control (1.38 [0.04; 7.60]) at p < 0.05. A similar difference (p < 0.05) is also observed in the hippocampal area CA1. A tendency (p > 0.05) to decrease the number of CD31+ endothelial cells in the dentate gyrus of the hippocampus (21.52 [17.56; 24.50]) in animals of the experimental group compared with the control group (23.08[21.18; 29.84]) was detected. A similar situation is observed in the CA2 and CA3 areas of the hippocampus.Conclusion. Neurodegenerative changes in the hippocampus of animals with a transgenic AD model are associated with impaired microcirculation in the brain tissue as a result of a reduction in the diameter and branching of blood vessels, and damage and increased permeability of BBB. |
first_indexed | 2024-04-10T01:05:07Z |
format | Article |
id | doaj.art-410603192bca456395d6f69158bd2ecc |
institution | Directory Open Access Journal |
issn | 1682-0363 1819-3684 |
language | English |
last_indexed | 2024-04-10T01:05:07Z |
publishDate | 2021-01-01 |
publisher | Siberian State Medical University (Tomsk) |
record_format | Article |
series | Бюллетень сибирской медицины |
spelling | doaj.art-410603192bca456395d6f69158bd2ecc2023-03-13T09:58:26ZengSiberian State Medical University (Tomsk)Бюллетень сибирской медицины1682-03631819-36842021-01-01194465210.20538/1682-0363-2020-4-46-522721Aberrant angiogenesis in brain tissue in experimental Alzheimer’s diseaseYa. V. Gorina0Yu. K. Komleva1E. D. Osipova2A. V. Morgun3N. A. Malinovskaya4O. L. Lopatina5A. B. Salmina6Красноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоКрасноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоКрасноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоКрасноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоКрасноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоКрасноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоКрасноярский государственный медицинский университет (КрасГМУ) имени профессора В.Ф. Войно-ЯсенецкогоThe aim was to study the molecular mechanisms of the violation of the structural and functional integrity ofthe blood-brain barrier in chronic neurodegeneration of the Alzheimer’s type associated with the development of cerebral angiopathy.Materials and methods. The transgenic model of Alzheimer’s disease is the B6SLJ-Tg line mice (APPSwFlLon,PSEN1 * M146L * L286V) 6799Vas group which includes 9 months aged males. The control group included C57BL / 6 x SJL mice, males aged 9 months.Results. The total length of the vessels in the area of the dentate gyrus is 2.5 times greater in transgenic animal models of Alzheimer’s disease than in animals of the control group (p < 0.01). The average diameter of blood vessels in all areas of the hippocampus is smaller compared with the control (p < 0.05). Transgenic modeling of neurodegeneration in the CA2 zone of the hippocampus increases the relative area of tissue with increased permeability of blood-brain barrier (BBB) (17.80 [9.15; 36.75]) compared to control (1.38 [0.04; 7.60]) at p < 0.05. A similar difference (p < 0.05) is also observed in the hippocampal area CA1. A tendency (p > 0.05) to decrease the number of CD31+ endothelial cells in the dentate gyrus of the hippocampus (21.52 [17.56; 24.50]) in animals of the experimental group compared with the control group (23.08[21.18; 29.84]) was detected. A similar situation is observed in the CA2 and CA3 areas of the hippocampus.Conclusion. Neurodegenerative changes in the hippocampus of animals with a transgenic AD model are associated with impaired microcirculation in the brain tissue as a result of a reduction in the diameter and branching of blood vessels, and damage and increased permeability of BBB.https://bulletin.ssmu.ru/jour/article/view/4149ангиогенезгематоэнцефалический барьерcd31болезнь альцгеймера |
spellingShingle | Ya. V. Gorina Yu. K. Komleva E. D. Osipova A. V. Morgun N. A. Malinovskaya O. L. Lopatina A. B. Salmina Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease Бюллетень сибирской медицины ангиогенез гематоэнцефалический барьер cd31 болезнь альцгеймера |
title | Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease |
title_full | Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease |
title_fullStr | Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease |
title_full_unstemmed | Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease |
title_short | Aberrant angiogenesis in brain tissue in experimental Alzheimer’s disease |
title_sort | aberrant angiogenesis in brain tissue in experimental alzheimer s disease |
topic | ангиогенез гематоэнцефалический барьер cd31 болезнь альцгеймера |
url | https://bulletin.ssmu.ru/jour/article/view/4149 |
work_keys_str_mv | AT yavgorina aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease AT yukkomleva aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease AT edosipova aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease AT avmorgun aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease AT namalinovskaya aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease AT ollopatina aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease AT absalmina aberrantangiogenesisinbraintissueinexperimentalalzheimersdisease |