Cargando…

Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction

Inflammation is a critical feature of aging and its related diseases, including cardiovascular diseases. Recent epidemiological studies demonstrated that abdominal aortic aneurysm (AAA), an aging-related vascular pathological condition, is associated with cognitive decline. However, the underlying m...

Descripción completa

Detalles Bibliográficos
Autores principales: Hashizume, Tsuyoshi, Son, Bo-Kyung, Taniguchi, Sakiko, Ito, Koichi, Noda, Yoshihiro, Endo, Tamao, Nanao-Hamai, Michiko, Ogawa, Sumito, Akishita, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411753/
https://www.ncbi.nlm.nih.gov/pubmed/30858535
http://dx.doi.org/10.1038/s41598-019-40726-z
_version_ 1783402446220951552
author Hashizume, Tsuyoshi
Son, Bo-Kyung
Taniguchi, Sakiko
Ito, Koichi
Noda, Yoshihiro
Endo, Tamao
Nanao-Hamai, Michiko
Ogawa, Sumito
Akishita, Masahiro
author_facet Hashizume, Tsuyoshi
Son, Bo-Kyung
Taniguchi, Sakiko
Ito, Koichi
Noda, Yoshihiro
Endo, Tamao
Nanao-Hamai, Michiko
Ogawa, Sumito
Akishita, Masahiro
author_sort Hashizume, Tsuyoshi
collection PubMed
description Inflammation is a critical feature of aging and its related diseases, including cardiovascular diseases. Recent epidemiological studies demonstrated that abdominal aortic aneurysm (AAA), an aging-related vascular pathological condition, is associated with cognitive decline. However, the underlying mechanism, especially the role of vascular inflammation, is largely unknown because of lack of an available animal model. In this study, we examined whether vascular inflammation affects synaptic and cognitive dysfunction, using an AAA mouse model. In young (3 months) and middle-aged (12 months) C57BL/6J mice, AAA was induced by angiotensin II infusion with calcium chloride application. After 4 weeks of induction, aortic diameter was significantly increased and excessive Mac3-positive inflammatory cells infiltrated the destroyed aorta in middle-aged mice. AAA-induced middle-aged mice further exhibited cognitive impairment. Neuronal loss was observed in the CA3 region of the hippocampus. IBA1/MHCII-double-positive microglia activation was also seen in the hippocampus, suggesting that vascular inflammation drives neuroinflammation and subsequent cognitive dysfunction. Furthermore, we found that senescence-accelerated mice prone 8 exhibited robust AAA formation and a marked decrease of cognitive and synaptic function in the hippocampus mediated by inflammation. In conclusion, this novel murine model convincingly suggested the occurrence of vascular inflammation-derived cognitive dysfunction.
format Online
Article
Text
id pubmed-6411753
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64117532019-03-13 Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction Hashizume, Tsuyoshi Son, Bo-Kyung Taniguchi, Sakiko Ito, Koichi Noda, Yoshihiro Endo, Tamao Nanao-Hamai, Michiko Ogawa, Sumito Akishita, Masahiro Sci Rep Article Inflammation is a critical feature of aging and its related diseases, including cardiovascular diseases. Recent epidemiological studies demonstrated that abdominal aortic aneurysm (AAA), an aging-related vascular pathological condition, is associated with cognitive decline. However, the underlying mechanism, especially the role of vascular inflammation, is largely unknown because of lack of an available animal model. In this study, we examined whether vascular inflammation affects synaptic and cognitive dysfunction, using an AAA mouse model. In young (3 months) and middle-aged (12 months) C57BL/6J mice, AAA was induced by angiotensin II infusion with calcium chloride application. After 4 weeks of induction, aortic diameter was significantly increased and excessive Mac3-positive inflammatory cells infiltrated the destroyed aorta in middle-aged mice. AAA-induced middle-aged mice further exhibited cognitive impairment. Neuronal loss was observed in the CA3 region of the hippocampus. IBA1/MHCII-double-positive microglia activation was also seen in the hippocampus, suggesting that vascular inflammation drives neuroinflammation and subsequent cognitive dysfunction. Furthermore, we found that senescence-accelerated mice prone 8 exhibited robust AAA formation and a marked decrease of cognitive and synaptic function in the hippocampus mediated by inflammation. In conclusion, this novel murine model convincingly suggested the occurrence of vascular inflammation-derived cognitive dysfunction. Nature Publishing Group UK 2019-03-11 /pmc/articles/PMC6411753/ /pubmed/30858535 http://dx.doi.org/10.1038/s41598-019-40726-z Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hashizume, Tsuyoshi
Son, Bo-Kyung
Taniguchi, Sakiko
Ito, Koichi
Noda, Yoshihiro
Endo, Tamao
Nanao-Hamai, Michiko
Ogawa, Sumito
Akishita, Masahiro
Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction
title Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction
title_full Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction
title_fullStr Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction
title_full_unstemmed Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction
title_short Establishment of Novel Murine Model showing Vascular Inflammation-derived Cognitive Dysfunction
title_sort establishment of novel murine model showing vascular inflammation-derived cognitive dysfunction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411753/
https://www.ncbi.nlm.nih.gov/pubmed/30858535
http://dx.doi.org/10.1038/s41598-019-40726-z
work_keys_str_mv AT hashizumetsuyoshi establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT sonbokyung establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT taniguchisakiko establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT itokoichi establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT nodayoshihiro establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT endotamao establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT nanaohamaimichiko establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT ogawasumito establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction
AT akishitamasahiro establishmentofnovelmurinemodelshowingvascularinflammationderivedcognitivedysfunction