TY - JOUR
T1 - Protective Effect of Rivaroxaban Against Amyloid Pathology and Neuroinflammation Through Inhibiting PAR-1 and PAR-2 in Alzheimer's Disease Mice
AU - Bian, Zhihong
AU - Liu, Xia
AU - Feng, Tian
AU - Yu, Haibo
AU - Hu, Xiao
AU - Hu, Xinran
AU - Bian, Yuting
AU - Sun, Hongming
AU - Tadokoro, Koh
AU - Takemoto, Mami
AU - Yunoki, Taijun
AU - Nakano, Yumiko
AU - Fukui, Yusuke
AU - Morihara, Ryuta
AU - Abe, Koji
AU - Yamashita, Toru
N1 - Funding Information:
This work was partly supported by Bayer Yakuhin, Ltd.
Publisher Copyright:
© 2022-IOS Press. All rights reserved.
PY - 2022
Y1 - 2022
N2 - Background: Recent studies have revealed that atrial fibrillation (AF) patients have a high risk of developing cognitive impairment, vascular dementia, and Alzheimer's disease (AD). Some reports suggest that the application of oral anticoagulant with an appropriate dose may have a preventive effect on AD. However, which oral anticoagulant drug is more appropriate for preventing AD and the underlying mechanism(s) is still unknown. Objective: The aim of the present study was to assess the treatment effect of rivaroxaban administration as well as investigate the roles of PAR-1 and PAR-2 in the AD+CAA mice model. Methods: In the present study, we compared a traditional oral anticoagulant, warfarin, and a direct oral anticoagulant (DOAC), rivaroxaban, via long-term administration to an AD with cerebral amyloid angiopathy (CAA) mice model. Results: Rivaroxaban treatment attenuated neuroinflammation, blood-brain barrier dysfunction, memory deficits, and amyloid-β deposition through PAR-1/PAR-2 inhibition in the AD+CAA mice model compared with warfarin and no-treatment groups. Conclusion: The present study demonstrates that rivaroxaban can attenuate AD progress and can be a potential choice to prevent AD.
AB - Background: Recent studies have revealed that atrial fibrillation (AF) patients have a high risk of developing cognitive impairment, vascular dementia, and Alzheimer's disease (AD). Some reports suggest that the application of oral anticoagulant with an appropriate dose may have a preventive effect on AD. However, which oral anticoagulant drug is more appropriate for preventing AD and the underlying mechanism(s) is still unknown. Objective: The aim of the present study was to assess the treatment effect of rivaroxaban administration as well as investigate the roles of PAR-1 and PAR-2 in the AD+CAA mice model. Methods: In the present study, we compared a traditional oral anticoagulant, warfarin, and a direct oral anticoagulant (DOAC), rivaroxaban, via long-term administration to an AD with cerebral amyloid angiopathy (CAA) mice model. Results: Rivaroxaban treatment attenuated neuroinflammation, blood-brain barrier dysfunction, memory deficits, and amyloid-β deposition through PAR-1/PAR-2 inhibition in the AD+CAA mice model compared with warfarin and no-treatment groups. Conclusion: The present study demonstrates that rivaroxaban can attenuate AD progress and can be a potential choice to prevent AD.
KW - Alzheimer's disease
KW - cerebral amyloid angiopathy chronic cerebral hypoperfusion
KW - rivaroxaban
KW - warfarin
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U2 - 10.3233/JAD-215318
DO - 10.3233/JAD-215318
M3 - Article
C2 - 35001892
AN - SCOPUS:85126388669
SN - 1387-2877
VL - 86
SP - 111
EP - 123
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 1
ER -