دورية أكاديمية

Aβ1–40-Induced Platelet Adhesion Is Ameliorated by Rosmarinic Acid through Inhibition of NADPH Oxidase/PKC-δ/Integrin αIIbβ3 Signaling

التفاصيل البيبلوغرافية
العنوان: Aβ1–40-Induced Platelet Adhesion Is Ameliorated by Rosmarinic Acid through Inhibition of NADPH Oxidase/PKC-δ/Integrin αIIbβ3 Signaling
المؤلفون: Bo Kyung Lee, Hye Jin Jee, Yi-Sook Jung
المصدر: Antioxidants, Vol 10, Iss 11, p 1671 (2021)
بيانات النشر: MDPI AG, 2021.
سنة النشر: 2021
المجموعة: LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: platelet, rosmarinic acid (RA), β-amyloid (Aβ), NADPH oxidase, integrin αIIbβ3, Therapeutics. Pharmacology, RM1-950
الوصف: In platelets, oxidative stress reportedly increases platelet adhesion to vessels, thus promoting the vascular pathology of various neurodegenerative diseases, including Alzheimer’s disease (AD). Recently, it has been shown that β-amyloid (Aβ) can increase oxidative stress in platelets; however, the underlying mechanism remains elusive. In the present study, we aimed to elucidate the signaling pathway of platelet adhesion induced by Aβ1–40, the major form of circulating Aβ, through Western blotting, immunofluorescence confocal microscopy, and fluorescence-activated cell sorting analysis. Additionally, we examined whether rosmarinic acid (RA), a natural polyphenol antioxidant, can modulate these processes. Our results show that Aβ1–40-induced platelet adhesion is mediated through NADPH oxidase/ROS/PKC-δ/integrin αIIbβ3 signaling, and these signaling pathways are significantly inhibited by RA. Collectively, these results suggest that RA may have beneficial effects on platelet-associated vascular pathology in AD.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2076-3921
Relation: https://www.mdpi.com/2076-3921/10/11/1671; https://doaj.org/toc/2076-3921
DOI: 10.3390/antiox10111671
URL الوصول: https://doaj.org/article/26ea9b04d8714705bc2a1daa0ac45495
رقم الأكسشن: edsdoj.26ea9b04d8714705bc2a1daa0ac45495
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20763921
DOI:10.3390/antiox10111671