氧化应激
硫辛酸
抗氧化剂
炎症
化学
药理学
生物化学
免疫学
医学
作者
Xinyi Li,Mengjiao Zhang,Anni Chen,Xinqi Wang,Lan Yang,Yingjian Zhu,Zhaojun Li
出处
期刊:ACS omega
[American Chemical Society]
日期:2024-11-25
卷期号:9 (49): 48642-48649
被引量:6
标识
DOI:10.1021/acsomega.4c07745
摘要
Oxidative stress and inflammation are key pathological features of atherosclerotic plaques. Numerous nanomedicines have been developed to alleviate oxidative stress and reduce inflammation within plaques. However, nonbioactive carrier materials reduce the bioavailability of nanomedicines and may pose potential biological toxicity. In this study, we utilized the unique amphiphilic chemical structure of lipoic acid (LA) to prepare LA nanoparticles (LA NPs) via a self-assembly method. Leveraging the inherent anti-inflammatory and antioxidant properties of LA, these NPs were used for the treatment of atherosclerosis. In an inflammatory macrophage model, LA NPs exhibited superior anti-inflammatory activity compared to free LA. Through ultrasound imaging and pathological methods, we discovered that LA NPs demonstrated nice antiatherosclerotic effects in an atherosclerotic mice model. Immunofluorescence analysis further indicated that the antiatherosclerotic effects of LA were associated with the alleviation of oxidative stress within the plaques, reduced macrophage infiltration, and downregulation of inflammatory cytokine levels. Therefore, LA NPs offer a promising therapeutic strategy for the treatment of atherosclerosis.
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