Author:
Sun Yuxiang,Xu Tianze,Qian Yike,Chen Qiaoyun,Xiong Fei,Du Wenxian,Xu Li
Abstract
AbstractCeria nanoparticles (CeO2NPs) exhibit great potential in cardiovascular disease and nonalcoholic fatty liver disease due to its excellent antioxidant capacity. However, the profitable effect of CeO2NPs on many diseases is almost all attributed to the regulation of ROS. Apart from the general antioxidant function, there seems to be no more distinct mechanism to reflect its unique multi-disease improvement effect. Here, we for the first time reveal a new discovery of CeO2NPs in mimicking nitric oxide synthase (NOS) by catalyzing L-arginine (L-Arg) to produce nitric oxide (NO) or the derivatives. NOS-like activity of CeO2NPs is original and associated with multiple factors like substrate concentration, pH, temperature and time, etc. where oxygen vacancy ratio plays a more critical role. Meanwhile, NOS-like activity of CeO2NPs successfully elevates NO secretion in endothelial cells and macrophages without expanding eNOS/iNOS expression. Importantly, NOS-like activity of CeO2NPs and the responsive endogenous NO promote the re-distribution of blood lipids and stabilize eNOS expression but suppress iNOS, thus collectively alleviate the accumulation of vascular plaque. Altogether, we provide a new angle of view to survey the outstanding potential of CeO2NPs, apart from the inevitable antioxidant capacity, the covert but possible and more critical NOS-like enzymatic activity is more noteworthy.
Funder
National Natural Science Foundation of China
Lvyang Jinfeng Plan for Excellent Doctor of Yangzhou City
Research Launch Fund of Yangzhou University
Open Research Fund of Key Laboratory of Biomarkers and In Vitro Diagnosis Translation of Zhejiang province
National Key Research and Development Program of China
Publisher
Springer Science and Business Media LLC
Cited by
2 articles.
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