| Literature DB >> 32955857 |
Haiyun Li1,2, Jiao Yan1,2, Dejing Meng1,2, Rui Cai1,2, Xinshuang Gao1,2, Yinglu Ji1, Liming Wang3,2,4, Chunying Chen5,2,6, Xiaochun Wu1,2.
Abstract
Cardiovascular disease is a leading cause of death, and one of the effective therapeutic strategies for cardiovascular disease is to provide a controlled, constant supply of nitric oxide (NO) in a mild manner; however, this has proved challenging in the clinic. To address this problem, we built a nitric oxide synthase (NOS)-like nanoplatform (NanoNOS) that consists of a noble metal nanoparticle core and a mesoporous silica shell and demonstrated the ability of NanoNOS to catalyze production of NO in vitro. Mechanistic studies show that the catalysis consists of a three-step reaction: the oxidation of NADPH to produce O2- via oxidase-like activity and the subsequent dismutation of O2- to H2O2 via SOD-like activity, followed by H2O2-mediated oxidation of l-arginine to produce NO via a nonenzymatic pathway. The generation of NO is precisely regulated by both the content of the NanoNOS species and the plasmon excitation. We found that NanoNOS greatly suppressed injury-driven monocyte-endothelial cell adhesion, suggesting the NanoNOS treatment could help prevent cardiovascular disease. With such a design as well as plasmon excitation that allows for controlled and constant catalytic activity, NanoNOS technology could have a variety of biomedical applications.Entities:
Keywords: arginine; cardiovascular disease; catalysis; gold nanorod; nanoplatform; nitric oxide; nitric oxide synthase
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Year: 2020 PMID: 32955857 DOI: 10.1021/acsnano.0c03629
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881