Nano-Cell Interactions Lab., Department of Biochemistry and Tissue Biology, Institute of Biology, University of Campinas, Campinas, SP, Brazil.
Institute of Chemistry, University of Campinas, Campinas, SP, Brazil; Department of Chemistry, Institute of Exact and Biologic Sciences, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.
Nanomedicine. 2020 Feb;24:102130. doi: 10.1016/j.nano.2019.102130. Epub 2019 Nov 21.
Many studies have shown that silver nanoparticles (AgNP) induce oxidative stress, and it is commonly assumed that this is the main mechanism of AgNP cytotoxicity. Most of these studies rely on antioxidants to establish this cause-and-effect relationship; nevertheless, details on how these antioxidants interact with the AgNP are often overlooked. This work aimed to investigate the molecular mechanisms underlying the use of antioxidants with AgNP nanoparticles. Thus, we studied the molecular interaction between the thiol-antioxidants (N-acetyl-L-Cysteine, L-Cysteine, and glutathione) or non-thiol-antioxidants (Trolox) with chemically and biologically synthesized AgNP. Both antioxidants could mitigate ROS production in Huh-7 hepatocarcinoma cells, but only thiol-antioxidants could prevent the cytotoxic effect, directly binding to the AgNP leading to aggregation. Our findings show that data interpretation might not be straightforward when using thiol-antioxidants to study the interactions between metallic nanoparticles and cells. This artifact exemplifies potential pitfalls that could hinder the progress of nanotechnology and the understanding of the nanotoxicity mechanism.
许多研究表明,银纳米粒子(AgNP)会诱导氧化应激,而这被普遍认为是 AgNP 细胞毒性的主要机制。这些研究大多依赖于抗氧化剂来建立这种因果关系;然而,关于这些抗氧化剂如何与 AgNP 相互作用的细节往往被忽视。本工作旨在研究抗氧化剂与 AgNP 纳米粒子共同作用的分子机制。因此,我们研究了巯基抗氧化剂(N-乙酰-L-半胱氨酸、L-半胱氨酸和谷胱甘肽)或非巯基抗氧化剂(Trolox)与化学合成和生物合成的 AgNP 之间的分子相互作用。两种抗氧化剂都可以减少 Huh-7 肝癌细胞中的 ROS 产生,但只有巯基抗氧化剂可以防止细胞毒性作用,直接与 AgNP 结合导致聚集。我们的研究结果表明,当使用巯基抗氧化剂来研究金属纳米粒子与细胞之间的相互作用时,数据解释可能并不简单。这个人工制品说明了可能阻碍纳米技术进展和纳米毒性机制理解的潜在陷阱。