State Key Laboratory of Electroanalytical Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences , Changchun 130022, China.
Center for Nanomedicine and Department of Anesthesiology, Brigham and Women's Hospital, Harvard Medical School , Boston, Massachusetts 02115, United States.
J Am Chem Soc. 2017 Jan 18;139(2):856-862. doi: 10.1021/jacs.6b11013. Epub 2017 Jan 5.
Nanotechnology-mediated antioxidative therapy is emerging as a novel strategy for treating a myriad of important diseases through scavenging excessive reactive oxygen and nitrogen species (RONS), a mechanism critical in disease development and progression. However, similar to antioxidative enzymes, currently studied nanoantioxidants have demonstrated scavenging activity to specific RONS, and sufficient antioxidative effects against multiple RONS generated in diseases remain elusive. Here we propose to develop bioinspired melanin nanoparticles (MeNPs) for more potent and safer antioxidative therapy. While melanin is known to function as a potential radical scavenger, its antioxidative mechanisms are far from clear, and its applications for the treatment of RONS-associated diseases have yet to be well-explored. In this study, we provide for the first time exhaustive characterization of the activities of MeNPs against multiple RONS including O, HO, OH, NO, and ONOO, the main toxic RONS generated in diseases. The potential of MeNPs for antioxidative therapy has also been evaluated in vitro and in a rat model of ischemic stroke. In addition to the broad defense against these RONS, MeNPs can also attenuate the RONS-triggered inflammatory responses through suppressing the expression of inflammatory mediators and cytokines. In vivo results further demonstrate that these unique multi-antioxidative, anti-inflammatory, and biocompatible features of MeNPs contribute to their effective protection of ischemic brains with negligible side effects.
纳米技术介导的抗氧化治疗作为一种新兴策略,通过清除过多的活性氧和氮物种 (RONS) 来治疗多种重要疾病,这种机制在疾病的发展和进展中至关重要。然而,与抗氧化酶类似,目前研究的纳米抗氧化剂已经表现出对特定 RONS 的清除活性,但针对疾病中产生的多种 RONS 仍然难以达到足够的抗氧化效果。在这里,我们提出开发仿生黑色素纳米颗粒 (MeNPs) 以实现更有效和更安全的抗氧化治疗。尽管黑色素已知是一种潜在的自由基清除剂,但它的抗氧化机制还远不清楚,其在治疗与 RONS 相关疾病中的应用尚未得到充分探索。在这项研究中,我们首次全面表征了 MeNPs 对包括 O、HO、OH、NO 和 ONOO 在内的多种 RONS 的活性,这些是疾病中产生的主要毒性 RONS。我们还评估了 MeNPs 在体外和缺血性中风大鼠模型中的抗氧化治疗潜力。除了对这些 RONS 的广泛防御外,MeNPs 还可以通过抑制炎症介质和细胞因子的表达来减轻 RONS 引发的炎症反应。体内结果进一步证明,MeNPs 的这些独特的多抗氧化、抗炎和生物相容性特征有助于其有效保护缺血性大脑,而几乎没有副作用。