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Cur@SF NPs 通过协同铁螯合和抗氧化作用缓解弗里德里希共济失调症小鼠模型的症状。

Cur@SF NPs alleviate Friedreich's ataxia in a mouse model through synergistic iron chelation and antioxidation.

机构信息

Jiangsu Key Laboratory of Molecular Medicine, Medical School of Nanjing University, Nanjing, 210093, China.

State Key Laboratory of Pharmaceutical Biotechnology, Division of Iron Metabolism and Mitochondrial Function, Medical School of Nanjing University, Nanjing, 210093, China.

出版信息

J Nanobiotechnology. 2022 Mar 9;20(1):118. doi: 10.1186/s12951-022-01333-9.

Abstract

Abnormal iron metabolism, mitochondrial dysfunction and the derived oxidative damage are the main pathogeneses of Friedrich's ataxia (FRDA), a single-gene inherited recessive neurodegenerative disease characterized by progressive cerebellar and sensory ataxia. This disease is caused by frataxin (FXN) mutation, which reduces FXN expression and impairs iron sulfur cluster biogenesis. To date, there is no effective therapy to treat this condition. Curcumin is proposed harboring excellent ability to resist oxidative stress through Nrf2 activation and its newly found ability to chelate iron. However, its limitation is its poor water solubility and permeability. Here, we synthesized slow-release nanoparticles (NPs) by loading curcumin (Cur) into silk fibroin (SF) to form NPs with an average size of 150 nm (Cur@SF NPs), which exhibited satisfactory therapeutic effects on the improvement of FRDA manifestation in lymphoblasts (1 μM) derived from FRDA patients and in YG8R mice (150 mg/kg/5 days). Cur@SF NPs not only removed iron from the heart and diminished oxidative stress in general but also potentiate iron-sulfur cluster biogenesis, which compensates FXN deficiency to improve the morphology and function of mitochondria. Cur@SF NPs showed a significant advantage in neuron and myocardial function, thereby improving FRDA mouse behavior scores. These data encourage us to propose that Cur@SF NPs are a promising therapeutic compound in the application of FRDA disease.

摘要

异常的铁代谢、线粒体功能障碍和由此产生的氧化损伤是弗里德里希共济失调症(FRDA)的主要发病机制,FRDA 是一种单基因遗传性退行性神经疾病,其特征是进行性小脑和感觉共济失调。这种疾病是由 frataxin(FXN)突变引起的,它降低了 FXN 的表达并损害了铁硫簇的生物发生。迄今为止,还没有有效的治疗方法来治疗这种疾病。姜黄素通过激活 Nrf2 及其新发现的螯合铁的能力,被认为具有很好的抵抗氧化应激的能力。然而,它的局限性是水溶性和渗透性差。在这里,我们通过将姜黄素(Cur)载入丝素蛋白(SF)中来合成缓释纳米颗粒(NPs),形成平均粒径为 150nm 的 NPs(Cur@SF NPs),在 FRDA 患者来源的淋巴母细胞(1μM)和 YG8R 小鼠(150mg/kg/5 天)中对 FRDA 表现的改善显示出令人满意的治疗效果。Cur@SF NPs 不仅从心脏中去除了铁并减轻了总体氧化应激,而且还增强了铁硫簇的生物发生,从而补偿了 FXN 的缺乏,改善了线粒体的形态和功能。Cur@SF NPs 在神经元和心肌功能方面表现出显著优势,从而改善了 FRDA 小鼠的行为评分。这些数据鼓励我们提出 Cur@SF NPs 是 FRDA 疾病应用中很有前途的治疗化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdf/8905737/ec943fab35b5/12951_2022_1333_Fig1_HTML.jpg

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