An RGD-Conjugated Prodrug Nanoparticle with Blood-Brain-Barrier Penetrability for Neuroprotection Against Cerebral Ischemia-Reperfusion Injury.

IF 6 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Antioxidants Pub Date : 2024-11-01 DOI:10.3390/antiox13111339
Ayijiang Taledaohan, Maer Maer Tuohan, Renbo Jia, Kai Wang, Liujia Chan, Yijiang Jia, Feng Wang, Yuji Wang
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Abstract

Cerebral ischemia-reperfusion injury significantly contributes to global morbidity and mortality. Loganin is a natural product with various neuroprotective effects; however, it lacks targeted specificity for particular cells or receptors, which may result in reduced therapeutic efficacy and an increased risk of side effects. To address the limitations of loganin, we developed LA-1, a novel compound incorporating an Arg-Gly-Asp (RGD) peptide to target integrin receptor αvβ3, enhancing brain-targeting efficacy. LA-1 exhibited optimal nanoscale properties, significantly improved cell viability, reduced ROS production, and enhanced survival rates in vitro. In vivo, LA-1 decreased infarct sizes, improved neurological function, and reduced oxidative stress and neuroinflammation. Proteomic analysis showed LA-1 modulates PI3K/Akt and Nrf2/HO-1 pathways, providing targeted neuroprotection. These findings suggest LA-1's potential for clinical applications in treating cerebral ischemia-reperfusion injury.

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一种具有血脑屏障穿透性的 RGD 共轭原药纳米粒子,可用于脑缺血再灌注损伤的神经保护。
脑缺血再灌注损伤是导致全球发病率和死亡率的重要原因。洛加宁是一种天然产物,具有多种神经保护作用;但它对特定细胞或受体缺乏靶向特异性,可能导致疗效降低和副作用风险增加。针对洛加宁的局限性,我们开发了一种新型化合物 LA-1,它含有 Arg-Gly-Asp (RGD) 肽,可靶向整合素受体 αvβ3,从而提高脑靶向疗效。LA-1 具有最佳的纳米级特性,在体外能显著提高细胞活力、减少 ROS 生成并提高存活率。在体内,LA-1能缩小脑梗塞面积,改善神经功能,减少氧化应激和神经炎症。蛋白质组分析表明,LA-1 可调节 PI3K/Akt 和 Nrf2/HO-1 通路,提供有针对性的神经保护。这些研究结果表明,LA-1具有治疗脑缺血再灌注损伤的临床应用潜力。
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来源期刊
Antioxidants
Antioxidants Biochemistry, Genetics and Molecular Biology-Physiology
CiteScore
10.60
自引率
11.40%
发文量
2123
审稿时长
16.3 days
期刊介绍: Antioxidants (ISSN 2076-3921), provides an advanced forum for studies related to the science and technology of antioxidants. It publishes research papers, reviews and communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files and software regarding the full details of the calculation or experimental procedure, if unable to be published in a normal way, can be deposited as supplementary electronic material.
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