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简便制备负载外泌体微小RNA和白藜芦醇的氧化还原纳米颗粒作为糖化抑制剂以减轻糖尿病性白内障的进展和发展

Facile fabrication of redox nanoparticles loaded with exosomal-miRNAs and resveratrol as glycation inhibitor in alleviating the progression and development of diabetic cataract.

作者信息

Chen Xia, Xi Qian, Sun Fei, Zou Lin, Li Yingxuan

机构信息

Department of Endocrinology, Gongli Hospital of Shanghai Pudong New Area, Shanghai, 200135, China.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 Apr;398(4):4247-4263. doi: 10.1007/s00210-024-03535-4. Epub 2024 Oct 24.

Abstract

Diabetic cataract (DC) represents a highly prevalent ocular manifestation resulting from diabetes often culminating in vision impairment among individuals with diabetes. Regrettably, the armamentarium of pharmaceutical interventions capable of both delaying and thwarting the onset of DC remains conspicuously sparse. Based on contemporary investigations, the pathogenesis of DC is prominently influenced by oxidative harm to the crystalline lens and the nonenzymatic glycosylation of lens proteins. Consequently, we have developed self-regenerating cerium oxide nanoparticles (CeO NPs), enveloped with resveratrol (RSV) and exosomal-microRNA (miRNA) to alleviate the effects of DC in an in vitro model. Moreover, the inclusion of RSV within CeO NPs serves a dual purpose. It can act as an antioxidant, minimizing glycation, and induce oxidative stress by effectively neutralizing reactive oxygen species (ROS). Additionally, it serves as a glycation inhibitor effectively preventing the cross-linking. Consequently, it helps minimize the glucose level in hemoglobin and inhibits the formation of advanced glycation end products (AGEs). Likewise, the CeO-exosomal-miRNA when treated alone found to slightly impede the viability of human lens epithelial cells (HLEC) and induce apoptosis by suppressing the expression of α-crystalline gene (CRYAA). Particularly, miRNAs target genes associated with oxidative stress pathways, protein glycation, and the generation of AGEs, hence preventing structural damage to lens proteins. Compared with CeO, RSV-CeO, and miRNA-RSV-CeO, the presence of miRNA-RSV-CeO led to a significant decrease in hemoglobin glycation. Remarkably, miRNA-RSV-CeO NPs attenuate the formation of malondialdehyde (MDA) and conjugated dienes (CD) with a relative value of 14.63 and 11.37 nmol/mg. As per the report, this method presents a promising opportunity to implement the proposed material combination for attenuating diabetic cataracts.

摘要

糖尿病性白内障(DC)是糖尿病常见的眼部表现,常导致糖尿病患者视力受损。遗憾的是,能够延缓和阻止DC发病的药物干预手段明显匮乏。根据当代研究,DC的发病机制主要受晶状体氧化损伤和晶状体蛋白非酶糖基化的影响。因此,我们开发了包裹白藜芦醇(RSV)和外泌体微小RNA(miRNA)的自再生氧化铈纳米颗粒(CeO NPs),以减轻体外模型中DC的影响。此外,在CeO NPs中加入RSV有双重作用。它可以作为抗氧化剂,减少糖基化,并通过有效中和活性氧(ROS)诱导氧化应激。此外,它还可以作为糖基化抑制剂,有效防止交联。因此,它有助于降低血红蛋白中的葡萄糖水平,抑制晚期糖基化终产物(AGEs)的形成。同样,单独处理的CeO-外泌体-miRNA发现会轻微阻碍人晶状体上皮细胞(HLEC)的活力,并通过抑制α-晶状体蛋白基因(CRYAA)的表达诱导细胞凋亡。特别是,miRNAs靶向与氧化应激途径、蛋白质糖基化和AGEs生成相关的基因,从而防止晶状体蛋白的结构损伤。与CeO、RSV-CeO和miRNA-RSV-CeO相比,miRNA-RSV-CeO的存在导致血红蛋白糖基化显著降低。值得注意的是,miRNA-RSV-CeO NPs使丙二醛(MDA)和共轭二烯(CD)的形成减少,相对值分别为14.63和11.37 nmol/mg。根据报告,该方法为实施所提出的减轻糖尿病性白内障的材料组合提供了一个有前景的机会。

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