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四氧化三锰纳米酶通过减少骨关节炎中的氧化应激来保护软骨免受退变。

Trimanganese Tetroxide Nanozyme protects Cartilage against Degeneration by Reducing Oxidative Stress in Osteoarthritis.

机构信息

Department of Neurosurgery, Qilu Hospital, Cheeloo College of Medicine and Institute of Brain and Brain-Inspired Science, Shandong University, Jinan, 250012, P. R. China.

State Key Laboratory of Crystal Materials, Shandong University, Jinan, 250100, P. R. China.

出版信息

Adv Sci (Weinh). 2023 Jun;10(17):e2205859. doi: 10.1002/advs.202205859. Epub 2023 Apr 23.

Abstract

Osteoarthritis, a chronic degenerative cartilage disease, is the leading cause of movement disorders among humans. Although the specific pathogenesis and associated mechanisms remain unclear, oxidative stress-induced metabolic imbalance in chondrocytes plays a crucial role in the occurrence and development of osteoarthritis. In this study, a trimanganese tetroxide (Mn O ) nanozyme with superoxide dismutase (SOD)-like and catalase (CAT)-like activities is designed to reduce oxidative stress-induced damage and its therapeutic effect is investigated. In vitro, Mn O nanozymes are confirmed to reprogram both the imbalance of metabolism in chondrocytes and the uncontrolled inflammatory response stimulated by hydrogen peroxide. In vivo, a cross-linked chondroitin sulfate (CS) hydrogel is designed as a substrate for Mn O nanozymes to treat osteoarthritis in mouse models. As a result, even in the early stage of OA (4 weeks), the therapeutic effect of the Mn O @CS hydrogel is observed in both cartilage metabolism and inflammation. Moreover, the Mn O @CS hydrogel maintained its therapeutic effects for at least 7 days, thus revealing a broad scope for future clinical applications. In conclusion, these results suggest that the Mn O @CS hydrogel is a potentially effective therapeutic treatment for osteoarthritis, and a novel therapeutic strategy for osteoarthritis based on nanozymes is proposed.

摘要

骨关节炎是一种慢性退行性软骨疾病,是人类运动障碍的主要原因。虽然其具体发病机制和相关机制尚不清楚,但软骨细胞中氧化应激诱导的代谢失衡在骨关节炎的发生和发展中起着关键作用。在这项研究中,设计了一种具有超氧化物歧化酶(SOD)样和过氧化氢酶(CAT)样活性的四氧化三锰(MnO)纳米酶,以减轻氧化应激诱导的损伤,并研究其治疗效果。在体外,MnO 纳米酶被证实可以重新编程软骨细胞代谢失衡和过氧化氢刺激的失控炎症反应。在体内,设计了交联硫酸软骨素(CS)水凝胶作为 MnO 纳米酶的基质来治疗小鼠模型中的骨关节炎。结果表明,即使在 OA 的早期(4 周),MnO@CS 水凝胶在软骨代谢和炎症方面都显示出治疗效果。此外,MnO@CS 水凝胶至少能维持 7 天的治疗效果,从而为未来的临床应用提供了广阔的前景。总之,这些结果表明,MnO@CS 水凝胶是一种治疗骨关节炎的潜在有效方法,为基于纳米酶的骨关节炎治疗提出了一种新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f074/10265103/93fb6bb4c1a5/ADVS-10-2205859-g006.jpg

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