文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

硒掺杂碳量子点通过清除活性氧来有效改善继发性脊髓损伤。

Selenium-Doped Carbon Quantum Dots Efficiently Ameliorate Secondary Spinal Cord Injury via Scavenging Reactive Oxygen Species.

机构信息

Department of Orthopaedic Surgery, China-Japan Union Hospital of Jilin University, Changchun 130033, People's Republic of China.

Key Laboratory of Polymer Ecomaterials, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China.

出版信息

Int J Nanomedicine. 2020 Dec 14;15:10113-10125. doi: 10.2147/IJN.S282985. eCollection 2020.


DOI:10.2147/IJN.S282985
PMID:33363370
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7754097/
Abstract

BACKGROUND: The excess production of reactive oxygen species (ROS) after traumatic spinal cord injury (TSCI) has been identified as a leading cause of secondary injury, which can significantly exacerbate acute damage in the injured spinal cord. Thus, scavenging of ROS has emerged as an effective route to ameliorate secondary spinal cord injury. PURPOSE: Selenium-doped carbon quantum dots (Se-CQDs) with the ability to scavenge reactive oxygen species were prepared and used for efficiently ameliorating secondary injury in TSCI. METHODS: Water-soluble Se-CQDs were easily synthesized via hydrothermal treatment of l-selenocystine. The chemical structure, size, and morphology of the Se-CQDs were characterized in detail. The biocompatibility and protective effects of the Se-CQDs against HO-induced oxidative damage were investigated in vitro. Moreover, the behavioral test, bladder function, histological observation, Western blot were used to investigate the neuroprotective effect of Se-CQDs in a rat model of contusion TSCI. RESULTS: The obtained Se-CQDs exhibited good biocompatibility and remarkable protective effect against HO-induced oxidative damage in astrocytes and PC12 cells. Moreover, Se-CQDs displayed marked anti-inflammatory and anti-apoptotic activities, which thereby reduced the formation of glial scars and increased the survival of neurons with unscathed myelin sheaths in vivo. As a result, Se-CQDs were capable of largely improving locomotor function of rats with TSCI. CONCLUSION: This study suggests that Se-CQDs can be used as a promising therapeutic platform for ameliorating secondary injury in TSCI.

摘要

背景:创伤性脊髓损伤(TSCI)后活性氧(ROS)的过度产生已被确定为继发性损伤的主要原因,这会显著加重损伤脊髓的急性损伤。因此,清除 ROS 已成为改善继发性脊髓损伤的有效途径。

目的:制备具有清除活性氧能力的硒掺杂碳量子点(Se-CQDs),并用于有效改善 TSCI 的继发性损伤。

方法:通过水热处理 L-硒代半胱氨酸很容易合成水溶性 Se-CQDs。详细表征了 Se-CQDs 的化学结构、尺寸和形态。体外研究了 Se-CQDs 对 HO 诱导的氧化损伤的生物相容性和保护作用。此外,行为测试、膀胱功能、组织学观察和 Western blot 用于研究 Se-CQDs 在大鼠挫伤性 TSCI 模型中的神经保护作用。

结果:所获得的 Se-CQDs 表现出良好的生物相容性和对星形胶质细胞和 PC12 细胞中 HO 诱导的氧化损伤的显著保护作用。此外,Se-CQDs 表现出明显的抗炎和抗细胞凋亡活性,从而减少了神经胶质瘢痕的形成,并增加了未受损髓鞘神经元的存活。结果,Se-CQDs 能够大大改善 TSCI 大鼠的运动功能。

结论:本研究表明,Se-CQDs 可用作改善 TSCI 继发性损伤的有前途的治疗平台。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/bb8f0b32fab3/IJN-15-10113-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/7ba6179331d1/IJN-15-10113-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/96e741aa2878/IJN-15-10113-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/68a104d8de99/IJN-15-10113-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/b59a76a37063/IJN-15-10113-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/bb7f61df3ee2/IJN-15-10113-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/20e28a3f3968/IJN-15-10113-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/bb8f0b32fab3/IJN-15-10113-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/7ba6179331d1/IJN-15-10113-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/96e741aa2878/IJN-15-10113-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/68a104d8de99/IJN-15-10113-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/b59a76a37063/IJN-15-10113-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/bb7f61df3ee2/IJN-15-10113-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/20e28a3f3968/IJN-15-10113-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3495/7754097/bb8f0b32fab3/IJN-15-10113-g0007.jpg

相似文献

[1]
Selenium-Doped Carbon Quantum Dots Efficiently Ameliorate Secondary Spinal Cord Injury via Scavenging Reactive Oxygen Species.

Int J Nanomedicine. 2020

[2]
Injectable Hydrogel Loaded with CDs and FTY720 Combined with Neural Stem Cells for the Treatment of Spinal Cord Injury.

Int J Nanomedicine. 2024

[3]
Neuroprotective effect of Scutellaria baicalensis on spinal cord injury in rats.

J Neurochem. 2009-8

[4]
The Neuroprotective Effect of Puerarin in Acute Spinal Cord Injury Rats.

Cell Physiol Biochem. 2016

[5]
Selenium attenuates ROS-mediated apoptotic cell death of injured spinal cord through prevention of mitochondria dysfunction; in vitro and in vivo study.

Cell Physiol Biochem. 2008

[6]
Epigallocatechin-3-gallate selenium nanoparticles for neuroprotection by scavenging reactive oxygen species and reducing inflammation.

Front Bioeng Biotechnol. 2022-9-8

[7]
Selenium-Doped Carbon Quantum Dots for Free-Radical Scavenging.

Angew Chem Int Ed Engl. 2017-7-13

[8]
Self-Assembly of Selenium-Doped Carbon Quantum Dots as Antioxidants for Hepatic Ischemia-Reperfusion Injury Management.

Small. 2023-7

[9]
Tamoxifen and estradiol improved locomotor function and increased spared tissue in rats after spinal cord injury: their antioxidant effect and role of estrogen receptor alpha.

Brain Res. 2014-5-2

[10]
Designing multifunctionalized selenium nanoparticles to reverse oxidative stress-induced spinal cord injury by attenuating ROS overproduction and mitochondria dysfunction.

J Mater Chem B. 2019-3-21

引用本文的文献

[1]
Intravenously injected poly(amino acid) nanoformulation relieves spinal cord injury through synergistical modulation of microenvironments.

Mater Today Bio. 2025-8-22

[2]
Antioxidant nanozymes: current status and future perspectives in spinal cord injury treatments.

Theranostics. 2025-5-8

[3]
Research Progress on Biomaterials for Spinal Cord Repair.

Int J Nanomedicine. 2025-2-11

[4]
Advancements in Antioxidant-Based Therapeutics for Spinal Cord Injury: A Critical Review of Strategies and Combination Approaches.

Antioxidants (Basel). 2024-12-26

[5]
Regulation of dynamic spatiotemporal inflammation by nanomaterials in spinal cord injury.

J Nanobiotechnology. 2024-12-19

[6]
Intravenous administration exosomes derived from human amniotic mesenchymal stem cells improves neurological recovery after acute traumatic spinal cord injury in rats.

Iran J Basic Med Sci. 2024

[7]
Functional biomaterials for modulating the dysfunctional pathological microenvironment of spinal cord injury.

Bioact Mater. 2024-5-30

[8]
Injectable Hydrogel Loaded with CDs and FTY720 Combined with Neural Stem Cells for the Treatment of Spinal Cord Injury.

Int J Nanomedicine. 2024

[9]
Polyacrylic Acid-Coated Selenium-Doped Carbon Dots Inhibit Ferroptosis to Alleviate Chemotherapy-Associated Acute Kidney Injury.

Adv Sci (Weinh). 2024-7

[10]
CD44-targeting hyaluronic acid-selenium nanoparticles boost functional recovery following spinal cord injury.

J Nanobiotechnology. 2024-1-23

本文引用的文献

[1]
Aligned collagen scaffold combination with human spinal cord-derived neural stem cells to improve spinal cord injury repair.

Biomater Sci. 2020-9-21

[2]
Selenium-Doped Carbon Quantum Dots Act as Broad-Spectrum Antioxidants for Acute Kidney Injury Management.

Adv Sci (Weinh). 2020-4-29

[3]
Transplanting neural progenitor cells to restore connectivity after spinal cord injury.

Nat Rev Neurosci. 2020-6-9

[4]
Carbon dots as versatile nanoarchitectures for the treatment of neurological disorders and their theranostic applications: A review.

Adv Colloid Interface Sci. 2020-2-19

[5]
Implantation of a functional TEMPO-hydrogel induces recovery from rat spinal cord transection through promoting nerve regeneration and protecting bladder tissue.

Biomater Sci. 2020-3-17

[6]
Clinical Neurorestorative Therapeutic Guidelines for Spinal Cord Injury (IANR/CANR version 2019).

J Orthop Translat. 2019-11-11

[7]
Selective Modulation of A1 Astrocytes by Drug-Loaded Nano-Structured Gel in Spinal Cord Injury.

ACS Nano. 2019-12-30

[8]
Synthesis of Sulfur-Selenium Doped Carbon Quantum Dots for Biological Imaging and Scavenging Reactive Oxygen Species.

Sci Rep. 2019-12-23

[9]
Nanoparticles with antioxidant enzymes protect injured spinal cord from neuronal cell apoptosis by attenuating mitochondrial dysfunction.

J Control Release. 2020-1-10

[10]
A MnO Nanoparticle-Dotted Hydrogel Promotes Spinal Cord Repair Regulating Reactive Oxygen Species Microenvironment and Synergizing with Mesenchymal Stem Cells.

ACS Nano. 2019-12-2

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索