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本文引用的文献

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Spinal mitochondrial-derived ROS contributes to remifentanil-induced postoperative hyperalgesia via modulating NMDA receptor in rats.脊髓线粒体源性活性氧通过调节大鼠N-甲基-D-天冬氨酸受体促成瑞芬太尼诱导的术后痛觉过敏。
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Central Nervous System Injury and Nicotinamide Adenine Dinucleotide Phosphate Oxidase: Oxidative Stress and Therapeutic Targets.中枢神经系统损伤与烟酰胺腺嘌呤二核苷酸磷酸氧化酶:氧化应激与治疗靶点
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A simple method for the synthesis of porous polymeric vesicles and their application as MR contrast agents.一种合成多孔聚合物囊泡的简单方法及其作为磁共振造影剂的应用。
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Reactive Oxygen Species Donors Increase the Responsiveness of Dorsal Horn Neurons and Induce Mechanical Hyperalgesia in Rats.活性氧供体增加大鼠背根神经节神经元的反应性并诱导机械性痛觉过敏。
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Oral nonsteroidal anti-inflammatory drugs for neuropathic pain.用于神经性疼痛的口服非甾体抗炎药。
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Intrathecal Administration of Tempol Reduces Chronic Constriction Injury-Induced Neuropathic Pain in Rats by Increasing SOD Activity and Inhibiting NGF Expression.鞘内注射Tempol通过增加超氧化物歧化酶(SOD)活性和抑制神经生长因子(NGF)表达减轻大鼠慢性压迫性损伤诱导的神经性疼痛。
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Anti-hyperalgesic and anti-nociceptive potentials of standardized grape seed proanthocyanidin extract against CCI-induced neuropathic pain in rats.标准化葡萄籽原花青素提取物对CCI诱导的大鼠神经性疼痛的抗痛觉过敏和抗伤害感受作用
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Drug delivery, cell-based therapies, and tissue engineering approaches for spinal cord injury.用于脊髓损伤的药物递送、基于细胞的疗法和组织工程方法。
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10
Supression of chronic central pain by superoxide dismutase in rats with spinal cord injury: Inhibition of the NMDA receptor implicated.超氧化物歧化酶对脊髓损伤大鼠慢性中枢性疼痛的抑制作用:与N-甲基-D-天冬氨酸受体抑制有关。
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载超氧化物歧化酶的多孔聚合物泡囊作为高效抗氧化剂治疗神经病理性疼痛。

Superoxide Dismutase-Loaded Porous Polymersomes as Highly Efficient Antioxidants for Treating Neuropathic Pain.

机构信息

Department of Bioengineering, University of Pennsylvania, 210 South 33rd Street, 240 Skirkanich Hall, Philadelphia, PA, 19104, USA.

Department of Systems Pharmacology and Translational Therapeutics, Center for Translational Targeted Therapeutics and Nanomedicine of the Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.

出版信息

Adv Healthc Mater. 2017 Sep;6(17). doi: 10.1002/adhm.201700500. Epub 2017 Jul 3.

DOI:10.1002/adhm.201700500
PMID:28671302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5591629/
Abstract

A highly efficient antioxidant is developed by encapsulating superoxide dismutase (SOD) within the aqueous interior of porous polymersomes. The porous polymersomes provide a permeable membrane that allows free superoxide radicals to pass into the aqueous interior and interact with the encapsulated antioxidant enzyme SOD. In vivo studies in the rat demonstrate that administration of SOD-encapsulated porous polymersomes can prevent neuropathic pain after nerve root compression more effectively than treatment with free antioxidant enzyme alone.

摘要

一种高效抗氧化剂是通过将超氧化物歧化酶(SOD)封装在多孔聚合物泡囊的水相内部来开发的。多孔聚合物泡囊提供了一个可渗透的膜,允许游离的超氧自由基进入水相内部并与封装的抗氧化酶 SOD 相互作用。在大鼠体内研究中,与单独使用游离抗氧化酶治疗相比,给予 SOD 封装的多孔聚合物泡囊可更有效地预防神经根压迫后的神经病理性疼痛。