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本文引用的文献

1
Suppression of NF-κB activity via nanoparticle-based siRNA delivery alters early cartilage responses to injury.基于纳米颗粒的 siRNA 递送来抑制 NF-κB 活性可改变早期软骨对损伤的反应。
Proc Natl Acad Sci U S A. 2016 Oct 11;113(41):E6199-E6208. doi: 10.1073/pnas.1608245113. Epub 2016 Sep 28.
2
Inflammation in joint injury and post-traumatic osteoarthritis.关节损伤与创伤后骨关节炎中的炎症
Osteoarthritis Cartilage. 2015 Nov;23(11):1825-34. doi: 10.1016/j.joca.2015.08.015.
3
Single intra-articular dexamethasone injection immediately post-surgery in a rabbit model mitigates early inflammatory responses and post-traumatic osteoarthritis-like alterations.在兔模型中,术后立即进行单次关节内注射地塞米松可减轻早期炎症反应和创伤后骨关节炎样改变。
J Orthop Res. 2015 Dec;33(12):1826-34. doi: 10.1002/jor.22972. Epub 2015 Jul 7.
4
Targeting pro-inflammatory cytokines following joint injury: acute intra-articular inhibition of interleukin-1 following knee injury prevents post-traumatic arthritis.针对关节损伤后的促炎细胞因子:膝关节损伤后对白细胞介素-1进行急性关节腔内抑制可预防创伤后关节炎。
Arthritis Res Ther. 2014 Jun 25;16(3):R134. doi: 10.1186/ar4591.
5
Early response of mouse joint tissue to noninvasive knee injury suggests treatment targets.早期非侵入性膝关节损伤对小鼠关节组织的反应提示了治疗靶点。
Arthritis Rheumatol. 2014 May;66(5):1256-65. doi: 10.1002/art.38375.
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Mechanisms of nanoparticle-mediated siRNA transfection by melittin-derived peptides.蜂毒素衍生肽介导的纳米颗粒 siRNA 转染的机制。
ACS Nano. 2013 Oct 22;7(10):8605-15. doi: 10.1021/nn403311c. Epub 2013 Sep 26.
7
Post-traumatic osteoarthritis: from mouse models to clinical trials.创伤后骨关节炎:从小鼠模型到临床试验。
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8
Melittin derived peptides for nanoparticle based siRNA transfection.蜂毒素衍生肽用于基于纳米颗粒的 siRNA 转染。
Biomaterials. 2013 Apr;34(12):3110-9. doi: 10.1016/j.biomaterials.2013.01.037. Epub 2013 Feb 4.
9
Effects of intraarticular IL1-Ra for acute anterior cruciate ligament knee injury: a randomized controlled pilot trial (NCT00332254).关节内注射 IL1-Ra 治疗急性前交叉韧带膝关节损伤的随机对照初步试验(NCT00332254)。
Osteoarthritis Cartilage. 2012 Apr;20(4):271-8. doi: 10.1016/j.joca.2011.12.009. Epub 2012 Jan 10.
10
Intraarticular injection of anakinra in osteoarthritis of the knee: a multicenter, randomized, double-blind, placebo-controlled study.膝关节骨关节炎中阿那白滞素关节内注射:一项多中心、随机、双盲、安慰剂对照研究。
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靶向核因子κB的纳米疗法减轻关节损伤后的急性疼痛。

Nanotherapy Targeting NF-κB Attenuates Acute Pain After Joint Injury.

作者信息

Yan Huimin, Duan Xin, Collins Kelsey H, Springer Luke E, Guilak Farshid, Wickline Samuel A, Rai M Farooq, Pan Hua, Pham Christine T N

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, MO.

Department of Orthopaedic Surgery, Washington University School of Medicine, St. Louis, MO.

出版信息

Precis Nanomed. 2019;2(1):245-248. doi: 10.33218/prnano2(1).181129.1. Epub 2019 Jan 12.

DOI:10.33218/prnano2(1).181129.1
PMID:31681908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6824724/
Abstract

Inflammation after joint injury leads to joint responses that result in eventual osteoarthritis development. Blockade of inflammation, by suppressing NF-κB expression, has been shown to reduce joint injury-induced chondrocyte apoptosis and reactive synovitis . Herein, we demonstrate that the suppression of NF-κB p65 expression also significantly mitigates the acute pain sensitivity induced by mechanical injury to the joint. These results suggest that early intervention with anti-NF-κB nanotherapy mitigates both structural and pain-related outcomes, which in turn may impact the progression of post-traumatic osteoarthritis.

摘要

关节损伤后的炎症会引发关节反应,最终导致骨关节炎的发展。通过抑制NF-κB表达来阻断炎症,已被证明可减少关节损伤诱导的软骨细胞凋亡和反应性滑膜炎。在此,我们证明抑制NF-κB p65表达也能显著减轻关节机械损伤引起的急性疼痛敏感性。这些结果表明,抗NF-κB纳米疗法的早期干预可减轻结构和疼痛相关的后果,进而可能影响创伤后骨关节炎的进展。