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本文引用的文献

1
Osteoarthritis year in review 2017: clinical.2017 年骨关节炎年度回顾:临床篇。
Osteoarthritis Cartilage. 2018 Mar;26(3):319-325. doi: 10.1016/j.joca.2017.11.014. Epub 2017 Dec 8.
2
Osteoarthritis biomarkers: year in review.骨关节炎生物标志物:年度回顾。
Osteoarthritis Cartilage. 2018 Mar;26(3):312-318. doi: 10.1016/j.joca.2017.10.016. Epub 2017 Oct 26.
3
Immunomodulatory potential of nanocurcumin-based formulation.基于纳米姜黄素的制剂的免疫调节潜力。
Inflammopharmacology. 2017 Dec;25(6):609-619. doi: 10.1007/s10787-017-0395-3. Epub 2017 Sep 18.
4
Liposomal curcumin and its application in cancer.脂质体姜黄素及其在癌症中的应用。
Int J Nanomedicine. 2017 Aug 21;12:6027-6044. doi: 10.2147/IJN.S132434. eCollection 2017.
5
Curcumin-loaded poly lactic-co-glycolic acid nanoparticles effects on mono-iodoacetate -induced osteoarthritis in rats.载姜黄素聚乳酸-乙醇酸共聚物纳米粒对大鼠单碘乙酸盐诱导骨关节炎的影响
Vet Res Forum. 2017 Spring;8(2):155-161. Epub 2017 Jun 15.
6
Effect of vitamin E on oxidative stress level in blood, synovial fluid, and synovial tissue in severe knee osteoarthritis: a randomized controlled study.维生素E对重度膝关节骨关节炎患者血液、滑液及滑膜组织氧化应激水平的影响:一项随机对照研究
BMC Musculoskelet Disord. 2017 Jun 29;18(1):281. doi: 10.1186/s12891-017-1637-7.
7
Nanoformulated natural therapeutics for management of streptozotocin-induced diabetes: potential use of curcumin nanoformulation.用于治疗链脲佐菌素诱导糖尿病的纳米制剂天然疗法:姜黄素纳米制剂的潜在用途
Nanomedicine (Lond). 2017 Jul;12(14):1689-1711. doi: 10.2217/nnm-2017-0106. Epub 2017 Jun 21.
8
Articular inflammation induced by an enzymatically-inactive Lys49 phospholipase A: activation of endogenous phospholipases contributes to the pronociceptive effect.无酶活性的赖氨酸49磷脂酶A诱导的关节炎症:内源性磷脂酶的激活促成伤害感受效应。
J Venom Anim Toxins Incl Trop Dis. 2017 Mar 23;23:18. doi: 10.1186/s40409-017-0104-0. eCollection 2017.
9
Radiation-induced surge of macrophage foam cell formation, oxidative damage, and cytokine release is attenuated by a nanoformulation of curcumin.姜黄素纳米制剂可减轻辐射诱导的巨噬细胞泡沫细胞形成、氧化损伤和细胞因子释放激增。
Int J Radiat Biol. 2017 Mar;93(3):303-314. doi: 10.1080/09553002.2016.1242817. Epub 2016 Nov 3.
10
Protein oxidation, nitration and glycation biomarkers for early-stage diagnosis of osteoarthritis of the knee and typing and progression of arthritic disease.用于膝关节骨关节炎早期诊断以及关节炎疾病分型和病情进展的蛋白质氧化、硝化和糖基化生物标志物。
Arthritis Res Ther. 2016 Oct 27;18(1):250. doi: 10.1186/s13075-016-1154-3.

高生物利用度姜黄素粉可抑制单碘乙酸盐(MIA)诱导的骨关节炎大鼠的关节软骨损伤。

Highly bioavailable curcumin powder suppresses articular cartilage damage in rats with mono-iodoacetate (MIA)-induced osteoarthritis.

作者信息

Park Hyun-Ji, Lee Chul-Kyu, Song Si-Hwan, Yun Jee-Hye, Lee Ahsa, Park Hee-Jung

机构信息

Gyeonggi Bio Research Center, Chemon Inc., Gwanggyo-ro, Yeongtong-gu, Suwon, Gyeonggi-do 16229 Korea.

2Handok Inc., 132 Teheran Street, Gangnam-gu, Seoul, 06235 Korea.

出版信息

Food Sci Biotechnol. 2019 Oct 5;29(2):251-263. doi: 10.1007/s10068-019-00679-5. eCollection 2020 Feb.

DOI:10.1007/s10068-019-00679-5
PMID:32064134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6992805/
Abstract

This study was performed to investigate the effects of highly bioavailable curcumin as Theracurmin (TC) in rats with monosodium iodoacetate (MIA)-induced osteoarthritis (OA). Seventy-seven male Wistar rats were divided into six groups: normal, negative control (MIA only), positive control (Cerebrex), and three experimental groups treated with 500, 1300, or 2600 mg/kg of TC for 5 weeks. MIA injection-induced OA caused 30% weight-bearing imbalance whereas weight bearing imbalance was significantly improved in the TC groups. Mankin scores revealed TC treatment had significantly ameliorated cartilage damage and chondrocyte decrease. The expressions of nitrotyrosine, tumor necrosis factor-α, phosphorylated nuclear factor kappa B cells, and cleaved caspase-3 were markedly increased in rat with MIA-induced OA, but the TC-treated groups exhibited a significant reduction in the number of immunoreactive cells in a dose-dependent manner. In conclusion, administration of TC contributes to the anti-arthritic effect in rat with MIA-induced OA.

摘要

本研究旨在探讨高生物利用度姜黄素(Theracurmin,TC)对碘乙酸钠(MIA)诱导的大鼠骨关节炎(OA)的影响。77只雄性Wistar大鼠分为六组:正常组、阴性对照组(仅注射MIA)、阳性对照组(使用Cerebrex)以及三个实验组,分别用500、1300或2600 mg/kg的TC处理5周。注射MIA诱导的OA导致30%的负重失衡,而TC组的负重失衡得到显著改善。Mankin评分显示,TC治疗显著改善了软骨损伤和软骨细胞减少的情况。在MIA诱导的OA大鼠中,硝基酪氨酸、肿瘤坏死因子-α、磷酸化核因子κB细胞和裂解的半胱天冬酶-3的表达显著增加,但TC治疗组的免疫反应细胞数量呈剂量依赖性显著减少。总之,给予TC有助于对MIA诱导的OA大鼠产生抗关节炎作用。