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姜黄素的神经保护作用通过调节 iNOS、COX-2、TGF-β1/2、MMP-9 和 BDNF 的表达缓解大鼠腰椎间盘退变。

Neuroprotective effects of curcumin alleviate lumbar intervertebral disc degeneration through regulating the expression of iNOS, COX‑2, TGF‑β1/2, MMP‑9 and BDNF in a rat model.

机构信息

Department of Orthopedics, The First Affiliated Hospital of Chinese PLA General Hospital, Beijing 100048, P.R. China.

出版信息

Mol Med Rep. 2017 Nov;16(5):6864-6869. doi: 10.3892/mmr.2017.7464. Epub 2017 Sep 12.

Abstract

Curcumin is a natural product with antimutagenic, antitumor, antioxidant and neuroprotective properties. However, to the best of our knowledge, curcumin has yet to be investigated for the treatment of lumbar intervertebral disc degeneration LIDD). The aim of the present study was to investigate whether curcumin can alleviate LIDD through regulating the expression of inducible nitric oxide synthase (iNOS), cyclooxygenase (COX)‑2, transforming growth factor (TGF)‑β1/2, matrix metalloproteinase (MMP)‑9 and brain‑derived neurotrophic factor (BDNF) in a rat model of LIDD. The results of the present study suggest that pretreatment with curcumin can prevent the development of LIDD in rats. It was revealed that treatment with curcumin significantly reduced interleukin (IL)‑1β and IL‑6, iNOS, COX‑2 and MMP‑9 levels in rats with LIDD. In addition, treatment with curcumin reduced the mRNA expression levels of TGF‑β1 and TGF‑β2, whereas it increased the mRNA expression levels of BDNF in rats with LIDD. In conclusion, the present findings indicate that curcumin may exert protective effects on LIDD development, exerting its action through the regulation of iNOS, COX‑2, TGF‑β1/2, MMP‑9 and BDNF.

摘要

姜黄素是一种具有抗突变、抗肿瘤、抗氧化和神经保护作用的天然产物。然而,据我们所知,姜黄素尚未被用于治疗腰椎间盘退行性变(LIDD)。本研究旨在探讨姜黄素是否可以通过调节诱导型一氧化氮合酶(iNOS)、环氧化酶(COX)-2、转化生长因子(TGF)-β1/2、基质金属蛋白酶(MMP)-9 和脑源性神经营养因子(BDNF)的表达来治疗 LIDD。本研究结果表明,姜黄素预处理可以预防大鼠 LIDD 的发生。结果显示,姜黄素治疗可显著降低 LIDD 大鼠白细胞介素(IL)-1β和 IL-6、iNOS、COX-2 和 MMP-9 的水平。此外,姜黄素治疗可降低 TGF-β1 和 TGF-β2 的 mRNA 表达水平,同时增加 LIDD 大鼠 BDNF 的 mRNA 表达水平。综上所述,本研究结果表明,姜黄素可能对 LIDD 的发展具有保护作用,其作用机制可能是通过调节 iNOS、COX-2、TGF-β1/2、MMP-9 和 BDNF。

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