4.3 Article

Achyranthes bidentate saponins protect rat articular chondrocytes against interleukin-1β-induced inflammation and apoptosis in vitro

期刊

KAOHSIUNG JOURNAL OF MEDICAL SCIENCES
卷 33, 期 2, 页码 62-68

出版社

WILEY
DOI: 10.1016/j.kjms.2016.11.004

关键词

Achyranthes bidentata saponins; Apoptosis; Chondrocyte; Inflammation; Osteoarthritis

资金

  1. Promotion Program for Young and Middle-aged Teacher in Science and Technology Research of Huaqiao University [ZQN-PY420]
  2. Key Project of Quanzhou City Science and Technology Program [2011Z8]
  3. Natural Science Foundation of Fujian Province of China [2015J01364]

向作者/读者索取更多资源

Achyranthes bidentate Blume (Niuxi) is often employed for treatment of arthritis in Traditional Chinese Medicine and possesses anti-inflammatory properties. Phytochemical and pharmacological studies proved the oleanane-type saponins to be the main bioactive principles. In the present study, protective effects of A. bidentata saponins (ABS) on inflammation and apoptosis in interleukine-1 beta (IL-1 beta)-induced chondrocytes were investigated. Rat chondrocytes were pretreated with ABS at 3 mu g/mL, 10 mu g/mL, and 30 mu g/mL, and subsequently stimulated with IL-1 beta (10 ng/mL). Methylthiazolyldiphenyl-tetrazolium bromide assay and annexin V/propidium iodide dual staining demonstrated that ABS could protect IL-1 beta-induced chondrocyte injury. ABS suppressed IL-1 beta-induced apoptosis by suppressing the activation of caspase-3, inhibiting levels of proapoptotic proteins Bax and Bad, decreasing p53 protein phosphorylation, and promoting the expression of antiapoptotic protein Bcl-x(L) and proliferating cell nuclear antigen. IL-1 beta-induced inflammation and matrix degradation were also alleviated by ABS through the downregulation of the expressions of matrix metalloproteinases 3 and 9 and cyclooxygenase-2. Moreover, ABS inhibited IL-1 beta-induced nuclear factor kappa B activation in rat chondrocytes. We demonstrated, for the first time, the protective effects of ABS on IL-1 beta-stimulated chondrocytes and their molecular mechanisms. Thus, it is suggested that ABS might be a potential drug in the treatment of osteoarthritis. Copyright (C) 2016, Kaohsiung Medical University. Published by Elsevier Taiwan LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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