4.2 Article

Total Saponins from Nigella glandulifera Seeds Ameliorate Adjuvant-Induced Rheumatoid Arthritis in Rats by Inhibition of an Inflammatory Response and Bone Erosion

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BIOMED RESEARCH INTERNATIONAL
卷 2021, 期 -, 页码 -

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HINDAWI LTD
DOI: 10.1155/2021/6613527

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资金

  1. National Natural Science Foundation of China [81660655, U1803281]
  2. Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences [2018RC350013]

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The study investigated the antiarthritic effects of total saponins from Nigella glandulifera seeds in rats with adjuvant-induced rheumatoid arthritis. It was found that the saponins inhibited arthritis by restoring the secretion and expression of inflammatory cytokines, increasing regulatory T cells, and protecting bone. This suggests that total saponins from Nigella glandulifera seeds could be a potential novel treatment for rheumatoid arthritis.
Rheumatoid arthritis (RA) is a widespread inflammatory disease whose clinical manifestations are joint swelling, pain, and disability, affecting approximately 1% of individuals worldwide. Conventional anti-RA drugs currently used in clinic have severe side effects. The present study is aimed at investigating the antiarthritic effects of total saponins from Nigella glandulifera seeds (TSNGS) in rats with adjuvant-induced rheumatoid arthritis (AIA). Arthritis score, paw swelling, and body weight were monitored throughout the period of TSNGS treatment. The histopathological features and levels of cytokines, including IFN-gamma, TNF-alpha, IL-1 beta, IL-4, IL-6, IL-10, and IL-17A, and OPG/RANKL signaling, were measured to determine the amelioration by TSNGS and its potential mechanisms on the inflammatory response and bone erosion. The differentiation of regulatory T cells (Tregs) in serum was assessed by flow cytometry. The results demonstrate that TSNGS at 10 mg/kg, 50 mg/kg, and 250 mg/kg inhibited AIA-induced clinical score, paw swelling, and histological changes. TSNGS reduced the immune-inflammatory reaction by restoring the secretion and expression of inflammatory cytokines and elevating the proportion of CD4(+) CD25(+) Tregs, accompanied by an increase in transcription factor Foxp3 levels. TSNGS also displayed bone protection by upregulation of the OPG/RANKL pathway. Collectively, TSNGS inhibited arthritis in AIA rats and so represents a potential novel treatment for RA.

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