4.4 Article

Panax notoginseng saponins alleviate osteoporosis and joint destruction in rabbits with antigen-induced arthritis

Journal

EXPERIMENTAL AND THERAPEUTIC MEDICINE
Volume 22, Issue 5, Pages -

Publisher

SPANDIDOS PUBL LTD
DOI: 10.3892/etm.2021.10737

Keywords

antigen-induced arthritis; Panax notoginseng saponins; rheumatoid arthritis; osteoporosis; joint destruction

Funding

  1. Shanghai Science and Technology Commission [19401935400]
  2. construction project of Li Fei Yue's National Famous TCM [MLZJGZS-2017001]
  3. Construction Project of Li Fei Yue's Shanghai Famous TCM Research Studio [SHGZS-2017010]
  4. National Natural Science Foundation of China [81302987]
  5. National Training Program for Innovative Talents of Traditional Chinese Medicine

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The study evaluated the therapeutic effect of Panax notoginseng saponins (PNS) on immune arthritis, showing that PNS significantly alleviated arthritic muscular atrophy and inflammation, and protected chondrocytes from damage. Additionally, rabbits treated with PNS exhibited improved bone density and microarchitecture.
Although a number of anti-rheumatic drugs and biologics may be used to alleviate the symptoms of rheumatoid arthritis (RA), these compounds have been associated with bone loss and joint destruction; thus, alternative treatment approaches are required. In the present study, various plant extracts were evaluated for their capacity to inhibit joint destruction, and Panax notoginseng saponins (PNS), obtained from the Traditional Chinese Medicine Panax notoginseng, was identified as such a compound. Therefore, a rabbit antigen-induced arthritis (AIA) model was generated by immunization with ovalbumin in Freund's complete adjuvant, followed by treatment with PNS for 3 months. The morphology of the quadriceps femoris muscle, cartilage chondrocytes and skeletal elements was histologically observed by transmission electron microscopy (TEM), as well as micro-computed tomography. The results revealed that PNS significantly reduced the histopathological alterations associated with arthritic muscular atrophy and inflammation. In addition, TEM demonstrated that PNS protected chondrocytes from RA-associated damage. Furthermore, the bone density and microarchitecture in rabbits treated with PNS were markedly improved compared with those of the model group. Collectively, these data indicated that treatment with PNS may relieve osteoporosis and prevent joint and bone destruction in AIA.

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