Literature DB >> 26980567

Chondroitin Sulfate and Glucosamine as Disease Modifying Anti- Osteoarthritis Dru gs (DMOADs).

Veronica Mantovani, Francesca Maccari, Nicola Volpi1.   

Abstract

Osteoarthritis is a disabling affliction expected to increase in the coming decades, and disease- modifying osteoarthritis drugs (DMOADs) would be highly desirable adjuncts to symptomatic relief and structure reconstruction as they may delay the disease process. Chondroitin sulfate and glucosamine have been observed to exert beneficial effects on the metabolism of various cells involved in osteoarthritis as well as in animal models and clinical trials. Clinical trials have reported beneficial effects of both these biological agents, alone or in combination, on pain and functions as well as their structure-modifying capacity reported and analyzed in recent meta-analyses. Nonetheless, the effectiveness of these bioactive (macro)molecules as DMOADs reported from randomized trials is mismatched. Current studies with varying levels of evidence suggest that chondroitin sulfate and glucosamine can modify the disease progression but at the same time there are not absolute certainties on their efficacy in modifying the course of the disease. This comprehensive review aims to clarify the role of these compounds in the therapeutic molecules/ drugs useful to patients affected by osteoarthritis.

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Year:  2016        PMID: 26980567     DOI: 10.2174/0929867323666160316123749

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  7 in total

1.  CHSY1 is upregulated and acts as tumor promotor in gastric cancer through regulating cell proliferation, apoptosis, and migration.

Authors:  Jingjing Liu; Zhenwei Tian; Tianzhou Liu; Dacheng Wen; Zhiming Ma; Yuanda Liu; Jiaming Zhu
Journal:  Cell Cycle       Date:  2021-08-19       Impact factor: 5.173

2.  Identification of chondroitin polymerizing factor (CHPF) as tumor promotor in cholangiocarcinoma through regulating cell proliferation, cell apoptosis and cell migration.

Authors:  Xiaohui Duan; Jianhui Yang; Bo Jiang; Wenbin Duan; Rongguang Wei; Hui Zhang; Xianhai Mao
Journal:  Cell Cycle       Date:  2021-03-02       Impact factor: 4.534

3.  Glycosaminoglycans and Proteoglycans.

Authors:  Vitor H Pomin; Barbara Mulloy
Journal:  Pharmaceuticals (Basel)       Date:  2018-02-27

4.  Seomae mugwort and jaceosidin attenuate osteoarthritic cartilage damage by blocking IκB degradation in mice.

Authors:  Hyemi Lee; Dain Jang; Jimin Jeon; Chanmi Cho; Sangil Choi; Seong Jae Han; Eunjeong Oh; Jiho Nam; Chan Hum Park; Yu Su Shin; Seung Pil Yun; Siyoung Yang; Li-Jung Kang
Journal:  J Cell Mol Med       Date:  2020-06-11       Impact factor: 5.310

5.  Anti‑chondrocyte apoptosis effect of genistein in treating inflammation‑induced osteoarthritis.

Authors:  Yang Zou; Qiming Liu; Piaoting Guo; Yang Huang; Zhengcong Ye; Jiong Hu
Journal:  Mol Med Rep       Date:  2020-06-18       Impact factor: 2.952

Review 6.  Non-invasive brain stimulation for osteoarthritis.

Authors:  Hui-Qi Zhu; Jing Luo; Xue-Qiang Wang; Xin-An Zhang
Journal:  Front Aging Neurosci       Date:  2022-09-29       Impact factor: 5.702

Review 7.  Current status of top 10 nutraceuticals used for Knee Osteoarthritis in India.

Authors:  Raju Vaishya; Amit Kumar Agarwal; Amish Shah; Vipul Vijay; Abhishek Vaish
Journal:  J Clin Orthop Trauma       Date:  2018-07-20
  7 in total

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