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Updated: Jan 31, 2026

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Published on: June 19, 2015
Proteoglycans isolated from the bramble shark cartilage show potential anti-osteoarthritic properties
Kizhakkeppurath Kumaran Ajeeshkumar1, Kalladath Venugopal Vishnu1, Raju Navaneethan1
1Biochemistry and Nutrition Division, ICAR-Central Institute of Fisheries Technology, Kochi, Kerala, India.
Abstract:
Osteoarthritis (OA) causes articular cartilage destruction, initiating pain and inflammation in the joints, resulting in joint disability. Medications are available to manage these symptoms; however, their effects on the disease progression are limited. Loss of proteoglycans (PGs) was reported to contribute articular cartilage destruction in OA. Therapeutics approaches were previously studied in the animal models of OA. In the present study, we investigated the oral efficacy of four dosages of PGs (25 mg/kg, 50 mg/kg, 100 mg/kg and 200 mg/kg), isolated from the bramble shark cartilage, in an animal model of OA. Indomethacin was used as a bioequivalent formulation. Primarily, the mass spectrum analysis of the purified PGs obtained from bramble shark cartilage revealed the presence of two unique peptides including AGWLSDGSVR and LDGNPINLSK, that showed sequence similarity with aggrecan core-protein and epiphycan, respectively. The levels of C-reactive protein and uric acid in the OA rats were reduced when treated with PGs. Histopathology analysis displayed less cartilage erosion and neovascularization in OA rats treated with PGs. The X-ray imaging presented higher bone density with 200 mg/kg dosage of PG treatment in OA rats. The expressions of the inflammatory modulators including TNF-α, IL-1β, MMP13, NOS2, IL-10 and COX-2 were found to be moderated with PG treatment. In addition, PG treatment maintained the activities of antioxidant enzymes, including SOD and catalase in the joint tissues with a higher GSH content, in a dose-dependent manner. Taken together, our preliminary findings report the anti-osteoarthritic properties of PGs and recommend to evaluate its efficacy and safety in randomized trials.
Insights
Proteoglycans (PGs) from bramble shark cartilage show promise in treating osteoarthritis (OA) by reducing inflammation and preserving cartilage. Further clinical trials are recommended for this potential OA therapy.
Area of Science:
- Biochemistry
- Pharmacology
- Biomedical Engineering
Background:
- Osteoarthritis (OA) is characterized by articular cartilage destruction, leading to joint pain, inflammation, and disability.
- Current medications offer limited effects on OA disease progression, highlighting the need for novel therapeutic strategies.
- Loss of proteoglycans (PGs) is a key factor in OA-related cartilage damage.
Purpose of the Study:
- To investigate the oral efficacy of proteoglycans (PGs) isolated from bramble shark cartilage in an animal model of osteoarthritis (OA).
- To evaluate the dose-dependent effects of PGs on OA-related pathological changes and inflammatory markers.
Main Methods:
- Purification and mass spectrum analysis of PGs from bramble shark cartilage, identifying unique peptides.
- Administration of four dosages of PGs (25-200 mg/kg) to an OA animal model, with indomethacin as a control.
- Assessment of therapeutic effects through analysis of C-reactive protein, uric acid, histopathology, X-ray imaging, inflammatory modulators, and antioxidant enzyme activities.
Main Results:
- PG treatment significantly reduced C-reactive protein and uric acid levels in OA rats.
- Histopathology revealed reduced cartilage erosion and neovascularization, while X-ray imaging showed increased bone density with higher PG dosages.
- PGs modulated inflammatory modulators (TNF-α, IL-1β, MMP13, NOS2, IL-10, COX-2) and maintained antioxidant enzyme activities (SOD, catalase, GSH) in a dose-dependent manner.
Conclusions:
- Proteoglycans (PGs) from bramble shark cartilage demonstrate significant anti-osteoarthritic properties in an animal model.
- PGs effectively reduce inflammation, preserve cartilage integrity, and enhance bone density.
- These preliminary findings support further evaluation of PGs in randomized clinical trials for osteoarthritis treatment.
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