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Impact of Symptomatic Slow-Acting Drugs on Inflammatory Pathways in Osteoarthritis: Therapeutic Advances and Future
Vitor Alfredo de Santana Silva1,2, Katarine Gabriely Aurista do Nascimento1,2, Priscila Gubert1,2
1Department of Biochemistry/Keizo Asami Institute-iLIKA, Federal University of Pernambuco (UFPE), Av. Prof. Moraes Rego, s/n, Cidade Universitária, CEP: 50670-420 Recife, Pernambuco, Brazil.
Abstract:
Osteoarthritis (OA) is a leading cause of physical disability, psychological distress, and a significant economic burden worldwide. Current treatments alleviate symptoms; however, disease progression remains largely uncontrolled, highlighting the urgent need for investigation of disease-modifying therapies. Symptomatic slow-acting drugs for osteoarthritis (SYSADOAs), such as glucosamine (GlcN), chondroitin sulfate (CS), and hyaluronic acid (HA), have gained increasing attention for their potential benefits in alleviating pain and mitigating the inflammatory and degenerative processes that characterize OA. These compounds modulate several homeostatic mechanisms, promoting anti-inflammatory, antioxidant, antiapoptotic, and anabolic countermensuring effects. Nevertheless, debates regarding their long-term efficacy and safety remain controversial, which explains why major osteoarthritis societies do not provide the same recommendations for the pharmacological treatment of OA. In this context, this review critically evaluates the current evidence surrounding HA, GlcN, and CS, highlighting their safety, mechanisms of action, and promising therapeutic perspectives for modifying the natural course of knee, hand, and hip OA.
Insights
Osteoarthritis (OA) treatments like glucosamine (GlcN), chondroitin sulfate (CS), and hyaluronic acid (HA) show potential for disease modification. This review examines their safety and efficacy for OA, offering therapeutic perspectives.
Area of Science:
- Orthopedics and Rheumatology
- Pharmacology
- Biochemistry
Background:
- Osteoarthritis (OA) is a major cause of disability and economic burden, with current treatments primarily managing symptoms.
- Disease-modifying therapies are urgently needed as OA progression is largely uncontrolled.
- Symptomatic slow-acting drugs for osteoarthritis (SYSADOAs), including glucosamine (GlcN), chondroitin sulfate (CS), and hyaluronic acid (HA), are gaining attention.
Purpose of the Study:
- To critically evaluate the current evidence on the safety, mechanisms of action, and therapeutic potential of HA, GlcN, and CS for OA.
- To explore their role in modifying the natural course of knee, hand, and hip OA.
- To address the ongoing debates regarding their long-term efficacy and safety.
Main Methods:
- Systematic review of existing scientific literature.
- Analysis of studies investigating the homeostatic, anti-inflammatory, antioxidant, antiapoptotic, and anabolic effects of HA, GlcN, and CS.
- Evaluation of clinical trial data on the efficacy and safety of these SYSADOAs.
Main Results:
- HA, GlcN, and CS modulate key homeostatic mechanisms involved in OA.
- These compounds demonstrate anti-inflammatory, antioxidant, antiapoptotic, and anabolic effects.
- Evidence regarding their long-term efficacy and safety remains debated, leading to varied recommendations.
Conclusions:
- HA, GlcN, and CS hold promise as disease-modifying agents for OA.
- Further research is needed to clarify their long-term benefits and establish consistent treatment guidelines.
- These SYSADOAs offer potential therapeutic perspectives for managing knee, hand, and hip OA progression.
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