Literature DB >> 15180452

The pathobiology of osteoarthritis and the rationale for using the chondroitin sulfate for its treatment.

Nicola Volpi1.   

Abstract

Structure-modifying osteoarthritis (OA) drugs are agents that reverse, retard, or stabilize the pathology of OA, thereby providing symptomatic relief in the long-term treatment. The objective of this review is to evaluate the literature on chondroitin sulfate (CS) with respect to the pathobiology of OA to ascertain whether this agent should be classified as a symptomatic slow-acting drug (SYSADOA), a compound that has a slow onset of action and improve OA symptoms after a couple of weeks. CS exhibits a wide range of biological activities and from a pharmacological point of view it produces a slow but gradual decrease of the clinical symptoms of OA and these benefits last for a long period after the end of treatment. Many literature data show that CS could have an anti-inflammatory activity and a chondroprotective action by modifying the structure of cartilage. These properties are also related to the oral adsorption of this molecule as high-molecular mass compounds having clusters of sulfate groups and high charge density capable of exert their chondroprotective activity in vivo.

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Year:  2004        PMID: 15180452     DOI: 10.2174/1568008043339929

Source DB:  PubMed          Journal:  Curr Drug Targets Immune Endocr Metabol Disord        ISSN: 1568-0088


  7 in total

1.  Immune modulation by chondroitin sulfate and its degraded disaccharide product in the development of an experimental model of multiple sclerosis.

Authors:  Juhua Zhou; Prakash Nagarkatti; Yin Zhong; Mitzi Nagarkatti
Journal:  J Neuroimmunol       Date:  2010-06       Impact factor: 3.478

Review 2.  Cartilage imaging: motivation, techniques, current and future significance.

Authors:  Thomas M Link; Robert Stahl; Klaus Woertler
Journal:  Eur Radiol       Date:  2006-11-09       Impact factor: 5.315

3.  Effect of chondroitin sulphate in a rabbit model of atherosclerosis aggravated by chronic arthritis.

Authors:  G Herrero-Beaumont; M E Marcos; O Sánchez-Pernaute; R Granados; L Ortega; E Montell; J Vergés; J Egido; R Largo
Journal:  Br J Pharmacol       Date:  2008-04-21       Impact factor: 8.739

4.  The effect of substitution of the N-acetyl groups of N-acetylgalactosamine residues in chondroitin sulfate on its degradation by chondroitinase ABC.

Authors:  Subbarao V Madhunapantula; Rajeshwara N Achur; Veer P Bhavanandan; D Channe Gowda
Journal:  Glycoconj J       Date:  2007-05-29       Impact factor: 2.916

5.  Rheological Behavior of a New Mucoadhesive Oral Formulation Based on Sodium Chondroitin Sulfate, Xyloglucan and Glycerol.

Authors:  Tiziana Maria Grazia Pecora; Barbara Ragazzo; Walter Bertin; Alessia Ragonese; Marco Mascagni; Paola Maffei; Rosario Pignatello
Journal:  J Funct Biomater       Date:  2021-04-28

6.  Short- and Long-Term Effectiveness of Supplementation with Non-Animal Chondroitin Sulphate on Inflammation, Oxidative Stress and Functional Status in Obese Subjects with Moderate Knee Osteoarthritis before and after Physical Stress: A Randomized, Double-Blind, Placebo-Controlled Trial.

Authors:  Mariangela Rondanelli; Niccolò Miraglia; Pietro Putignano; Gabriella Peroni; Milena Anna Faliva; Maurizio Naso; Clara Gasparri; Vittoria Infantino; Mara Nichetti; Nicola Volpi; Federica Capitani; Veronica Mantovani; Simone Perna
Journal:  Antioxidants (Basel)       Date:  2020-12-07

Review 7.  Immunomodulatory and anti-inflammatory effects of chondroitin sulphate.

Authors:  Patrick du Souich; Antonio G García; Josep Vergés; Eulàlia Montell
Journal:  J Cell Mol Med       Date:  2009-06-11       Impact factor: 5.310

  7 in total

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