Document Detail


Biological actions of curcumin on articular chondrocytes.
MedLine Citation:
PMID:  19836480     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
OBJECTIVES: Curcumin (diferuloylmethane) is the principal biochemical component of the spice turmeric and has been shown to possess potent anti-catabolic, anti-inflammatory and antioxidant, properties. This article aims to provide a summary of the actions of curcumin on articular chondrocytes from the available literature with the use of a text-mining tool. We highlight both the potential benefits and drawbacks of using this chemopreventive agent for treating osteoarthritis (OA). We also explore the recent literature on the molecular mechanisms of curcumin mediated alterations in gene expression mediated via activator protein 1 (AP-1)/nuclear factor-kappa B (NF-kappaB) signalling in chondrocytes, osteoblasts and synovial fibroblasts. METHODS: A computer-aided search of the PubMed/Medline database aided by a text-mining tool to interrogate the ResNet Mammalian database 6.0. RESULTS: Recent work has shown that curcumin protects human chondrocytes from the catabolic actions of interleukin-1 beta (IL-1beta) including matrix metalloproteinase (MMP)-3 up-regulation, inhibition of collagen type II and down-regulation of beta1-integrin expression. Curcumin blocks IL-1beta-induced proteoglycan degradation, AP-1/NF-kappaB signalling, chondrocyte apoptosis and activation of caspase-3. CONCLUSIONS: The available data from published in vitro and in vivo studies suggest that curcumin may be a beneficial complementary treatment for OA in humans and companion animals. Nevertheless, before initiating extensive clinical trials, more basic research is required to improve its solubility, absorption and bioavailability and gain additional information about its safety and efficacy in different species. Once these obstacles have been overcome, curcumin and structurally related biochemicals may become safer and more suitable nutraceutical alternatives to the non-steroidal anti-inflammatory drugs that are currently used for the treatment of OA.
Authors:
Y Henrotin; A L Clutterbuck; D Allaway; E M Lodwig; P Harris; M Mathy-Hartert; M Shakibaei; A Mobasheri
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Review     Date:  2009-10-08
Journal Detail:
Title:  Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society     Volume:  18     ISSN:  1522-9653     ISO Abbreviation:  Osteoarthr. Cartil.     Publication Date:  2010 Feb 
Date Detail:
Created Date:  2010-02-03     Completed Date:  2010-06-29     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9305697     Medline TA:  Osteoarthritis Cartilage     Country:  England    
Other Details:
Languages:  eng     Pagination:  141-9     Citation Subset:  IM    
Copyright Information:
Copyright 2009 Osteoarthritis Research Society International. All rights reserved.
Affiliation:
University of Li?ge, Institute of Pathology, Sart-Tilman, Li?ge, Belgium. yhenrotin@ulg.ac.be
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Antigens, CD18 / metabolism
Apoptosis / drug effects
Cartilage, Articular / cytology,  metabolism*
Caspase 3 / metabolism
Cells, Cultured
Chondrocytes / drug effects*,  metabolism
Collagen Type II / metabolism
Curcumin / pharmacology*
Enzyme Inhibitors / pharmacology*
Humans
Inflammation / physiopathology
Interleukin-1beta / metabolism
Matrix Metalloproteinase 3 / metabolism
NF-kappa B / physiology
Osteoarthritis / drug therapy,  prevention & control
Signal Transduction / drug effects*,  genetics,  physiology
Transcription Factor AP-1 / physiology
Grant Support
ID/Acronym/Agency:
BBSRC/S/M/2006/13141//Biotechnology and Biological Sciences Research Council
Chemical
Reg. No./Substance:
0/Antigens, CD18; 0/Collagen Type II; 0/Enzyme Inhibitors; 0/Interleukin-1beta; 0/NF-kappa B; 0/Transcription Factor AP-1; 458-37-7/Curcumin; EC 3.4.22.-/Caspase 3; EC 3.4.24.17/Matrix Metalloproteinase 3

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  A novel form of 4-1BBL has better immunomodulatory activity than an agonistic anti-4-1BB Ab without ...
Next Document:  Surgical management of MEN-1 and -2: state of the art.