Home LiteratureArticle Details
PMID: 12374621 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Green tea polyphenol epigallocatechin-3-gallate inhibits the IL-1 beta-induced activity and expression of cyclooxygenase-2 and nitric oxide synthase-2 in human chondrocytes.

Free radical biology & medicine ·Vol. 33 ·No. 8 ·2002-10-15 ·Pages 1097-105

Ahmed S, Rahman A, Hasnain A, Lalonde M, Goldberg VM, Haqqi TM

Abstract

We have previously shown that green tea polyphenols inhibit the onset and severity of collagen II-induced arthritis in mice. In the present study, we report the pharmacological effects of green tea polyphenol epigallocatechin-3-gallate (EGCG), on interleukin-1 beta (IL-1 beta)-induced expression and activity of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) in human chondrocytes derived from osteoarthritis (OA) cartilage. Stimulation of human chondrocytes with IL-1 beta (5 ng/ml) for 24 h resulted in significantly enhanced production of nitric oxide (NO) and prostaglandin E(2) (PGE(2)) when compared to untreated controls (p <.001). Pretreament of human chondrocytes with EGCG showed a dose-dependent inhibition in the production of NO and PGE(2) by 48% and 24%, respectively, and correlated with the inhibition of iNOS and COX-2 activities (p <.005). In addition, IL-1 beta-induced expression of iNOS and COX-2 was also markedly inhibited in human chondrocytes pretreated with EGCG (p <.001). Parallel to these findings, EGCG also inhibited the IL-1 beta-induced LDH release in chondrocytes cultures. Overall, the study suggests that EGCG affords protection against IL-1 beta-induced production of catabolic mediators NO and PGE(2) in human chondrocytes by regulating the expression and catalytic activity of their respective enzymes. Furthermore, our results also indicate that ECGC may be of potential therapeutic value for inhibiting cartilage resorption in arthritic joints.

MeSH Terms
Antioxidants/pharmacology Catechin/analogs & derivatives,pharmacology Cells, Cultured/drug effects Chondrocytes/drug effects,enzymology Cyclooxygenase 2 Depression, Chemical Dinoprostone/metabolism Dose-Response Relationship, Drug Enzyme Induction/drug effects Humans Interleukin-1/antagonists & inhibitors Isoenzymes/biosynthesis,genetics L-Lactate Dehydrogenase/metabolism Membrane Proteins Nitric Oxide/metabolism Nitric Oxide Synthase/biosynthesis,genetics Nitric Oxide Synthase Type II Osteoarthritis/metabolism,prevention & control Prostaglandin-Endoperoxide Synthases/biosynthesis,genetics Reactive Oxygen Species/metabolism Tea/chemistry
Chemicals
Antioxidants Interleukin-1 Isoenzymes Membrane Proteins Reactive Oxygen Species Tea Nitric Oxide Catechin epigallocatechin gallate L-Lactate Dehydrogenase NOS2 protein, human Nitric Oxide Synthase Nitric Oxide Synthase Type II Cyclooxygenase 2 PTGS2 protein, human Prostaglandin-Endoperoxide Synthases Dinoprostone
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Ahmed Salahuddin
Department of Orthopedics, Case Western Reserve University, Cleveland, OH 44106-4946, USA.
Rahman Ayesha
Hasnain Absarul
Lalonde Matthew
Goldberg Victor M
Haqqi Tariq M
Article Info
Journal
Free radical biology & medicine
Abbr.
Free Radic Biol Med
ISSN
0891-5849
Published
2002-10-15
Pages
1097-105
Language
English
Region
United States
NLM ID
8709159
Subset
IM
Grants
NIAMS NIH HHS · AR-20618 · United States
NIAMS NIH HHS · AR-37726 · United States
NIAMS NIH HHS · AR-44902 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]