Osteoarthritis (OA) is the most common musculoskeletal disease among the aging population in the United States and throughout the world. OA is characterized by degeneration of articular cartilage of the joints in hands, knees, spine and hips. While conditions predisposing to the development of OA have been identified, the actual causes remain unknown and the current treatment options are limited to relief of symptoms using NSAIDS. However, use of NSAIDS may be complicated by significant side effects that include gastrointestinal bleeding, cardiovascular adverse events and nephrotoxicity. Pomegranate fruit (Punica granatum L) is revered through the ages for its medicinal properties. Pomegranate fruit (PF) or its extract (PFE) is widely used in Unani and Ayurvedic medicinal systems in India for the treatment of diabetes and Colitis. Edible part of PF is rich in anthocyanins, a group of polyphenolic compounds that possess antioxidant and anti-inflammatory properties. We previously reported that PFE exert a potent inhibitory effect on IL-1?-induced activation of MAPK sub-groups p38-MAPK and JNK, transcription factor NF-?B and the expression of MMPs by human cartilage explants and chondrocytes in vitro. Recently we have shown that (1) oral consumption of PFE inhibited the development of collagen-induced arthritis in mice(CIA);and (2) bioavailable PFE constituents/metabolites inhibited COX-2 activity and IL-1?-induced production of NO and PGE2 in chondrocytes. Proposed studies capitalizes on these novel findings as here we will extend these studies and will determine the relevance of the in vitro findings to in vivo PFE use in an animal model of OA. We will test the hypothesis that """"""""oral consumption of PFE inhibits cartilage degradation and suppresses the progression of knee OA in rabbits induced by anterior cruciate ligament transection (ACLT)"""""""".
In aim -1 we will establish the identity and concentration of several of the known PFE-derived anthocyanins and ellagitanins (ET) that become bioavailable in plasma and synovial fluid (SF) in rabbits given different doses of PFE;
in aim -2 we will determine and compare the efficacy of plasma and SF containing PFE-derived ET and anthocyanins in inhibiting the IL-1?-induced catabolic responses in human and rabbit cartilage explants in vitro;
in aim -3 we will use the dose determined to be most relevant from above studies for feeding rabbits and evaluate the effect of oral consumption of PFE on articular cartilage degeneration in the ACLT model of OA. Public Health Relevance: Osteoarthritis (OA) is characterized by high high levels of IL-1?, excessive production of ROS and articular cartilage degeneration in the affected joints. However, its etiology and precise pathogenetic mechanisms remain unclear. Here, we will determine whether consumption of a standardized extract of pomegranate fruit (PFE) can slow or retard the artciular cartilage degeneration in vivo. The broad objectives of the proposed studies are (a) to identify the molecular mechanism in vitro associated with cartilage/chondroprotective activity of PFE;and (b) to test the relevance of in vitro studies to the in vivo situation using a widely used animal model of human OA. Our findings are likely to open the door for the development of novel therapeutic strategies for the treatment of OA.

Public Health Relevance

; First; Middle): Haqqi; Tariq M.Public Health Relevance/NarrativeOsteoarthritis (OA) is characterized by high high levels of IL-1 ; excessive production of ROS and articularcartilage degeneration in the affected joints. However; its etiology and precise pathogenetic mechanismsremain unclear. Here; we will determine whether consumption of a standardized extract of pomegranate fruit(PFE) can slow or retard the artciular cartilage degeneration in vivo. The broad objectives of the proposedstudies are (a) to identify the molecular mechanism in vitro associated with cartilage/chondroprotective activityof PFE; and (b) to test the relevance of in vitro studies to the in vivo situation using a widely used animal modelof human OA. Our findings are likely to open the door for the development of novel therapeutic strategies forthe treatment of OA.PHS 398/2590 (Rev. 11/07) Page Continuation Format Page

Agency
National Institute of Health (NIH)
Institute
National Center for Complementary & Alternative Medicine (NCCAM)
Type
Exploratory/Developmental Grants (R21)
Project #
7R21AT004026-02
Application #
8063331
Study Section
Special Emphasis Panel (ZAT1-PK (03))
Program Officer
Pontzer, Carol H
Project Start
2009-09-01
Project End
2011-08-31
Budget Start
2009-11-21
Budget End
2010-08-31
Support Year
2
Fiscal Year
2009
Total Cost
$120,525
Indirect Cost
Name
Case Western Reserve University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Bükülmez, Hülya; Khan, Fozia; Bartels, Cynthia F et al. (2014) Protective effects of C-type natriuretic peptide on linear growth and articular cartilage integrity in a mouse model of inflammatory arthritis. Arthritis Rheumatol 66:78-89
Haseeb, Abdul; Haqqi, Tariq M (2013) Immunopathogenesis of osteoarthritis. Clin Immunol 146:185-96
Akhtar, Nahid; Rasheed, Zafar; Ramamurthy, Sangeetha et al. (2010) MicroRNA-27b regulates the expression of matrix metalloproteinase 13 in human osteoarthritis chondrocytes. Arthritis Rheum 62:1361-71
Singh, Rashmi; Akhtar, Nahid; Haqqi, Tariq M (2010) Green tea polyphenol epigallocatechin-3-gallate: inflammation and arthritis. [corrected]. Life Sci 86:907-18