Long-term oral administration of glucosamine or chondroitin sulfate reduces destruction of cartilage and up-regulation of MMP-3 mRNA in a model of spontaneous osteoarthritis in Hartley guinea pigs

被引:52
作者
Taniguchi, Shin [1 ,2 ]
Ryu, Junnosuke [2 ]
Seki, Masayuki [2 ]
Sumino, Takanobu [2 ]
Tokuhashi, Yasuaki [2 ]
Esumi, Mariko [1 ]
机构
[1] Nihon Univ, Sch Med, Dept Pathol, Itabashi Ku, Tokyo 1738610, Japan
[2] Nihon Univ, Sch Med, Dept Orthopaed Surg, Itabashi Ku, Tokyo 1738610, Japan
关键词
osteoarthritis; glucosamine; chondroitin sulfate; Hartley guinea pig; MMP-3; KNEE OSTEOARTHRITIS; DOUBLE-BLIND; CHONDROCYTE APOPTOSIS; IN-VITRO; DEGRADATION; STROMELYSIN;
D O I
10.1002/jor.22003
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
100224 [整形外科学];
摘要
Histological and molecular changes were examined to investigate the effects of long-term administration of glucosamine (GlcN) and chondroitin sulfate (CS) in a model of spontaneous osteoarthritis (OA) in Hartley guinea pigs. Three groups of female 3-week-old Hartley guinea pigs received GlcN, CS, and neither agent, respectively. Five animals in each group were sacrificed at 8, 12, and 18 months of age. At 8 months of age, Hartley guinea pigs had severe degeneration of knee joint cartilage, chondrocyte apoptosis, marked reduction of tissue total RNA, decreases of aggrecan and collagen type 2 mRNAs, and increases in MMP-3 and MMP-8 mRNAs. Long-term administration of GlcN and CS reduced cartilage degeneration at 8 months of age. The marked loss of total RNA and the increase in MMP-3 mRNA were also inhibited by GlcN and CS. Thus, long-term oral administration of GlcN or CS inhibits OA progression, maintains total RNA and down-regulates MMP-3 mRNA in a spontaneous OA model in Hartley guinea pigs. (C) 2011 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 30:673678, 2012
引用
收藏
页码:673 / 678
页数:6
相关论文
共 30 条
[1]
Mechanisms of Disease: role of chondrocytes in the pathogenesis of osteoarthritis - structure, chaos and senescence [J].
Aigner, Thomas ;
Soeder, Stefan ;
Gebhard, Pia M. ;
McAlinden, Audrey ;
Haag, Jochen .
NATURE CLINICAL PRACTICE RHEUMATOLOGY, 2007, 3 (07) :391-399
[2]
Stimulation of proteoglycan production by glucosamine sulfate in chondrocytes isolated from human osteoarthritic articular cartilage in vitro [J].
Bassleer, C ;
Rovati, L ;
Franchimont, P .
OSTEOARTHRITIS AND CARTILAGE, 1998, 6 (06) :427-434
[3]
BENDELE AM, 1989, LAB ANIM SCI, V39, P115
[4]
Blanco FJ, 1998, ARTHRITIS RHEUM, V41, P284, DOI 10.1002/1529-0131(199802)41:2<284::AID-ART12>3.0.CO
[5]
2-T
[6]
Alternative therapy of earth elements increases the chondroprotective effects of chondroitin sulfate in mice [J].
Caraglia, M ;
Beninati, S ;
Giuberti, G ;
D'Alessandro, AM ;
Lentini, A ;
Abbruzzese, A ;
Bove, G ;
Landolfi, F ;
Rossi, F ;
Lampa, E ;
Costantino, M .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2005, 37 (05) :476-481
[7]
Randomized, double-blind, placebo-controlled glucosamine discontinuation trial in knee osteoarthritis [J].
Cibere, J ;
Kopec, JA ;
Thorne, A ;
Singer, J ;
Canvin, J ;
Robinson, DB ;
Pope, J ;
Hong, P ;
Grant, E ;
Esdaile, JM .
ARTHRITIS & RHEUMATISM-ARTHRITIS CARE & RESEARCH, 2004, 51 (05) :738-745
[8]
Glucosamine, chondroitin sulfate, and the two in combination for painful knee osteoarthritis [J].
Clegg, DO ;
Reda, DJ ;
Harris, CL ;
Klein, MA ;
O'Dell, JR ;
Hooper, MM ;
Bradley, JD ;
Bingham, CO ;
Weisman, MH ;
Jackson, CG ;
Lane, NE ;
Cush, JJ ;
Moreland, LW ;
Schumacher, HR ;
Oddis, CV ;
Wolfe, F ;
Molitor, JA ;
Yocum, DE ;
Schnitzer, TJ ;
Furst, DE ;
Sawitzke, AD ;
Shi, H ;
Brandt, KD ;
Moskowitz, RW ;
Williams, HJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (08) :795-808
[9]
CONTE A, 1995, ARZNEIMITTEL-FORSCH, V45-2, P918
[10]
DROVANTI A, 1980, CLIN THER, V3, P260