Ascorbic acid increases the severity of spontaneous knee osteoarthritis in a guinea pig model

被引:65
作者
Kraus, VB
Huebner, JL
Stabler, T
Flahiff, CM
Setton, LA
Fink, C
Vilim, V
Clark, AG
机构
[1] Duke Univ, Med Ctr, Durham, NC 27710 USA
[2] Inst Rheumatol, Prague, Czech Republic
来源
ARTHRITIS AND RHEUMATISM | 2004年 / 50卷 / 06期
关键词
D O I
10.1002/art.20291
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objective. To determine whether ascorbic acid might be of benefit for the treatment of spontaneous osteoarthritis (OA) when administered over a long period of time. Methods. We investigated the effects of 8 months' exposure to low, medium, and high doses of ascorbic acid on the in vivo development of histologic knee OA in the male Hartley guinea pig. The low dose represented the minimum amount needed to prevent scurvy. The medium dose was the amount present in standard laboratory guinea pig chow and resulted in plasma levels comparable with those achieved in a person consuming 200 mg/day (5 fruits and vegetables daily). The high dose was the amount shown in a previous study of the guinea pig to slow the progression of surgically induced OA. Results. We found an association between ascorbic acid supplementation and increased cartilage collagen content but, in contrast to findings in a previous study of surgically induced OA in the guinea pig, ascorbic acid worsened the severity of spontaneous OA. Active transforming growth factor beta (TGFbeta) was expressed in marginal osteophytes, whose size and number were significantly increased with increasing intake of ascorbic acid. Synovial fluid levels of cartilage oligomeric matrix protein, a biomarker of cartilage turnover, corroborated the histologic findings. Conclusion. Ascorbic acid has been shown to activate latent TGFbeta. Prolonged intraarticular exposure to TGFbeta has been shown to cause OA-like changes. We found expression of active TGFbeta in osteophytes, a prominent feature of the joint histology seen in association with ascorbic acid treatment. Thus, the deleterious effects of prolonged ascorbic acid exposure may be mediated in part by TGFJ3. This worsening of OA with ascorbic acid supplementation suggests that ascorbic acid intake should not be supplemented above the currently recommended dietary allowance (90 mg/day for men and 75 mg/day for women).
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页码:1822 / 1831
页数:10
相关论文
共 49 条
[1]
Overexpression of active TGF-beta-1 in the murine knee joint: evidence for synovial-layer-dependent chondro-osteophyte formation [J].
Bakker, AC ;
van de Loo, FAJ ;
van Beuningen, HM ;
Sime, P ;
van Lent, PLEM ;
van der Kraan, PM ;
Richards, CD ;
van den Berg, WB .
OSTEOARTHRITIS AND CARTILAGE, 2001, 9 (02) :128-136
[2]
Redox-mediated activation of latent transforming growth factor-beta 1 [J].
BarcellosHoff, MH ;
Dix, TA .
MOLECULAR ENDOCRINOLOGY, 1996, 10 (09) :1077-1083
[3]
EFFECTS OF BODY-WEIGHT RESTRICTION ON THE DEVELOPMENT AND PROGRESSION OF SPONTANEOUS OSTEOARTHRITIS IN GUINEA-PIGS [J].
BENDELE, AM ;
HULMAN, JF .
ARTHRITIS AND RHEUMATISM, 1991, 34 (09) :1180-1184
[4]
BENDELE AM, 1989, LAB ANIM SCI, V39, P115
[6]
Synovial fluid biomarker levels predict articular cartilage damage following complete medial meniscectomy in the canine knee [J].
Carlson, CS ;
Guilak, F ;
Vail, TP ;
Gardin, JF ;
Kraus, VB .
JOURNAL OF ORTHOPAEDIC RESEARCH, 2002, 20 (01) :92-100
[7]
Intracellular demonstration of active TGF beta 1 in B cells and plasma cells of autoimmune mice - IgG-Bound TGF beta 1 suppresses neutrophil function and host defense against Staphylococcus aureus infection [J].
Caver, TE ;
OSullivan, FX ;
Gold, LI ;
Gresham, HD .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (11) :2496-2506
[8]
CHOJKIER M, 1989, J BIOL CHEM, V264, P16957
[9]
SPECIFICALLY DECREASED COLLAGEN BIOSYNTHESIS IN SCURVY DISSOCIATED FROM AN EFFECT ON PROLINE HYDROXYLATION AND CORRELATED WITH BODY-WEIGHT LOSS - INVITRO STUDIES IN GUINEA-PIG CALVARIAL BONES [J].
CHOJKIER, M ;
SPANHEIMER, R ;
PETERKOFSKY, B .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 72 (03) :826-835
[10]
The effects of ascorbic acid on cartilage metabolism in guinea pig articular cartilage explants [J].
Clark, AG ;
Rohrbaugh, AL ;
Otterness, I ;
Kraus, VB .
MATRIX BIOLOGY, 2002, 21 (02) :175-184