Red Ginseng Saponin Extract Attenuates Murine Collagen-Induced Arthritis by Reducing Pro-inflammatory Responses and Matrix Metalloproteinase-3 Expression

被引:36
作者
Kim, Ki Rim [2 ,3 ]
Chung, Tae Yong [1 ]
Shin, Heungsop [4 ]
Son, Sung Ho [5 ]
Park, Kwang-Kyun [2 ,3 ]
Choi, Jong-Hoon [1 ]
Chung, Won-Yoon [2 ,3 ]
机构
[1] Yonsei Univ, Coll Dent, Dept Oral Diag & Oral Med, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Dent, Res Ctr Orofacial Hard Tissue Regenerat, Oral Sci Res Inst,Dept Oral Biol,Brain Korea Proj, Seoul 120752, South Korea
[3] Yonsei Univ, Grad Sch, Dept Appl Life Sci, Seoul 120749, South Korea
[4] Korea Polytech Univ, Dept Chem Engn & Biotechnol, Shihung 429450, South Korea
[5] Vitrosys Inc, Yeongju 750804, South Korea
关键词
Panax ginseng; ginsenoside; anti-arthritic; cytokine; matrix metalloproteinase-3; IN-VIVO MODELS; RHEUMATOID-ARTHRITIS; EXPERIMENTAL OSTEOARTHRITIS; OXIDATIVE STRESS; ORAL ABSORPTION; CELL INFILTRATE; DESTRUCTION; CARTILAGE; DISEASE; MICE;
D O I
10.1248/bpb.33.604
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ginseng, the root of Palmy ginseng C. A. MEYER, has been used as a food product and medicinal ingredient. In this study, we assessed the anti-arthritic effects of red ginseng saponin extract (RGSE), including ginsenosides Rg3, Rk1 and Rg5 as major components, on a murine type II collagen (CII)-induced arthritis (CIA), which is a valid animal model of human arthritis. Oral administration of RGSE at 10 mg/kg reduced the clinical arthritis score and paw swelling in the CIA mice, and inhibited joint space narrowing and histological arthritis, illustrating the severity of synovial hyperplasia, inflammatory cell infiltration, pannus formation, and erosion of cartilage. RGSE inhibited the expression of matrix metalloproteinase-3 and nitrotyrosine formation, and recovered the expression of superoxide dismutase in the joints of the CIA mice. Orally administered RGSE also reduced the levels of serum tumor necrosis factor-a and interleukin-1 beta in the CIA mice. CII- or lipopolysaccharide-stimulated cytokine production, in addition to CH-specific proliferation, was reduced in the spleen cells of the RGSE-treated CIA mice, as compared with those from vehicle-treated CIA mice. Furthermore, RGSE administration protected against CIA-induced oxidative tissue damage by restoring the increased malondialdehyde levels and the decreased glutathione levels and catalase activities almost to control levels. Therefore, RGSE may be a beneficial supplement which can improve human arthritis.
引用
收藏
页码:604 / 610
页数:7
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