Geranylgeranylacetone protects mice from dextran sulfate sodium-induced colitis

被引:37
作者
Ohkawara, T
Nishihira, J
Takeda, H
Miyashita, K
Kato, K
Kato, M
Sugiyama, T
Asaka, M
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Gastroenterol & Hematol, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] GeneticLab, Dept Res & Dev, Sapporo, Hokkaido, Japan
[3] Toyama Med & Pharmaceut Univ, Dept Internal Med 3, Toyama, Japan
关键词
cytokine; dextran sulfate sodium-induced colitis; geranylgeranylacetone; heat shock protein; inflammatory bowel disease;
D O I
10.1080/00365520510023161
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective. Geranylgeranylacetone (GGA) has recently been reported to induce heat shock protein (HSP) 70, which has a protective function against inflammation. We investigated the therapeutic effects of oral administration of GGA on dextran sulfate sodium (DSS)-induced colitis in mice. Material and methods. BALB/c mice were given 3% DSS solution orally for 7 days to induce colitis. The disease activity of colitis was assessed clinically every day, and histology in the colon was evaluated at 7 days post-DSS. The levels of myeloperoxidase (MPO) activity, tumor necrosis factor (TNF)-alpha and interferon (IFN)-gamma in the colon tissues were also examined. In addition, expression of HSPs 25, 40, 70 and 90 in the colon tissue was determined by Western blot analysis. Mice were orally administered GGA ( 50 - 500 mg/kg) when treatment of DSS started. Results. It was found that GGA significantly reduced the clinical severity of colitis and suppressed the levels of MPO activity, TNF-alpha and IFN-gamma induced by DSS in the colon. On the other hand, GGA enhanced the expression of HSP70 in the colon of mice given DSS. HSP70-positive cells were identified in the epithelial cells of the colon from mice treated with GGA and DSS. Conclusions. Taken together, these results suggest that GGA is a new anti-inflammatory drug that could be useful in the treatment of colitis such as inflammatory bowel disease.
引用
收藏
页码:1049 / 1057
页数:9
相关论文
共 38 条
[21]   Amelioration of dextran sulfate sodium-induced colitis by anti-macrophage migration inhibitory factor antibody in mice [J].
Ohkawara, T ;
Nishihira, J ;
Takeda, H ;
Hige, S ;
Kato, M ;
Sugiyama, T ;
Iwanaga, T ;
Nakamura, H ;
Mizue, Y ;
Asaka, M .
GASTROENTEROLOGY, 2002, 123 (01) :256-270
[22]   Single oral dose of geranylgeranylacetone induces heat-shock protein 72 and renders protection against ischemia/reperfusion injury in rat heart [J].
Ooie, T ;
Takahashi, N ;
Saikawa, T ;
Nawata, T ;
Arikawa, M ;
Yamanaka, K ;
Hara, M ;
Shimada, T ;
Sakata, T .
CIRCULATION, 2001, 104 (15) :1837-1843
[23]   Effect of preinduction of heat shock proteins on acetic acid-induced colitis in rats [J].
Otani, S ;
Otaka, M ;
Jin, M ;
Okuyama, A ;
Itoh, S ;
Iwabuchi, A ;
Sasahara, H ;
Itoh, H ;
Tashima, Y ;
Masamune, O .
DIGESTIVE DISEASES AND SCIENCES, 1997, 42 (04) :833-846
[24]   Role of cytokines in the pathogenesis of inflammatory bowel disease [J].
Papadakis, KA ;
Targan, SR .
ANNUAL REVIEW OF MEDICINE, 2000, 51 :289-298
[25]  
PAPPAS TN, 1987, ARCH SURG-CHICAGO, V122, P447
[26]   Heat shock proteins as regulators of the immune response [J].
Pockley, AG .
LANCET, 2003, 362 (9382) :469-476
[27]   MECHANISMS OF DISEASE Inflammatory Bowel Disease [J].
Abraham, Clara ;
Cho, Judy H. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (21) :2066-2078
[28]  
Sartor RB, 1997, AM J GASTROENTEROL, V92, pS5
[29]   Intestinal expression of human heat shock protein 90 in patients with Crohn's disease and ulcerative colitis [J].
Stahl, M ;
Ludwig, D ;
Fellermann, K ;
Stange, EF .
DIGESTIVE DISEASES AND SCIENCES, 1998, 43 (05) :1079-1087
[30]   A short-term study of chimeric monoclonal antibody cA2 to tumor necrosis factor alpha for Crohn's disease [J].
Targan, SR ;
Hanauer, SB ;
vanDeventer, SJH ;
Mayer, L ;
Present, DH ;
Braakman, T ;
DeWoody, KL ;
Schaible, TF ;
Rutgeerts, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (15) :1029-1035