4.4 Article

Prophylactic effects of Lonicera japonica extract on dextran sulphate sodium-induced colitis in a mouse model by the inhibition of the Th1/Th17 response

期刊

BRITISH JOURNAL OF NUTRITION
卷 109, 期 2, 页码 283-292

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114512001122

关键词

Inflammatory bowel disease; Lonicera japonica; Dextran sulphate sodium; Regulatory T cells; Th1/Th17 pathway

资金

  1. Basic Science Research Program through the National Research Foundation of Korea
  2. Ministry of Education, Science and Technology [2011-0013837, 2005-0049404]
  3. National Research Foundation of Korea [2011-0013837] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Inflammatory bowel diseases (IBD) are chronically relapsing inflammatory disorders of the intestine. Although some therapeutic agents, including steroids, are available for the treatment of IBD, these agents have limited use. Therefore, dietary supplements have emerged as possible interventions for IBD. Japanese honeysuckle flower, the flower of Lonicera japonica, is a well-known dietary supplement and has been used to prevent or treat various inflammatory diseases. In the present study, we investigated the effects of L. japonica on experimental murine colitis. Colitis was induced by 5% dextran sulphate sodium (DSS) in Balb/c mice. The water extract of L. japonica (LJE) at doses of 20, 100 or 500 mg/kg was orally administered to mice twice per day for 7 d. Body weight, colon length and a histological damage score were assessed to determine the effects on colitis. Cytokine profiles were assessed to examine the effects on helper T (Th) cell-related immunological responses. In addition, CD4(+)CD25(+)Foxp3(+)T cells were analysed in vivo and in vitro for investigating the effects on regulatory T (T-reg) cells. LJE showed dose-dependent inhibitory effects against colon shortening, weight loss and histological damage. LJE down-regulated IL-1 beta, TNF-alpha, interferon-gamma, IL-6, IL-12 and IL-17. However, LJE did not show any significant effects on IL-10, IL-23, transforming growth factor-beta 1 and T-reg cell populations. In conclusion, LJE showed protective effects against DSS-induced colitis via the Th1/Th17 pathway and not via T-reg cell-related mechanisms.

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