Glucagon-like peptide-1 as a treatment for chemotherapy-induced mucositis

被引:51
|
作者
Kissow, Hannelouise
Hartmann, Bolette
Holst, Jens Juul
Poulsen, Steen Seier
机构
[1] Univ Copenhagen, Dept Biomed Sci, Copenhagen, Denmark
[2] Univ Copenhagen, Novo Nordisk Fdn Ctr Basic Metab Res, Copenhagen, Denmark
关键词
Gut Hormones; Mucosal Repair; Mucosal Injury; Gastrointestinal Peptides; Chemotherapy; RECEPTOR; GROWTH; GLP-2; CELLS; PROGLUCAGON; INHIBITION; EXENDIN-4; MORTALITY; MASS;
D O I
10.1136/gutjnl-2012-303280
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background Glucagon-like peptide-2 (GLP-2) has been suggested for the treatment of mucositis, but the peptide has also been shown to accentuate colonic dysplasia in carcinogen-treated mice. Recently, an effect on intestinal growth was discovered for glucagon-like peptide-1 (GLP-1), Objective To determine whether endogenous GLP-1 contributes to the healing processes and if exogenous GLP-1 has a potential role in treating mucositis. Methods Mice were injected with 5-fluorouracil (5-FU) or saline to induce mucositis and were then treated with GLP-1, GLP-2, GLP-2 (3-33), exendin (9-39) or vehicle. The mice were sacrificed 48 or 96h after the 5-FU injections. The end points were intestinal weight, villus height, proliferation and histological scoring of mucositis severity. Rats were injected with 5-FU or saline, and after 48h, blood was drawn and analysed for GLP-1 and GLP-2 concentration. Results GLP-1 and GLP-2 significantly prevented the loss of mucosal mass and villus height and significantly decreased the mucositis severity score in the duodenum and jejunum 48h after chemotherapy. The effect was equivalent. Exendin (9-39) reduced the intestinal weight 96h after chemotherapy. The GLP-1 levels in blood were increased more than 10-fold, and GLP-2 levels were increased sevenfold. Conclusions GLP-1 and GLP-2 were secreted after intestinal injury, and recovery was delayed after treatment with exendin (9-39), indicating an important role for the peptides in the protection of the intestine from injury. GLP-1 treatment ameliorated mucositis, which suggests that mucositis and other acute intestinal disorders might benefit from treatment with GLP-1 analogues.
引用
收藏
页码:1724 / 1733
页数:10
相关论文
共 50 条
  • [1] Glucagon-like peptide 1 (GLP-1) as treatment for chemotherapy induced mucositis (CIM)
    Kissow, H.
    Hartmann, B.
    Holst, J.
    Poulsen, S.
    REGULATORY PEPTIDES, 2012, 177 : S24 - S24
  • [2] Glucagon-like peptide 2: A new treatment for chemotherapy-induced enteritis
    Tavakkolizadeh, A
    Shen, R
    Abraham, P
    Kormi, N
    Seifert, P
    Edelman, ER
    Jacobs, DO
    Zinner, MJ
    Ashley, SW
    Whang, EE
    JOURNAL OF SURGICAL RESEARCH, 2000, 91 (01) : 77 - 82
  • [3] Glucagon and glucagon-like peptide-1
    Livingston, JN
    Schoen, WR
    ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 34, 1999, 34 : 189 - 198
  • [4] Glucagon-like peptide-1
    Doyle, ME
    Egan, JM
    RECENT PROGRESS IN HORMONE RESEARCH, VOL 56, 2001, 56 : 377 - 399
  • [5] Glucagon-like peptide-1 and glucagon-like peptide-2
    Baggio, LL
    Drucker, DJ
    BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 18 (04) : 531 - 554
  • [6] On the treatment of diabetes mellitus with glucagon-like peptide-1
    Holst, JJ
    Deacon, C
    Toft-Nielsen, MB
    Bjerre-Knudsen, L
    VIP, PACAP, AND RELATED PEPTIDES: THIRD INTERNATIONAL SYMPOSIUM, 1998, 865 : 336 - 343
  • [7] Glucagon-like peptide-1 and satiety
    S. R. Bloom
    Nature, 1997, 385 : 214 - 214
  • [8] Glucagon-Like Peptide-1 and Diabetes
    Monami, Matteo
    EXPERIMENTAL DIABETES RESEARCH, 2011,
  • [9] Glucagon-like peptide-1 and satiety
    van, Dijk, G.
    Thiele, T.E.
    Seeley, R.J.
    Woods, S.C.
    Bernstein, I.L.
    Bloom, S.R.
    Nature, 1997, 385 (6613)
  • [10] Glucagon-like peptide-1 and satiety
    G. van Dijk
    T. E. Thiele
    R. J. Seeley
    S. C. Woods
    I. L. Bernstein
    Nature, 1997, 385 : 214 - 214