Low molecular weight heparin relieves experimental colitis in mice by downregulating IL-1β and inhibiting syndecan-1 shedding in the intestinal mucosa

PLoS One. 2013 Jul 18;8(7):e66397. doi: 10.1371/journal.pone.0066397. Print 2013.

Abstract

Low molecular weight heparin (LMWH) exhibits anti-inflammatory properties, but its effect on inflammation in colitis remains unclear. This study aimed to evaluate the therapeutic effects of LMWH on dextran sulfate sodium (DSS)-induced colitis in mice, in which acute colitis progresses to chronic colitis, and to explore the potential mechanism involved in this process. C57BL/6 mice were randomly divided into control, DSS, and DSS plus LMWH groups (n = 18). Disease activity was scored by a disease activity index (DAI). Histological changes were evaluated by hematoxylin and eosin (HE) staining. The mRNA levels of syndecan-1, interleukin (IL)-1β, and IL-10 were determined by quantitative reverse transcription polymerase chain reaction. Protein expression of syndecan-1 was detected by immunohistochemistry. The serum syndecan-1 level was examined by a dot immunobinding assay. LMWH ameliorated the disease activity of colitis induced by DSS administration in mice. Colon destruction with the appearance of crypt damage, goblet cell loss, and a larger ulcer was found on day 12 after DSS administration, which was greatly relieved by the treatment of LMWH. LMWH upregulated syndecan-1 expression in the intestinal mucosa and reduced the serum syndecan-1 level on days 12 and 20 after DSS administration (P<0.05 vs. DSS group). In addition, LMWH significantly decreased the expression of both IL-1β and IL-10 mRNA on days 12 and 20 (P<0.05 vs. DSS group). LMWH has therapeutic effects on colitis by downregulating inflammatory cytokines and inhibiting syndecan-1 shedding in the intestinal mucosa.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Colitis / drug therapy*
  • Colitis / etiology
  • DNA Primers / genetics
  • Dextran Sulfate / toxicity
  • Down-Regulation / drug effects*
  • Heparin, Low-Molecular-Weight / metabolism
  • Heparin, Low-Molecular-Weight / pharmacology*
  • Immunoblotting
  • Immunohistochemistry
  • Interleukin-10 / metabolism
  • Interleukin-1beta / metabolism*
  • Intestinal Mucosa / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Reverse Transcriptase Polymerase Chain Reaction
  • Syndecan-1 / blood*

Substances

  • DNA Primers
  • Heparin, Low-Molecular-Weight
  • Interleukin-1beta
  • Sdc1 protein, mouse
  • Syndecan-1
  • Interleukin-10
  • Dextran Sulfate

Grants and funding

Supported by the National Natural Science Foundation of China (YC, 81070291), the Program for New Century Excellent Talents in University (YC, China, NCET-10-0091), the Medical Research Fund of Guangdong Province (XJ, A2010364), and the Ministry of Education and Guangdong province University-industry cooperation projects (SDL 2011B090400018). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.