Extracellular DNA is Increased in Dextran Sulphate Sodium-Induced Colitis in Mice
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
30938673
DOI
10.14712/fb2018064050167
PII: file/5881/fb2018a0020.pdf
Knihovny.cz E-resources
- MeSH
- Biomarkers metabolism MeSH
- Deoxyribonucleases metabolism MeSH
- DNA blood metabolism MeSH
- Gastrointestinal Tract enzymology MeSH
- Colitis blood metabolism pathology MeSH
- Disease Models, Animal MeSH
- Mice, Inbred C57BL MeSH
- Dextran Sulfate MeSH
- Body Weight MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- Deoxyribonucleases MeSH
- DNA MeSH
- Dextran Sulfate MeSH
Ulcerative colitis and Crohn's disease constitute the two main forms of inflammatory bowel disease. Prevalence of these diseases increases. In the present day, inadequate and inefficient therapy causes complications and frequent relapse. Extracellular DNA (ecDNA) is the DNA that is outside of cells and may be responsible for activation of the inflammatory response. To determine whether colitis is associated with higher concentration of ecDNA we used male mice of the C57BL/6 strain. Colitis was induced by 2% dextran sulphate sodium (DSS). After 7 days, mice exhibited considerable weight loss compared to the control group. Also, there was a higher stool consistency score and the colon was significantly shorter in comparison to the control group. Higher concentration of ecDNA was found in the DSS group. Interestingly, deoxyribonuclease activity was lower in the colon of the DSS group compared with the negative control. These findings may point to ecDNA as a potential pathogenetic factor and marker of inflammation.
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