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PRECLINICAL PUBLICATION · 2018

Chitosan oligosaccharide ameliorates acute lung injury induced by blast injury through the DDAH1/ADMA pathway.

Mouse / Other

Evidence by therapy association

Study details and outcomes are extracted in the context of a specific intervention. Separate associations are retained rather than silently merged.

PMID 29415054 ↗2018Reported benefit

Chitosan oligosaccharide ameliorates acute lung injury induced by blast injury through the DDAH1/ADMA pathway.

MouseOtherKunmingMalen = 30 mice in 3 groups (control, acute lung injury, acute lung…Oral gavage80 mg/kg per dayStarted 14 days before blast injury

Model: Blast injury induced acute lung injury using a self-made explosive device with instantaneous shock wave overpressure of 321 plus or minus 24 PSI

Chitosan oligosaccharide pretreatment improved gas exchange, reduced pulmonary oedema, inflammation, oxidative stress and apoptosis, and increased DDAH1 while lowering ADMA and p38.

Extraction: extract · Supplied extraction confidence: 0.9. Machine-extracted fields require source verification.