Betulinic acid attenuates lung injury by modulation of inflammatory cytokine response in experimentally-induced polymicrobial sepsis in mice

•Betulinic acid improves survival of mice in septic-lung injury model.•Betulinic acid exerts anti-inflammatory effect in CLP-induced pro-inflammatory lung damage in mice.•Betulinic acid can be a therapeutic modality in treatment of pro-inflammatory lung injury in septic patients. Sepsis commonly pro...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2015-01, Vol.71 (1), p.101-108
Hauptverfasser: Lingaraju, Madhu Cholenahalli, Pathak, Nitya Nand, Begum, Jubeda, Balaganur, Venkanna, Bhat, Rafia Ahmad, Ramachandra, Harish Darasaguppe, Ayanur, Anjaneya, Ram, Mahendra, Singh, Vishakha, Kumar, Dhirendra, Kumar, Dinesh, Tandan, Surendra Kumar
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Sprache:eng
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Zusammenfassung:•Betulinic acid improves survival of mice in septic-lung injury model.•Betulinic acid exerts anti-inflammatory effect in CLP-induced pro-inflammatory lung damage in mice.•Betulinic acid can be a therapeutic modality in treatment of pro-inflammatory lung injury in septic patients. Sepsis commonly progresses to acute lung injury (ALI), an inflammatory lung disease with high morbidity and mortality. Septic ALI is characterized by excessive production of proinflammatory mediators. It remained refractory to present therapies and new therapies need to be developed to improve further clinical outcomes. Betulinic acid (BA), a pentacyclic lupane group triterpenoid has been shown to have anti-inflammatory activities in many studies. However, its therapeutic efficacy in polymicrobial septic ALI is yet unknown. Therefore, we investigated the effects of BA on septic ALI using cecal ligation and puncture (CLP) model in mice. Vehicle or BA (3, 10, and 30mg/kg) was administered intraperitoneally, 3 times (0, 24 and 48h) before CLP and CLP was done on 49thh of the study. Survival rate was observed till 120h post CLP. Lung tissues were collected for analysis by sacrificing mice 18h post CLP. BA at 10 and 30mg/kg dose significantly reduced sepsis-induced mortality and lung injury as implied by attenuated lung histopathological changes, decreased protein and neutrophils infiltration. BA also decreased lung NF-κB expression, cytokine, intercellular adhesion molecule-1, monocyte chemoattractant protein-1 and matrix metalloproteinase-9 levels. These evidences suggest that, the protective effects of BA on lungs are associated with defending action against inflammatory response and BA could be a potential modulatory agent of inflammation in sepsis-induced ALI.
ISSN:1043-4666
1096-0023
DOI:10.1016/j.cyto.2014.09.004