1. 3‐ O ‐trans‐caffeoyloleanolic acid improves acute lung injury via anti‐inflammation and antioxidative stress‐involved PI3K/AKT pathway
- Author
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Jianhua Huang, Xueping Nong, Yanling Chen, Aimei Zhang, and Lerong Chen
- Subjects
Lipopolysaccharides ,Male ,Phosphopeptides ,Lipopolysaccharide ,Acute Lung Injury ,Anti-Inflammatory Agents ,Nitric Oxide Synthase Type II ,Inflammation ,Pharmacology ,Lung injury ,medicine.disease_cause ,01 natural sciences ,Biochemistry ,Phosphatidylinositol 3-Kinases ,chemistry.chemical_compound ,In vivo ,Drug Discovery ,medicine ,Animals ,Humans ,Oleanolic Acid ,Protein kinase B ,PI3K/AKT/mTOR pathway ,Mice, Inbred BALB C ,010405 organic chemistry ,Chemistry ,Macrophages ,Organic Chemistry ,0104 chemical sciences ,Toll-Like Receptor 4 ,Oxidative Stress ,010404 medicinal & biomolecular chemistry ,Gene Expression Regulation ,TLR4 ,Molecular Medicine ,medicine.symptom ,Proto-Oncogene Proteins c-akt ,Oxidative stress ,Signal Transduction - Abstract
3-O-trans-caffeoyloleanolic acid (COA) is a pentacyclic triterpenoid compound, with significant anti-inflammatory effects. In this study, we report the protective effects of COA on lipopolysaccharide (LPS)-induced acute lung injury (ALI) and explored its mechanism of action. LPS was used to construct in vivo mouse ALI models to observe the effects of COA pretreatment on lung pathology, inflammation, and oxidative stress. In vitro, mouse alveolar macrophages MH-S cells were cultured and stimulated with LPS to investigate the effects of COA pretreatment on inflammation and oxidative stress. Western blotting was used to investigate the expression of iNOS, TLR4, p-p65, p-AKT, and p-PI3K from in vivo and in vitro samples. The results showed that COA significantly improved lung injury, inhibited neutrophil infiltration, prevented macrophage infiltration, inhibited the release of inflammatory factors, reduced oxidative stress, and down-regulated the expression of iNOS, TLR4, p-p65, p-AKT, and p-PI3K in ALI mice caused by LPS. In vitro, COA inhibited the release of inflammatory factors, reduced oxidative stress, and down-regulated the expression of iNOS, TLR4, p-p65, p-AKT, and p-PI3K in MH-S cells stimulated with LPS. Of interest, the protective effects of COA were significantly attenuated in MH-S cells pretreated with the PI3K phosphopeptide activator 740Y-P with no effect on TLR4 expression observed. Taken together, these findings confirm the protective effects of COA on ALI. We further demonstrate that the anti-inflammation and antioxidant effects of COA are mediated through its effects on PI3K/AKT and potentially TLR4.
- Published
- 2021