Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P43026 (
lipopolysaccharide
)
62,215
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Andrographolide sulfonate (Andro-S), a sulfonation derivative of andrographolide, is known to be effective in treating inflammation-related diseases, while the underlying mechanisms and global protein alterations in response to
Andro
-S remain unknown. This study aimed to investigate the pharmacological effects and potential targets of
Andro
-S in a murine model of acute lung injury (ALI). ALI was induced by aerosolized
lipopolysaccharide
(
LPS
) exposure before treatment with
Andro
-S. Inflammatory state of each treatment group was determined by histological analysis and quantification of inflammatory markers. Differentially expressed proteins in lung tissues were identified by an iTRAQ-based quantitative proteomic approach and further confirmed by immunohistochemistry analysis. Administration of
Andro
-S alleviated
LPS
-induced histological changes in the lung and reduced the expression of inflammatory markers in serum, bronchoalveolar fluid and lung tissues. Proteomic analysis identified 31 differentially expressed proteins from a total of 2,234 quantified proteins in the lung. According to bioinformatics analysis, neutrophil elastase (ELANE), cathepsin G (CTSG) and myeloperoxidase (MPO), three neutrophil-derived proteases related to immune system process and defense responses to fungi were chosen as potential targets of
Andro
-S. Further immunohistochemistry analysis confirmed the inhibitory effects of
Andro
-S on
LPS
-induced ELANE, CTSG and MPO up-regulation. These results indicate that
Andro
-S suppressed the severity of
LPS
-induced ALI, possibly by attenuating the expression of and neutrophil-derived proteases.
...
PMID:Andrographolide Sulfonate Attenuates Acute Lung Injury by Reducing Expression of Myeloperoxidase and Neutrophil-Derived Proteases in Mice. 3017 7