Andrographolide protects against LPS-induced acute lung injury by inactivation of NF-κB

PLoS One. 2013;8(2):e56407. doi: 10.1371/journal.pone.0056407. Epub 2013 Feb 21.

Abstract

Background: Nuclear factor-κB (NF-κB) is a central transcriptional factor and a pleiotropic regulator of many genes involved in acute lung injury. Andrographolide is found in the plant of Andrographis paniculata and widely used in Traditional Chinese Medicine, exhibiting potently anti-inflammatory property by inhibiting NF-κB activity. The purpose of our investigation was designed to reveal the effect of andrographolide on various aspects of LPS induced inflammation in vivo and in vitro.

Methods and results: In vivo, BALB/C mice were subjected to LPS injection with or without andrographolide treatments to induce ALI model. In vitro, MLE-12 cells were stimulated with LPS in the presence and absence of andrographolide. In vivo, pulmonary inflammation, pulmonary edema, ultrastructure changes of type II alveolar epithelial cells, MPO activity, total cells, neutrophils, macrophages, TNF-α, IL-6 and IL-1β in BALF, along with the expression of VCAM-1 and VEGF were dose-dependently attenuated by andrographolide. Meanwhile, in vitro, the expression of VCAM-1 and VEGF was also reduced by andrographolide. Moreover, our data showed that andrographolide significantly inhibited the ratios of phospho-IKKβ/total IKKβ, phospho-IκBα/total IκBα and phospho-NF-κB p65/total NF-κB p65, and NF-κB p65 DNA binding activities, both in vivo and in vitro.

Conclusions: These results indicate that andrographolide dose-dependently suppressed the severity of LPS-induced ALI, more likely by virtue of andrographolide-mediated NF-κB inhibition at the level of IKKβ activation. These results suggest andrographolide may be considered as an effective and safe drug for the potential treatment of ALI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / drug therapy*
  • Acute Lung Injury / genetics
  • Acute Lung Injury / metabolism*
  • Acute Lung Injury / pathology
  • Alveolar Epithelial Cells / pathology
  • Alveolar Epithelial Cells / ultrastructure
  • Animals
  • Bronchoalveolar Lavage Fluid
  • Cell Count
  • Cell Survival / drug effects
  • Cell Survival / genetics
  • Cytokines / metabolism
  • DNA / metabolism
  • Diterpenes / pharmacology
  • Diterpenes / therapeutic use*
  • Down-Regulation / drug effects
  • Gene Expression Regulation / drug effects
  • Lipopolysaccharides
  • Male
  • Mice
  • Mice, Inbred BALB C
  • NF-kappa B / metabolism*
  • Peroxidase / metabolism
  • Pneumonia / complications
  • Pneumonia / drug therapy
  • Pneumonia / genetics
  • Pneumonia / pathology
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Protein Binding / drug effects
  • Protein Binding / genetics
  • Pulmonary Edema / complications
  • Pulmonary Edema / drug therapy
  • Pulmonary Edema / genetics
  • Pulmonary Edema / pathology
  • Transcription Factor RelA / metabolism
  • Vascular Cell Adhesion Molecule-1 / genetics
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Cytokines
  • Diterpenes
  • Lipopolysaccharides
  • NF-kappa B
  • Protective Agents
  • Transcription Factor RelA
  • Vascular Cell Adhesion Molecule-1
  • Vascular Endothelial Growth Factor A
  • andrographolide
  • DNA
  • Peroxidase

Grants and funding

This study was supported by the National Natural Science Foundation of China (Grant No. 30971303). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.