Tectorigenin inhibits the inflammation of LPS-induced acute lung injury in mice

Chin J Nat Med. 2014 Nov;12(11):841-6. doi: 10.1016/S1875-5364(14)60126-6.

Abstract

Aim: In a previous study, the anti-inflammatory effects of tectorigenin were disclosed. In this study, the anti-inflammatory effects of tectorigenin on acute lung injury using a lipopolysaccharide (LPS)-induced acute lung injury (ALI) mouse model were investigated

Method: The cell-count in the bronchoalveolar lavage fluid (BALF) was measured. The animal lung edema degree was evaluated by the wet/dry weight (W/D) ratio. The superoxidase dismutase (SOD) activity and myeloperoxidase (MPO) activity was assayed using SOD and MPO kits, respectively. The levels of inflammatory mediators, including tumor necrosis factor-α (TNF-α), IL-1β, and IL-6 were assayed using an enzyme-linked immunosorbent assay method. Pathological changes of lung tissues were observed through HE staining. The inflammatory signal pathway related protein nuclear factor NF-κB p65 mRNA expression was measured by real-time PCR, and the protein level of NF-κB p65 was measured using Western blotting analysis.

Results: The data showed that treatment with the tectorigenin markedly attenuated the inflammatory cell numbers in the BALF, decreased nuclear factor NF-κB p65 mRNA level and protein level in the lungs, and improved SOD activity and inhibited MPO activity. Histological studies showed that tectorigenin substantially inhibited LPS-induced neutrophils in lung tissue compared with the model group.

Conclusion: The results indicated that tectorigenin had a protective effect on LPS-induced ALI in mice.

Keywords: Inflammation; LPS-induced acute lung injury; Tectorigenin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / chemically induced
  • Acute Lung Injury / drug therapy*
  • Acute Lung Injury / pathology
  • Animals
  • Bronchoalveolar Lavage Fluid / cytology
  • Cell Count
  • Female
  • Inflammation / drug therapy
  • Inflammation / pathology
  • Isoflavones / therapeutic use*
  • Lipopolysaccharides
  • Mice
  • Mice, Inbred BALB C
  • Peroxidase / analysis
  • Pulmonary Edema / pathology
  • Superoxide Dismutase / analysis

Substances

  • Isoflavones
  • Lipopolysaccharides
  • tectorigenin
  • Peroxidase
  • Superoxide Dismutase