Ruscogenin attenuates particulate matter-induced acute lung injury in mice via protecting pulmonary endothelial barrier and inhibiting TLR4 signaling pathway

Acta Pharmacol Sin. 2021 May;42(5):726-734. doi: 10.1038/s41401-020-00502-6. Epub 2020 Aug 27.

Abstract

The inhalation of particulate matter (PM) is closely related to respiratory damage, including acute lung injury (ALI), characterized by inflammatory fluid edema and disturbed alveolar-capillary permeability. Ruscogenin (RUS), the main active ingredient in the traditional Chinese medicine Ophiopogonis japonicus, has been found to exhibit anti-inflammatory activity and rescue LPS-induced ALI. In this study, we investigated whether and how RUS exerted therapeutic effects on PM-induced ALI. RUS (0.1, 0.3, 1 mg·kg-1·d-1) was orally administered to mice prior to or after intratracheal instillation of PM suspension (50 mg/kg). We showed that RUS administration either prior to or after PM challenge significantly attenuated PM-induced pathological injury, lung edema, vascular leakage and VE-cadherin expression in lung tissue. RUS administration significantly decreased the levels of cytokines IL-6 and IL-1β, as well as the levels of NO and MPO in both bronchoalveolar lavage fluid (BALF) and serum. RUS administration dose-dependently suppressed the phosphorylation of NF-κB p65 and the expression of TLR4 and MyD88 in lung tissue. Furthermore, TLR4 knockout partly diminished PM-induced lung injury, and abolished the protective effects of RUS in PM-instilled mice. In conclusion, RUS effectively alleviates PM-induced ALI probably by inhibition of vascular leakage and TLR4/MyD88 signaling. TLR4 might be crucial for PM to initiate pulmonary lesion and for RUS to exert efficacy against PM-induced lung injury.

Keywords: acute lung injury; bronchoalveolar lavage fluid; endothelial permeability; particulate matter; ruscogenin; toll like receptor 4.

MeSH terms

  • Acute Lung Injury / chemically induced
  • Acute Lung Injury / complications
  • Acute Lung Injury / drug therapy*
  • Acute Lung Injury / pathology
  • Animals
  • Anti-Inflammatory Agents / therapeutic use*
  • Endothelium / drug effects*
  • Gene Knockout Techniques
  • Inflammation / chemically induced
  • Inflammation / drug therapy
  • Inflammation / etiology
  • Inflammation / pathology
  • Lung / drug effects*
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Myeloid Differentiation Factor 88 / metabolism
  • Particulate Matter
  • Protective Agents / therapeutic use
  • Signal Transduction / drug effects*
  • Spirostans / therapeutic use*
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / metabolism

Substances

  • Anti-Inflammatory Agents
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Particulate Matter
  • Protective Agents
  • Spirostans
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • ruscogenin