151. Celastrol reduces lung inflammation induced by multiwalled carbon nanotubes in mice via NF-κb-signaling pathway.
- Author
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Qing TL, Jiang XY, Li JF, Shen Q, Zhao XY, Ren LJ, Dai XY, Zhang JQ, Shi WJ, Zhang XF, Zhang B, Yan L, Chen JK, and Zhu JB
- Subjects
- Animals, Male, Mice, Anti-Inflammatory Agents pharmacology, Bronchoalveolar Lavage Fluid cytology, Bronchoalveolar Lavage Fluid chemistry, Cytokines metabolism, Lung drug effects, Lung pathology, Lung metabolism, Mice, Inbred C57BL, Mice, Knockout, NF-kappa B metabolism, Nanotubes, Carbon toxicity, Pentacyclic Triterpenes pharmacology, Pneumonia chemically induced, Pneumonia drug therapy, Pneumonia prevention & control, Pneumonia metabolism, Signal Transduction drug effects, Triterpenes pharmacology
- Abstract
Multiwalled carbon nanotubes (MWCNTs) have numerous applications in the field of carbon nanomaterials. However, the associated toxicity concerns have increased significantly because of their widespread use. The inhalation of MWCNTs can lead to nanoparticle deposition in the lung tissue, causing inflammation and health risks. In this study, celastrol, a natural plant medicine with potent anti-inflammatory properties, effectively reduced the number of inflammatory cells, including white blood cells, neutrophils, and lymphocytes, and levels of inflammatory cytokines, such as IL-1β, IL-6, and TNF-α, in mice lungs exposed to MWCNTs. Moreover, celastrol inhibited the activation of the NF-κB-signaling pathway. This study confirmed these findings by demonstrating comparable reductions in inflammation upon exposure to MWCNTs in mice with the deletion of NF-κB (P50
-/- ). These results indicate the utility of celastrol as a promising pharmacological agent for preventing MWCNT-induced lung tissue inflammation.- Published
- 2024
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