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April 11, 2026Journal of Traditional and Complementary Medicine1 citationsOpen Access

Qingwen Baidu Decoction attenuates acute lung injury via macrophage exosomal miR-146a suppression of alveolar epithelial cell pyroptosis

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QYQiong YiJWJianxiang WangYJYaqing Jiang

Key Points

  • The study aims to investigate how Qingwen Baidu Decoction attenuates acute lung injury and the role of macrophage exosomal miR-146a.
  • Mouse models of LPS-induced acute lung injury were treated with QBD and/or antago-miR-146a.
  • Vascular permeability and total protein concentration of broncho-alveolar lavage fluid were assessed.
  • M2 macrophages were analyzed through immunofluorescence staining.
  • Exosomes and alveolar macrophages were isolated from broncho-alveolar lavage fluid.
  • TLR-4/NF-κB signaling and pyroptosis proteins were detected using western blotting and flow cytometry.
  • QBD treatment improved lung damage and enhanced M2 macrophage polarization.
  • Exosomal miR-146a uptake by AEC-II cells suppressed their pyroptosis through TLR4/NF-κB pathway inhibition.
  • Inhibition of miR-146a diminished the protective effects of QBD against acute lung injury.
  • Mid- to high-dose QBD increased miR-146a expression and secretion in M2 macrophages.

Abstract

The anti-inflammatory and anti-pyroptosis effects of traditional Chinese medicine Qingwen Baidu Decoction (QBD), as well as the potential involvement of miR-146a from M2 alveolar macrophage exosomes in acute lung injury (ALI) remain uncharacterized. This study aims to explore the mechanism by which QBD attenuates lipopolysaccharide (LPS)-induced ALI and the involvement of alveolar macrophage exosomal miR-146a. Mouse models of LPS-induced ALI were treated with QBD and/or antago-miR-146a. Vascular permeability was assessed by wet/dry (W/D) ratio and total protein concentration of broncho-alveolar lavage fluid (BALF). BALF neutrophils were stained with Wright-Giemsa stain and counted. M2 macrophages were assessed by immunofluorescence. The exosomes and alveolar macrophages were isolated from BALF. Alveolar epithelial type Ⅱ cells (AEC-II) were isolated from lung tissues and incubated with the exosomes. TLR-4/NF-κB signaling and pyroptosis proteins were detected by western blotting and flow cytometry. QBD treatment attenuated lung damage and enhanced M2 polarization. M2 secreted exosomal miR-146a was increased. The exosomal miR-146a can be taken up by AEC-II to suppress AEC-II pyroptosis via inhibiting TLR4/NF-κB signaling pathway. Mid- to high-dose QBD increased miR-146a expression, suppressed TLR4/NF-κB signaling, and attenuated ALI in vivo . Inhibition of miR-146a abolished the protective effect of QBD against ALI. QBD increased miR-146a expression and secretion in M2 macrophage exosomes, decreased TLR4/NF-κB signaling in AEC II cells, and suppressed AEC-II pyroptosis, attenuating septic lung injury.

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Cite This Study

Yi et al. (2026) studied this question.

synapsesocial.com/papers/69d9e58f78050d08c1b75ca7https://doi.org/10.1016/j.jtcme.2026.04.001
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