Preventive Effect of the Total Polyphenols from Nymphaea candida on Sepsis-Induced Acute Lung Injury in Mice via Gut Microbiota and NLRP3, TLR-4/NF-κB Pathway

Int J Mol Sci. 2024 Apr 12;25(8):4276. doi: 10.3390/ijms25084276.

Abstract

This study aimed to investigate the preventive effects of the total polyphenols from Nymphaea candida (NCTP) on LPS-induced septic acute lung injury (ALI) in mice and its mechanisms. NCTP could significantly ameliorate LPS-induced lung tissue pathological injury in mice as well as lung wet/dry ratio and MPO activities (p < 0.05). NCTP could significantly decrease the blood leukocyte, neutrophil, monocyte, basophil, and eosinophil amounts and LPS contents in ALI mice compared with the model group (p < 0.05), improving lymphocyte amounts (p < 0.05). Moreover, compared with the model group, NCTP could decrease lung tissue TNF-α, IL-6, and IL-1β levels (p < 0.05) and downregulate the protein expression of TLR4, MyD88, TRAF6, IKKβ, IκB-α, p-IκB-α, NF-κB p65, p-NF-κB p65, NLRP3, ASC, and Caspase1 in lung tissues (p < 0.05). Furthermore, NCTP could inhibit ileum histopathological injuries, restoring the ileum tight junctions by increasing the expression of ZO-1 and occludin. Simultaneously, NCTP could reverse the gut microbiota disorder, restore the diversity of gut microbiota, increase the relative abundance of Clostridiales and Lachnospiraceae, and enhance the content of SCFAs (acetic acid, propionic acid, and butyric acid) in feces. These results suggested that NCTP has preventive effects on septic ALI, and its mechanism is related to the regulation of gut microbiota, SCFA metabolism, and the TLR-4/NF-κB and NLRP3 pathways.

Keywords: NLRP3; Nymphaea candida; TLR-4/NF-κB pathway; acute lung injury; gut microbiota; inflammatory response; polyphenols; short-chain fatty acids.

MeSH terms

  • Acute Lung Injury* / etiology
  • Acute Lung Injury* / metabolism
  • Acute Lung Injury* / microbiology
  • Acute Lung Injury* / prevention & control
  • Animals
  • Gastrointestinal Microbiome* / drug effects
  • Lipopolysaccharides
  • Male
  • Mice
  • NF-kappa B* / metabolism
  • NLR Family, Pyrin Domain-Containing 3 Protein* / metabolism
  • Polyphenols* / pharmacology
  • Sepsis* / complications
  • Sepsis* / metabolism
  • Signal Transduction* / drug effects
  • Toll-Like Receptor 4* / metabolism

Substances

  • NLR Family, Pyrin Domain-Containing 3 Protein
  • Toll-Like Receptor 4
  • NF-kappa B
  • Polyphenols
  • Nlrp3 protein, mouse
  • Tlr4 protein, mouse
  • Lipopolysaccharides