Da-Yuan-Yin decoction polyphenol fraction attenuates acute lung injury induced by lipopolysaccharide

Pharm Biol. 2023 Dec;61(1):228-240. doi: 10.1080/13880209.2023.2166085.

Abstract

Context: Da-Yuan-Yin is a Chinese traditional prescription.

Objective: This study explores the therapeutic effects of the Da-Yuan-Yin decoction polyphenol fraction (DYY-4) on acute lung injury (ALI) in mice induced by lipopolysaccharide (LPS).

Materials and methods: The mice (n = 10) were orally administrated with DYY-4 (15, 30, and 60 mg/kg) or DXM (5 mg/kg), half an hour after LPS (2 mg/kg) instilled intratracheally. The protein content and the levels of inflammatory factors, the levels of complements, the mRNA expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), the level of myeloperoxidase (MPO) and superoxide dismutase (SOD), the expression of the IkB kinase (IKK) and nuclear factor-kappa B (NF-κB), the lung wet-to-dry weight (W/D) ratio and lung tissue were evaluated, 24 h after LPS challenge. Network pharmacology predicted potential targets.

Results: DYY-4 (30, 60 mg/kg, p < 0.01, p < 0.01) decreased the lung W/D ratio, total protein concentration, the levels of C3, C3c and C5a, the levels of TNF-α, IL-6, and IL-1β, while increased the levels of IL-4 and IL-10. DYY-4 (60 mg/kg) decreased the levels of C5aR1, C5b-9 and COX-2 mRNA (p < 0.05), the levels of MPO and iNOS mRNA, the activation of the IKK/NF-κB pathway (p < 0.01), and increased the levels of IL-13 and SOD (p < 0.01). DYY-4 (60 mg/kg) relieved the lung tissue pathological changes and reduced the C3c deposition.

Discussion and conclusions: Network pharmacology combined with animal experiments revealed the targets of DYY-4 alleviating ALI.

Keywords: Complement; IKK; NF-κB; inflammatory factors; network pharmacology; oxidase.

MeSH terms

  • Acute Lung Injury* / chemically induced
  • Acute Lung Injury* / drug therapy
  • Acute Lung Injury* / prevention & control
  • Animals
  • Cyclooxygenase 2 / genetics
  • Lipopolysaccharides / toxicity
  • Lung
  • Mice
  • NF-kappa B* / metabolism
  • Polyphenols / adverse effects
  • RNA, Messenger
  • Superoxide Dismutase

Substances

  • NF-kappa B
  • Lipopolysaccharides
  • Polyphenols
  • Cyclooxygenase 2
  • Superoxide Dismutase
  • RNA, Messenger

Grants and funding

This work was supported by Science and Technology Department of Suzhou, China under Grant [No. SYS2020079], Jiangsu Health Commission Medical Research Projects, China under Grant [No. Z2020063] and 2018 Qinglan Project of the Yong and Middle-aged Academic Leader of Jiangsu College.