Ephedra sinica polysaccharide alleviates airway inflammations of mouse asthma-like induced by PM2.5 and ovalbumin via the regulation of gut microbiota and short chain fatty acid

J Pharm Pharmacol. 2022 Nov 25;74(12):1784-1796. doi: 10.1093/jpp/rgac078.

Abstract

Objectives: Epidemiological investigations show that long-term exposure to PM2.5 is directly related to asthma-like and other respiratory diseases. This study aims to further explore the pharmacological effect of Ephedra sinica polysaccharide (ESP) on lung injury caused by atmospheric PM2.5.

Methods: To achieve the aim, we explored the therapeutic effect of ESP on an aggravated asthma-like mouse induced by PM2.5 combined with ovalbumin (OVA), and explored mechanisms underlying the connection between gut microbiota and lung function.

Key findings: Preliminary results showed that ESP alleviated the symptoms of aggravated allergic asthma-like in mice; reduced the number of eosinophils in BALF; reduced the levels of serum Ig-E, IL-6, TNF-α, and IL-1β. Further qRT-PCR detected that ESP inhibited the NF-κB pathway. The final analysis detected by 16S rRNA and short chain fatty acid (SCFA) confirmed that ESP increased relative proportions of Bacteroides, Lactobacillus, Prevotella, Butyricicoccus and Paraprevotella, but decreased that of Enterococcus and Ruminococcus; increased acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, and isohexanic acid in the meanwhile.

Conclusions: The study showed that ESP has a potential for future therapeutical applications in the prevention and treatment of asthma-like disease induced by PM2.5 and OVA via regulation of gut microbiota and SCFA.

Keywords: Ephedra sinica polysaccharide; PM2.5; aggravated asthma-like disease; gut microbiota; lung; short chain fatty acid.

MeSH terms

  • Animals
  • Asthma* / chemically induced
  • Asthma* / drug therapy
  • Asthma* / metabolism
  • Disease Models, Animal
  • Ephedra sinica*
  • Fatty Acids, Volatile / metabolism
  • Gastrointestinal Microbiome*
  • Inflammation / metabolism
  • Lung / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin / pharmacology
  • Particulate Matter / metabolism
  • Particulate Matter / toxicity
  • Polysaccharides / pharmacology
  • Polysaccharides / therapeutic use
  • RNA, Ribosomal, 16S / metabolism

Substances

  • Ovalbumin
  • RNA, Ribosomal, 16S
  • Polysaccharides
  • Particulate Matter
  • Fatty Acids, Volatile