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

Author:

Liu Jun-Xi12,Yuan Hong-Yu1,Li Ya-Nan3,Wei Zhen1,Liu Yang4,Liang Jun1ORCID

Affiliation:

1. Key Laboratory of Basic and Application Research of Beiyao (Heilongjiang University of Chinese Medicine), Ministry of Education , Harbin , PR China

2. Department of Pharmacy, Heilongjiang Nursing College , Harbin , PR China

3. Harbin Environmental Monitoring Center Station , Harbin , PR China

4. Shanghai Personalbio Biotechnology Co., Ltd , Xuhui District, Shanghai , PR China

Abstract

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.

Funder

National Natural Science Foundation of China

National Key Research and Development Project of China

Applied Technology Research and Development Plan of Heilongjiang Province

University Research and Development Projects of Heilongjiang Province

Heilongjiang Natural Science Funds

Heilongjiang Touyan Innovation Team Program

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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