Fecal Microbiota Transplantation Alleviates Airway Inflammation in Asthmatic Rats by Increasing the Level of Short-Chain Fatty Acids in the Intestine
- PMID: 39775370
- PMCID: PMC12234594
- DOI: 10.1007/s10753-024-02233-w
Fecal Microbiota Transplantation Alleviates Airway Inflammation in Asthmatic Rats by Increasing the Level of Short-Chain Fatty Acids in the Intestine
Abstract
Asthma is a prevalent chronic inflammatory disorder of the respiratory tract that not only manifests with respiratory symptoms but also often involves intestinal flora disorders and gastrointestinal dysfunction. Recent studies have confirmed the close relationship between the gut and lungs, known as the "gut-lung axis" theory. Fecal microbiota transplantation (FMT), a method for restoring normal intestinal flora, has shown promise in treating common gastrointestinal diseases. The "gut-lung axis" theory suggests that FMT may have significant therapeutic potential for asthma. In this study, we established an Ovalbumin (OVA)-induced rat model of asthma to investigate the protective effect of FMT on airway inflammation and the restoration of intestinal short-chain fatty acids (SCFAs), aiming to explore its underlying mechanism. Rats in the Control group underwent fecal treatment via gavage (Control-FMT, C-FMT group), while rats in the Asthma group underwent fecal treatment via gavage after asthma induction (Asthma-FMT, A-FMT group). Following a two-week period of continuous intragastric administration, various measurements were conducted to assess pulmonary function, peripheral blood neutrophil, lymphocyte, and eosinophil content, lung tissue pathology, and collagen fiber deposition in the lungs. Additionally, neutrophil and eosinophil content in bronchoalveolar lavage fluid (BALF), expression levels of Interleukin-4 (IL-4), IL-5, IL-13, IL-17, IL-33, leukotrienes (LT), thymic stromal lymphopoietin (TSLP), prostaglandin D2 (PGD2) protein and mRNA in lung tissue, and SCFAs content in stool were evaluated. In the C-FMT group, lung function significantly improved, inflammatory cell content in peripheral blood and BALF decreased, lung tissue pathology and collagen fiber deposition significantly improved, the protein and mRNA levels of lung inflammatory factors IL-4, IL-5, IL-13, IL-17, IL-33, LT, TSLP, PGD2 were significantly decreased, and SCFAs such as acetate (C2), propionate (C3), butyrate (C4), isobutyric acid (I-C4), valeric acid (C5), and isovaleric acid (I-C5) content in stool significantly increased. However, the indexes in the A-FMT group did not show significant recovery, and the treatment effect on asthma symptoms in rats was inferior to that in the C-FMT group. Asthma induced intestinal flora disorders in rats, and FMT treatment improved the inflammatory response in asthmatic rat models and corrected their intestinal SCFAs disorders. Encouraging the recovery of intestinal SCFAs may play a significant role, and beneficial bacteria present in feces may improve asthma symptoms by promoting the remodeling of intestinal flora. This experiment provides further scientific evidence supporting the "gut-lung axis" theory.
Keywords: Airway inflammation; Asthma; Fecal bacteria transplantation; Gut-lung axis; Short-chain fatty acid.
© 2025. The Author(s).
Conflict of interest statement
Declarations. We confirming the study is reported in accordance with ARRIVE guidelines. All animal procedures were conducted in strict compliance with the National Institue of Health Guide for Use and Care of Laboratory Animals and approved by Institutional Animal Ethical Care Committee of Hunan University of Chinese Medicine Experimental Animal Center. This article does not contain any studies with human participants performed by any of the authors. Ethical Approval: The handling and care of the animals during the experiment were conducted following the provisions of the Guiding Opinions on the Kindness of Experimental Animals, with ethical approval number LL2021032407. Competing Interest: The authors declare no competing interests.
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- (No. 2021JJ30513, No. 2017JJ3245)/Natural Science Foundation of Hunan Province
- No. 20B444/Education Department of Hunan Province
- (No. 81603705)/National Natural Science Foundation of China
- ( No. 2017M612567)/Postdoctoral Science Foundation of China
- (2024XJZA008)/Hunan University of Chinese Medicine research project
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