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                <identifier>oai:data.mendeley.com/sn9b54bmxn.1</identifier>
                <datestamp>2025-12-25T03:07:13Z</datestamp>
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    <dc:creator>hu, ruitao</dc:creator>
    <dc:title>Liuweidihuang Pill ameliorates Pulmonary Fibrosis through anti-inflammation and modulating gut microbiome in mice</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>Background: Pulmonary fibrosis is a chronic lung disease. Liuweidihuang pill is a TCM prescription primarily indicated for a range of disorders related to kidney-yin deficiency. Emerging pharmacological evidence indicates LD also has anti-inflammatory and antioxidant properties, suggesting its potential in attenuating inflammatory diseases, including PF. However, the efficacy and mechanism of LD in PF therapy is unclear.

Purpose: This study aimed to investigate the effects and mechanisms  of LD on bleomycin-induced PF in mice, and elucidate the underlying mechanism.

Methods: Mice were intratracheally administered bleomycin and simultaneously treated with LD. Pathological changes in lung tissue were evaluated with HE and Masson staining. Levels of pro-inflammatory factors and hydroxyproline content were assessed in lung tissue and serum using ELISA. The chemical components of LD were analyzed using UPLC-MS/MS. Gut microbiome in mice was examined using 16S ribosomal DNA sequencing. To investigate the contributions of gut microbiota and LD&apos;s absorbed components, we employed fecal microbiota transplantation, probiotic VSL#3 treatment, and in vitro assays with drug-containing serum.

Results: Our findings demonstrated that LD treatment reduced the lung index, alleviated inflammation and decreased interstitial fibrosis in PF mice. The expression of inflammatory cytokines, α-smooth muscle actin protein expression and hydroxyproline content were reduced in LD-treated mice compared to PF group. The study also revealed alterations in gut microbiota following LD treatment. Meanwhile, VSL#3 partially improved lung pathology, while FMT and drug-containing serum showed limited efficacy in both in vivo and in vitro tests.

Conclusion: Taken together, LD shows promise in delaying bleomycin-induced PF progression by modulating gut microbiota and inhibiting inflammatory factors. This study highlights LD&apos;s potential as a therapeutic agent for PF.</dc:description>
    <dc:subject>Pharmacology</dc:subject>
    <dc:subject>Traditional Medicine</dc:subject>
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    <dc:identifier>doi:10.17632/sn9b54bmxn.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/sn9b54bmxn.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2025-12-25T03:07:13Z</dc:date>
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