Qingxuan Zhike Granules Modulate Gut Dysbiosis and Enhance Intestinal Repair in Murine Mycoplasma pneumonia

Shiyu Liu1, Bowen Li2, Meiling Wang3

  • 1Department of Pediatrics, Yunnan University of Traditional Chinese Medicine's First Affiliated Hospital, Kunming, Yunnan 650021, P.R. China.

Insights

Qingxuan Zhike Granules (QXZKG) effectively treat pediatric Mycoplasma pneumoniae pneumonia (MPP) by improving gut microbiota and intestinal repair. This treatment supports the gut-lung axis, reducing inflammation and enhancing barrier function.

Area of Science:

  • Microbiology
  • Immunology
  • Pharmacology

Background:

  • Pediatric Mycoplasma pneumoniae pneumonia (MPP) poses significant health challenges.
  • The gut-lung axis, involving gut microbiota and intestinal barrier function, is increasingly recognized in respiratory diseases.
  • Qingxuan Zhike Granules (QXZKG) is a traditional remedy with potential therapeutic applications.

Purpose of the Study:

  • To investigate the therapeutic efficacy of QXZKG in pediatric MPP.
  • To elucidate the mechanisms of QXZKG, focusing on gut microbiota modulation and intestinal repair via the gut-lung axis.

Main Methods:

  • Established a BALB/c mouse model of MPP for in vivo studies.
  • Assessed disease activity, histopathology, inflammatory markers, tight junction proteins, gut microbiota, and serum LPS.
  • Utilized an in vitro co-culture system to evaluate QXZKG effects on intestinal cells and immune cells.

Main Results:

  • QXZKG dose-dependently improved MPP symptoms and alleviated lung and intestinal tissue damage.
  • QXZKG reduced pro-inflammatory factors, increased intestinal tight junction proteins, and decreased serum LPS.
  • QXZKG restored gut microbiota diversity, increased beneficial bacteria, and inhibited opportunistic pathogens.

Conclusions:

  • QXZKG demonstrates therapeutic efficacy in pediatric MPP by modulating gut microbiota and enhancing intestinal barrier function.
  • The findings suggest QXZKG acts through the gut-lung axis to suppress systemic inflammation.
  • These results provide evidence for the expanded clinical use of QXZKG in treating pediatric MPP.

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