Frontiers in Pharmacology (Sep 2024)

Mechanistic study of leukopenia treatment by Qijiao shengbai Capsule via the Bcl2/Bax/CASAPSE3 pathway

  • Siyue Jiang,
  • Siyue Jiang,
  • Pengjiao Wang,
  • Pengjiao Wang,
  • Xiaodong Sun,
  • Xiaodong Sun,
  • Min Zhang,
  • Min Zhang,
  • Shuo Zhang,
  • Shuo Zhang,
  • Yu Cao,
  • Yu Cao,
  • Yuben Wang,
  • Yuben Wang,
  • Li Liu,
  • Li Liu,
  • Xiuli Gao,
  • Xiuli Gao

DOI
https://doi.org/10.3389/fphar.2024.1451553
Journal volume & issue
Vol. 15

Abstract

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BackgroundLeukopenia can be caused by chemotherapy, which suppresses bone marrow function and can impact the effectiveness of cancer treatment. Qijiao Shengbai Capsule (QJSB) is commonly used to treat leukopenia, but the specific bioactive components and mechanisms of action are not well understood.Objectives and resultsThis study aimed to analyze the active ingredients of QJSB and its potential targets for treating leukopenia using network pharmacology and molecular docking. Through a combination of serum pharmacochemistry, multi-omics, network pharmacology, and validation experiments in a murine leukopenia model, the researchers sought to understand how QJSB improves leukopenia. The study identified 16 key components of QJSB that act in vivo to increase the number of white blood cells in leukopenic mice. Multi-omics analysis and network pharmacology revealed that the PI3K-Akt and MAPK signaling pathways are important in the treatment of leukopenia with QJSB. Five specific targets (JUN, FOS, BCl-2, CASPAS-3) were identified as key targets.ConclusionValidation experiments confirmed that QJSB regulates genes related to cell growth and inhibits apoptosis, suggesting that apoptosis may play a crucial role in leukopenia development and that QJSB may improve immune function by regulating apoptotic proteins and increasing CD4+ T cell count in leukopenic mice.

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