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Mechanistic study of leukopenia treatment by Qijiao shengbai Capsule via the Bcl2/Bax/CASAPSE3 pathway.
Jiang, Siyue; Wang, Pengjiao; Sun, Xiaodong; Zhang, Min; Zhang, Shuo; Cao, Yu; Wang, Yuben; Liu, Li; Gao, Xiuli.
Afiliação
  • Jiang S; State Key Laboratory of Functions and Applications of Medicinal Plants and School of Pharmacy, Guizhou Medical University, Guiyang, China.
  • Wang P; Center of Microbiology and Biochemical Pharmaceutical Engineering, Guizhou Medical University, Guiyang, China.
  • Sun X; State Key Laboratory of Functions and Applications of Medicinal Plants and School of Pharmacy, Guizhou Medical University, Guiyang, China.
  • Zhang M; Center of Microbiology and Biochemical Pharmaceutical Engineering, Guizhou Medical University, Guiyang, China.
  • Zhang S; State Key Laboratory of Functions and Applications of Medicinal Plants and School of Pharmacy, Guizhou Medical University, Guiyang, China.
  • Cao Y; Center of Microbiology and Biochemical Pharmaceutical Engineering, Guizhou Medical University, Guiyang, China.
  • Wang Y; State Key Laboratory of Functions and Applications of Medicinal Plants and School of Pharmacy, Guizhou Medical University, Guiyang, China.
  • Liu L; Center of Microbiology and Biochemical Pharmaceutical Engineering, Guizhou Medical University, Guiyang, China.
  • Gao X; State Key Laboratory of Functions and Applications of Medicinal Plants and School of Pharmacy, Guizhou Medical University, Guiyang, China.
Front Pharmacol ; 15: 1451553, 2024.
Article em En | MEDLINE | ID: mdl-39295929
ABSTRACT

Background:

Leukopenia 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

results:

This 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.

Conclusion:

Validation 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pharmacol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Pharmacol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça