Journal of Oral Science Research ›› 2026, Vol. 42 ›› Issue (2): 126-133.DOI: 10.13701/j.cnki.kqyxyj.2026.02.008

Previous Articles     Next Articles

Study on Mechanism of Baicalin Regulating Proliferation and Angiogenesis of Dental Pulp Stem Cells through PI3K/AKT Signaling Axis

CHENG Gang1, WU Xiuyin1, LI Yuexiu2, MI Jing2, WU Qishan2*   

  1. 1. Department of Stomatology, The Affiliated People's Hospital of Shandong First Medical University, Jinan 271199, China;
    2. Department of Stomatology, Tai 'an City Central Hospital (Tai'an City Central Hospital Affiliated to Qingdao University, Taishan Medical Care Center), Tai'an 271000, China
  • Received:2025-04-21 Published:2026-02-28

Abstract: Objective: To explore the effect of baicalin on the proliferation and angiogenesis of dental pulp stem cells (DPSC), and to investigate the regulatory mechanism of phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT) signal axis in this process. Methods: Human DPSC were cultured and divided into the control group (complete medium), the 10 μmol/L group, the 20 μmol/L group, the 50 μmol/L group, and the 100 μmol/L group (complete medium + different concentrations of baicalin) according to the concentration of baicalin. The effect of different concentrations of baicalin on the viability of DPSC was observed. The changes of the PI3K/AKT signaling axis were further explored. Meanwhile, LY294002 (a PI3K/AKT inhibitor) was added to the 50 μmol/L group to observe its regulatory effect on the proliferation and angiogenesis of DPSC. Results: Baicalin could enhance the activity of DPSC, inhibit their apoptosis, and the effect was more obvious in the 50 μmol/L group (P<0.05). Compared with other groups, the expressions of PI3K, AKT mRNA, p-PI3K/PI3K, and p-AKT/AKT in the 50 μmol/L group were significantly increased (P<0.05). Compared with the 50 μmol/L group, the proliferation ability of DPSC in the 50 μmol/L+LY294002 group was significantly weakened and the number of migrations was significantly reduced. The expressions of vascular endothelial growth factor (VEGF) and angiopoietin-2 (Ang-2) were significantly decreased. Conclusion: Baicalein can promote the proliferation and angiogenesis of DPSC. This process is related to the activation of the PI3K/AKT signaling pathway and the increased expression levels of VEGF and Ang-2, providing theoretical support for the application of baicalein in DPSC.

Key words: baicalin, dental pulp stem cells, cell proliferation, angiogenesis, regulatory mechanism