In total, 102 chemical components, 10 prototype components, and 16 metabolites absorbed in the brain were identified in XYP. Network pharmacology analysis showed the compounds sharing 420 common targets with depression. TP53, EGFR, PTGS2, ESR1, PPARG, and other 68 targets were considered core targets, mainly enriched in PI3K-Akt and MAPK signaling pathways. Further analysis revealed associated apoptosis and inflammatory response. Molecular docking revealed that paeoniflorin, liquiritin, and atractylenolide III were found to have the highest binding energy to TP53, ESR1 and PPARG, which can affect signaling pathways to regulate inflammatory responses and cell apoptosis.
This study was shown to provide experimental evidence for elucidating XYP response compounds and the formation of quality control. That said, the scientists only analyzed the active components in XYP, overlooking the active components potentially playing an antidepressant effect molecular mechanism. They intend to address this in future research efforts.
References
(1) Zhou, S.; Wang, Y.; Xie, M.; et al. Uncovering the Antidepressant Active Ingredients and Related Molecular Mechanisms of Xiaoyao Pill Using Integrated Pharmacological Strategy. J. Chromatogr. B 2025, 1255, 124502. DOI: 10.1016/j.jchromb.2025.124502
(2) Mental Health in China. World Health Organization 2025. https://www.who.int/china/health-topics/mental-health (accessed 2025-5-30)
(3) Xue, Z.; Huang, Z.; Cheng, S-L.; Wang, X-H.; Zhou, X.; Ma, Q-Y.; Chen, J-X. Efficacy and Safety of Xiaoyao Pills for Mild to Moderate Depression: Study Protocol for a Randomized Controlled Trial. Trials 2022, 23 (10). DOI: 10.1186/s13063-021-05909-y
(4) Lubeck, B. What is Xiao Yao San? Verywell Health 2024. https://www.verywellhealth.com/xiao-yao-wan-88943 (accessed 2025-6-2)