Zhang Guangjie, Feng Yining, Huang Li, Ren Chenxi, Gao Mingyuan, Zhang Jie, Guan Tianzhu
School of Biology and Food Engineering, Anyang Institute of Technology, Anyang 455000, China.
School of Food Science and Engineering, Yangzhou University, Yangzhou 225127, China.
Molecules. 2025 Aug 15;30(16):3393. doi: 10.3390/molecules30163393.
Hederagenin, a pentacyclic triterpenoid saponin from various medicinal plants, shows immense therapeutic potential; however, its inherent low bioavailability severely hinders its clinical translation. This comprehensive review synthesizes recent studies on the health benefits of hederagenin and its glycosides, critically the chemical modification strategies and pharmacological mechanisms aimed at optimizing its bioactivity. Key findings reveal that its broad anticancer and anti-inflammatory activities largely stem from its capacity to modulate crucial cellular signaling pathways, including the NF-κB, PI3K/Akt, and MAPK. Structural modification, particularly intelligent derivatization at the C-28 position, is a central strategy to overcome its pharmacokinetic deficiencies and significantly boost cytotoxicity. Furthermore, its unique pro-oxidant function within cancer cells, achieved by inhibiting the Nrf2-ARE antioxidant pathway, offers a novel approach for selective chemotherapeutics. For the clinical translation of hederagenin, we propose a strategic focus on derivatization through multi-target hybrids and sophisticated delivery systems. This approach is essential for addressing its pharmacokinetic barriers while strategically leveraging its context-dependent pro-oxidant effects.
常春藤皂苷元是一种从多种药用植物中提取的五环三萜皂苷,具有巨大的治疗潜力;然而,其固有的低生物利用度严重阻碍了其临床应用。这篇综述综合了常春藤皂苷元及其糖苷对健康益处的最新研究,重点探讨了旨在优化其生物活性的化学修饰策略和药理机制。主要研究结果表明,其广泛的抗癌和抗炎活性主要源于其调节关键细胞信号通路的能力,包括NF-κB、PI3K/Akt和MAPK。结构修饰,特别是在C-28位进行智能衍生化,是克服其药代动力学缺陷并显著提高细胞毒性的核心策略。此外,通过抑制Nrf2-ARE抗氧化途径在癌细胞内实现的独特促氧化功能,为选择性化疗提供了一种新方法。对于常春藤皂苷元的临床应用,我们建议将战略重点放在通过多靶点杂合物和精密给药系统进行衍生化上。这种方法对于解决其药代动力学障碍,同时战略性地利用其依赖于环境的促氧化作用至关重要。