Lu Xiaobei, Sun Yapeng, Zhang Zhaoyi, Sun Zhigang, Wang Shaohui, Xu Erping
Traditional Chinese Medicine (Zhong Jing) School, Henan University of Chinese Medicine, Zhengzhou, China.
Department of Proctology, Third Affiliated Hospital of Henan University of Traditional Chinese Medicine, Zhengzhou, China.
Front Pharmacol. 2025 Apr 9;16:1573684. doi: 10.3389/fphar.2025.1573684. eCollection 2025.
Ulcerative colitis (UC), a chronic inflammatory bowel disease, is driven by dysregulated immune responses and persistent intestinal inflammation. Pyroptosis, a caspase/gasdermin-mediated inflammatory cell death that exacerbates mucosal damage through excessive cytokine release and epithelial barrier disruption. Although pyroptosis is considered to be a key mechanism in the pathogenesis of UC, the systematic assessment of the role of natural products in targeting the pyroptosis pathway remains a critical research gap. The purpose of this review is to investigate the regulatory effects of natural products on pyroptosis in UC and elucidate the mechanisms of action and potential therapeutic effects. Key findings highlight polyphenols (e.g., resveratrol), flavonoids (e.g., Quercetin), and terpenoids as promising agents that inhibit NLRP3 inflammasome activation, suppress gasdermin D cleavage, and restore barrier integrity, thereby reducing pro-inflammatory cytokine release in preclinical UC models. Current evidence shows enhanced efficacy and safety when these compounds are combined with standard therapies, but clinical translation requires overcoming three key barriers: limited human trial data, uncharacterized polypharmacology, and suboptimal pharmacokinetics needing formulation refinement. Future research should prioritize standardized animal-to-human translational models, mechanistic studies on synergistic pathways, and rigorous clinical validation to harness the full potential of natural products in pyroptosis-targeted UC therapies.
溃疡性结肠炎(UC)是一种慢性炎症性肠病,由免疫反应失调和持续性肠道炎症驱动。细胞焦亡是一种由半胱天冬酶/gasdermin介导的炎症性细胞死亡,通过过度释放细胞因子和破坏上皮屏障加剧黏膜损伤。尽管细胞焦亡被认为是UC发病机制中的关键机制,但对天然产物在靶向细胞焦亡途径中作用的系统评估仍然是一个关键的研究空白。本综述的目的是研究天然产物对UC中细胞焦亡的调节作用,并阐明其作用机制和潜在治疗效果。主要发现突出了多酚类(如白藜芦醇)、黄酮类(如槲皮素)和萜类化合物是有前景的药物,它们可抑制NLRP3炎性小体激活、抑制gasdermin D裂解并恢复屏障完整性,从而减少临床前UC模型中促炎细胞因子的释放。目前的证据表明,这些化合物与标准疗法联合使用时疗效和安全性增强,但临床转化需要克服三个关键障碍:人体试验数据有限、多药理学特征不明以及药代动力学欠佳需要改进制剂。未来的研究应优先考虑标准化的动物到人类转化模型、协同途径的机制研究以及严格的临床验证,以充分发挥天然产物在靶向细胞焦亡的UC治疗中的潜力。