Taufani Indra Putra, Tasminatun Sri, Harimurti Sabtanti, Yang Liang-Yo, Huang Chih-Yang, Situmorang Jiro Hasegawa
Graduate Institute of Pharmacy, China Medical University, Taichung, Taiwan.
Department of Pharmacist Profession Education, Faculty of Medicine and Health Sciences, Universitas Muhammadiyah Yogyakarta, Yogyakarta, Indonesia.
Biol Trace Elem Res. 2024 Aug 29. doi: 10.1007/s12011-024-04360-9.
Iron toxicity intricately links with ferroptosis, a unique form of cell death, and is significantly influenced by lipid peroxidation. Despite its critical role in various diseases and drug development, the association between iron toxicity and ferroptosis remains relatively unexplored. Accidental iron ingestion has emerged as a growing concern, resulting in a spectrum of symptoms ranging from gastrointestinal discomfort to severe outcomes, including mortality. This research introduces tannic acid (TA), which contains numerous phenol groups, as a powerful antiferroptotic agent. In male Wistar rats, even a modest dose of TA (7.5 mg/kg) significantly curtailed thiobarbituric acid reactive substances (TBARS), a well-established indicator of lipid peroxidation, and mitigated iron accumulation induced by ferrous sulfate (FeSO) in the liver and kidney. The evidence supporting TA's protective function against iron-triggered liver and kidney dysfunction was substantiated by assessing specifically the levels of blood urea nitrogen (BUN) and alanine aminotransferase (ALT). In cell models using ferroptosis inducers such as iron-salophene (FeSP) and RAS-selective lethal 3 (RSL3), tannic acid (TA) exhibited superior protective capabilities compared to the traditional iron chelator, deferoxamine (DFO). Nrf2 and HO-1, regulators of antioxidant defense genes, are implicated in controlling ferroptosis. The expression of Nrf2 and HO-1 increased with TA treatment in the presence of FeSP, indicating their role in reducing lipid ROS levels. Additionally, TA significantly reduced the heightened levels of COX2, a marker associated with ferroptosis. In summary, the remarkable antiferroptosis activity of TA is likely due to its combined iron-chelating and antioxidant properties. With its safety profile for oral consumption, TA may offer benefits in cases of accidental iron ingestion and conditions like hemochromatosis.
铁毒性与铁死亡(一种独特的细胞死亡形式)密切相关,并受到脂质过氧化的显著影响。尽管其在各种疾病和药物开发中起着关键作用,但铁毒性与铁死亡之间的关联仍相对未被充分探索。意外铁摄入已成为一个日益令人担忧的问题,会导致一系列症状,从胃肠道不适到严重后果,包括死亡。本研究引入了含有众多酚基团的单宁酸(TA)作为一种强大的抗铁死亡剂。在雄性Wistar大鼠中,即使是适度剂量的TA(7.5毫克/千克)也能显著减少硫代巴比妥酸反应性物质(TBARS,一种公认的脂质过氧化指标),并减轻硫酸亚铁(FeSO)在肝脏和肾脏中诱导的铁积累。通过具体评估血尿素氮(BUN)和丙氨酸转氨酶(ALT)水平,证实了支持TA对铁引发的肝脏和肾脏功能障碍具有保护作用的证据。在使用铁 - 萨洛芬(FeSP)和RAS选择性致死3(RSL3)等铁死亡诱导剂的细胞模型中,单宁酸(TA)表现出比传统铁螯合剂去铁胺(DFO)更强的保护能力。Nrf2和HO - 1是抗氧化防御基因的调节因子,参与控制铁死亡。在FeSP存在的情况下,TA处理使Nrf2和HO - 1的表达增加,表明它们在降低脂质ROS水平中的作用。此外,TA显著降低了与铁死亡相关的标志物COX2的升高水平。总之,TA显著的抗铁死亡活性可能归因于其铁螯合和抗氧化特性的结合。鉴于其口服安全性,TA可能在意外铁摄入和血色素沉着症等病症中发挥益处。