单宁酸可抑制肾细胞中铁盐酚复合物诱导的铁突变,防止铁超载诱导的大鼠肝肾功能障碍

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Indra Putra Taufani, Sri Tasminatun, Sabtanti Harimurti, Liang-Yo Yang, Chih-Yang Huang, Jiro Hasegawa Situmorang
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引用次数: 0

摘要

铁毒性与铁变态反应(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。尽管铁在各种疾病和药物开发中起着至关重要的作用,但铁中毒与铁变态反应之间的联系仍相对缺乏研究。意外摄入铁已成为一个日益令人担忧的问题,会导致一系列症状,从肠胃不适到严重后果,包括死亡。本研究将含有大量酚基的单宁酸(TA)作为一种强有力的抗铁锈色素沉着剂。在雄性 Wistar 大鼠体内,即使是适量的单宁酸(7.5 毫克/千克)也能显著减少硫代巴比妥酸活性物质(TBARS)(一种公认的脂质过氧化指标),并减轻硫酸亚铁(FeSO4)在肝脏和肾脏中引起的铁积累。通过具体评估血尿素氮(BUN)和丙氨酸氨基转移酶(ALT)的水平,证实了支持 TA 对铁引发的肝肾功能障碍具有保护作用的证据。在使用铁-沙洛芬(FeSP)和RAS-选择性致死3(RSL3)等铁变态反应诱导剂的细胞模型中,单宁酸(TA)比传统的铁螯合剂去铁胺(DFO)表现出更强的保护能力。Nrf2和HO-1是抗氧化防御基因的调节因子,它们与控制铁变态反应有关。在有 FeSP 存在的情况下,TA 处理后 Nrf2 和 HO-1 的表达增加,表明它们在降低脂质 ROS 水平方面发挥作用。此外,TA 还能明显降低 COX2 水平的升高,而 COX2 是与铁变态反应相关的标志物。总之,TA 具有显著的抗铁细胞沉积活性,这可能是由于它兼具螯合铁和抗氧化的特性。TA口服安全,可为意外摄入铁和血色沉着病等情况带来益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tannic Acid Suppresses Ferroptosis Induced by Iron Salophene Complex in Kidney Cells and Prevents Iron Overload-Induced Liver and Kidney Dysfunction in Rats.

Tannic Acid Suppresses Ferroptosis Induced by Iron Salophene Complex in Kidney Cells and Prevents Iron Overload-Induced Liver and Kidney Dysfunction in Rats.

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 (FeSO4) 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.

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CiteScore
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