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乳铁蛋白通过螯合铁和调节铁代谢对急性酒精性肝损伤的预防作用。

Preventive effects of lactoferrin on acute alcohol-induced liver injury via iron chelation and regulation of iron metabolism.

机构信息

College of Food Science and Engineering, Jilin University, Changchun, Jilin 130062, China; State Key Laboratory for Zoonotic Diseases, Key Laboratory for Zoonosis Research, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun 130012, China.

College of Food Science and Engineering, Jilin University, Changchun, Jilin 130062, China.

出版信息

J Dairy Sci. 2024 Aug;107(8):5316-5329. doi: 10.3168/jds.2023-24490. Epub 2024 Apr 11.

Abstract

Lactoferrin is widely found in milk and has the ability to bind iron. Previous studies have reported that lactoferrin was effective in the prevention and treatment of acute alcohol-induced liver injury (AALI). Ferroptosis is a recently discovered cell death and is involved in the development of AALI. However, the potential role of lactoferrin in acute alcohol-induced ferroptosis is still unclear. In this study, we observed that lactoferrin (10, 20, and 40 μg/mL) significantly mitigated alcohol (300 mM)-induced injury in vitro. Additionally, lactoferrin (100 and 200 mg/kg BW) significantly alleviated alcohol (4.8 g/kg BW)-induced injury in vivo. Our results showed that lactoferrin inhibited alcohol-induced upregulation of the ferroptosis marker protein ACSL4 and downregulation of GPX4. Meanwhile, lactoferrin treatment successfully reversed the elevated malondialdehyde (MDA) levels and the reduced glutathione (GSH) levels caused by alcohol treatment. These results may indicate that lactoferrin significantly decreased ferroptosis in vivo and in vitro. Lactoferrin has the potential to chelate iron, and our results showed that lactoferrin (20 μg/mL) significantly reduced iron ions and the expression of the ferritin heavy chain (FTH) under FeCl (100 μM) treatment. It was demonstrated that lactoferrin had a significant iron-chelating effect and reduced iron overload caused by FeCl in AML12 cells. Next, we examined iron content and the expression of iron metabolism marker proteins transferrin receptor (TFR), divalent metal transporter 1 (DMT1), FTH, and ferroportin (FPN). Our results showed that lactoferrin alleviated iron overload induced by acute alcohol. The expression of TFR and DMT1 was downregulated, and FPN and FTH were upregulated after lactoferrin treatment in vivo and in vitro. Above all, the study suggested that lactoferrin can alleviate AALI by mitigating acute alcohol-induced ferroptosis. Lactoferrin may offer new strategies for the prevention or treatment of AALI.

摘要

乳铁蛋白广泛存在于牛奶中,具有结合铁的能力。先前的研究报告称,乳铁蛋白在预防和治疗急性酒精性肝损伤(AALI)方面有效。铁死亡是一种新发现的细胞死亡方式,与 AALI 的发展有关。然而,乳铁蛋白在急性酒精诱导的铁死亡中的潜在作用尚不清楚。在这项研究中,我们观察到乳铁蛋白(10、20 和 40 μg/mL)显著减轻了体外酒精(300 mM)诱导的损伤。此外,乳铁蛋白(100 和 200 mg/kg BW)显著减轻了体内酒精(4.8 g/kg BW)诱导的损伤。我们的结果表明,乳铁蛋白抑制了酒精诱导的铁死亡标志物蛋白 ACSL4 的上调和 GPX4 的下调。同时,乳铁蛋白处理成功逆转了酒精处理引起的丙二醛(MDA)水平升高和谷胱甘肽(GSH)水平降低。这些结果可能表明乳铁蛋白显著减少了体内和体外的铁死亡。乳铁蛋白具有螯合铁的能力,我们的结果表明,乳铁蛋白(20 μg/mL)显著减少了铁离子和铁蛋白重链(FTH)在 FeCl(100 μM)处理下的表达。结果表明,乳铁蛋白具有显著的铁螯合作用,减少了 AML12 细胞中 FeCl 引起的铁过载。接下来,我们检查了铁含量和铁代谢标志物蛋白转铁蛋白受体(TFR)、二价金属转运蛋白 1(DMT1)、FTH 和铁蛋白(FPN)的表达。我们的结果表明,乳铁蛋白缓解了急性酒精引起的铁过载。体内和体外乳铁蛋白处理后,TFR 和 DMT1 的表达下调,FPN 和 FTH 的表达上调。综上所述,该研究表明,乳铁蛋白通过减轻急性酒精诱导的铁死亡来缓解 AALI。乳铁蛋白可能为预防或治疗 AALI 提供新策略。

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