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Ameliorative effects of -lipoic acid on high-fat diet-induced oxidative stress and glucose uptake impairment of T cells

机译:- 对 - 对高脂饮食诱导的氧化应激和T细胞葡萄糖摄取损伤的改善作用

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摘要

The incidence of obesity and metabolic disease continues to rise, mainly associated with consumption of a high-fat diet (HFD). Previous studies have indicated that HFD could disturb the immune system, leading to immunodeficiency and inflammation. Several mechanisms have been postulated to account for immunodeficiency associated with HFD, one being oxidative stress. To further investigate the effects of HFD on glucose metabolism and proliferative capability of T cells and the protective effects of -lipoic acid (LA), male C57BL/6J mice were fed a normal chow (10% fat), an HFD (60% fat), an LA supplement (HFD +0.1%LA), and a N-acetyl-L-cysteine supplement (HFD +0.1% NAC) for 10 weeks. Results showed that 10-week HFD increased intracellular reactive oxygen species (ROS) production, induced oxidative stress state formation, inhibited glucose uptake, decreased ATP concentration, reduced proliferative rate, and dampened IL-2 production of T cells of mice. Administration of LA significantly alleviated these changes induced by HFD. These findings reveal that oxidative stress of T cells caused by HFD may be a key factor leading to glucose metabolism reduction and proliferative capability and function impairment of T cells. LA, as a potent agonist, could promote Nrf2 nuclear translocation and up-regulate expression of Nrf2 target genes (Ho-1 and Prdx1), which can eliminate excess ROS and restore redox balance of cells.
机译:肥胖和代谢疾病的发病率持续上升,主要与高脂饮食(HFD)的消耗相关。以前的研究表明,HFD可能会扰乱免疫系统,导致免疫缺陷和炎症。已经假设了几种机制以考虑与HFD相关的免疫缺陷,一种是氧化应激。为了进一步研究HFD对T细胞的葡萄糖代谢和增殖能力的影响以及 - 己酸(La)的保护作用,将雄性C57BL / 6J小鼠喂养正常的食物(10%脂肪),HFD(60%脂肪),La补充(HFD + 0.1%La)和N-乙酰基-1-半胱氨酸补充剂(HFD + 0.1%NAc)10周。结果表明,10周的HFD增加细胞内反应性氧(ROS)生产,诱导氧化应激状态形成,抑制葡萄糖摄取,降低浓度,降低增殖率,并抑制小鼠的T细胞的IL-2产生。 La的管理显着减轻了HFD诱导的这些变化。这些发现表明,由HFD引起的T细胞的氧化应激可能是导致葡萄糖代谢降低和增殖能力和T细胞的功能损伤的关键因素。作为一种有效的激动剂,可以促进NRF2核转位和上调NRF2靶基因(HO-1和PRDX1)的表达,这可以消除过量的ROS和恢复细胞的氧化还原平衡。

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