Anion exchanger1 (AE1/SLC4A1) function is impaired in red blood cells from prediabetic subjects: Potential benefits of finger lime (Citrus australasica, Faustrime cultivar) juice extract

IF 2.8 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Function Pub Date : 2024-08-02 DOI:10.1002/cbf.4105
Alessia Remigante, Sara Spinelli, Lucrezia Gambardella, Elisabetta Straface, Giovanna Cafeo, Marina Russo, Daniele Caruso, Paola Dugo, Silvia Dossena, Angela Marino, Rossana Morabito
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Abstract

Prediabetes is a risk state that defines a high chance of developing diabetes and cardiovascular disease. Oxidative stress mediated by hyperglycemia-induced production of reactive species could play a crucial role in this context. In the present study, we investigated whether the anion exchange capability mediated by AE1 (SLC4A1), which is sensitive to oxidative stress, was altered in human red blood cells (RBCs) obtained from prediabetic volunteers. In addition, we assessed the precise composition of bioactive compounds and the potential benefits of finger lime juice extract (Citrus australasica, Faustrime cultivar) in counteracting oxidative stress-related functional alterations. Human RBCs from normal and prediabetic volunteers were incubated with 50 µg/mL juice extract for 2 h at 25°C. Juice extract restored alterations of the anion exchange capability mediated by AE1 and prevented the structural rearrangements of AE1 and α/β-spectrin in prediabetic RBCs. AE1 functional and structural alterations were not associated with an increase in lipid peroxidation or protein oxidation at the level of the plasma membrane. An increased production of intracellular ROS, which provoked the oxidation of hemoglobin to methemoglobin, both reverted by juice extract, was instead observed. Importantly, juice extract also induced a reduction in glycated hemoglobin levels in prediabetic RBCs. Finally, juice extract blunted the overactivation of the endogenous antioxidant enzymes catalase and superoxide dismutase and prevented glutathione depletion in prediabetic RBCs. These findings contribute to clarifying cellular and molecular mechanisms related to oxidative stress and glycation events that may influence RBC and systemic homeostasis in prediabetes, identify AE1 as a sensitive biomarker of RBC structural and function alterations in prediabetes and propose finger lime juice extract as a natural antioxidant for the treatment and/or prevention of the complications associated with the prediabetic condition.

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糖尿病前期患者的红细胞中阴离子交换器1(AE1/SLC4A1)功能受损:指柠檬(Citrus australasica, Faustrime cultivar)果汁提取物的潜在益处。
糖尿病前期是一种风险状态,决定了患糖尿病和心血管疾病的几率很高。在这种情况下,由高血糖诱导产生的活性物质所介导的氧化应激可能起着至关重要的作用。在本研究中,我们调查了从糖尿病前期志愿者体内获得的人类红细胞(RBCs)中由 AE1(SLC4A1)介导的阴离子交换能力是否发生了改变,AE1 对氧化应激很敏感。此外,我们还评估了指柠檬汁提取物(Citrus australasica,Faustrime 栽培品种)中生物活性化合物的精确成分及其在抵消氧化应激相关功能改变方面的潜在益处。将正常和糖尿病前期志愿者的人体红细胞与 50 µg/mL 的果汁提取物在 25°C 下培养 2 小时。果汁提取物恢复了由 AE1 介导的阴离子交换能力的改变,并防止了糖尿病前期红细胞中 AE1 和 α/β-spectrin 的结构重排。AE1 功能和结构的改变与质膜水平的脂质过氧化或蛋白质氧化的增加无关。相反,观察到细胞内 ROS 生成增加,导致血红蛋白氧化成高铁血红蛋白,而果汁提取物可使这两种现象恢复。重要的是,果汁提取物还能降低糖尿病前期红细胞的糖化血红蛋白水平。最后,果汁提取物能减弱内源性抗氧化酶过氧化氢酶和超氧化物歧化酶的过度活化,并防止糖尿病前期红细胞中谷胱甘肽的耗竭。这些发现有助于阐明与氧化应激和糖化事件有关的细胞和分子机制,这些机制可能会影响糖尿病前期红细胞和全身的平衡,确定 AE1 是糖尿病前期红细胞结构和功能改变的敏感生物标志物,并建议将指柠檬汁提取物作为一种天然抗氧化剂,用于治疗和/或预防与糖尿病前期相关的并发症。
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来源期刊
Cell Biochemistry and Function
Cell Biochemistry and Function 生物-生化与分子生物学
CiteScore
6.20
自引率
0.00%
发文量
93
审稿时长
6-12 weeks
期刊介绍: Cell Biochemistry and Function publishes original research articles and reviews on the mechanisms whereby molecular and biochemical processes control cellular activity with a particular emphasis on the integration of molecular and cell biology, biochemistry and physiology in the regulation of tissue function in health and disease. The primary remit of the journal is on mammalian biology both in vivo and in vitro but studies of cells in situ are especially encouraged. Observational and pathological studies will be considered providing they include a rational discussion of the possible molecular and biochemical mechanisms behind them and the immediate impact of these observations to our understanding of mammalian biology.
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