氢化水对细胞内抗氧化剂、葡萄糖摄取、胰岛素信号、sirt1和端粒酶活性的影响

R. Settineri, Jin Ji, C.-H. Luo, Rita R. Ellithorpe, Gonzalo Ferreira de Mattos, S. Rosenblatt, J. Lavalle, Antonio Jinenez, S. Ohta, G. Nicolson
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引用次数: 3

摘要

在几项临床试验中,氢已被证明是完全安全的,没有不良事件,并且在文献中没有关于长期接触氢的毒性或不良反应的警告。在氧化应激和基因表达变化导致细胞损伤的许多情况下,氢分子已被证明是一种有用的和方便的新型抗氧化剂和基因表达调节剂。我们的细胞内生物标志物研究表明,利用细胞抗氧化试验(CAA),含有2.6 ppm溶解氢的氢化水饮料配方能够穿透细胞膜,并在人肝细胞(HePG2)中发挥抗氧化剂的作用。该试验使用荧光探针作为活性氧(ROS)(如过氧自由基)对细胞损伤的标记,并将其与已知的抗氧化剂标准槲皮素进行比较。使用该系统,氧化损伤以剂量依赖的方式减少。一毫升氢化水的抗氧化能力相当于0.05µmol槲皮素。当在人结肠细胞系(Caco-2细胞)中检测时,氢化水显示出对细胞内荧光葡萄糖衍生物(2-NBDG)的剂量和时间依赖性通透性抑制,表明葡萄糖摄取减少。在另一项研究中,氢化水对Akt磷酸化(Ser473)(胰岛素信号的生物标志物)的影响在人类骨骼肌细胞中被监测。氢化水处理显著提高Akt (Ser473)的磷酸化水平,且呈剂量依赖性。利用SIRT1表达作为人类脐带细胞(HUVECs)衰老的生物标志物,研究了氢化水的抗衰老作用。氢化水增加剂量依赖性SIRT1基因表达。当细胞用含有25%氢化水配方的培养基处理时,氢化水也使端粒酶活性(HUVEC细胞中的抗衰老生物标志物)提高了148%。氢化水引起的端粒酶活性增加可能能够保护端粒免受降解,这表明氢化水可能用于年龄相关疾病的治疗干预。这些研究表明,商业氢化水提高了一些细胞内生物标志物的水平或活性,这些生物标志物与抗氧化活性、葡萄糖摄取、胰岛素信号传导、sirt1和端粒酶活性有关。工业意义:本研究中使用的氢分子表明,某些商业来源的氢化水可以提供与其他来源的氢分子类似的抗氧化剂和基因表达修饰。这里评估的生物标志物很好地反映了氢化水与健康状况和衰老有关的生物活性。
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Effects of Hydrogenized Water on Intracellular Biomarkers for Antioxidants, Glucose Uptake, Insulin Signaling and SIRT 1 and Telomerase Activity
Hydrogen has been shown in several clinical trials to be completely safe without adverse events and there are no warnings in the literature of its toxicity or adverse effects during long-term exposure. Molecular hydrogen has proven useful and convenient as a novel antioxidant and modifier of gene expression in many conditions where oxidative stress and changes in gene expression result in cellular damage. Our intracellular biomarker studies have shown that a hydrogenized water drink formula containing 2.6 ppm dissolved hydrogen was able to penetrate cellular membranes and function as an antioxidant in human liver cells (HePG2) utilizing the Cellular Antioxidant Assay (CAA). This assay uses the protection of a florescent probe as a marker for cellular damage by reactive oxygen species (ROS), such as peroxyl radical, and compares this to the known antioxidant standard, Quercetin. Using this system oxidative damage was reduced in a dose-dependent manner. One ml of hydrogenized water was found to possess antioxidant capacity equivalent to 0.05 µmole of quercetin. When examined in a human colon cell line (Caco-2 cells), hydrogenized water demonstrated a dose- and time-dependent permeability inhibition of an intracellular fluorescent glucose derivative (2-NBDG), indicating decreased glucose uptake. In another study, the impact of hydrogenized water on Akt phosphorylation (Ser473), a biomarker for insulin signaling, was monitored in human skeletal muscle cells. The hydrogenized water treatment markedly elevated the level of phosphorylation of Akt (Ser473) in a dose-dependent manner. The anti-aging effects of hydrogenized water were examined utilizing SIRT1 expression as a biomarker of aging in human umbilical cells (HUVECs). Hydrogenized water increased dose-dependent SIRT1 gene expression. Hydrogenized water also increased telomerase activity (an anti-aging biomarker in HUVEC cells) up to 148% when cells were treated with media containing 25% hydrogenized water formula. Increased telomerase activity caused by hydrogenized water may be able to protect telomeres from degradation, suggesting the possible use of hydrogenized water in therapeutic interventions of age-related diseases. These studies show that commercial hydrogenized water improved the levels or activities of a few intracellular biomarkers specific for antioxidant activity, glucose uptake, insulin signaling and SIRT 1 and telomerase activities. Industrial Relevance: The molecular hydrogen used in this study indicates that certain commercial sources of hydrogenized water can provide similar antioxidant and gene expression modifications seen in other sources of molecular hydrogen. The biomarkers evaluated here lend well to hydrogenized water’s biological activity relating to health conditions and aging.
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