首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Circulating Human hepcidin-25 concentrations display a diurnal rhythm, increase with prolonged fasting, and are reduced by growth hormone administration
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Circulating Human hepcidin-25 concentrations display a diurnal rhythm, increase with prolonged fasting, and are reduced by growth hormone administration

机译:循环中人类hepcidin-25的浓度表现出昼夜节律,随着禁食时间的延长而增加,并因施用生长激素而降低

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BACKGROUND: Hepcidin-25 reduces iron absorption by binding to the intestinal iron transporter ferroportin and causing its degradation. Currently, little is known about the basal regulation of circulating hepcidin-25. In addition, although erythropoietin administration has been reported to decrease the circulating hepcidin concentration, information is limited regarding how other stimulators of erythropoiesis, such as growth hormone (GH), might alter hepcidin-25 concentrations. METHODS: We used a sensitive and specific hepcidin-25 dual-monoclonal antibody sandwich immunoassay to measure hepcidin-25 in healthy human volunteers at various time points throughout the day and during 3 days of fasting and subsequent refeeding. We also measured hepcidin-25 concentrations in healthy volunteers after GH administration. RESULTS: In healthy individuals, hepcidin-25 concentrations displayed a diurnal variation, with concentrations being lowest in the early morning and steadily increasing throughout the day before declining during the evening hours, a pattern that was not influenced by food intake. Prolonged fasting produced statistically significant increases in hepcidin-25 concentrations. Refeeding reversed this process, and GH administration markedly decreased hepcidin-25 concentrations. CONCLUSIONS: Our results indicate that in humans, hepcidin-25 exhibits diurnal changes that can be altered by prolonged fasting, which increases hepcidin-25 concentrations approximately 3-fold after 3 days of fasting, possibly owing to a suppression of erythropoiesis that may occur during the fasting state to preserve tissue iron concentrations. In contrast, GH administration decreased hepcidin-25 concentrations by approximately 65%, presumably by stimulating erythropoiesis. These results indicate that circulating hepcidin-25 concentrations display much more dynamic and rapid variation than might have been anticipated previously.
机译:背景:Hepcidin-25通过与肠铁转运蛋白铁转运蛋白结合并引起其降解来减少铁吸收。目前,关于循环铁调素25的基础调节知之甚少。另外,尽管已经报道施用促红细胞生成素会降低循环铁调素的浓度,但是关于促红细胞生成的其他刺激物(例如生长激素(GH))如何改变hepcidin-25浓度的信息仍然有限。方法:我们使用灵敏且特异性的hepcidin-25双单克隆抗体夹心免疫分析法在一天中的不同时间点以及禁食和随后的3天喂食期间的不同时间点,对健康人类志愿者的hepcidin-25进行了测量。 GH给药后,我们还测量了健康志愿者体内的hepcidin-25浓度。结果:在健康个体中,hepcidin-25的浓度表现出昼夜变化,其浓度在清晨最低,并在一天中稳定增加,然后在傍晚时间下降,这种变化不受食物摄入量的影响。长期禁食会导致hepcidin-25浓度有统计学显着增加。再次喂食逆转了这一过程,GH的施用显着降低了hepcidin-25的浓度。结论:我们的结果表明,在人类中,hepcidin-25表现出昼夜变化,可通过禁食时间延长而改变,禁食3天后hepcidin-25的浓度大约增加3倍,这可能是由于抑制红细胞生成过程空腹状态以保持组织中铁的浓度。相反,GH的施用可能通过刺激红细胞生成而使hepcidin-25的浓度降低了约65%。这些结果表明,循环铁调素25的浓度比以前预期的动态和快速变化大得多。

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