Oral copper loading test in humans

Mojgan Rahmaniyan, Kelley E. Johnston, Tsunenobu Tamura
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Abstract

There has been no report of normal responses of plasma copper and/or ceruloplasmin concentrations after an oral loading dose of unlabeled copper in humans. To establish a normal plasma response curve following an oral dose, we performed a copper-loading test (10 mg elemental copper as copper sulfate) in six healthy adult subjects and monitored plasma copper and ceruloplasmin concentrations for 3.5 h. We found that there were no significant changes in plasma copper and ceruloplasmin concentrations following the oral dose in the subjects. The test was originally intended to evaluate whether there was copper malabsorption in a female patient who developed signs of copper deficiency with her plasma copper levels below 3.0 μmol/l after multiple gastrointestinal surgeries. She did not respond to oral copper sulfate administration but responded to a sublingual application of copper glycinate. These findings suggest that she does not have adequate intestinal copper absorption. In conclusion, the use of unlabeled copper, such as copper sulfate, for an oral loading test, seemingly simple and economical, does not appear to be a suitable means to evaluate copper absorption in humans and is discouraged. In case of copper malabsorption, sublingual administration of copper may be worth trying. J. Trace Elem. Exp. Med. 16: 61–66, 2003. © 2003 Wiley-Liss, Inc.
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人体口服铜负荷试验
目前还没有关于人类口服负载剂量的未标记铜后血浆铜和/或铜蓝蛋白浓度的正常反应的报告。为了建立口服剂量后的正常血浆反应曲线,我们对6名健康成年受试者进行了铜负荷试验(10 mg元素铜,硫酸铜),并监测了3.5小时的血浆铜和铜蓝蛋白浓度。我们发现,受试者口服剂量后,血浆铜和铜蓝蛋白浓度没有显著变化。该测试最初旨在评估一名女性患者是否存在铜吸收不良,该患者在多次胃肠道手术后出现铜缺乏症状,血浆铜水平低于3.0μmol/l。她对口服硫酸铜没有反应,但对舌下应用甘氨酸铜有反应。这些发现表明她没有足够的肠道铜吸收。总之,使用未标记的铜,如硫酸铜,进行口服负荷试验,看似简单且经济,似乎不是评估人体铜吸收的合适方法,因此不鼓励使用。在铜吸收不良的情况下,舌下给药铜可能值得一试。J.Trace Elem。实验医学。16:61-662003。©2003 Wiley-Liss,股份有限公司。
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International Society For Trace Element Research In Humans (ISTERH) Seventh International Conference, Bangkok, Thailand, November 7–12, 2004 Response† Erratum Fluoride: A toxic or therapeutic agent in the treatment of osteoporosis? Interleukin-1α, tumor necrosis factor-α, and interleukin-12 secreted by zinc-induced murine macrophages in vivo and in vitro
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