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本文引用的文献

1
Copper signalling: causes and consequences.铜信号转导:病因与后果。
Cell Commun Signal. 2018 Oct 22;16(1):71. doi: 10.1186/s12964-018-0277-3.
2
Role of Copper in the Onset of Alzheimer's Disease Compared to Other Metals.与其他金属相比,铜在阿尔茨海默病发病中的作用。
Front Aging Neurosci. 2018 Jan 23;9:446. doi: 10.3389/fnagi.2017.00446. eCollection 2017.
3
Copper dyshomeostasis in Wilson disease and Alzheimer's disease as shown by serum and urine copper indicators.血清和尿液铜指标显示 Wilson 病和阿尔茨海默病中的铜动态平衡失调。
J Trace Elem Med Biol. 2018 Jan;45:181-188. doi: 10.1016/j.jtemb.2017.11.005. Epub 2017 Nov 8.
4
Copper signaling in the brain and beyond.大脑及其他部位的铜信号。
J Biol Chem. 2018 Mar 30;293(13):4628-4635. doi: 10.1074/jbc.R117.000176. Epub 2017 Oct 30.
5
Oxidative stress and the amyloid beta peptide in Alzheimer's disease.阿尔茨海默病中的氧化应激与淀粉样β肽。
Redox Biol. 2018 Apr;14:450-464. doi: 10.1016/j.redox.2017.10.014. Epub 2017 Oct 18.
6
Glycation of Lys-16 and Arg-5 in amyloid-β and the presence of Cu play a major role in the oxidative stress mechanism of Alzheimer's disease.淀粉样β蛋白中赖氨酸-16和精氨酸-5的糖基化以及铜的存在在阿尔茨海默病的氧化应激机制中起主要作用。
J Biol Inorg Chem. 2017 Dec;22(8):1211-1222. doi: 10.1007/s00775-017-1497-5. Epub 2017 Oct 16.
7
Serum Copper, Zinc, and Iron Levels in Patients with Alzheimer's Disease: A Meta-Analysis of Case-Control Studies.阿尔茨海默病患者的血清铜、锌和铁水平:病例对照研究的荟萃分析
Front Aging Neurosci. 2017 Sep 15;9:300. doi: 10.3389/fnagi.2017.00300. eCollection 2017.
8
Evidence for widespread, severe brain copper deficiency in Alzheimer's dementia.阿尔茨海默病患者大脑广泛存在严重铜缺乏的证据。
Metallomics. 2017 Aug 16;9(8):1106-1119. doi: 10.1039/c7mt00074j.
9
The Case for Abandoning Therapeutic Chelation of Copper Ions in Alzheimer's Disease.放弃阿尔茨海默病中铜离子治疗性螯合的理由。
Front Neurosci. 2017 Jun 2;11:317. doi: 10.3389/fnins.2017.00317. eCollection 2017.
10
Diabetes and Alzheimer's Disease: Can Elevated Free Copper Predict the Risk of the Disease?糖尿病与阿尔茨海默病:游离铜升高能否预测疾病风险?
J Alzheimers Dis. 2017;56(3):1055-1064. doi: 10.3233/JAD-161033.

暴露与效应的批判性评价:对制定摄入铜的监管健康标准的启示。

Critical Review of Exposure and Effects: Implications for Setting Regulatory Health Criteria for Ingested Copper.

机构信息

Exponent, Inc., 475 14th Street, Suite 400, Oakland, CA, 94612, USA.

Exponent, Inc., 15375 SE 30th Place, Suite 250, Bellevue, WA, 98027, USA.

出版信息

Environ Manage. 2020 Jan;65(1):131-159. doi: 10.1007/s00267-019-01234-y. Epub 2019 Dec 12.

DOI:10.1007/s00267-019-01234-y
PMID:31832729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6960211/
Abstract

Decades of study indicate that copper oral exposures are typically not a human health concern. Ingesting high levels of soluble copper salts can cause acute gastrointestinal symptoms and, in uncommon cases, liver toxicity in susceptible individuals with repeated exposure. This focused toxicological review evaluated the current literature since the last comprehensive reviews (2007-2010). Our review identified limitations in the existing United States and international guidance for determining an oral reference dose (RfD) for essential metals like copper. Instead, an alternative method using categorical regression analysis to develop an optimal dose that considers deficiency, toxicity, and integrates information from human and animal studies was reviewed for interpreting an oral RfD for copper. We also considered subchronic or chronic toxicity from genetic susceptibility to copper dysregulation leading to rare occurrences of liver and other organ toxicity with elevated copper exposure. Based on this approach, an oral RfD of 0.04 mg Cu/kg/day would be protective of acute or chronic toxicity in adults and children. This RfD is also protective for possible genetic susceptibility to elevated copper exposure and allows for background dietary exposures. This dose is not intended to be protective of patients with rare genetic disorders for copper sensitivity within typical nutritional intake ranges, nor is it protective for those with excessive supplement intake. Less soluble mineral forms of copper in soil have reduced bioavailability as compared with more soluble copper in water and diet, which should be considered in using this RfD for risk assessments of copper.

摘要

数十年的研究表明,口服铜暴露通常不会对人类健康造成影响。摄入高浓度的可溶性铜盐会导致急性胃肠道症状,在反复暴露于敏感个体中,极少数情况下会导致肝脏毒性。本次重点毒理学评价评估了自上次全面审查(2007-2010 年)以来的现有文献。我们的审查发现,目前美国和国际上确定必需金属(如铜)口服参考剂量(RfD)的指导方针存在局限性。相反,我们审查了一种替代方法,即使用分类回归分析来开发最佳剂量,该方法考虑了缺乏、毒性,并整合了来自人类和动物研究的信息,以解释铜的口服 RfD。我们还考虑了因铜失调的遗传易感性导致的亚慢性或慢性毒性,这会导致罕见的肝脏和其他器官毒性,以及铜暴露升高。基于这种方法,口服 RfD 为 0.04mg Cu/kg/天,可预防成人和儿童的急性或慢性毒性。该 RfD 还可预防因铜暴露升高而导致的潜在遗传易感性,同时允许背景膳食暴露。该剂量不是为了保护在典型营养摄入范围内对铜敏感的罕见遗传疾病患者,也不是为了保护因补充剂摄入过多而对铜敏感的患者。与水和饮食中更易溶解的铜相比,土壤中较少溶解的矿物形式的铜生物利用度较低,在使用该 RfD 进行铜风险评估时应考虑这一点。