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首页医源资料库在线期刊美国临床营养学杂志2005年82卷第6期

Use of mathematical modeling to study copper metabolism in humans

来源:《美国临床营养学杂志》
摘要:comThomasDBLyonDepartmentofClinicalBiochemistryRoyalInfirmaryGlasgowUnitedKingdomDearSir:InarecentarticleintheJournal,Harveyetal(1)describedamathematicalmodelusedtostudycoppermetabolisminhumans。Themodelinvolvedthesubdivisionofbodycopperintocompartment......

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Walter S Watson

Southern General Hospital
Nuclear Medicine Department
Govan Road
Glasgow G51 4TF
United Kingdom
E-mail: wswatson{at}f2s.com

Thomas DB Lyon

Department of Clinical Biochemistry
Royal Infirmary
Glasgow
United Kingdom

Dear Sir:

In a recent article in the Journal, Harvey et al (1) described a mathematical model used to study copper metabolism in humans. The model involved the subdivision of body copper into compartments that ideally have some physiologic relevance. The amount of copper in each of the compartments and the flow rates of copper between the compartments could be quantified with the use of tracer data as input in the model.

One of the results of the model was that the half-life of ceruloplasmin was 27 d, which the authors suggested compared well with the value of 20 d that was previously reported by one of us (TDBL) (2). In that 1995 article, the "biological half-time of copper in plasma ... was found to be 19.5 ± 5 days (mean ± SD)". However, as stated in that article, this was not the half-life of ceruloplasmin. Although ceruloplasmin-bound copper accounts for >90% of plasma copper, the biological half-life of copper in plasma after ingestion of a copper tracer is not the half-life of ceruloplasmin, because the half-life of copper is influenced not only by the exit from the ceruloplasmin compartment but also by the input of recycled copper into the compartment from other longer-lived compartments. Evidence for this is included in that 1995 article, ie, the biological half-life for clearance of the tracer from the plasma pool was increased to a median half-life of 43 d in Wilsons disease heterozygotes, in whom, as previously described (3), decreased biliary excretion of copper results in a greater whole-body half-life than in control subjects.

Harvey et al (1) also state that "Only one compartmental model of copper metabolism has been developed for humans"—that of Scott and Turnlund (4). However, many articles published since the 1960s have described compartmental models for human copper metabolism (5–9).

ACKNOWLEDGMENTS

The authors had no conflicts of interest.

REFERENCES


作者: Walter S Watson
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