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人体3-甲基组氨酸代谢的房室模型。

A compartmental model of 3-methylhistidine metabolism in humans.

作者信息

Rathmacher J A, Flakoll P J, Nissen S L

机构信息

Department of Animal Science, Iowa State University, Ames 50011, USA.

出版信息

Am J Physiol. 1995 Jul;269(1 Pt 1):E193-8. doi: 10.1152/ajpendo.1995.269.1.E193.

Abstract

Urinary 3-methylhistidine (3MH) excretion has been proposed as a noninvasive in vivo marker of muscle protein breakdown, but such analysis requires quantitative collection of urine and yields few details about the metabolism of 3MH. In this study, we propose that data from a single bolus dose of tracer and serial blood samples over 72 h can be described by a kinetic model that defines 3MH metabolism in humans. Plasma concentration of the tracer was described by a linear time-invariant three-compartment model. The model defines masses and fluxes of 3MH within the subjects and, in particular, the intracellular de novo production of 3MH. The de novo production of 3MH as calculated by the model was not different from that calculated via the traditional collection of urinary 3MH (3.09 vs 2.57 mumol.kg-1.day-1, respectively; P > 0.30). These data indicate that 3MH production can be measured by a compartmental model that can be used to measure muscle proteolysis without quantitative urine collections.

摘要

尿中3-甲基组氨酸(3MH)排泄已被提议作为肌肉蛋白分解的一种非侵入性体内标志物,但这种分析需要定量收集尿液,且关于3MH代谢的细节信息很少。在本研究中,我们提出,单次推注示踪剂的数据以及72小时内的系列血样数据可用一个动力学模型来描述,该模型定义了人类3MH的代谢。示踪剂的血浆浓度由一个线性时不变三室模型描述。该模型定义了受试者体内3MH的质量和通量,特别是3MH的细胞内从头合成。模型计算得出的3MH从头合成量与通过传统收集尿3MH计算得出的量无差异(分别为3.09与2.57 μmol·kg⁻¹·天⁻¹;P>0.30)。这些数据表明,3MH的生成可用一个房室模型来测量,该模型可用于在无需定量收集尿液的情况下测量肌肉蛋白水解。

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