首页> 外文期刊>The Journal of toxicological sciences >Human plasma and urinary metabolic profiles of trimethylamine and trimethylamine N-oxide extrapolated using a simple physiologically based pharmacokinetic model
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Human plasma and urinary metabolic profiles of trimethylamine and trimethylamine N-oxide extrapolated using a simple physiologically based pharmacokinetic model

机译:使用简单的生理基于生理学药代动力学模型将人血浆和三甲胺N-氧化物的尿胺和三甲胺N-氧化物的尿代谢谱

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Trimethylamine, a dietary- and medicinal carnitine-derived amine, is extensively metabolized by liver to non-malodorous trimethylamine N-oxide. Although trimethylamine and trimethylamine N-oxide under daily dietary consumption or carnitine treatment are generally regarded as nontoxic, they have been, and remain, of toxicological and clinical interest because of their potential association with atherosclerosis. The aim of the current study was to model the pharmacokinetics of trimethylamine after oral administration of trimethylamine in humans and compare the results with reported measured values. Adjusted biomonitoring equivalents from rat studies based on reported plasma concentrations were scaled to human equivalents using known species allometric scaling factors. In vitro metabolic clearance data were obtained using rat and human liver microsomal preparations. Renal clearances in humans for trimethylamine and trimethylamine N-oxide were calculated with a clearance concept approach using reported 24-hr urinary excretion rates and assumed areas under plasma concentration curves. The resulting modeled plasma and urinary concentration curves by simple physiologically based pharmacokinetic models (or semi-physiological pharmacokinetic models) were consistent with reported concentrations. This study provides important information to help simulate human plasma levels of trimethylamine and trimethylamine N-oxide in trimethylamine loading tests and during treatment with prescribed medicinal 1-carnitine, showing the similar range as that resulting from daily dietary foodstuff consumption along with little toxicological impacts. The present models could estimate relationship between plasma and urine concentrations of trimethylamine or trimethylamine N-oxide and the daily oral doses by both forward and reverse dosimetry from viewpoint of human risk assessment.
机译:三甲胺是一种从饮食和药物中提取的肉碱胺,由肝脏广泛代谢为无臭味的三甲胺N-氧化物。尽管日常饮食或肉碱治疗下的三甲胺和三甲胺N-氧化物通常被视为无毒,但由于其与动脉粥样硬化的潜在关联,它们一直并仍然具有毒理学和临床意义。本研究的目的是模拟人体口服三甲胺后三甲胺的药代动力学,并将结果与报告的测量值进行比较。根据报告的血浆浓度对大鼠研究中的生物监测当量进行调整,并使用已知的物种异速生长比例因子将其换算为人类当量。使用大鼠和人肝微粒体制剂获得体外代谢清除率数据。根据报告的24小时尿排泄率和血浆浓度曲线下的假定面积,采用清除率概念方法计算三甲胺和三甲胺N-氧化物对人类肾脏的清除率。通过简单的生理药代动力学模型(或半生理药代动力学模型)模拟的血浆和尿液浓度曲线与报告浓度一致。本研究提供了重要信息,有助于在三甲胺负荷试验中以及在使用规定的药用1-肉碱治疗期间,模拟人体血浆中三甲胺和三甲胺N-氧化物的水平,显示出与日常饮食食品消费产生的范围相似,且毒理学影响很小。目前的模型可以从人类风险评估的角度,通过正向和反向剂量测定来估计血浆和尿液中三甲胺或三甲胺N-氧化物浓度与每日口服剂量之间的关系。

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