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描述大鼠体内铅分布的药代动力学模型。

Pharmacokinetic model to describe the disposition of lead in the rat.

作者信息

Bornemann L D, Colburn W A

出版信息

J Toxicol Environ Health. 1985;16(3-4):631-9. doi: 10.1080/15287398509530769.

DOI:10.1080/15287398509530769
PMID:4087323
Abstract

A pharmacokinetic model was developed to describe the disposition of lead in the rat. The model can be used to predict the effect of acute high-dose as well as low-dose exposure to lead. These results suggest that the model should be able to predict the effect of chronic low-dose exposures as well. Plasma, bone, liver, and bile profiles were generated from this model using previously published data. The results obtained supported the existing theory that lead demonstrates a dose-dependent pharmacokinetic profile in the rat.

摘要

建立了一个药代动力学模型来描述大鼠体内铅的处置情况。该模型可用于预测急性高剂量以及低剂量铅暴露的影响。这些结果表明,该模型应该也能够预测慢性低剂量暴露的影响。利用先前发表的数据从该模型生成了血浆、骨骼、肝脏和胆汁的分布图。所获得的结果支持了现有的理论,即铅在大鼠体内呈现出剂量依赖性药代动力学特征。

相似文献

1
Pharmacokinetic model to describe the disposition of lead in the rat.描述大鼠体内铅分布的药代动力学模型。
J Toxicol Environ Health. 1985;16(3-4):631-9. doi: 10.1080/15287398509530769.
2
"Severe chronic lead insult that maintains body burdens of lead related to those in the skeleton": observations by Dr. Clair Patterson conclusively demonstrated.“严重的慢性铅中毒,使人体铅负荷维持在与骨骼中铅负荷相关的水平”:克莱尔·帕特森博士的观察结果确凿地证明了这一点。
Environ Res. 1998 Aug;78(2):140-51. doi: 10.1006/enrs.1997.3830.
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Factors affecting the absorption and excretion of lead in the rat.影响大鼠体内铅吸收与排泄的因素。
Gastroenterology. 1978 Apr;74(4):731-40.
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Lead in bone: storage site, exposure source, and target organ.骨骼中的铅:储存部位、暴露源及靶器官。
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A physiologically based model of chromium kinetics in the rat.大鼠体内铬动力学的生理基础模型。
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