Disappearance of radioactivity from perfusate of isolated rat liver after administration of different doses of tritiated DH-ergotoxine.

I Tilser, J Martínková, V Chmelar
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Abstract

In ergot alkaloids a disproportion between the size of the peroral dose and the achieved area under the curve concentrations was described. This process can be explained by nonlinearity in the absorption, distribution or elimination of alkaloids. The aim of the present paper is to find whether elimination of tritiated DH-ergotoxine (3HDHE) in the liver is a linear, dose-independent process. Therefore on the model of the isolated rat liver disappearance of radioactivity in perfusate after the administration of two doses of 3HDHE, viz. 60 ng g-1 of the liver and 3030 ng g-1 of the liver, was investigated. The disappearance curves of radioactivity expressed as the percentage of the administered dose did not significantly differ between both groups. No significant changes between the groups were found either in the size of pharmacokinetic parameters, or in the portion of the administered radioactivity excreted in bile. Therefore the present authors think that disappearance of radioactivity in perfusate of the isolated liver after administration of 3HDHE is a linear process following first-order kinetics.

给药不同剂量的氚化dh -麦角毒素对离体大鼠肝脏灌注液放射性消失的影响。
在麦角生物碱中,口服剂量的大小与曲线下达到的浓度面积之间的不比例被描述。这个过程可以用生物碱的吸收、分布或消除的非线性来解释。本论文的目的是发现是否消除氚化dh -麦角毒素(3HDHE)在肝脏是一个线性的,剂量无关的过程。因此,在离体大鼠肝脏模型上,研究了两种剂量的3HDHE(即肝脏60 ng g-1和肝脏3030 ng g-1)对灌注液放射性消失的影响。以给药剂量百分比表示的放射性消失曲线在两组间无显著差异。两组之间在药代动力学参数的大小或在给药的放射性在胆汁中排泄的部分没有发现明显的变化。因此,作者认为3HDHE给药后离体肝脏灌注液中放射性的消失是一个一级动力学的线性过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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