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测定氨基比林消除率以控制人体肝脏的代谢能力。

The determination of aminopyrin elimination for control of the metabolic capacity of the liver in man.

作者信息

Haustein K O, Hüller G, Sensing H

出版信息

Eur J Clin Invest. 1982 Apr;12(2):157-64. doi: 10.1111/j.1365-2362.1982.tb00953.x.

Abstract

The kinetics of plasma and breath elimination of aminopyrine after 14C-aminopyrine given orally were studied using an open one-compartment model and first order rates of elimination. The study comprised eight healthy volunteers and two groups with histologically verified chronic liver diseases (cirrhosis, n = 12, and chronic aggressive hepatitis, n = 12). Elimination rates from plasma and breath were significantly reduced in the group with cirrhosis, but only so in chronic aggressive hepatitis when they were expressed relative to each other. Monomethylaminopyrine was eliminated more rapidly compared to aminopyrine, and the rate of formaldehyde formation was positively correlated to the excretion rate of CO2 (r = 0.53, P less than 0.002). No correlation was found with clinical or other laboratory data in the groups of liver diseases studied. The test is a quantitative indicator of the drug metabolizing mixed function oxidases of the endoplasmatic reticulum of the liver, and may reflect the degree of damage to this system in chronic liver disease.

摘要

采用开放一室模型和一级消除速率,研究了口服14C-氨基比林后血浆和呼出气体中氨基比林的消除动力学。该研究包括8名健康志愿者以及两组经组织学证实患有慢性肝病的患者(肝硬化,n = 12;慢性活动性肝炎,n = 12)。肝硬化组血浆和呼出气体的消除速率显著降低,但慢性活动性肝炎组仅在两者相互比较时才如此。与氨基比林相比,单甲基氨基比林消除更快,甲醛形成速率与二氧化碳排泄速率呈正相关(r = 0.53,P<0.002)。在所研究的肝病组中,未发现与临床或其他实验室数据存在相关性。该试验是肝脏内质网药物代谢混合功能氧化酶的定量指标,可能反映慢性肝病中该系统的损伤程度。

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