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使用吲哚菁绿或半乳糖连续输注法测定大鼠肝血流量。

Determination of hepatic blood flow in the rat using sequential infusions of indocyanine green or galactose.

作者信息

Pollack G M, Brouwer K L, Demby K B, Jones J A

机构信息

Division of Pharmaceutics, School of Pharmacy, University of North Carolina, Chapel Hill 27599.

出版信息

Drug Metab Dispos. 1990 Mar-Apr;18(2):197-202.

PMID:1971573
Abstract

A method was developed for the estimation of hepatic blood flow in the rat using sequential infusions of one of two model substrates, indocyanine green or galactose. Either substrate was infused to steady state (achieved within 6 min of the start of indocyanine green infusion and within 40 min of the start of galactose infusion) through either the femoral or portal vein, and three steady state blood samples were obtained. Following a 30-min washout period, the same substrate was infused a second time through the alternate blood vessel. Using a pharmacokinetic approach, hepatic blood flow was estimated from the mean steady state concentrations during the two infusions and the infusion rate. The present method yielded hepatic blood flow estimates of 2.03 +/- 0.13 ml/min/g of liver (indocyanine green) and 2.28 +/- 0.49 ml/min/g of liver (galactose) in two groups of four adult male rats. A Monte-Carlo simulation experiment was conducted to assess the potential error introduced into the blood flow calculation by the moderate transhepatic extraction ratio of the two model substrates (0.386 +/- 0.049 for indocyanine green; 0.439 +/- 0.139 for galactose). The simulation experiment predicted calculational errors between 7.4% (indocyanine green) and 19.5% (galactose), based on the hepatic extraction ratio and the precision of the analytical method for the two compounds. The predicted errors were in good agreement with the variability in blood flow estimates observed experimentally (6.5% for indocyanine green; 21.4% for galactose). The steady state approach employed appears to be associated with superior reproducibility as compared to previously reported methods utilizing bolus dose administration of marker compounds and calculations based upon AUC estimates.

摘要

开发了一种使用两种模型底物(吲哚菁绿或半乳糖)之一进行连续输注来估算大鼠肝血流量的方法。通过股静脉或门静脉将任一底物输注至稳态(吲哚菁绿输注开始后6分钟内、半乳糖输注开始后40分钟内达到稳态),并采集三份稳态血样。在30分钟的洗脱期后,通过另一条血管再次输注相同的底物。采用药代动力学方法,根据两次输注期间的平均稳态浓度和输注速率估算肝血流量。在两组各四只成年雄性大鼠中,本方法得出的肝血流量估计值分别为:吲哚菁绿组2.03±0.13 ml/min/g肝脏,半乳糖组2.28±0.49 ml/min/g肝脏。进行了蒙特卡洛模拟实验,以评估两种模型底物的中等经肝提取率(吲哚菁绿为0.386±0.049;半乳糖为0.439±0.139)给血流量计算带来的潜在误差。模拟实验预测,基于肝提取率和两种化合物分析方法的精密度,计算误差在7.4%(吲哚菁绿)至19.%(半乳糖)之间。预测误差与实验观察到的血流量估计值的变异性(吲哚菁绿为6.5%;半乳糖为21.4%)高度一致。与先前报道的使用标记化合物大剂量给药和基于AUC估计进行计算的方法相比,所采用的稳态方法似乎具有更高的重现性。

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