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Model‐Based Prediction of Plasma Concentration and Enterohepatic Circulation of Total Bile Acids in Humans

机译:基于模型的人类总胆汁酸血浆浓度和肝肠循环的预测

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Bile acids released postprandially can modify the rate and extent of lipophilic compounds’ absorption. This study aimed to predict the enterohepatic circulation (EHC) of total bile acids (TBAs) in response to caloric intake from their spillover in plasma. A model for TBA EHC was combined with a previously developed gastric emptying (GE) model. Longitudinal gallbladder volumes and TBA plasma concentration data from 30 subjects studied after ingestion of four different test drinks were supplemented with literature data. Postprandial gallbladder refilling periods were implemented to improve model predictions. The TBA hepatic extraction was reduced with the high‐fat drink. Basal and nutrient‐induced gallbladder emptying rates were altered by type 2 diabetes (T2D). The model was predictive of the central trend and the variability of gallbladder volume and TBA plasma concentration for all test drinks. Integration of this model within physiological pharmacokinetic modeling frameworks could improve the predictions for lipophilic compounds’ absorption considerably.
机译:餐后释放的胆汁酸可以改变亲脂性化合物吸收的速率和程度。这项研究旨在预测总胆汁酸(TBA)的肠肝循环(EHC),以响应其从血浆中溢出时的热量摄入。将TBA EHC模型与先前开发的胃排空(GE)模型相结合。摄入四种不同的测试饮料后,对30位研究对象的纵向胆囊体积和TBA血浆浓度数据进行了补充。餐后胆囊补充期的实施可以改善模型预测。高脂饮料减少了TBA肝提取。 2型糖尿病(T2D)改变了基础和营养导致的胆囊排空率。该模型可预测所有测试饮料的中心趋势以及胆囊体积和TBA血浆浓度的变化。将该模型整合到生理药代动力学建模框架中可以大大改善对亲脂性化合物吸收的预测。

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