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Exenatide effects on gastric emptying rate and the glucose rate of appearance in plasma: A A quantitative assessment using an integrative systems pharmacology model

机译:杂氮对胃排空率的影响及等离子体外观的葡萄糖速率:使用综合体系药理学模型进行定量评估

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摘要

This study aimed to quantify the effect of the immediate release (IR) of exenatide, a short‐acting glucagon‐like peptide‐1 (GLP‐1) receptor agonist (GLP‐1RA), on gastric emptying rate (GER) and the glucose rate of appearance (GluRA), and evaluate the influence of drug characteristics and food‐related factors on postprandial plasma glucose (PPG) stabilization under GLP‐1RA treatment. A quantitative systems pharmacology (QSP) approach was used, and the proposed model was based on data from published sources including: (1) GLP‐1 and exenatide plasma concentration‐time profiles; (2) GER estimates under placebo, GLP‐1 or exenatide IR dosing; and (3) GluRA measurements upon food intake. According to the model's predictions, the recommended twice‐daily 5‐ and 10‐μg exenatide IR treatment is associated with GluRA flattening after morning and evening meals (48%‐49%), whereas the midday GluRA peak is affected to a lesser degree (5%‐30%) due to lower plasma drug concentrations. This effect was dose‐dependent and influenced by food carbohydrate content, but not by the lag time between exenatide injection and meal ingestion. Hence, GER inhibition by exenatide IR represents an important additional mechanism of its effect on PPG.
机译:本研究旨在量化艾塞那肽的直接释放(IR),一种短发血胰葡萄糖样肽-1(GLP-1)受体激动剂(GLP-1RA)的效果,胃排空率(GER)和葡萄糖外观速率(Glura),并评估药物特征和食物相关因素对GLP-1RA治疗后的药物血浆葡萄糖(PPG)稳定性的影响。使用定量系统药理学(QSP)方法,所提出的模型基于来自已发表的来源的数据,包括:(1)GLP-1和杂交等离子体浓度 - 时间谱; (2)GER估计安慰剂,GLP-1或exenatide IR给药; (3)食物摄入量的Glura测量。根据该模型的预测,推荐的两次5-和10-μgeNEnatide IR治疗与早晨和晚餐后的Glura扁平化有关(48%-49%),而午间的Glura Peak受到较小程度的影响(由于较低的血浆药物浓度,5%-30%。这种效果是剂量依赖性和受食物碳水化合物含量的影响,但不是由艾塞那肽注射和膳食摄取之间的滞后时间。因此,通过eXenatide IR抑制IR代表其对PPG作用的重要额外机制。

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