论文标题

人类对脂多糖引起的炎症反应的统一模型

A unified model for the human response to lipopolysaccharide-induced inflammation

论文作者

Windoloski, Kristen A., Bansgaard, Elisabeth O., Dobreva, Atanaska, Ottesen, Johnny T., Olufsen, Mette S.

论文摘要

这项研究开发了一个统一的模型,可预测全身对内毒素的反应。我们使用微分方程模拟动力学,检查对脂多糖(LPS)注入的响应。该模型跟踪促炎和抗炎细胞因子(TNF- $α$,IL-6,IL-10),皮质激素释放激素(CRH),肾上腺皮质激素激素(ACTH)和皮质醇的浓度,以及在低素坐骨培训中的皮质醇(HPA)。每日激素变异通过跟踪CRH时包括昼夜节律振荡,将每日荷尔蒙变化整合到模型中。此外,该模型跟踪心率,血压,体温和疼痛感知。研究的数量在数分钟到几天之间的时间尺度上的功能。为了了解内毒素在这段巨大的时间范围内如何影响身体,我们研究了对LPS给药方法变化的反应(单剂量,重复剂量和连续剂量),以及给药的时间以及释放到系统中的内毒素的数量。我们将模型校准为2 ng/kg LPS注射的文献数据。结果表明,LPS在清晨或傍晚给药会产生更明显的激素反应。在给药后24小时,从身体中消除了大多数LPS效应,炎症的主要影响在系统中持续了48小时,并且反复的剂量模拟表明,在初次注射后残留效应仍然超过10天。我们还表明,如果LPS给药方法或总剂量增加,则系统响应会放大,从而带来更大的低血压和发育风险。

This study develops a unified model predicting the whole-body response to endotoxin. We simulate dynamics using differential equations examining the response to a lipopolysaccharide (LPS) injection. The model tracks pro- and anti-inflammatory cytokines (TNF-$α$, IL-6, IL-10), concentrations of corticotropin-releasing hormone (CRH), adrenocorticotropic hormone (ACTH), and cortisol in the hypothalamic-pituitary-adrenal (HPA) axis. Daily hormonal variations are integrated into the model by including circadian oscillations when tracking CRH. Additionally, the model tracks heart rate, blood pressure, body temperature, and pain perception. Studied quantities function on timescales ranging from minutes to days. To understand how endotoxin impacts the body over this vast span of timescales, we examine the response to variations in LPS administration methods (single dose, repeated dose, and continuous dose) as well as the timing of the administration and the amount of endotoxin released into the system. We calibrate the model to literature data for a 2 ng/kg LPS bolus injection. Results show that LPS administration during early morning or late evening generates a more pronounced hormonal response. Most of the LPS effects are eliminated from the body 24 hours after administration, the main impact of inflammation remains in the system for 48 hours, and repeated dose simulations show that residual effects remain more than 10 days after the initial injection. We also show that if the LPS administration method or total dosage is increased, the system response is amplified, posing a greater risk of hypotension and pyrexia.

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