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Extracellular dopamine concentration control: Computational model of feedback control.

机译:细胞外多巴胺浓度控制:反馈控制的计算模型。

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摘要

Dopamine is one of the central neurotransmitters; its homeostatic concentration is highly maintained through release and re-uptake. Dopamine release is mediated at presynaptic vesicles and controlled by dopamine receptors. Dopamine release regulation by dopamine receptors is mediated by negative feedback. This negative feedback is a function of dopamine receptor occupancy by dopamine or dopamine agonists. Dopamine re-uptake is regulated presynaptically by Dopamine Transporter (DAT).; The object of this study was to develop a computational system to describe and predict the behavior of the complex process of extracellular dopamine concentration control. The uniqueness and advantage of presented modeling work is that it models extracellular dopamine concentration control as a complex of both re-uptake and feedback mechanisms.; Mathematical modeling was based on published pharmacokinetic parameters for dopamine re-uptake and binding in rat striatum, and computational data generated by presented study. The dopamine system modeling was conducted for the following conditions: (1) basal conditions; (2) increased/decreased dopamine release; (3) presence of dopamine agonist/antagonist in the system.; Results of mathematical modeling showed that proposed computational model is successfully predicting outcomes of complex extracellular dopamine concentration control system. It was demonstrated computationally that both re-uptake by dopamine transporter and negative feedback mediated by receptors are necessary components to maintain low, nM, extracellular dopamine concentration under basal conditions. Mathematical modeling demonstrated the critical role of feedback to maintain stable extracellular dopamine concentration under conditions of increased/decreased dopamine release. The model-generated results predicting extracellular dopamine concentration change under conditions equivalent to the presence of dopamine agonist/antagonist were in good accordance with published experimental data.; In addition to the mathematical modeling and computational programming, the value of this thesis work is that it demonstrates how data mining and computational conclusions can be done based on the integration of the results from independent experimental studies. A strong trend in the modern bioscience is a computational analysis based on data generated by biological research. This thesis work is an example of successful biological system modeling based on published experimental data.
机译:多巴胺是中枢神经递质之一。通过释放和再摄取可以高度维持其体内稳态浓度。多巴胺释放在突触前囊泡中介导,并受多巴胺受体控制。多巴胺受体对多巴胺释放的调节是由负反馈介导的。该负反馈是多巴胺或多巴胺激动剂对多巴胺受体占有的函数。多巴胺再摄取是由多巴胺转运蛋白(DAT)突触地调节的。这项研究的目的是开发一种计算系统,以描述和预测细胞外多巴胺浓度控制这一复杂过程的行为。所提出的建模工作的独特性和优势在于,它可以将细胞外多巴胺浓度控制建模为重摄取和反馈机制的复合体。数学建模基于已公布的大鼠纹状体中多巴胺再摄取和结合的药代动力学参数,以及本研究产生的计算数据。在以下条件下进行多巴胺系统建模:(1)基础条件; (2)增加/减少多巴胺的释放; (3)系统中存在多巴胺激动剂/拮抗剂。数学建模结果表明,所提出的计算模型可以成功预测复杂的细胞外多巴胺浓度控制系统的结果。通过计算证明,多巴胺转运蛋白的再摄取和受体介导的负反馈都是在基础条件下维持低nM细胞外多巴胺浓度的必要成分。数学模型表明,在多巴胺释放增加/减少的条件下,反馈对于维持稳定的细胞外多巴胺浓度至关重要。该模型产生的结果预测在与多巴胺激动剂/拮抗剂存在相同的条件下细胞外多巴胺浓度的变化与已发表的实验数据完全吻合。除了数学建模和计算编程外,本论文的价值还在于它展示了如何基于独立实验研究的结果的整合来完成数据挖掘和计算结论。现代生物科学的一个重要趋势是根据生物学研究产生的数据进行计算分析。本文工作是基于已公开的实验数据成功进行生物系统建模的一个例子。

著录项

  • 作者

    Koshkina, Elena.;

  • 作者单位

    Drexel University.;

  • 授予单位 Drexel University.;
  • 学科 Biology Neuroscience.; Mathematics.; Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2006
  • 页码 121 p.
  • 总页数 121
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 神经科学;数学;生物医学工程;
  • 关键词

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