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Modeling and Analyzing Pattern Formation Mechanisms Derived from Nonlinear Physiological and Neuronal Systems

Modeling and Analyzing Pattern Formation Mechanisms Derived from Nonlinear Physiological and Neuronal Systems
非线性生理和神经系统衍生的模式形成机制的建模和分析
批准号:
203241-2012
负责人:
Li, YueXian
金额:
$0.87万
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2014
资助国家:
加拿大
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

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中文摘要
翻译
本研究旨在模拟和分析细胞生理学和神经科学中的非线性系统所产生的时间、空间和时空模式形成机制。分析和数值方法/开发的非线性常,偏和积分微分方程,描述这些系统的研究。不像封闭的物理系统,朝着增加的无序状态进化,生物系统通常是开放的,并进化成越来越复杂的结构/模式。了解驱动这些模式形成的机制是生物学研究的主要目标之一,对于揭示它们的功能和开发控制它们的潜在方法至关重要。由于这些过程的非线性和动态性质,数学方法往往是必不可少的,以实现理解,否则很难,甚至不可能获得只使用实验工具。这项研究的主题是:(1)单细胞行为和神经内分泌细胞激素的同步节律分泌;(2)耦合细胞中的一般同步机制;(3)可兴奋的单细胞和多细胞介质中的波传播;(4)噪声在生物模式形成中的影响。在开发模型时,我们使用最新实验的数据和结果。一旦开发出一个模型,我们就寻求深入理解每一种新行为背后的数学原理。一个模型描述的同步和脉冲式GnRH释放的产生在弥漫性分布的GnRH神经元是一个很好的例子。这些项目与实验细胞生理学前沿发展之间的密切关系证明了拟议研究的新奇和潜在影响。在这些模型中产生的方程的数学理解的进展将加深我们对非线性微分方程的理解,以前很少探索,并有可能被应用到解决相关领域的其他问题。
英文摘要
This research is aimed at modeling and analyzing temporal, spatial, and spatio-temporal pattern-formation mechanisms arising from nonlinear systems in cell physiology and neural sciences. Analytical and numerical methods are employed/developed in the study of the nonlinear ordinary, partial, and integral differential equations that describe these systems. Unlike closed physical systems that evolve toward a state of increased disorder, biological systems are typically open and evolving into structures/patterns of increasing complexity. Understanding the mechanisms driving the formation of these patterns is one of the major goals of biological research and is vital in revealing their functions and developing potential ways of controlling them. Due to the nonlinear and dynamical nature of these processes, mathematical methods are often essential in achieving an understanding that is otherwise difficult or even impossible to obtain using only experimental tools. The topics of this proposed research are: (1) single-cell behaviors and synchronized rhythmic secretion of hormones from neuroendocrine cells; (2) general synchronization mechanisms in coupled cells; (3) the wave propagation in excitable single- and multi-cellular media; and (4) effects of noise in the formation of biological patterns. When developing models, we use data and results from most recent experiments. Once a model is developed, we seek in-depth understanding of the mathematics behind each novel behavior. A model describing the synchronization and generation of pulsatile GnRH release in diffusely distributed GnRH neurons is a good example. The novelty and potential impact of the proposed research is evidenced by the close relationship between these projects and the frontier developments in experimental cell physiology. Progress in the mathematical understanding of the equations arising in these models will deepen our understanding of nonlinear differential equations that were poorly explored previously and has the potential of being applied to solving other problems of interest in related areas.
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Modeling and Analyzing Pattern Formation Mechanisms Derived from Nonlinear Physiological and Neuronal Systems
  • 批准号:
    203241-2012
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $0.87万
  • 财政年份:
    2015
  • 负责人:
    Li, YueXian
  • 依托单位:
Modeling and Analyzing Pattern Formation Mechanisms Derived from Nonlinear Physiological and Neuronal Systems
  • 批准号:
    203241-2012
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $0.87万
  • 财政年份:
    2012
  • 负责人:
    Li, YueXian
  • 依托单位:
Modeling and analyzing mechanisms that generate oscillations and waves in cells and neurons
  • 批准号:
    203241-2007
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $1.46万
  • 财政年份:
    2011
  • 负责人:
    Li, YueXian
  • 依托单位:
Modeling and analyzing mechanisms that generate oscillations and waves in cells and neurons
  • 批准号:
    203241-2007
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $1.46万
  • 财政年份:
    2010
  • 负责人:
    Li, YueXian
  • 依托单位:
国内基金
海外基金
Computational Methods for Analyzing Toponome Data