Neuromodulation and Robustness of Neurons and Networks

神经元和网络的神经调节和鲁棒性

• 批准号: 10530594
• 负责人: EVE E MARDER
• 金额: $ 96.04万
• 依托单位: BRANDEIS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-12-01 至 2024-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10530594
• 关键词: Address; Animals; Behavior; Biological; Brain; Compensation; Computer Models; Crustacea; Funding; Future; Ganglia; Goals; Human; Individual; Invertebrates; Ion Channel; Measures; Membrane Proteins; Modeling; National Institute of Neurological Disorders and Stroke; Nervous System; Neuromodulator Receptors; Neurons; Regulation; Synapses; Temperature; Time; Work; experimental study; flexibility; neuroregulation; receptor; response

Project Summary/Abstract This is a request to consolidate three ongoing NINDS-funded proposals that deal with neuromodulation (R37 NS 17813), temperature compensation (R01 NS 81012), and computational models of homeostatic regulation of intrinsic excitability (Project #4 of P01 NS07949). Together these projects comprise a coherent attempt to understand brain circuit stability in the face of: a) extensive neuromodulation, b) constant and rapid turnover of ion channels and receptors, and c) degenerate and multiple solutions at the single neuron and circuit level. These questions arise from years of computational and experimental work using the small circuits of the crustacean stomatogastric ganglion (STG), but address general problems relevant to all nervous systems, from invertebrates to humans. Future experiments will combine experimental and computational work to understand the correlations in biological parameters in neurons and networks that allow any given parameter to be variable while the circuit itself retains robustness. Animal to animal variability in response to perturbations will be measured, the strengths of all of the synapses in STG circuits will be measured, and the regulation of multiple neuromodulator receptors by single neurons will be studied. Additionally, self-tuning models will be developed to find sets of neuronal parameters that allow neurons to maintain stability in response to perturbations. This work will illuminate the extent to which the same animal can potentially generate similar behavior by substantially different (degenerate) circuit mechanisms at different times. If so, this can shed light on how larger circuits may switch between a number of degenerate circuit mechanisms to generate stable behaviors over time.

项目总结/摘要 这是一项要求，以巩固三个正在进行的NINDS资助的建议，处理 具有神经调节（R37 NS 17813）、温度补偿（R 01 NS 81012）和 内在兴奋性的稳态调节的计算模型（项目#4， P01 NS07949）。这些项目共同构成了一个连贯的尝试， 面对以下情况时的脑回路稳定性：a）广泛的神经调节，B）恒定和快速 离子通道和受体的转换，以及c）在离子通道和受体处的简并和多个溶液。 单神经元和电路水平。这些问题源于多年的计算和 实验工作使用甲壳动物口胃神经节的小回路 (STG)，但解决与所有神经系统相关的一般问题，从无脊椎动物 对人类未来的实验将结合联合收割机的实验和计算工作， 了解神经元和网络中生物参数的相关性， 任何给定的参数是可变的，而电路本身保持鲁棒性。动物 将测量动物对扰动的反应变异性， STG回路中的突触将被测量，并且多个突触的调节将被测量。 将研究单个神经元的神经调质受体。此外，自调整 将开发模型来找到允许神经元 保持稳定以应对扰动。这项工作将阐明的程度， 相同的动物可以潜在地产生类似的行为， 不同的（退化）电路机制在不同的时间。如果是这样的话， 更大的电路如何在许多退化电路机制之间切换， 随着时间的推移产生稳定的行为。