Multiscale Model of Neural Control of Breathing

呼吸神经控制的多尺度模型

• 批准号: 8535256
• 负责人: Alona Ben-Tal
• 金额: $ 54.44万
• 依托单位: DREXEL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-01 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8535256
• 关键词: 4-nitrophenethyl bromide; Abdomen; Ablation; Address; Adult; Affect; Animal Model; Apnea; Area; Attenuated; Biological; Biological Models; Biomedical Engineering; Blood; Blood Circulation; Brain; Brain Stem; Breathing; Carbon Dioxide; Cardiovascular system; Cell Nucleus; Cell model; Cells; Chemoreceptors; Chest; Chronic; Collaborations; Complex; Computer Simulation; Data; Data Set; Databases; Depressed mood; Development; Disease; Economic Inflation; Equilibrium; Feedback; Frequencies; Generations; Glycine; Goals; Health; Heart failure; Hodgkin Disease; Homeostasis; Hypercapnia; Hypocapnia; Hypoxia; In Situ; In Vitro; Individual; Injection of therapeutic agent; Investigation; Knowledge; Life; Link; Literature; Location; Lung; Lung diseases; Mammals; Maps; Mathematics; Mechanics; Mechanoreceptors; Mediating; Medical; Mental Depression; Metabolic; Methods; Modeling; Motor; Motor Activity; Movement; Muscle; Muscle Contraction; National Institute of Neurological Disorders and Stroke; Network-based; Neurons; Nitric Oxide Synthase; Nucleus solitarius; Organ; Output; Oxygen; Paper; Partial Pressure; Participant; Pathway interactions; Pattern; Peripheral; Physiological; Physiology; Play; Pontine structure; Population; Preparation; Process; Property; Pulmonary Stretch Receptors; Pump; Randomized; Rattus; Regulation; Research; Respiration; Respiratory Diaphragm; Respiratory System; Respiratory Transport; Role; Scientist; Series; Signal Transduction; Simulate; Source; Stimulus; Structure of phrenic nerve; Synapses; System; Systems Analysis; Testing; Time; Tissues; United States National Institutes of Health; Universities; Vagotomy; Validation; Weight; base; central pattern generator; computational neuroscience; computer framework; conditioning; data modeling; expiration; extracellular; feeding; gamma-Aminobutyric Acid; in vivo; lung volume; mRNA Expression; model development; multi-scale modeling; multicore processor; multidisciplinary; multilevel analysis; neural model; neuromechanism; neurophysiology; neuroregulation; programs; raphe nuclei; receptor; relating to nervous system; research study; respiratory; response; simulation; translational neuroscience; web site

DESCRIPTION (provided by applicant): Respiration in mammals is a primal homeostatic process, regulating levels of oxygen (O2) and carbon dioxide (CO2) in blood and tissues and is crucial for life. Rhythmic respiratory movements must occur continuously throughout life and originate from neural activity generated by specially organized circuits in the brain stem constituting the respiratory central pattern generator (CPG). The respiratory CPG generates rhythmic patterns of motor activity that produce coordinated movements of the respiratory pump (diaphragm, thorax, and abdomen), controlling lung inflation and deflation, and upper airway muscles, controlling airflow. These coordinated rhythmic movements drive exchange and transport of O2 and CO2 that maintain physiological homeostasis of the brain and body. Uncovering complex multilevel and multiscale mechanisms operating in the respiratory system, leading to mechanistic understanding of breathing, including breathing in different disease states requires a Physiome-type approach that relies on the development and explicit implementation of multiscale computational models of particular organs and physiological functions. The specific aims of this multi-institutional project are: (1) develop a Physiome-type, predictive, multiscale computational model of neural control of breathing that links multiple physiological mechanisms and processes involved in the vital function of breathing but operating at different scales of functional and structural organization, (2) validate this model in a series of complementary experimental investigations and (3) use the model as a computational framework for formulating predictions about possible sources and mechanisms of respiratory pattern alteration associated with heart failure. The project brings together a multidisciplinary team of scientists with long standing collaboration and complementary expertise in respiration physiology, neuroscience and translational medical studies (Thomas E. Dick, Case Western Reserve University; Julian F.R. Paton, University of Bristol, UK; Robert F. Rogers, Drexel University; Jeffrey C. Smith, NINDS, NIH, intramural), mathematics, system analysis and bioengineering (Alona Ben-Tal, Massey University, NZ), and computational neuroscience and neural control (Ilya A. Rybak, Drexel University). The end result of our proposed cross-disciplinary modeling and experimental studies will be the development and implementation of a new, fully operational, multiscale model of the integrated neurophysiological control system for breathing based on the current state of physiological knowledge. This model can then be used as a computational framework for formulating predictions about possible neural mechanisms of respiratory diseases and suggesting possible treatments.

描述（由申请人提供）：哺乳动物的呼吸是一个原始的稳态过程，调节血液和组织中的氧气（O2）和二氧化碳（CO2）水平，对生命至关重要。有节奏的呼吸运动必须在一生中持续发生，并且起源于脑干中构成呼吸中枢模式发生器（CPG）的特殊组织回路产生的神经活动。呼吸CPG产生有节奏的运动活动模式，产生呼吸泵（隔膜、胸腔和腹部）的协调运动，控制肺的膨胀和收缩，以及上呼吸道肌肉，控制气流。这些协调的有节奏的运动驱动O2和CO2的交换和运输，维持大脑和身体的生理稳态。揭示呼吸系统中复杂的多层次和多尺度机制，从而导致对呼吸的机制理解，包括不同疾病状态下的呼吸，需要一种生理组类型的方法，这种方法依赖于特定器官和生理功能的多尺度计算模型的开发和明确实施。这个多机构项目的具体目标是：(1)建立一个生理组型的、可预测的、多尺度的呼吸神经控制计算模型，该模型将涉及呼吸重要功能的多种生理机制和过程联系起来，但在不同的功能和结构组织尺度上运作；(2)在一系列互补的实验研究中验证该模型；(3)将该模型作为计算框架，用于制定与心力衰竭相关的呼吸模式改变的可能来源和机制的预测。该项目汇集了一个多学科的科学家团队，他们在呼吸生理学、神经科学和转化医学研究方面有着长期的合作和互补的专业知识(托马斯·迪克，凯斯西储大学，朱利安·f·r·帕顿，英国布里斯托尔大学，罗伯特·f·罗杰斯，德雷塞尔大学；Jeffrey C. Smith， NINDS， NIH，校内)，数学，系统分析和生物工程（Alona Ben-Tal，梅西大学，新西兰），计算神经科学和神经控制（Ilya A. Rybak，德雷塞尔大学）。我们提出的跨学科建模和实验研究的最终结果将是开发和实施一个新的、完全可操作的、基于当前生理知识状态的呼吸综合神经生理控制系统的多尺度模型。然后，这个模型可以用作计算框架，用于制定有关呼吸系统疾病可能的神经机制的预测，并提出可能的治疗方法。