Effects of standard fMRI calibrations on the diverse microvascular blood flow and oxygenation responses in cortical layers

标准功能磁共振成像校准对皮质层不同微血管血流和氧合反应的影响

• 批准号: 10673193
• 负责人: Ikbal Sencan-Egilmez
• 金额: $ 23.97万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-08-01 至 2025-07-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10673193
• 关键词: Affect; Age; Aging; Anesthesia procedures; Animal Model; Area; BRAIN initiative; Biophysics; Blood Vessels; Blood capillaries; Blood flow; Brain; Brain Mapping; Brain Pathology; Breathing; Caffeine; Calibration; Carbon Dioxide; Catheters; Cerebrovascular Circulation; Cerebrum; Chronic; Clinical; Complex; Computer Models; Coupled; Data; Development; Diameter; Environment; Faculty; Functional Magnetic Resonance Imaging; Gases; General Hospitals; Goals; Health; Human; Hypercapnia; Hyperoxia; Image; Imaging Device; Injections; Intake; Intraventricular; Ipsilateral; Link; Maps; Massachusetts; Measurement; Mentors; Metabolism; Methodology; Methods; Modeling; Morphology; Mus; Nature; Neurons; Neurosciences; Noise; Optics; Oxygen; Partial Pressure; Pathologic; Pharmacologic Substance; Positioning Attribute; Procedures; Radiology Specialty; Research; Research Design; Research Methodology; Resolution; Rest; Shoulder; Signal Transduction; Technology; Time; Tissues; Training; Vibrissae; Visual; Work; arterial spin labeling; arteriole; awake; biomedical imaging; biophysical model; blood oxygen level dependent; career development; experimental study; healthy aging; hemodynamics; imaging modality; improved; insight; interdisciplinary collaboration; medical schools; metabolic rate; microscopic imaging; middle age; neuroimaging; neurovascular coupling; new technology; next generation; novel; pressure; response; tenure track; tool; training opportunity; two-photon; venule

This proposed project focuses on quantifying the spatial and temporal diversity in cortical oxygen metabolism and neurovascular coupling, and informing next generation of biophysical models of the Blood Oxygen Level Dependent (BOLD) functional Magnetic Resonance Imaging (fMRI) measurements by integrating new technological and conceptual approaches. Broad and long term objectives of this application are (1) to bridge understanding of brain in action at multiple scales in spatial (subcapillary to whole- brain) and temporal (µs to months) domains, (2) to contribute discovering diversity of hemodynamic responses across cortical tissue layers, functional areas, and microvascular branches, and (3) to support the modelling efforts of BOLD signal by to quantifying hemodynamic responses in cortex of healthy-aging awake mice. Realizing these objectives would contribute to the joined efforts towards improving human health through accomplishing BRAIN Initiative goals of understanding the brain in action, discovering diversity, mapping/linking activity across spatial and temporal scales, and understanding the biophysical basis of fMRI signal. The specific aims of the proposed project can be summarized as: (1) to develop faster, deeper, longitudinal measurements of the cerebral blood flow (CBF), partial pressure of oxygen (pO2), and cerebral metabolic rate of oxygen (CMRO2), (2) to quantify the diversity of CMRO2 and CBF responses to functional activation across different cortical functional areas, cortical layers, and microvasculature types in healthy-aging mouse, and (3) to quantify the effects of standard fMRI calibrations (e.g. hypercapnia, hyperoxia, and caffeine) on the CMRO2 and CBF at rest and during functional activation. The research design and methods that will be used in this project will include (1) developing faster and deeper chronic imaging of absolute oxygen concentration to assess relation between cortical pO2, CMRO2, and blood flow changes during brain activation across the cortical areas and layers, and (2) realistic measurements of the oxygenation, blood flow, and metabolism responses to functional activation at the microvascular scales in healthy-aging mice and in response to calibration procedures that are commonly used in BOLD fMRI imaging. The research environment of Dr. Sencan (the Athinoula A. Martinos Center for Biomedical Imaging at Massachusetts General Hospital and Radiology Department in Harvard Medical School) is equipped with state-of-the-art technologies required to execute the proposed project and is rich with opportunities for training in neuroscience, career development, and interdisciplinary collaborations. She has a team of mentors, collaborators and advisors with diverse and strong expertise, who are committed to support Dr. Sencan’s research, and her career development. All these factors will facilitate the successful execution of the proposed project, the completion of Dr. Sencan’s training in neuroimaging, and her transition to an independent tenure-track faculty position.

该项目的重点是量化皮质氧代谢和神经血管耦合的空间和时间多样性，并通过整合新的技术和概念方法，为下一代血氧水平依赖（BOLD）功能性磁共振成像（fMRI）测量的生物物理模型提供信息。该应用的广泛和长期目标是（1）在空间的多个尺度上桥接对大脑活动的理解（毛细血管下至全脑）和颞叶（µs至月）领域，（2）有助于发现皮质组织层、功能区和微血管分支的血流动力学反应的多样性，（3）通过对健康老龄清醒小鼠大脑皮层血流动力学反应的定量研究，支持BOLD信号的建模工作。实现这些目标将有助于通过实现BRAIN倡议的目标来改善人类健康，这些目标包括了解大脑的活动，发现多样性，在空间和时间尺度上映射/链接活动，以及了解功能磁共振成像信号的生物物理基础。拟议项目的具体目标可概括为：（1）开发脑血流量（CBF）、氧分压（pO 2）和脑氧代谢率（CMRO 2）的更快、更深的纵向测量，（2）量化CMRO 2和CBF对不同皮质功能区、皮质层、和微血管类型，以及（3）量化标准fMRI校准（例如高碳酸血症，高氧和咖啡因）对静息和功能激活期间CMRO 2和CBF的影响。本项目中使用的研究设计和方法将包括（1）开发更快、更深的绝对氧浓度慢性成像，以评估皮质pO 2、CMRO 2和脑激活期间跨皮质区域和层的血流变化之间的关系，以及（2）对氧合、血流、以及代谢对健康老龄小鼠微血管尺度功能激活的反应，以及对BOLD fMRI成像中常用的校准程序的反应。Sencan博士的研究环境（Athinoula A.位于马萨诸塞州总医院和哈佛医学院放射科的Martinos生物医学成像中心）配备了执行拟议项目所需的最先进的技术，并拥有丰富的神经科学培训、职业发展和跨学科合作的机会。她拥有一支由导师、合作者和顾问组成的团队，他们拥有丰富的专业知识，致力于支持Sencan博士的研究和她的职业发展。所有这些因素都将促进拟议项目的成功执行，完成Sencan博士在神经影像学方面的培训，以及她向独立终身教职的过渡。