动态校准功能磁共振成像中的神经血管和神经代谢耦合:块设计和事件相关范式的瞬时氧化神经能量学。

Frontiers in neuroenergetics Pub Date : 2010-08-19 eCollection Date: 2010-01-01 DOI:10.3389/fnene.2010.00018
Fahmeed Hyder, Basavaraju G Sanganahalli, Peter Herman, Daniel Coman, Natasja J G Maandag, Kevin L Behar, Hal Blumenfeld, Douglas L Rothman
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引用次数: 41

摘要

功能磁共振成像(fMRI)与血氧水平依赖(BOLD)对比是绘制大脑活动的重要工具。对定量功能磁共振成像的兴趣重新唤起了人们对氧化神经能量学重要性的认识,氧化神经能量学是由脑氧消耗代谢率(cro2)反映的,它支持脑功能。BOLD信号与潜在神经生理参数之间的关系已经被阐明,从而可以通过“校准功能磁共振成像”来确定mro2的动态变化,这需要对BOLD信号以及脑血流量(CBF)和脑容量(CBV)进行多模态测量。但是,与局部场电位(LFP)和/或多单元活动(MUA)的神经活动记录相比,校准的fMRI得出的doCMRO2稳态或瞬态变化如何?在这里,我们主要讨论最近的动物研究结果,这些研究结果允许高磁场研究,以获得卓越的BOLD灵敏度,以及多模态CBV和CBF测量,并结合活化部位的LFP和MUA记录。一个关键的观察结果是,虽然神经活动和感觉刺激特征之间的关系从线性到非线性不等,但充血成分(BOLD、CBF、CBV)和神经活动(LFP、MUA)之间的关联几乎总是线性的。更重要的是,结果表明inCMRO2的变化与LFP或MUA的独立测量之间有很好的一致性。紧密的神经血管和神经代谢耦合,观察到从稳态条件到事件分开
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Neurovascular and Neurometabolic Couplings in Dynamic Calibrated fMRI: Transient Oxidative Neuroenergetics for Block-Design and Event-Related Paradigms.

Neurovascular and Neurometabolic Couplings in Dynamic Calibrated fMRI: Transient Oxidative Neuroenergetics for Block-Design and Event-Related Paradigms.

Neurovascular and Neurometabolic Couplings in Dynamic Calibrated fMRI: Transient Oxidative Neuroenergetics for Block-Design and Event-Related Paradigms.

Neurovascular and Neurometabolic Couplings in Dynamic Calibrated fMRI: Transient Oxidative Neuroenergetics for Block-Design and Event-Related Paradigms.

Functional magnetic resonance imaging (fMRI) with blood-oxygenation level dependent (BOLD) contrast is an important tool for mapping brain activity. Interest in quantitative fMRI has renewed awareness in importance of oxidative neuroenergetics, as reflected by cerebral metabolic rate of oxygen consumption(CMRO2), for supporting brain function. Relationships between BOLD signal and the underlying neurophysiological parameters have been elucidated to allow determination of dynamic changes inCMRO2 by "calibrated fMRI," which require multi-modal measurements of BOLD signal along with cerebral blood flow (CBF) and volume (CBV). But how doCMRO2 changes, steady-state or transient, derived from calibrated fMRI compare with neural activity recordings of local field potential (LFP) and/or multi-unit activity (MUA)? Here we discuss recent findings primarily from animal studies which allow high magnetic fields studies for superior BOLD sensitivity as well as multi-modal CBV and CBF measurements in conjunction with LFP and MUA recordings from activated sites. A key observation is that while relationships between neural activity and sensory stimulus features range from linear to non-linear, associations between hyperemic components (BOLD, CBF, CBV) and neural activity (LFP, MUA) are almost always linear. More importantly, the results demonstrate good agreement between the changes inCMRO2 and independent measures of LFP or MUA. The tight neurovascular and neurometabolic couplings, observed from steady-state conditions to events separated by <200 ms, suggest rapid oxygen equilibration between blood and tissue pools and thus calibrated fMRI at high magnetic fields can provide high spatiotemporal mapping ofCMRO2 changes.

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