Mangia Silvia, Giove Federico, Tkác Ivan, Logothetis Nikos K, Henry Pierre-Gilles, Olman Cheryl A, Maraviglia Bruno, Di Salle Francesco, Uğurbil Kâmil
Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J Cereb Blood Flow Metab. 2009 Mar;29(3):441-63. doi: 10.1038/jcbfm.2008.134. Epub 2008 Nov 12.
Unraveling the energy metabolism and the hemodynamic outcomes of excitatory and inhibitory neuronal activity is critical not only for our basic understanding of overall brain function, but also for the understanding of many brain disorders. Methodologies of magnetic resonance spectroscopy (MRS) and magnetic resonance imaging (MRI) are powerful tools for the noninvasive investigation of brain metabolism and physiology. However, the temporal and spatial resolution of in vivo MRS and MRI is not suitable to provide direct evidence for hypotheses that involve metabolic compartmentalization between different cell types, or to untangle the complex neuronal microcircuitry, which results in changes of electrical activity. This review aims at describing how the current models of brain metabolism, mainly built on the basis of in vitro evidence, relate to experimental findings recently obtained in vivo by (1)H MRS, (13)C MRS, and MRI. The hypotheses related to the role of different metabolic substrates, the metabolic neuron-glia interactions, along with the available theoretical predictions of the energy budget of neurotransmission will be discussed. In addition, the cellular and network mechanisms that characterize different types of increased and suppressed neuronal activity will be considered within the sensitivity-constraints of MRS and MRI.
揭示兴奋性和抑制性神经元活动的能量代谢及血流动力学结果,不仅对我们从根本上理解大脑整体功能至关重要,而且对于理解许多脑部疾病也至关重要。磁共振波谱(MRS)和磁共振成像(MRI)方法是用于无创研究脑代谢和生理学的强大工具。然而,体内MRS和MRI的时间和空间分辨率并不适合为涉及不同细胞类型之间代谢区室化的假设提供直接证据,也无法理清导致电活动变化的复杂神经元微电路。本综述旨在描述目前主要基于体外证据建立的脑代谢模型,如何与最近通过氢质子磁共振波谱(¹H MRS)、碳-13磁共振波谱(¹³C MRS)和MRI在体内获得的实验结果相关联。将讨论与不同代谢底物的作用、代谢性神经元-胶质细胞相互作用相关的假设,以及神经传递能量预算的现有理论预测。此外,将在MRS和MRI的敏感性限制范围内考虑表征不同类型神经元活动增强和抑制的细胞及网络机制。