Bonvento Gilles, Valette Julien, Flament Julien, Mochel Fanny, Brouillet Emmanuel
1 Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Département de la Recherche Fondamentale (DRF), Institut d'Imagerie Biomédicale (I2BM), Molecular Imaging Research Center (MIRCen), CNRS UMR 9199, Université Paris-Sud, Université Paris-Saclay, Fontenay-aux-Roses, France.
2 INSERM US 27, Molecular Imaging Research Center (MIRCen), Fontenay-aux-Roses, France.
J Cereb Blood Flow Metab. 2017 Jun;37(6):1927-1943. doi: 10.1177/0271678X17697989. Epub 2017 Mar 9.
Changes in energy metabolism are generally considered to play an important role in neurodegenerative diseases such as Alzheimer's, Parkinson's, and Huntington's diseases. Whether these changes are causal or simply a part of self-defense mechanisms is a matter of debate. Furthermore, energy defects have often been discussed solely in the context of their probable neuronal origin without considering the cellular heterogeneity of the brain. Recent data point towards the existence of a tri-cellular compartmentation of brain energy metabolism between neurons, astrocytes, and oligodendrocytes, each cell type having a distinctive metabolic profile. Still, the number of methods to follow energy metabolism in patients is extremely limited and existing clinical techniques are blind to most cellular processes. There is a need to better understand how brain energy metabolism is regulated in health and disease through experiments conducted at different scales in animal models to implement new methods in the clinical setting. The purpose of this review is to offer a brief overview of the broad spectrum of methodological approaches that have emerged in recent years to probe energy metabolism in more detail. We conclude that multi-modal neuroimaging is needed to follow non-cell autonomous energy metabolism dysregulation in neurodegenerative diseases.
能量代谢的变化通常被认为在诸如阿尔茨海默病、帕金森病和亨廷顿病等神经退行性疾病中起重要作用。这些变化是因果性的还是仅仅是自我防御机制的一部分,这是一个有争议的问题。此外,能量缺陷常常仅在其可能的神经元起源的背景下进行讨论,而没有考虑大脑的细胞异质性。最近的数据表明,神经元、星形胶质细胞和少突胶质细胞之间存在脑能量代谢的三细胞区室化,每种细胞类型都有独特的代谢特征。然而,跟踪患者能量代谢的方法数量极其有限,现有的临床技术对大多数细胞过程视而不见。有必要通过在动物模型中进行不同规模的实验,更好地了解健康和疾病状态下脑能量代谢是如何调节的,以便在临床环境中应用新方法。本综述的目的是简要概述近年来出现的广泛的方法学途径,以便更详细地探究能量代谢。我们得出结论,需要多模态神经成像来跟踪神经退行性疾病中非细胞自主能量代谢失调。