Temporal and spatial evolution of various functional neurons during demyelination induced by cuprizone

• Published in: Journal of neurophysiology 2021-11, Vol.126 (5), p.1756-1771
• Main Authors: An, Jun, He, Yan, Yin, Jun-Jun, Ding, Zhi-Bin, Han, Qing-Xian, Chen, Yang-Yang, Wang, Qing, Chai, Zhi, Yu, Jie-Zhong, Song, Li-Juan, Xiao, Bao-Guo, Ma, Cun-Gen
• Format: Article
• Language: English
• Subjects: Animals; Astrocytes - drug effects; Astrocytes - metabolism; Axons - drug effects; Axons - metabolism; Axons - pathology; Cuprizone - administration & dosage; Cuprizone - pharmacology; Demyelinating Diseases - chemically induced; Demyelinating Diseases - metabolism; Disease Models, Animal; Glutamic Acid - metabolism; Mice; Monoamine Oxidase Inhibitors - administration & dosage; Monoamine Oxidase Inhibitors - pharmacology; Multiple Sclerosis - metabolism; Myelin Sheath - drug effects; Myelin Sheath - metabolism; Neurons - drug effects; Neurons - metabolism; Neurons - pathology
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.00224.2021

Multiple sclerosis (MS) is an inflammatory, demyelinating, and neurodegenerative disease of the central nervous system (CNS). Here we report the temporal and spatial evolution of various functional neurons during demyelination in a cuprizone (CPZ)-induced mouse model. CPZ did not significantly induce the damage of axons and neurons after 2 wk of feeding. However, after 4-6 wk of CPZ feeding, axons and neurons were markedly reduced in the cortex, posterior thalamic nuclear group, and hippocampus. Simultaneously, the expression of TPH tryptophan neurons and VGLUT1 glutamate neurons was obviously decreased, and the expression of TH dopaminergic neurons was slightly decreased in the tail part of the substantia nigra striatum, whereas the number of ChAT cholinergic neurons was not significantly different in the brain. In the second week of feeding, CPZ caused a higher level of glutamate secretion and upregulated the expression of EAAT2 on astrocytes, which should contribute to rapid and sufficient glutamate uptake and removal. This finding reveals that astrocyte-driven glutamate reuptake protected the CNS from excitotoxicity by rapid reuptake of glutamate in 4-6 wk of CPZ feeding. At this stage, although NG2 oligodendroglia progenitor cells (OPCs) were enhanced in the demyelination foci, the myelin sheath was still absent. In conclusion, we comprehensively observed the temporal and spatial evolution of various functional neurons. Our results will assist with understanding how demyelination affects neurons during CPZ-induced demyelination and provide novel information for neuroprotection in myelin regeneration and demyelinating diseases. Our results further indicate temporal and spatial evolution of various functional neurons during the demyelination in a cuprizone (CPZ)-induced mouse model, which mainly occur 4-6 wk after CPZ feeding. At the same time, the axonal compartment is damaged and, consequently, neuronal death occurs, while glutamate neurons are lost obviously. The astrocyte-mediated glutamate reuptake could protect the neurons from the excitatory effects of glutamate.