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Oral treatment of 4-methylumbelliferone reduced perineuronal nets and improved recognition memory in mice

神经周围网 海马体 医学 神经可塑性 海马结构 中枢神经系统 免疫组织化学 萎缩 麻醉 脊髓 神经科学 内科学 药理学 化学 心理学
作者
Jana Dubišová,Jana Burianová,Lucie Svobodová,Pavol Makovický,Noelia Martínez-Varea,Anda Cimpean,James W. Fawcett,Jessica C. F. Kwok,Šárka Kubinová
出处
期刊:Brain Research Bulletin [Elsevier BV]
卷期号:181: 144-156 被引量:32
标识
DOI:10.1016/j.brainresbull.2022.01.011
摘要

Hyaluronan (HA) is a core constituent of perineuronal nets (PNNs) that surround subpopulations of neurones. The PNNs control synaptic stabilization in both the developing and adult central nervous system, and disruption of PNNs has shown to reactivate neuroplasticity. We investigated the possibility of memory prolongation by attenuating PNN formation using 4-methylumbelliferone (4-MU), an inhibitor of HA synthesis. Adult C57BL/6 mice were fed with chow containing 5% (w/w) 4-MU for 6 months, at a dose ~6.7 mg/g/day. The oral administration of 4-MU reduced the glycosaminoglycan level in the brain to 72% and the spinal cord to 50% when compared to the controls. Spontaneous object recognition test (SOR) performed at 2, 3, 6 and 7 months showed a significant increase in SOR score in the 6-months treatment group 24 h after object presentation. The effect however did not persist in the washout group (1-month post treatment). Immunohistochemistry confirmed a reduction of PNNs, with shorter and less arborization of aggrecan staining around dendrites in hippocampus after 6 months of 4-MU treatment. Histopathological examination revealed mild atrophy in articular cartilage but it did not affect the motor performance as demonstrated in rotarod test. In conclusion, systemic oral administration of 4-MU for 6 months reduced PNN formation around neurons and enhanced memory retention in mice. However, the memory enhancement was not sustained despite the reduction of PNNs, possibly due to the lack of memory enhancement training during the washout period. Our results suggest that 4-MU treatment might offer a strategy for PNN modulation in memory enhancement.
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