Oral treatment of 4-methylumbelliferone reduced perineuronal nets and improved recognition memory in mice
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
MR/S011110/1
Medical Research Council - United Kingdom
PubMed
35066096
PubMed Central
PMC8867078
DOI
10.1016/j.brainresbull.2022.01.011
PII: S0361-9230(22)00013-2
Knihovny.cz E-zdroje
- Klíčová slova
- Extracellular matrix, Hyaluronan, Memory, Neuroplasticity, Perineuronal net,
- MeSH
- agrekany účinky léků MeSH
- aplikace orální MeSH
- centrální nervový systém účinky léků MeSH
- chování zvířat účinky léků MeSH
- extracelulární matrix účinky léků MeSH
- hymekromon aplikace a dávkování farmakologie MeSH
- kyselina hyaluronová metabolismus MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- neuroplasticita účinky léků MeSH
- oligodendroglie účinky léků MeSH
- rozpoznávání (psychologie) účinky léků MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- agrekany MeSH
- hymekromon MeSH
- kyselina hyaluronová MeSH
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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