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- W2486213928 endingPage "2040" @default.
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- W2486213928 abstract "Subtle white matter abnormalities have emerged as a hallmark of brain alterations in magnetic resonance imaging or upon autopsy of mentally ill subjects. However, it is unknown whether such reduction of white matter and myelin contributes to any disease-relevant phenotype or simply constitutes an epiphenomenon, possibly even treatment-related. Here, we have re-analyzed Mbp heterozygous mice, the unaffected parental strain of shiverer, a classical neurological mutant. Between 2 and 20 months of age, Mbp(+/-) versus Mbp(+/+) littermates were deeply phenotyped by combining extensive behavioral/cognitive testing with MRI, 1H-MR spectroscopy, electron microscopy, and molecular techniques. Surprisingly, Mbp-dependent myelination was significantly reduced in the prefrontal cortex. We also noticed a mild but progressive hypomyelination of the prefrontal corpus callosum and low-grade inflammation. While most behavioral functions were preserved, Mbp(+/-) mice exhibited defects of sensorimotor gating, as evidenced by reduced prepulse-inhibition, and a late-onset catatonia phenotype. Thus, subtle but primary abnormalities of CNS myelin can be the cause of a persistent cortical network dysfunction including catatonia, features typical of neuropsychiatric conditions. GLIA 2016;64:2025-2040." @default.
- W2486213928 created "2016-08-23" @default.
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- W2486213928 date "2016-07-29" @default.
- W2486213928 modified "2023-10-17" @default.
- W2486213928 title "Cortical network dysfunction caused by a subtle defect of myelination" @default.
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- W2486213928 doi "https://doi.org/10.1002/glia.23039" @default.
- W2486213928 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5129527" @default.
- W2486213928 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27470661" @default.
- W2486213928 hasPublicationYear "2016" @default.
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