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Isolated catatonia-like executive dysfunction in mice with forebrain-specific loss of myelin integrity. | LitMetric

AI Article Synopsis

  • Advanced brain aging is marked by defects in intracortical myelin, which lead to neuroinflammation and behavioral issues, similar to those seen in certain mutant mice.
  • Newly engineered mice lacking a key myelin protein showed milder myelin defects confined to specific brain areas, allowing for normal basic motor-sensory functions.
  • Despite normal social behaviors, these mutants exhibited catatonia-like symptoms and executive function impairments, indicating that myelin integrity is crucial for cortical connectivity and could shed light on human neuropsychiatric disorders.

Article Abstract

A key feature of advanced brain aging includes structural defects of intracortical myelin that are associated with secondary neuroinflammation. A similar pathology is seen in specific myelin mutant mice that model 'advanced brain aging' and exhibit a range of behavioral abnormalities. However, the cognitive assessment of these mutants is problematic because myelin-dependent motor-sensory functions are required for quantitative behavioral readouts. To better understand the role of cortical myelin integrity for higher brain functions, we generated mice lacking , encoding the major integral myelin membrane protein, selectively in ventricular zone stem cells of the mouse forebrain. In contrast to conventional null mutants, subtle myelin defects were restricted to the cortex, hippocampus, and underlying callosal tracts. Moreover, forebrain-specific mutants exhibited no defects of basic motor-sensory performance at any age tested. Surprisingly, several behavioral alterations reported for conventional null mice (Gould et al., 2018) were absent and even social interactions appeared normal. However, with novel behavioral paradigms, we determined catatonia-like symptoms and isolated executive dysfunction in both genders. This suggests that loss of myelin integrity has an impact on cortical connectivity and underlies specific defects of executive function. These observations are likewise relevant for human neuropsychiatric conditions and other myelin-related diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9998085PMC
http://dx.doi.org/10.7554/eLife.70792DOI Listing

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