AI Article Synopsis

  • Alzheimer's disease (AD) is the leading type of dementia, and this study focuses on the distribution of amyloid-beta (Aβ) plaques in various brain regions of 5xFAD mice, revealing significant memory deficits compared to normal mice.
  • High concentrations of Aβ plaques were found in areas like the somatosensory cortex and hippocampus, while other regions like the amygdala had low or no plaque presence.
  • The findings indicate a positive correlation between Aβ deposition and several brain regions, shedding light on how these plaques may contribute to the development of AD.

Article Abstract

Alzheimer's disease (AD) is the most common form of dementia. Although previous studies have selectively investigated the localization of amyloid-beta (Aβ) deposition in certain brain regions, a comprehensive characterization of the rostro-caudal distribution of Aβ plaques in the brain and their inter-regional correlation remain unexplored. Our results demonstrated remarkable working and spatial memory deficits in 9-month-old 5xFAD mice compared to wildtype mice. High Aβ plaque load was detected in the somatosensory cortex, piriform cortex, thalamus, and dorsal/ventral hippocampus; moderate levels of Aβ plaques were observed in the motor cortex, orbital cortex, visual cortex, and retrosplenial dysgranular cortex; and low levels of Aβ plaques were located in the amygdala, and the cerebellum; but no Aβ plaques were found in the hypothalamus, raphe nuclei, vestibular nucleus, and cuneate nucleus. Interestingly, the deposition of Aβ plaques was positively associated with brain inter-regions including the prefrontal cortex, somatosensory cortex, medial amygdala, thalamus, and the hippocampus. In conclusion, this study provides a comprehensive morphological profile of Aβ deposition in the brain and its inter-regional correlation. This suggests an association between Aβ plaque deposition and specific brain regions in AD pathogenesis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371463PMC
http://dx.doi.org/10.3389/fnagi.2022.964336DOI Listing

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