4.5 Article

Longitudinal characterization of neuroanatomical changes in the Fischer 344 rat brain during normal aging and between sexes

期刊

NEUROBIOLOGY OF AGING
卷 109, 期 -, 页码 216-228

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.neurobiolaging.2021.10.003

关键词

Normative aging; Magnetic resonance imaging; Regional volumetry; Longitudinal study; Sex differences

资金

  1. Canadian Institutes of Health Research [PJT-148751]
  2. Fonds de la Recherche en SanteduQuebec [00 0 0 035275]

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Through a comprehensive longitudinal examination of morphometric changes in 73 brain regions in F344 rats during normative aging, vulnerability to aging was identified within certain brain regions, with sex differences particularly notable in specific areas such as the caudoputamen, hippocampus, nucleus accumbens, and thalamus.
Animal models are widely used to study the pathophysiology of disease and to evaluate the efficacy of novel interventions, crucial steps towards improving disease outcomes in humans. The Fischer 344 (F344) wildtype rat is a common experimental background strain for transgenic models of disease and is one of the most frequently used models in aging research. Despite frequency of use, characterization of agerelated neuroanatomical change has not been performed in the F344 rat. To this end, we present a comprehensive longitudinal examination of morphometric change in 73 brain regions and at a voxel-wise level during normative aging in vivo in a mixed-sexcohort of F344 rats. We identified the greatest vulnerability to aging within the cortex, caudoputamen, hindbrain, and internal capsule, while the influence of sex was strongest in the caudoputamen, hippocampus, nucleus accumbens, and thalamus, many of which are implicated in memory and motor control circuits frequently affected by aging and neurodegenerative disease. These findings provide a baseline for neuroanatomical changes associated with aging in male and female F344 rats, to which data from transgenic models or other background strains can be compared. (c) 2021 Elsevier Inc. All rights reserved.

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