Age-Related Brain Atrophy and the Positive Effects of Behavioral Enrichment in Middle-Aged Beagles

Aging dogs serve as a valuable preclinical model for Alzheimer's disease (AD) due to their natural age-related development of β-amyloid (Aβ) plaques, human-like metabolism, and large brains that are ideal for studying structural brain aging trajectories from serial neuroimaging. Here we examine...

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Veröffentlicht in:The Journal of neuroscience 2024-05, Vol.44 (20), p.e2366232024
Hauptverfasser: Noche, Jessica A, Radhakrishnan, Hamsanandini, Ubele, Margo F, Boaz, Kathy, Mefford, Jennifer L, Jones, Erin D, van Rooyen, Hollie Y, Perpich, Jessica A, McCarty, Katie, Meacham, Beverly, Smiley, Jeffrey, Bembenek Bailey, Stasia A, Puskás, László G, Powell, David K, Sordo, Lorena, Phelan, Michael J, Norris, Christopher M, Head, Elizabeth, Stark, Craig E L
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Sprache:eng
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Zusammenfassung:Aging dogs serve as a valuable preclinical model for Alzheimer's disease (AD) due to their natural age-related development of β-amyloid (Aβ) plaques, human-like metabolism, and large brains that are ideal for studying structural brain aging trajectories from serial neuroimaging. Here we examined the effects of chronic treatment with the calcineurin inhibitor (CNI) tacrolimus or the nuclear factor of activated T cells (NFAT)-inhibiting compound Q134R on age-related canine brain atrophy from a longitudinal study in middle-aged beagles (36 females, 7 males) undergoing behavioral enrichment. Annual MRI was analyzed using modern, automated techniques for region-of-interest-based and voxel-based volumetric assessments. We found that the frontal lobe showed accelerated atrophy with age, while the caudate nucleus remained relatively stable. Remarkably, the hippocampus increased in volume in all dogs. None of these changes were influenced by tacrolimus or Q134R treatment. Our results suggest that behavioral enrichment can prevent atrophy and increase the volume of the hippocampus but does not prevent aging-associated prefrontal cortex atrophy.
ISSN:0270-6474
1529-2401
1529-2401
DOI:10.1523/JNEUROSCI.2366-23.2024