Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory

The current longitudinal study examined factors (sex, physical function, response to novelty, ability to adapt to a shift in light/dark cycle, brain connectivity), which might predict the emergence of impaired memory during aging. Male and female Fisher 344 rats were tested at 6, 12, and 18 months o...

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Main Authors: Marcelo Febo, Asha Rani, Brittney Yegla, Jolie Barter, Ashok Kumar, Christopher A. Wolff, Karyn Esser, Thomas C. Foster
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Aging Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnagi.2020.00034/full
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spelling doaj-2f5e49f825f34b04a82dcb34b4c4cb432020-11-25T00:30:55ZengFrontiers Media S.A.Frontiers in Aging Neuroscience1663-43652020-02-011210.3389/fnagi.2020.00034512171Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial MemoryMarcelo Febo0Asha Rani1Brittney Yegla2Jolie Barter3Ashok Kumar4Christopher A. Wolff5Karyn Esser6Thomas C. Foster7Thomas C. Foster8Department of Psychiatry, McKnight Brain Institute, University of Florida, Gainesville, FL, United StatesDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, United StatesDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, United StatesDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, United StatesDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, United StatesDepartment of Physiology and Functional Genomics, Myology Institute, University of Florida, Gainesville, FL, United StatesDepartment of Physiology and Functional Genomics, Myology Institute, University of Florida, Gainesville, FL, United StatesDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL, United StatesGenetics and Genomics Program, University of Florida, Gainesville, FL, United StatesThe current longitudinal study examined factors (sex, physical function, response to novelty, ability to adapt to a shift in light/dark cycle, brain connectivity), which might predict the emergence of impaired memory during aging. Male and female Fisher 344 rats were tested at 6, 12, and 18 months of age. Impaired spatial memory developed in middle-age (12 months), particularly in males, and the propensity for impairment increased with advanced age. A reduced response to novelty was observed over the course of aging, which is inconsistent with cross-sectional studies. This divergence likely resulted from differences in the history of environmental enrichment/impoverishment for cross-sectional and longitudinal studies. Animals that exhibited lower level exploration of the inner region on the open field test exhibited better memory at 12 months. Furthermore, males that exhibited a longer latency to enter a novel environment at 6 months, exhibited better memory at 12 months. For females, memory at 12 months was correlated with the ability to behaviorally adapt to a shift in light/dark cycle. Functional magnetic resonance imaging of the brain, conducted at 12 months, indicated that the decline in memory was associated with altered functional connectivity within different memory systems, most notably between the hippocampus and multiple regions such as the retrosplenial cortex, thalamus, striatum, and amygdala. Overall, some factors, specifically response to novelty at an early age and the capacity to adapt to shifts in light cycle, predicted spatial memory in middle-age, and spatial memory is associated with corresponding changes in brain connectivity. We discuss similarities and differences related to previous longitudinal and cross-sectional studies, as well as the role of sex differences in providing a theoretical framework to guide future longitudinal research on the trajectory of cognitive decline. In addition to demonstrating the power of longitudinal studies, these data highlight the importance of middle-age for identifying potential predictive indicators of sexual dimorphism in the trajectory in brain and cognitive aging.https://www.frontiersin.org/article/10.3389/fnagi.2020.00034/fullSexual dimorphismsepisodic memorycognitive functionlife spanlongitudinal
collection DOAJ
language English
format Article
sources DOAJ
author Marcelo Febo
Asha Rani
Brittney Yegla
Jolie Barter
Ashok Kumar
Christopher A. Wolff
Karyn Esser
Thomas C. Foster
Thomas C. Foster
spellingShingle Marcelo Febo
Asha Rani
Brittney Yegla
Jolie Barter
Ashok Kumar
Christopher A. Wolff
Karyn Esser
Thomas C. Foster
Thomas C. Foster
Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory
Frontiers in Aging Neuroscience
Sexual dimorphisms
episodic memory
cognitive function
life span
longitudinal
author_facet Marcelo Febo
Asha Rani
Brittney Yegla
Jolie Barter
Ashok Kumar
Christopher A. Wolff
Karyn Esser
Thomas C. Foster
Thomas C. Foster
author_sort Marcelo Febo
title Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory
title_short Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory
title_full Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory
title_fullStr Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory
title_full_unstemmed Longitudinal Characterization and Biomarkers of Age and Sex Differences in the Decline of Spatial Memory
title_sort longitudinal characterization and biomarkers of age and sex differences in the decline of spatial memory
publisher Frontiers Media S.A.
series Frontiers in Aging Neuroscience
issn 1663-4365
publishDate 2020-02-01
description The current longitudinal study examined factors (sex, physical function, response to novelty, ability to adapt to a shift in light/dark cycle, brain connectivity), which might predict the emergence of impaired memory during aging. Male and female Fisher 344 rats were tested at 6, 12, and 18 months of age. Impaired spatial memory developed in middle-age (12 months), particularly in males, and the propensity for impairment increased with advanced age. A reduced response to novelty was observed over the course of aging, which is inconsistent with cross-sectional studies. This divergence likely resulted from differences in the history of environmental enrichment/impoverishment for cross-sectional and longitudinal studies. Animals that exhibited lower level exploration of the inner region on the open field test exhibited better memory at 12 months. Furthermore, males that exhibited a longer latency to enter a novel environment at 6 months, exhibited better memory at 12 months. For females, memory at 12 months was correlated with the ability to behaviorally adapt to a shift in light/dark cycle. Functional magnetic resonance imaging of the brain, conducted at 12 months, indicated that the decline in memory was associated with altered functional connectivity within different memory systems, most notably between the hippocampus and multiple regions such as the retrosplenial cortex, thalamus, striatum, and amygdala. Overall, some factors, specifically response to novelty at an early age and the capacity to adapt to shifts in light cycle, predicted spatial memory in middle-age, and spatial memory is associated with corresponding changes in brain connectivity. We discuss similarities and differences related to previous longitudinal and cross-sectional studies, as well as the role of sex differences in providing a theoretical framework to guide future longitudinal research on the trajectory of cognitive decline. In addition to demonstrating the power of longitudinal studies, these data highlight the importance of middle-age for identifying potential predictive indicators of sexual dimorphism in the trajectory in brain and cognitive aging.
topic Sexual dimorphisms
episodic memory
cognitive function
life span
longitudinal
url https://www.frontiersin.org/article/10.3389/fnagi.2020.00034/full
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