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Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease

Alzheimer's disease (AD), a prevalent form of dementia, is characterized by the decline of cognitive abilities with age. Available treatment options for AD are limited, making it a significant public health concern. Recent research suggests that metabolic dysfunction plays a role in the develop...

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Autores principales: Srivastava, Hemant, Lasher, Alexander Tate, Nagarajan, Akash, Sun, Liou Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352566/
https://www.ncbi.nlm.nih.gov/pubmed/37095621
http://dx.doi.org/10.1111/acel.13854
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author Srivastava, Hemant
Lasher, Alexander Tate
Nagarajan, Akash
Sun, Liou Y.
author_facet Srivastava, Hemant
Lasher, Alexander Tate
Nagarajan, Akash
Sun, Liou Y.
author_sort Srivastava, Hemant
collection PubMed
description Alzheimer's disease (AD), a prevalent form of dementia, is characterized by the decline of cognitive abilities with age. Available treatment options for AD are limited, making it a significant public health concern. Recent research suggests that metabolic dysfunction plays a role in the development of AD. In addition, insulin therapy has been shown to improve memory in patients with cognitive decline. In this study, we report the first examination of body composition, peripheral insulin sensitivity, and glucose tolerance in relation to behavioral assessments of learning, memory, and anxiety in the TgF344‐AD rat model of AD. Results from glucose and insulin tolerance tests show that female TgF344‐AD rats exhibit impaired glucose clearance and reduced insulin sensitivity at both 9 and 12 months of age, while males display no differences at 9 months and even improved glucose clearance at 12 months. Results from the Morris Water Maze assessment of learning and memory reveal that male TgF344‐AD rats display impairments at both 9 and 12 months of age, while female TgF344‐AD rats only show impairments at 12 months. Furthermore, results from open field and elevated plus maze tests suggest that female TgF344‐AD rats display increased anxiety at 9 months of age; however, no differences were detected in males or at 12 months of age. Overall, our findings suggest that impairments in metabolism, commonly associated with type 2 diabetes, occur before or simultaneously with cognitive decline and anxiety in a sexually dimorphic manner in the TgF344‐AD rat model.
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spelling pubmed-103525662023-07-19 Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease Srivastava, Hemant Lasher, Alexander Tate Nagarajan, Akash Sun, Liou Y. Aging Cell Research Articles Alzheimer's disease (AD), a prevalent form of dementia, is characterized by the decline of cognitive abilities with age. Available treatment options for AD are limited, making it a significant public health concern. Recent research suggests that metabolic dysfunction plays a role in the development of AD. In addition, insulin therapy has been shown to improve memory in patients with cognitive decline. In this study, we report the first examination of body composition, peripheral insulin sensitivity, and glucose tolerance in relation to behavioral assessments of learning, memory, and anxiety in the TgF344‐AD rat model of AD. Results from glucose and insulin tolerance tests show that female TgF344‐AD rats exhibit impaired glucose clearance and reduced insulin sensitivity at both 9 and 12 months of age, while males display no differences at 9 months and even improved glucose clearance at 12 months. Results from the Morris Water Maze assessment of learning and memory reveal that male TgF344‐AD rats display impairments at both 9 and 12 months of age, while female TgF344‐AD rats only show impairments at 12 months. Furthermore, results from open field and elevated plus maze tests suggest that female TgF344‐AD rats display increased anxiety at 9 months of age; however, no differences were detected in males or at 12 months of age. Overall, our findings suggest that impairments in metabolism, commonly associated with type 2 diabetes, occur before or simultaneously with cognitive decline and anxiety in a sexually dimorphic manner in the TgF344‐AD rat model. John Wiley and Sons Inc. 2023-04-24 /pmc/articles/PMC10352566/ /pubmed/37095621 http://dx.doi.org/10.1111/acel.13854 Text en © 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Srivastava, Hemant
Lasher, Alexander Tate
Nagarajan, Akash
Sun, Liou Y.
Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease
title Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease
title_full Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease
title_fullStr Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease
title_full_unstemmed Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease
title_short Sexual dimorphism in the peripheral metabolic homeostasis and behavior in the TgF344‐AD rat model of Alzheimer's disease
title_sort sexual dimorphism in the peripheral metabolic homeostasis and behavior in the tgf344‐ad rat model of alzheimer's disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10352566/
https://www.ncbi.nlm.nih.gov/pubmed/37095621
http://dx.doi.org/10.1111/acel.13854
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