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A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin

AIMS: To explore the novel linkage between a Western diet combining high saturated fat, sugar, and salt (HFSS) and neurological dysfunctions during aging as well as Metformin intervention, we assessed cerebral cortex abnormalities associated with sensory and motor dysfunctions and cellular and molec...

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Autores principales: Hong, Song, Nagayach, Aarti, Lu, Yan, Peng, Hongying, Duong, Quoc‐Viet A., Pham, Nicholas B., Vuong, Christopher A., Bazan, Nicolas G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611779/
https://www.ncbi.nlm.nih.gov/pubmed/34510763
http://dx.doi.org/10.1111/cns.13726
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author Hong, Song
Nagayach, Aarti
Lu, Yan
Peng, Hongying
Duong, Quoc‐Viet A.
Pham, Nicholas B.
Vuong, Christopher A.
Bazan, Nicolas G.
author_facet Hong, Song
Nagayach, Aarti
Lu, Yan
Peng, Hongying
Duong, Quoc‐Viet A.
Pham, Nicholas B.
Vuong, Christopher A.
Bazan, Nicolas G.
author_sort Hong, Song
collection PubMed
description AIMS: To explore the novel linkage between a Western diet combining high saturated fat, sugar, and salt (HFSS) and neurological dysfunctions during aging as well as Metformin intervention, we assessed cerebral cortex abnormalities associated with sensory and motor dysfunctions and cellular and molecular insights in brains using HFSS‐fed mice during aging. We also explored the effect of Metformin treatment on these mice. METHODS: C57BL/6 mice were fed with HFSS and treated with metformin from 20 to 22 months of age, resembling human aging from 56 to 68 years of age (an entry phase of the aged portion of lifespan). RESULTS: The motor and sensory cortexes in mice during aging after HFSS diet showed: (A) decreased motor‐muscular and sensory functions; (B) reduced inflammation‐resolving Arg‐1(+) microglia; (C) increased inflammatory iNOs(+) microglia and TNFα levels; (D) enhanced abundance of amyloid‐β peptide and of phosphorylated Tau. Metformin attenuated these changes. CONCLUSION: A HFSS‐combined diet caused motor‐muscular and sensory dysfunctions, neuroinflammation, and neurodegeneration, whereas metformin counteracted these effects. Our findings show neuroinflammatory consequences of a HFSS diet in aging. Metformin curbs the HFSS‐related neuroinflammation eliciting neuroprotection.
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spelling pubmed-86117792021-11-30 A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin Hong, Song Nagayach, Aarti Lu, Yan Peng, Hongying Duong, Quoc‐Viet A. Pham, Nicholas B. Vuong, Christopher A. Bazan, Nicolas G. CNS Neurosci Ther Original Articles AIMS: To explore the novel linkage between a Western diet combining high saturated fat, sugar, and salt (HFSS) and neurological dysfunctions during aging as well as Metformin intervention, we assessed cerebral cortex abnormalities associated with sensory and motor dysfunctions and cellular and molecular insights in brains using HFSS‐fed mice during aging. We also explored the effect of Metformin treatment on these mice. METHODS: C57BL/6 mice were fed with HFSS and treated with metformin from 20 to 22 months of age, resembling human aging from 56 to 68 years of age (an entry phase of the aged portion of lifespan). RESULTS: The motor and sensory cortexes in mice during aging after HFSS diet showed: (A) decreased motor‐muscular and sensory functions; (B) reduced inflammation‐resolving Arg‐1(+) microglia; (C) increased inflammatory iNOs(+) microglia and TNFα levels; (D) enhanced abundance of amyloid‐β peptide and of phosphorylated Tau. Metformin attenuated these changes. CONCLUSION: A HFSS‐combined diet caused motor‐muscular and sensory dysfunctions, neuroinflammation, and neurodegeneration, whereas metformin counteracted these effects. Our findings show neuroinflammatory consequences of a HFSS diet in aging. Metformin curbs the HFSS‐related neuroinflammation eliciting neuroprotection. John Wiley and Sons Inc. 2021-09-12 /pmc/articles/PMC8611779/ /pubmed/34510763 http://dx.doi.org/10.1111/cns.13726 Text en © 2021 The Authors. CNS Neuroscience & Therapeutics published by 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 Original Articles
Hong, Song
Nagayach, Aarti
Lu, Yan
Peng, Hongying
Duong, Quoc‐Viet A.
Pham, Nicholas B.
Vuong, Christopher A.
Bazan, Nicolas G.
A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin
title A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin
title_full A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin
title_fullStr A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin
title_full_unstemmed A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin
title_short A high fat, sugar, and salt Western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: Ameliorative action of metformin
title_sort high fat, sugar, and salt western diet induces motor‐muscular and sensory dysfunctions and neurodegeneration in mice during aging: ameliorative action of metformin
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611779/
https://www.ncbi.nlm.nih.gov/pubmed/34510763
http://dx.doi.org/10.1111/cns.13726
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