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Brain Formaldehyde is Related to Water Intake behavior

A promising strategy for the prevention of Alzheimer’s disease (AD) is the identification of age-related changes that place the brain at risk for the disease. Additionally, AD is associated with chronic dehydration, and one of the significant changes that are known to result in metabolic dysfunction...

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Autores principales: Li, Ting, Su, Tao, He, Yingge, Lu, Jihui, Mo, Weichuan, Wei, Yan, He, Rongqiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JKL International LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036952/
https://www.ncbi.nlm.nih.gov/pubmed/27699080
http://dx.doi.org/10.14336/AD.2016.0323
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author Li, Ting
Su, Tao
He, Yingge
Lu, Jihui
Mo, Weichuan
Wei, Yan
He, Rongqiao
author_facet Li, Ting
Su, Tao
He, Yingge
Lu, Jihui
Mo, Weichuan
Wei, Yan
He, Rongqiao
author_sort Li, Ting
collection PubMed
description A promising strategy for the prevention of Alzheimer’s disease (AD) is the identification of age-related changes that place the brain at risk for the disease. Additionally, AD is associated with chronic dehydration, and one of the significant changes that are known to result in metabolic dysfunction is an increase in the endogenous formaldehyde (FA) level. Here, we demonstrate that the levels of uric formaldehyde in AD patients were markedly increased compared with normal controls. The brain formaldehyde levels of wild-type C57 BL/6 mice increased with age, and these increases were followed by decreases in their drinking frequency and water intake. The serum arginine vasopressin (AVP) concentrations were also maintained at a high level in the 10-month-old mice. An intravenous injection of AVP into the tail induced decreases in the drinking frequency and water intake in the mice, and these decreases were associated with increases in brain formaldehyde levels. An ELISA assay revealed that the AVP injection increased both the protein level and the enzymatic activity of semicarbazide-sensitive amine oxidase (SSAO), which is an enzyme that produces formaldehyde. In contrast, the intraperitoneal injection of formaldehyde increased the serum AVP level by increasing the angiotensin II (ANG II) level, and this change was associated with a marked decrease in water intake behavior. These data suggest that the interaction between formaldehyde and AVP affects the water intake behaviors of mice. Furthermore, the highest concentration of formaldehyde in vivo was observed in the morning. Regular water intake is conducive to eliminating endogenous formaldehyde from the human body, particularly when water is consumed in the morning. Establishing good water intake habits not only effectively eliminates excess formaldehyde and other metabolic products but is also expected to yield valuable approaches to reducing the risk of AD prior to the onset of the disease.
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spelling pubmed-50369522016-10-04 Brain Formaldehyde is Related to Water Intake behavior Li, Ting Su, Tao He, Yingge Lu, Jihui Mo, Weichuan Wei, Yan He, Rongqiao Aging Dis Original Article A promising strategy for the prevention of Alzheimer’s disease (AD) is the identification of age-related changes that place the brain at risk for the disease. Additionally, AD is associated with chronic dehydration, and one of the significant changes that are known to result in metabolic dysfunction is an increase in the endogenous formaldehyde (FA) level. Here, we demonstrate that the levels of uric formaldehyde in AD patients were markedly increased compared with normal controls. The brain formaldehyde levels of wild-type C57 BL/6 mice increased with age, and these increases were followed by decreases in their drinking frequency and water intake. The serum arginine vasopressin (AVP) concentrations were also maintained at a high level in the 10-month-old mice. An intravenous injection of AVP into the tail induced decreases in the drinking frequency and water intake in the mice, and these decreases were associated with increases in brain formaldehyde levels. An ELISA assay revealed that the AVP injection increased both the protein level and the enzymatic activity of semicarbazide-sensitive amine oxidase (SSAO), which is an enzyme that produces formaldehyde. In contrast, the intraperitoneal injection of formaldehyde increased the serum AVP level by increasing the angiotensin II (ANG II) level, and this change was associated with a marked decrease in water intake behavior. These data suggest that the interaction between formaldehyde and AVP affects the water intake behaviors of mice. Furthermore, the highest concentration of formaldehyde in vivo was observed in the morning. Regular water intake is conducive to eliminating endogenous formaldehyde from the human body, particularly when water is consumed in the morning. Establishing good water intake habits not only effectively eliminates excess formaldehyde and other metabolic products but is also expected to yield valuable approaches to reducing the risk of AD prior to the onset of the disease. JKL International LLC 2016-10-01 /pmc/articles/PMC5036952/ /pubmed/27699080 http://dx.doi.org/10.14336/AD.2016.0323 Text en Copyright: © 2016 Li T, et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Original Article
Li, Ting
Su, Tao
He, Yingge
Lu, Jihui
Mo, Weichuan
Wei, Yan
He, Rongqiao
Brain Formaldehyde is Related to Water Intake behavior
title Brain Formaldehyde is Related to Water Intake behavior
title_full Brain Formaldehyde is Related to Water Intake behavior
title_fullStr Brain Formaldehyde is Related to Water Intake behavior
title_full_unstemmed Brain Formaldehyde is Related to Water Intake behavior
title_short Brain Formaldehyde is Related to Water Intake behavior
title_sort brain formaldehyde is related to water intake behavior
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036952/
https://www.ncbi.nlm.nih.gov/pubmed/27699080
http://dx.doi.org/10.14336/AD.2016.0323
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