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Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism

The bifunctional enzyme soluble epoxide hydrolase (sEH) is found in all regions of the brain. It has two different catalytic activities, each assigned to one of its terminal domains: the C-terminal domain presents hydrolase activity, whereas the N-terminal domain exhibits phosphatase activity. The e...

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Autores principales: Domingues, Michelle Flores, Callai-Silva, Natalia, Piovesan, Angela Regina, Carlini, Celia Regina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000630/
https://www.ncbi.nlm.nih.gov/pubmed/32063836
http://dx.doi.org/10.3389/fnmol.2019.00325
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author Domingues, Michelle Flores
Callai-Silva, Natalia
Piovesan, Angela Regina
Carlini, Celia Regina
author_facet Domingues, Michelle Flores
Callai-Silva, Natalia
Piovesan, Angela Regina
Carlini, Celia Regina
author_sort Domingues, Michelle Flores
collection PubMed
description The bifunctional enzyme soluble epoxide hydrolase (sEH) is found in all regions of the brain. It has two different catalytic activities, each assigned to one of its terminal domains: the C-terminal domain presents hydrolase activity, whereas the N-terminal domain exhibits phosphatase activity. The enzyme’s C-terminal domain has been linked to cardiovascular protective and anti-inflammatory effects. Cholesterol-related disorders have been associated with sEH, which plays an important role in the metabolism of cholesterol precursors. The role of sEH’s phosphatase activity has been so far poorly investigated in the context of the central nervous system physiology. Given that brain cholesterol disturbances play a role in the onset of Alzheimer’s disease (AD) as well as of other neurodegenerative diseases, understanding the functions of this enzyme could provide pivotal information on the pathophysiology of these conditions. Moreover, the sEH phosphatase domain could represent an underexplored target for drug design and therapeutic strategies to improve symptoms related to neurodegenerative diseases. This review discusses the function of sEH in mammals and its protein structure and catalytic activities. Particular attention was given to the distribution and expression of sEH in the human brain, deepening into the enzyme’s phosphatase activity and its participation in brain cholesterol synthesis. Finally, this review focused on the metabolism of cholesterol and its association with AD.
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spelling pubmed-70006302020-02-14 Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism Domingues, Michelle Flores Callai-Silva, Natalia Piovesan, Angela Regina Carlini, Celia Regina Front Mol Neurosci Neuroscience The bifunctional enzyme soluble epoxide hydrolase (sEH) is found in all regions of the brain. It has two different catalytic activities, each assigned to one of its terminal domains: the C-terminal domain presents hydrolase activity, whereas the N-terminal domain exhibits phosphatase activity. The enzyme’s C-terminal domain has been linked to cardiovascular protective and anti-inflammatory effects. Cholesterol-related disorders have been associated with sEH, which plays an important role in the metabolism of cholesterol precursors. The role of sEH’s phosphatase activity has been so far poorly investigated in the context of the central nervous system physiology. Given that brain cholesterol disturbances play a role in the onset of Alzheimer’s disease (AD) as well as of other neurodegenerative diseases, understanding the functions of this enzyme could provide pivotal information on the pathophysiology of these conditions. Moreover, the sEH phosphatase domain could represent an underexplored target for drug design and therapeutic strategies to improve symptoms related to neurodegenerative diseases. This review discusses the function of sEH in mammals and its protein structure and catalytic activities. Particular attention was given to the distribution and expression of sEH in the human brain, deepening into the enzyme’s phosphatase activity and its participation in brain cholesterol synthesis. Finally, this review focused on the metabolism of cholesterol and its association with AD. Frontiers Media S.A. 2020-01-29 /pmc/articles/PMC7000630/ /pubmed/32063836 http://dx.doi.org/10.3389/fnmol.2019.00325 Text en Copyright © 2020 Domingues, Callai-Silva, Piovesan and Carlini. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Domingues, Michelle Flores
Callai-Silva, Natalia
Piovesan, Angela Regina
Carlini, Celia Regina
Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism
title Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism
title_full Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism
title_fullStr Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism
title_full_unstemmed Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism
title_short Soluble Epoxide Hydrolase and Brain Cholesterol Metabolism
title_sort soluble epoxide hydrolase and brain cholesterol metabolism
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7000630/
https://www.ncbi.nlm.nih.gov/pubmed/32063836
http://dx.doi.org/10.3389/fnmol.2019.00325
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