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Modulation of the Circadian Rhythm and Oxidative Stress as Molecular Targets to Improve Vascular Dementia: A Pharmacological Perspective
The circadian rhythms generated by the master biological clock located in the brain's hypothalamus influence central physiological processes. At the molecular level, a core set of clock genes interact to form transcription-translation feedback loops that provide the molecular basis of the circa...
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Published in: | International journal of molecular sciences 2024-04, Vol.25 (8), p.4401 |
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description | The circadian rhythms generated by the master biological clock located in the brain's hypothalamus influence central physiological processes. At the molecular level, a core set of clock genes interact to form transcription-translation feedback loops that provide the molecular basis of the circadian rhythm. In animal models of disease, a desynchronization of clock genes in peripheral tissues with the central master clock has been detected. Interestingly, patients with vascular dementia have sleep disorders and irregular sleep patterns. These alterations in circadian rhythms impact hormonal levels, cardiovascular health (including blood pressure regulation and blood vessel function), and the pattern of expression and activity of antioxidant enzymes. Additionally, oxidative stress in vascular dementia can arise from ischemia-reperfusion injury, amyloid-beta production, the abnormal phosphorylation of tau protein, and alterations in neurotransmitters, among others. Several signaling pathways are involved in the pathogenesis of vascular dementia. While the precise mechanisms linking circadian rhythms and vascular dementia are still being studied, there is evidence to suggest that maintaining healthy sleep patterns and supporting proper circadian rhythm function may be important for reducing the risk of vascular dementia. Here, we reviewed the main mechanisms of action of molecular targets related to the circadian cycle and oxidative stress in vascular dementia. |
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At the molecular level, a core set of clock genes interact to form transcription-translation feedback loops that provide the molecular basis of the circadian rhythm. In animal models of disease, a desynchronization of clock genes in peripheral tissues with the central master clock has been detected. Interestingly, patients with vascular dementia have sleep disorders and irregular sleep patterns. These alterations in circadian rhythms impact hormonal levels, cardiovascular health (including blood pressure regulation and blood vessel function), and the pattern of expression and activity of antioxidant enzymes. Additionally, oxidative stress in vascular dementia can arise from ischemia-reperfusion injury, amyloid-beta production, the abnormal phosphorylation of tau protein, and alterations in neurotransmitters, among others. Several signaling pathways are involved in the pathogenesis of vascular dementia. While the precise mechanisms linking circadian rhythms and vascular dementia are still being studied, there is evidence to suggest that maintaining healthy sleep patterns and supporting proper circadian rhythm function may be important for reducing the risk of vascular dementia. Here, we reviewed the main mechanisms of action of molecular targets related to the circadian cycle and oxidative stress in vascular dementia.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms25084401</identifier><identifier>PMID: 38673986</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Analysis ; Animals ; Antioxidants ; Atherosclerosis ; Binswanger's disease ; Biological clocks ; Blood pressure ; Body temperature ; Circadian Clocks - genetics ; Circadian Rhythm ; Dementia ; Dementia, Vascular - metabolism ; Development and progression ; Disease ; Genes ; Genetic aspects ; Genetic engineering ; Genetic transcription ; Heart attacks ; Hormones ; Humans ; Melatonin ; Memory ; Metabolism ; Neurophysiology ; Oxidative Stress ; Physiological aspects ; Physiology ; Sapropterin dihydrochloride ; Sleep disorders ; Vascular dementia</subject><ispartof>International journal of molecular sciences, 2024-04, Vol.25 (8), p.4401</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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At the molecular level, a core set of clock genes interact to form transcription-translation feedback loops that provide the molecular basis of the circadian rhythm. In animal models of disease, a desynchronization of clock genes in peripheral tissues with the central master clock has been detected. Interestingly, patients with vascular dementia have sleep disorders and irregular sleep patterns. These alterations in circadian rhythms impact hormonal levels, cardiovascular health (including blood pressure regulation and blood vessel function), and the pattern of expression and activity of antioxidant enzymes. Additionally, oxidative stress in vascular dementia can arise from ischemia-reperfusion injury, amyloid-beta production, the abnormal phosphorylation of tau protein, and alterations in neurotransmitters, among others. Several signaling pathways are involved in the pathogenesis of vascular dementia. While the precise mechanisms linking circadian rhythms and vascular dementia are still being studied, there is evidence to suggest that maintaining healthy sleep patterns and supporting proper circadian rhythm function may be important for reducing the risk of vascular dementia. 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While the precise mechanisms linking circadian rhythms and vascular dementia are still being studied, there is evidence to suggest that maintaining healthy sleep patterns and supporting proper circadian rhythm function may be important for reducing the risk of vascular dementia. Here, we reviewed the main mechanisms of action of molecular targets related to the circadian cycle and oxidative stress in vascular dementia.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38673986</pmid><doi>10.3390/ijms25084401</doi><orcidid>https://orcid.org/0000-0002-3769-5649</orcidid><orcidid>https://orcid.org/0000-0001-8087-3597</orcidid><orcidid>https://orcid.org/0009-0004-5528-1898</orcidid><orcidid>https://orcid.org/0000-0002-4105-4641</orcidid><orcidid>https://orcid.org/0000-0002-1968-4815</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Animals Antioxidants Atherosclerosis Binswanger's disease Biological clocks Blood pressure Body temperature Circadian Clocks - genetics Circadian Rhythm Dementia Dementia, Vascular - metabolism Development and progression Disease Genes Genetic aspects Genetic engineering Genetic transcription Heart attacks Hormones Humans Melatonin Memory Metabolism Neurophysiology Oxidative Stress Physiological aspects Physiology Sapropterin dihydrochloride Sleep disorders Vascular dementia |
title | Modulation of the Circadian Rhythm and Oxidative Stress as Molecular Targets to Improve Vascular Dementia: A Pharmacological Perspective |
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