Rho‐associated protein kinases as therapeutic targets for both vascular and parenchymal pathologies in Alzheimer's disease
The causes of late‐onset Alzheimer's disease are unclear and likely multifactorial. Rho‐associated protein kinases (ROCKs) are ubiquitously expressed signaling messengers that mediate a wide array of cellular processes. Interestingly, they play an important role in several vascular and brain pa...
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Veröffentlicht in: | Journal of neurochemistry 2018-03, Vol.144 (5), p.659-668 |
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description | The causes of late‐onset Alzheimer's disease are unclear and likely multifactorial. Rho‐associated protein kinases (ROCKs) are ubiquitously expressed signaling messengers that mediate a wide array of cellular processes. Interestingly, they play an important role in several vascular and brain pathologies implicated in Alzheimer's etiology, including hypertension, hypercholesterolemia, blood–brain barrier disruption, oxidative stress, deposition of vascular and parenchymal amyloid‐beta peptides, tau hyperphosphorylation, and cognitive decline. The current review summarizes the functions of ROCKs with respect to the various risk factors and pathologies on both sides of the blood–brain barrier and present support for targeting ROCK signaling as a multifactorial and multi‐effect approach for the prevention and amelioration of late‐onset Alzheimer's disease.
This article is part of the Special Issue “Vascular Dementia”.
We reviewed evidence that supports using inhibitors of ROCKs to treat Alzheimer Disease (AD). The multifaceted AD pathologies on both sides of the blood–brain barrier can be ameliorated by inhibition of ROCKs providing a potentially viable therapeutic strategy.
This article is part of the Special Issue “Vascular Dementia”. |
doi_str_mv | 10.1111/jnc.14130 |
format | Article |
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This article is part of the Special Issue “Vascular Dementia”.
We reviewed evidence that supports using inhibitors of ROCKs to treat Alzheimer Disease (AD). The multifaceted AD pathologies on both sides of the blood–brain barrier can be ameliorated by inhibition of ROCKs providing a potentially viable therapeutic strategy.
This article is part of the Special Issue “Vascular Dementia”.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/jnc.14130</identifier><identifier>PMID: 28722749</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Alzheimer Disease - metabolism ; Alzheimer Disease - pathology ; Alzheimer Disease - therapy ; Alzheimer's disease ; amyloid‐beta peptide ; Animals ; Blood ; Blood-Brain Barrier - metabolism ; Blood-Brain Barrier - pathology ; Brain ; Brain - blood supply ; Brain - metabolism ; Brain - pathology ; Cognitive ability ; dementia ; Dementia disorders ; Etiology ; Humans ; Hypercholesterolemia ; Hypertension ; Kinases ; Neurodegenerative diseases ; Oxidative stress ; Parenchymal Tissue ; Peptides ; Phosphorylation ; Protein kinase ; rho-Associated Kinases - metabolism ; Risk analysis ; Risk Factors ; ROCK ; Rocks ; Signal Transduction ; Signaling ; tau ; Tau protein ; Therapeutic applications ; Vascular dementia</subject><ispartof>Journal of neurochemistry, 2018-03, Vol.144 (5), p.659-668</ispartof><rights>2017 International Society for Neurochemistry</rights><rights>2017 International Society for Neurochemistry.</rights><rights>Copyright © 2018 International Society for Neurochemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4540-8290d6a3a15fdbbbe98bb1a7f579d6f1a037d57832ac4b81c88a2988d044dcbe3</citedby><cites>FETCH-LOGICAL-c4540-8290d6a3a15fdbbbe98bb1a7f579d6f1a037d57832ac4b81c88a2988d044dcbe3</cites><orcidid>0000-0002-7428-9105</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjnc.14130$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjnc.14130$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,1432,27922,27923,45572,45573,46407,46831</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28722749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lai, Aaron Y.</creatorcontrib><creatorcontrib>McLaurin, JoAnne</creatorcontrib><title>Rho‐associated protein kinases as therapeutic targets for both vascular and parenchymal pathologies in Alzheimer's disease</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>The causes of late‐onset Alzheimer's disease are unclear and likely multifactorial. Rho‐associated protein kinases (ROCKs) are ubiquitously expressed signaling messengers that mediate a wide array of cellular processes. Interestingly, they play an important role in several vascular and brain pathologies implicated in Alzheimer's etiology, including hypertension, hypercholesterolemia, blood–brain barrier disruption, oxidative stress, deposition of vascular and parenchymal amyloid‐beta peptides, tau hyperphosphorylation, and cognitive decline. The current review summarizes the functions of ROCKs with respect to the various risk factors and pathologies on both sides of the blood–brain barrier and present support for targeting ROCK signaling as a multifactorial and multi‐effect approach for the prevention and amelioration of late‐onset Alzheimer's disease.
This article is part of the Special Issue “Vascular Dementia”.
We reviewed evidence that supports using inhibitors of ROCKs to treat Alzheimer Disease (AD). The multifaceted AD pathologies on both sides of the blood–brain barrier can be ameliorated by inhibition of ROCKs providing a potentially viable therapeutic strategy.
This article is part of the Special Issue “Vascular Dementia”.</description><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - therapy</subject><subject>Alzheimer's disease</subject><subject>amyloid‐beta peptide</subject><subject>Animals</subject><subject>Blood</subject><subject>Blood-Brain Barrier - metabolism</subject><subject>Blood-Brain Barrier - pathology</subject><subject>Brain</subject><subject>Brain - blood supply</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Cognitive ability</subject><subject>dementia</subject><subject>Dementia disorders</subject><subject>Etiology</subject><subject>Humans</subject><subject>Hypercholesterolemia</subject><subject>Hypertension</subject><subject>Kinases</subject><subject>Neurodegenerative diseases</subject><subject>Oxidative stress</subject><subject>Parenchymal Tissue</subject><subject>Peptides</subject><subject>Phosphorylation</subject><subject>Protein kinase</subject><subject>rho-Associated Kinases - metabolism</subject><subject>Risk analysis</subject><subject>Risk Factors</subject><subject>ROCK</subject><subject>Rocks</subject><subject>Signal Transduction</subject><subject>Signaling</subject><subject>tau</subject><subject>Tau protein</subject><subject>Therapeutic applications</subject><subject>Vascular dementia</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUtuFDEQhi0EIpPAggsgSyySLDrxqx9eRqOEhyKQEKxb1XZ12kN3e7DdoEEsOAJn5CQxmcACidpULb76VKWfkGecnfFc55vZnHHFJXtAVlzVvFC81A_JijEhCsmUOCCHMW4Y45Wq-GNyIJpaiFrpFfn-fvC_fvyEGL1xkNDSbfAJ3Uw_uRkiRgqRpgEDbHFJztAE4QZTpL0PtPNpoF8gmmWEQGHOyxBwNsNugjHPafCjv3FZkn0X47cB3YThOFLrImb5E_KohzHi0_t-RD5eXX5Yvyqu3718vb64LowqFSsaoZmtQAIve9t1Heqm6zjUfVlrW_UcmKxtWTdSgFFdw03TgNBNY5lS1nQoj8jJ3pt_-7xgTO3kosFxhBn9EluuBZNa1rrK6It_0I1fwpyvawXjmpVc3lGne8oEH2PAvt0GN0HYtZy1vyNpcyTtXSSZfX5vXLoJ7V_yTwYZON8DX92Iu_-b2jdv13vlLX2smBk</recordid><startdate>201803</startdate><enddate>201803</enddate><creator>Lai, Aaron Y.</creator><creator>McLaurin, JoAnne</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7428-9105</orcidid></search><sort><creationdate>201803</creationdate><title>Rho‐associated protein kinases as therapeutic targets for both vascular and parenchymal pathologies in Alzheimer's disease</title><author>Lai, Aaron Y. ; McLaurin, JoAnne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4540-8290d6a3a15fdbbbe98bb1a7f579d6f1a037d57832ac4b81c88a2988d044dcbe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - therapy</topic><topic>Alzheimer's disease</topic><topic>amyloid‐beta peptide</topic><topic>Animals</topic><topic>Blood</topic><topic>Blood-Brain Barrier - metabolism</topic><topic>Blood-Brain Barrier - pathology</topic><topic>Brain</topic><topic>Brain - blood supply</topic><topic>Brain - metabolism</topic><topic>Brain - pathology</topic><topic>Cognitive ability</topic><topic>dementia</topic><topic>Dementia disorders</topic><topic>Etiology</topic><topic>Humans</topic><topic>Hypercholesterolemia</topic><topic>Hypertension</topic><topic>Kinases</topic><topic>Neurodegenerative diseases</topic><topic>Oxidative stress</topic><topic>Parenchymal Tissue</topic><topic>Peptides</topic><topic>Phosphorylation</topic><topic>Protein kinase</topic><topic>rho-Associated Kinases - metabolism</topic><topic>Risk analysis</topic><topic>Risk Factors</topic><topic>ROCK</topic><topic>Rocks</topic><topic>Signal Transduction</topic><topic>Signaling</topic><topic>tau</topic><topic>Tau protein</topic><topic>Therapeutic applications</topic><topic>Vascular dementia</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lai, Aaron Y.</creatorcontrib><creatorcontrib>McLaurin, JoAnne</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lai, Aaron Y.</au><au>McLaurin, JoAnne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rho‐associated protein kinases as therapeutic targets for both vascular and parenchymal pathologies in Alzheimer's disease</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2018-03</date><risdate>2018</risdate><volume>144</volume><issue>5</issue><spage>659</spage><epage>668</epage><pages>659-668</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><abstract>The causes of late‐onset Alzheimer's disease are unclear and likely multifactorial. Rho‐associated protein kinases (ROCKs) are ubiquitously expressed signaling messengers that mediate a wide array of cellular processes. Interestingly, they play an important role in several vascular and brain pathologies implicated in Alzheimer's etiology, including hypertension, hypercholesterolemia, blood–brain barrier disruption, oxidative stress, deposition of vascular and parenchymal amyloid‐beta peptides, tau hyperphosphorylation, and cognitive decline. The current review summarizes the functions of ROCKs with respect to the various risk factors and pathologies on both sides of the blood–brain barrier and present support for targeting ROCK signaling as a multifactorial and multi‐effect approach for the prevention and amelioration of late‐onset Alzheimer's disease.
This article is part of the Special Issue “Vascular Dementia”.
We reviewed evidence that supports using inhibitors of ROCKs to treat Alzheimer Disease (AD). The multifaceted AD pathologies on both sides of the blood–brain barrier can be ameliorated by inhibition of ROCKs providing a potentially viable therapeutic strategy.
This article is part of the Special Issue “Vascular Dementia”.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>28722749</pmid><doi>10.1111/jnc.14130</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-7428-9105</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alzheimer Disease - metabolism Alzheimer Disease - pathology Alzheimer Disease - therapy Alzheimer's disease amyloid‐beta peptide Animals Blood Blood-Brain Barrier - metabolism Blood-Brain Barrier - pathology Brain Brain - blood supply Brain - metabolism Brain - pathology Cognitive ability dementia Dementia disorders Etiology Humans Hypercholesterolemia Hypertension Kinases Neurodegenerative diseases Oxidative stress Parenchymal Tissue Peptides Phosphorylation Protein kinase rho-Associated Kinases - metabolism Risk analysis Risk Factors ROCK Rocks Signal Transduction Signaling tau Tau protein Therapeutic applications Vascular dementia |
title | Rho‐associated protein kinases as therapeutic targets for both vascular and parenchymal pathologies in Alzheimer's disease |
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