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Non-electrophilic TRPA1 agonists, menthol, carvacrol and clotrimazole, open epithelial tight junctions via TRPA1 activation
Abstract Activation of the transient receptor potential A1 channel (TRPA1) by electrophilic agonists was reported to induce the opening of tight junctions (TJs). Because compounds that increase TJ permeability can be paracellular permeability enhancers, we investigated the effect of non-electrophili...
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Published in: | Journal of biochemistry (Tokyo) 2020-10, Vol.168 (4), p.407-415 |
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container_title | Journal of biochemistry (Tokyo) |
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creator | Mukaiyama, Minagi Usui, Takeo Nagumo, Yoko |
description | Abstract
Activation of the transient receptor potential A1 channel (TRPA1) by electrophilic agonists was reported to induce the opening of tight junctions (TJs). Because compounds that increase TJ permeability can be paracellular permeability enhancers, we investigated the effect of non-electrophilic TRPA1 activators, including food ingredients (menthol and carvacrol) and medication (clotrimazole), on epithelial permeability. We show that all three compounds induced increase of the permeability of fluorescein isothiocyanate-conjugated dextran (4 kDa) and decrease of transepithelial electrical resistance, accompanied by Ca2+ influx and cofilin activation in epithelial MDCK II monolayers. These phenotypes were attenuated by pretreatment of a TRPA1 antagonist, suggesting TRPA1-mediated opening of TJs. These results suggest that non-electrophilic TRPA1 activators with established safety can be utilized to regulate epithelial barriers. |
doi_str_mv | 10.1093/jb/mvaa057 |
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Activation of the transient receptor potential A1 channel (TRPA1) by electrophilic agonists was reported to induce the opening of tight junctions (TJs). Because compounds that increase TJ permeability can be paracellular permeability enhancers, we investigated the effect of non-electrophilic TRPA1 activators, including food ingredients (menthol and carvacrol) and medication (clotrimazole), on epithelial permeability. We show that all three compounds induced increase of the permeability of fluorescein isothiocyanate-conjugated dextran (4 kDa) and decrease of transepithelial electrical resistance, accompanied by Ca2+ influx and cofilin activation in epithelial MDCK II monolayers. These phenotypes were attenuated by pretreatment of a TRPA1 antagonist, suggesting TRPA1-mediated opening of TJs. These results suggest that non-electrophilic TRPA1 activators with established safety can be utilized to regulate epithelial barriers.</description><identifier>ISSN: 0021-924X</identifier><identifier>EISSN: 1756-2651</identifier><identifier>DOI: 10.1093/jb/mvaa057</identifier><identifier>PMID: 32428205</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Animals ; Antifungal Agents - pharmacology ; Antipruritics - pharmacology ; Cells, Cultured ; Clotrimazole - pharmacology ; Cymenes - pharmacology ; Dogs ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Menthol - pharmacology ; Tight Junctions - drug effects ; Tight Junctions - metabolism ; TRPA1 Cation Channel - agonists ; TRPA1 Cation Channel - metabolism</subject><ispartof>Journal of biochemistry (Tokyo), 2020-10, Vol.168 (4), p.407-415</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the Japanese Biochemical Society. All rights reserved 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of the Japanese Biochemical Society. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-a48ef35c11e4df2ca20ac5068876944b4899912adf948cd94d326ad3718d75d23</citedby><cites>FETCH-LOGICAL-c368t-a48ef35c11e4df2ca20ac5068876944b4899912adf948cd94d326ad3718d75d23</cites><orcidid>0000-0002-6266-0181</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32428205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukaiyama, Minagi</creatorcontrib><creatorcontrib>Usui, Takeo</creatorcontrib><creatorcontrib>Nagumo, Yoko</creatorcontrib><title>Non-electrophilic TRPA1 agonists, menthol, carvacrol and clotrimazole, open epithelial tight junctions via TRPA1 activation</title><title>Journal of biochemistry (Tokyo)</title><addtitle>J Biochem</addtitle><description>Abstract
Activation of the transient receptor potential A1 channel (TRPA1) by electrophilic agonists was reported to induce the opening of tight junctions (TJs). Because compounds that increase TJ permeability can be paracellular permeability enhancers, we investigated the effect of non-electrophilic TRPA1 activators, including food ingredients (menthol and carvacrol) and medication (clotrimazole), on epithelial permeability. We show that all three compounds induced increase of the permeability of fluorescein isothiocyanate-conjugated dextran (4 kDa) and decrease of transepithelial electrical resistance, accompanied by Ca2+ influx and cofilin activation in epithelial MDCK II monolayers. These phenotypes were attenuated by pretreatment of a TRPA1 antagonist, suggesting TRPA1-mediated opening of TJs. These results suggest that non-electrophilic TRPA1 activators with established safety can be utilized to regulate epithelial barriers.</description><subject>Animals</subject><subject>Antifungal Agents - pharmacology</subject><subject>Antipruritics - pharmacology</subject><subject>Cells, Cultured</subject><subject>Clotrimazole - pharmacology</subject><subject>Cymenes - pharmacology</subject><subject>Dogs</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Menthol - pharmacology</subject><subject>Tight Junctions - drug effects</subject><subject>Tight Junctions - metabolism</subject><subject>TRPA1 Cation Channel - agonists</subject><subject>TRPA1 Cation Channel - metabolism</subject><issn>0021-924X</issn><issn>1756-2651</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEtLAzEUhYMoWh8bf4BkI4h0NK95LUvxBaIiFdwNt0nGpmQm4yQzoP55p7R16epyDx8fnIPQKSVXlOT8ejm_rnoAEqc7aETTOIlYEtNdNCKE0Shn4v0AHXq_XL2M8310wJlgGSPxCP08uTrSVsvQumZhrJF49voyoRg-XG188GNc6TosnB1jCW0PsnUWQ62wtC60poJvZ_UYu0bXWDcmLLQ1YHEwH4uAl10tg3G1x72BrXhIelilx2ivBOv1yeYeobfbm9n0Pnp8vnuYTh4jyZMsRCAyXfJYUqqFKpkERkDGJMmyNMmFmIssz3PKQJW5yKTKheIsAcVTmqk0VowfoYu1t2ndZ6d9KCrjpbYWau06XzBBYk5SwpIBvVyjQ03vW10Wzapj-1VQUqzGLpbzYjP2AJ9tvN280uoP3a47AOdrwHXNf6JfUPyItw</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Mukaiyama, Minagi</creator><creator>Usui, Takeo</creator><creator>Nagumo, Yoko</creator><general>Oxford University Press</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>7X8</scope><orcidid>https://orcid.org/0000-0002-6266-0181</orcidid></search><sort><creationdate>20201001</creationdate><title>Non-electrophilic TRPA1 agonists, menthol, carvacrol and clotrimazole, open epithelial tight junctions via TRPA1 activation</title><author>Mukaiyama, Minagi ; Usui, Takeo ; Nagumo, Yoko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-a48ef35c11e4df2ca20ac5068876944b4899912adf948cd94d326ad3718d75d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Antifungal Agents - pharmacology</topic><topic>Antipruritics - pharmacology</topic><topic>Cells, Cultured</topic><topic>Clotrimazole - pharmacology</topic><topic>Cymenes - pharmacology</topic><topic>Dogs</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Menthol - pharmacology</topic><topic>Tight Junctions - drug effects</topic><topic>Tight Junctions - metabolism</topic><topic>TRPA1 Cation Channel - agonists</topic><topic>TRPA1 Cation Channel - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukaiyama, Minagi</creatorcontrib><creatorcontrib>Usui, Takeo</creatorcontrib><creatorcontrib>Nagumo, Yoko</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biochemistry (Tokyo)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukaiyama, Minagi</au><au>Usui, Takeo</au><au>Nagumo, Yoko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Non-electrophilic TRPA1 agonists, menthol, carvacrol and clotrimazole, open epithelial tight junctions via TRPA1 activation</atitle><jtitle>Journal of biochemistry (Tokyo)</jtitle><addtitle>J Biochem</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>168</volume><issue>4</issue><spage>407</spage><epage>415</epage><pages>407-415</pages><issn>0021-924X</issn><eissn>1756-2651</eissn><abstract>Abstract
Activation of the transient receptor potential A1 channel (TRPA1) by electrophilic agonists was reported to induce the opening of tight junctions (TJs). Because compounds that increase TJ permeability can be paracellular permeability enhancers, we investigated the effect of non-electrophilic TRPA1 activators, including food ingredients (menthol and carvacrol) and medication (clotrimazole), on epithelial permeability. We show that all three compounds induced increase of the permeability of fluorescein isothiocyanate-conjugated dextran (4 kDa) and decrease of transepithelial electrical resistance, accompanied by Ca2+ influx and cofilin activation in epithelial MDCK II monolayers. These phenotypes were attenuated by pretreatment of a TRPA1 antagonist, suggesting TRPA1-mediated opening of TJs. These results suggest that non-electrophilic TRPA1 activators with established safety can be utilized to regulate epithelial barriers.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>32428205</pmid><doi>10.1093/jb/mvaa057</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6266-0181</orcidid></addata></record> |
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subjects | Animals Antifungal Agents - pharmacology Antipruritics - pharmacology Cells, Cultured Clotrimazole - pharmacology Cymenes - pharmacology Dogs Epithelial Cells - drug effects Epithelial Cells - metabolism Menthol - pharmacology Tight Junctions - drug effects Tight Junctions - metabolism TRPA1 Cation Channel - agonists TRPA1 Cation Channel - metabolism |
title | Non-electrophilic TRPA1 agonists, menthol, carvacrol and clotrimazole, open epithelial tight junctions via TRPA1 activation |
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