Effects of transient receptor potential (TRP) channel agonists and antagonists on slowly adapting type II mechanoreceptors in the rat sinus hair follicle
The possible functional role of transient receptor potential (TRP) channels was investigated by testing various TRP agonists and antagonists in an isolated rat sinus hair follicle preparation. Extracellular recordings from slowly adapting type II mechanoreceptor units were made. The antagonist capsa...
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description | The possible functional role of transient receptor potential (TRP) channels was investigated by testing various TRP agonists and antagonists in an isolated rat sinus hair follicle preparation. Extracellular recordings from slowly adapting type II mechanoreceptor units were made. The antagonist capsazepine depressed spontaneous and mechanically evoked activity, with an IC50 of 82 µM. In one‐third of units, capsazepine caused a selective depression of mechanically evoked firing, such that the existing spontaneous firing was interrupted by an absence of activity during the mechanical stimulus. The broad spectrum TRP blocker ruthenium red (30 µM) had inconsistent effects, although in some units a delayed onset (following wash) bursting and paroxysmal firing ensued. The agonist icilin (50–100 µM) had an excitatory effect on spontaneous firing, and (‐)‐menthol (200 µM) had inconsistent effects. Cinnamaldehyde (1–2 mM) depressed all types of activity equally, mechanically evoked and spontaneous. Camphor (0.5–2 mM) also depressed all types of activity, although it had a preferential effect on spontaneous activity. Capsaicin (1–10 µM) and allyl isothiocyanate (50–100 µM) had no clear effects. These results rule out any role for TRPA1 and TRPV1 channels in mechanotransduction processes of slowly adapting type II mechanoreceptors. |
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Extracellular recordings from slowly adapting type II mechanoreceptor units were made. The antagonist capsazepine depressed spontaneous and mechanically evoked activity, with an IC50 of 82 µM. In one‐third of units, capsazepine caused a selective depression of mechanically evoked firing, such that the existing spontaneous firing was interrupted by an absence of activity during the mechanical stimulus. The broad spectrum TRP blocker ruthenium red (30 µM) had inconsistent effects, although in some units a delayed onset (following wash) bursting and paroxysmal firing ensued. The agonist icilin (50–100 µM) had an excitatory effect on spontaneous firing, and (‐)‐menthol (200 µM) had inconsistent effects. Cinnamaldehyde (1–2 mM) depressed all types of activity equally, mechanically evoked and spontaneous. Camphor (0.5–2 mM) also depressed all types of activity, although it had a preferential effect on spontaneous activity. Capsaicin (1–10 µM) and allyl isothiocyanate (50–100 µM) had no clear effects. These results rule out any role for TRPA1 and TRPV1 channels in mechanotransduction processes of slowly adapting type II mechanoreceptors.</description><identifier>ISSN: 1085-9489</identifier><identifier>EISSN: 1529-8027</identifier><identifier>DOI: 10.1111/j.1529-8027.2009.00242.x</identifier><identifier>PMID: 20021572</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject><![CDATA[Acrolein - administration & dosage ; Acrolein - analogs & derivatives ; Acrolein - pharmacology ; Action Potentials - drug effects ; Animals ; Ankyrins ; Calcium Channels - metabolism ; camphor ; Camphor - administration & dosage ; Camphor - pharmacology ; capsaicin ; Capsaicin - administration & dosage ; Capsaicin - analogs & derivatives ; Capsaicin - pharmacology ; capsazepine ; cinnamaldehyde ; Evoked Potentials - drug effects ; Hair Follicle - drug effects ; Hair Follicle - physiology ; icilin ; In Vitro Techniques ; Isothiocyanates - administration & dosage ; Isothiocyanates - pharmacology ; Male ; mechanogated channels ; Mechanoreceptors - drug effects ; Mechanoreceptors - physiology ; Menthol - pharmacology ; Physical Stimulation ; Pyrimidinones - administration & dosage ; Pyrimidinones - pharmacology ; Rats ; Rats, Wistar ; ruthenium red ; Ruthenium Red - pharmacology ; tetraethylammonium ; Time Factors ; Transient Receptor Potential Channels - agonists ; Transient Receptor Potential Channels - antagonists & inhibitors ; Transient Receptor Potential Channels - metabolism ; TRPA1 Cation Channel ; TRPC Cation Channels ; TRPV Cation Channels - agonists ; TRPV Cation Channels - antagonists & inhibitors ; TRPV Cation Channels - metabolism]]></subject><ispartof>Journal of the peripheral nervous system, 2009-12, Vol.14 (4), p.300-309</ispartof><rights>2009 Peripheral Nerve Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5032-ee3dc08e7e535aba3c77db0f86b451474bf81b333a335d23eefae27ffe47ccb73</citedby><cites>FETCH-LOGICAL-c5032-ee3dc08e7e535aba3c77db0f86b451474bf81b333a335d23eefae27ffe47ccb73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1529-8027.2009.00242.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1529-8027.2009.00242.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20021572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cahusac, Peter M.B.</creatorcontrib><title>Effects of transient receptor potential (TRP) channel agonists and antagonists on slowly adapting type II mechanoreceptors in the rat sinus hair follicle</title><title>Journal of the peripheral nervous system</title><addtitle>J Peripher Nerv Syst</addtitle><description>The possible functional role of transient receptor potential (TRP) channels was investigated by testing various TRP agonists and antagonists in an isolated rat sinus hair follicle preparation. Extracellular recordings from slowly adapting type II mechanoreceptor units were made. The antagonist capsazepine depressed spontaneous and mechanically evoked activity, with an IC50 of 82 µM. In one‐third of units, capsazepine caused a selective depression of mechanically evoked firing, such that the existing spontaneous firing was interrupted by an absence of activity during the mechanical stimulus. The broad spectrum TRP blocker ruthenium red (30 µM) had inconsistent effects, although in some units a delayed onset (following wash) bursting and paroxysmal firing ensued. The agonist icilin (50–100 µM) had an excitatory effect on spontaneous firing, and (‐)‐menthol (200 µM) had inconsistent effects. Cinnamaldehyde (1–2 mM) depressed all types of activity equally, mechanically evoked and spontaneous. Camphor (0.5–2 mM) also depressed all types of activity, although it had a preferential effect on spontaneous activity. Capsaicin (1–10 µM) and allyl isothiocyanate (50–100 µM) had no clear effects. These results rule out any role for TRPA1 and TRPV1 channels in mechanotransduction processes of slowly adapting type II mechanoreceptors.</description><subject>Acrolein - administration & dosage</subject><subject>Acrolein - analogs & derivatives</subject><subject>Acrolein - pharmacology</subject><subject>Action Potentials - drug effects</subject><subject>Animals</subject><subject>Ankyrins</subject><subject>Calcium Channels - metabolism</subject><subject>camphor</subject><subject>Camphor - administration & dosage</subject><subject>Camphor - pharmacology</subject><subject>capsaicin</subject><subject>Capsaicin - administration & dosage</subject><subject>Capsaicin - analogs & derivatives</subject><subject>Capsaicin - pharmacology</subject><subject>capsazepine</subject><subject>cinnamaldehyde</subject><subject>Evoked Potentials - drug effects</subject><subject>Hair Follicle - drug effects</subject><subject>Hair Follicle - physiology</subject><subject>icilin</subject><subject>In Vitro Techniques</subject><subject>Isothiocyanates - administration & dosage</subject><subject>Isothiocyanates - pharmacology</subject><subject>Male</subject><subject>mechanogated channels</subject><subject>Mechanoreceptors - drug effects</subject><subject>Mechanoreceptors - physiology</subject><subject>Menthol - pharmacology</subject><subject>Physical Stimulation</subject><subject>Pyrimidinones - administration & dosage</subject><subject>Pyrimidinones - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>ruthenium red</subject><subject>Ruthenium Red - pharmacology</subject><subject>tetraethylammonium</subject><subject>Time Factors</subject><subject>Transient Receptor Potential Channels - agonists</subject><subject>Transient Receptor Potential Channels - antagonists & inhibitors</subject><subject>Transient Receptor Potential Channels - metabolism</subject><subject>TRPA1 Cation Channel</subject><subject>TRPC Cation Channels</subject><subject>TRPV Cation Channels - agonists</subject><subject>TRPV Cation Channels - antagonists & inhibitors</subject><subject>TRPV Cation Channels - metabolism</subject><issn>1085-9489</issn><issn>1529-8027</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkctuEzEUhkcIRC_wCsgrLosJvozjmQWLUrUlVVQoLerS8njONA6OPdiOmjwKb4uHtFkiLFk-R_6_Y1lfUSCCJySvj8sJ4bQpa0zFhGLcTDCmFZ1snhWH-4vnucY1L5uqbg6KoxiXGBPRkOZlcZAZSrigh8Xvs74HnSLyPUpBuWjAJRRAw5B8QINPuTfKove33799QHqhnAOL1L13JmZMuS7vtO-9Q9H6B7tFqlNDMu4epe0AaDZDKxhp_zQ7IuNQWgAKKqFo3DqihTIB9d5aoy28Kl70ykZ4_XgeFz_Oz25Pv5Tzrxez05N5qTlmtARgncY1COCMq1YxLUTX4r6ethUnlajaviYtY0wxxjvKAHoFVORfV0LrVrDj4t1u7hD8rzXEJFcmarBWOfDrKAWrKGaYTHPy7T-TlNApZZzkYL0L6uBjDNDLIZiVCltJsBwFyqUcPcnRkxwFyr8C5Sajbx7fWLcr6Pbgk7Ec-LQLPBgL2_8eLC-vbniuMl_u-KwLNntehZ9yKpjg8u7qQtLPl9fi5u5aztkfWVC8LQ</recordid><startdate>200912</startdate><enddate>200912</enddate><creator>Cahusac, Peter M.B.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>200912</creationdate><title>Effects of transient receptor potential (TRP) channel agonists and antagonists on slowly adapting type II mechanoreceptors in the rat sinus hair follicle</title><author>Cahusac, Peter M.B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5032-ee3dc08e7e535aba3c77db0f86b451474bf81b333a335d23eefae27ffe47ccb73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acrolein - administration & dosage</topic><topic>Acrolein - analogs & derivatives</topic><topic>Acrolein - pharmacology</topic><topic>Action Potentials - drug effects</topic><topic>Animals</topic><topic>Ankyrins</topic><topic>Calcium Channels - metabolism</topic><topic>camphor</topic><topic>Camphor - administration & dosage</topic><topic>Camphor - pharmacology</topic><topic>capsaicin</topic><topic>Capsaicin - administration & dosage</topic><topic>Capsaicin - analogs & derivatives</topic><topic>Capsaicin - pharmacology</topic><topic>capsazepine</topic><topic>cinnamaldehyde</topic><topic>Evoked Potentials - drug effects</topic><topic>Hair Follicle - drug effects</topic><topic>Hair Follicle - physiology</topic><topic>icilin</topic><topic>In Vitro Techniques</topic><topic>Isothiocyanates - administration & dosage</topic><topic>Isothiocyanates - pharmacology</topic><topic>Male</topic><topic>mechanogated channels</topic><topic>Mechanoreceptors - drug effects</topic><topic>Mechanoreceptors - physiology</topic><topic>Menthol - pharmacology</topic><topic>Physical Stimulation</topic><topic>Pyrimidinones - administration & dosage</topic><topic>Pyrimidinones - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>ruthenium red</topic><topic>Ruthenium Red - pharmacology</topic><topic>tetraethylammonium</topic><topic>Time Factors</topic><topic>Transient Receptor Potential Channels - agonists</topic><topic>Transient Receptor Potential Channels - antagonists & inhibitors</topic><topic>Transient Receptor Potential Channels - metabolism</topic><topic>TRPA1 Cation Channel</topic><topic>TRPC Cation Channels</topic><topic>TRPV Cation Channels - agonists</topic><topic>TRPV Cation Channels - antagonists & inhibitors</topic><topic>TRPV Cation Channels - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cahusac, Peter M.B.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the peripheral nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cahusac, Peter M.B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of transient receptor potential (TRP) channel agonists and antagonists on slowly adapting type II mechanoreceptors in the rat sinus hair follicle</atitle><jtitle>Journal of the peripheral nervous system</jtitle><addtitle>J Peripher Nerv Syst</addtitle><date>2009-12</date><risdate>2009</risdate><volume>14</volume><issue>4</issue><spage>300</spage><epage>309</epage><pages>300-309</pages><issn>1085-9489</issn><eissn>1529-8027</eissn><abstract>The possible functional role of transient receptor potential (TRP) channels was investigated by testing various TRP agonists and antagonists in an isolated rat sinus hair follicle preparation. Extracellular recordings from slowly adapting type II mechanoreceptor units were made. The antagonist capsazepine depressed spontaneous and mechanically evoked activity, with an IC50 of 82 µM. In one‐third of units, capsazepine caused a selective depression of mechanically evoked firing, such that the existing spontaneous firing was interrupted by an absence of activity during the mechanical stimulus. The broad spectrum TRP blocker ruthenium red (30 µM) had inconsistent effects, although in some units a delayed onset (following wash) bursting and paroxysmal firing ensued. The agonist icilin (50–100 µM) had an excitatory effect on spontaneous firing, and (‐)‐menthol (200 µM) had inconsistent effects. Cinnamaldehyde (1–2 mM) depressed all types of activity equally, mechanically evoked and spontaneous. Camphor (0.5–2 mM) also depressed all types of activity, although it had a preferential effect on spontaneous activity. Capsaicin (1–10 µM) and allyl isothiocyanate (50–100 µM) had no clear effects. These results rule out any role for TRPA1 and TRPV1 channels in mechanotransduction processes of slowly adapting type II mechanoreceptors.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20021572</pmid><doi>10.1111/j.1529-8027.2009.00242.x</doi><tpages>10</tpages></addata></record> |
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subjects | Acrolein - administration & dosage Acrolein - analogs & derivatives Acrolein - pharmacology Action Potentials - drug effects Animals Ankyrins Calcium Channels - metabolism camphor Camphor - administration & dosage Camphor - pharmacology capsaicin Capsaicin - administration & dosage Capsaicin - analogs & derivatives Capsaicin - pharmacology capsazepine cinnamaldehyde Evoked Potentials - drug effects Hair Follicle - drug effects Hair Follicle - physiology icilin In Vitro Techniques Isothiocyanates - administration & dosage Isothiocyanates - pharmacology Male mechanogated channels Mechanoreceptors - drug effects Mechanoreceptors - physiology Menthol - pharmacology Physical Stimulation Pyrimidinones - administration & dosage Pyrimidinones - pharmacology Rats Rats, Wistar ruthenium red Ruthenium Red - pharmacology tetraethylammonium Time Factors Transient Receptor Potential Channels - agonists Transient Receptor Potential Channels - antagonists & inhibitors Transient Receptor Potential Channels - metabolism TRPA1 Cation Channel TRPC Cation Channels TRPV Cation Channels - agonists TRPV Cation Channels - antagonists & inhibitors TRPV Cation Channels - metabolism |
title | Effects of transient receptor potential (TRP) channel agonists and antagonists on slowly adapting type II mechanoreceptors in the rat sinus hair follicle |
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