{"id":1527,"date":"2017-10-20T10:12:18","date_gmt":"2017-10-20T01:12:18","guid":{"rendered":"http:\/\/misterx95.myds.me\/?p=1527"},"modified":"2017-10-20T10:14:47","modified_gmt":"2017-10-20T01:14:47","slug":"17-10-20","status":"publish","type":"post","link":"https:\/\/misterx95.myds.me\/wordpress\/?p=1527","title":{"rendered":"17.10.20"},"content":{"rendered":"<h1><span class=\"highlight\">Involvement<\/span> of <span class=\"highlight\">TRPV4<\/span> in <span class=\"highlight\">Serotonin<\/span>-Evoked Scratching.<\/h1>\n<div class=\"auths\"><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Akiyama%20T%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Akiyama T<\/a><sup>1<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Ivanov%20M%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Ivanov M<\/a><sup>2<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Nagamine%20M%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Nagamine M<\/a><sup>2<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Davoodi%20A%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Davoodi A<\/a><sup>2<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Carstens%20MI%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Carstens MI<\/a><sup>2<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Ikoma%20A%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Ikoma A<\/a><sup>3<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Cevikbas%20F%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Cevikbas F<\/a><sup>3<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Kempkes%20C%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Kempkes C<\/a><sup>3<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Buddenkotte%20J%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Buddenkotte J<\/a><sup>4<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Steinhoff%20M%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Steinhoff M<\/a><sup>5<\/sup>, <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Carstens%20E%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=26763435\">Carstens E<\/a><sup>6<\/sup>.<\/div>\n<div class=\"afflist\">\n<div class=\"ui-helper-reset\"><\/div>\n<div class=\"ui-helper-reset\"><strong>Abstract<\/strong><\/div>\n<\/div>\n<div class=\"abstr\">\n<div class=\"\">\n<p>Several thermosensitive transient receptor potential channels (transient receptor potential vanilloid type-1, -3; transient receptor potential cation channel, subfamily A, member 1) have been implicated in itch. In contrast, the role of transient receptor potential vanilloid type-4 (<span class=\"highlight\">TRPV4<\/span>) in itch is unknown. Therefore, we investigated if <span class=\"highlight\">TRPV4<\/span>, a temperature-sensitive cation channel, plays an important role in acute itch in mice. Four different pruritogens, including <span class=\"highlight\">serotonin<\/span> (5-hydroxytryptamine [5-HT]), histamine, SLIGRL (protease-activated receptors 2\/mas-related G-protein-coupled receptor C11 agonist), and chloroquine (mas-related G-protein-coupled receptor A3 agonist), were intradermally injected into mice and itch-related scratching behavior was assessed. <span class=\"highlight\">TRPV4<\/span> knockout mice exhibited significantly fewer 5-HT-evoked scratching bouts compared with wild-type mice. Notably, no differences between <span class=\"highlight\">TRPV4<\/span> knockout and wild-type mice were observed in the number of scratch bouts elicited by SLIGRL and histamine. Pretreatment with a <span class=\"highlight\">TRPV4<\/span> antagonist significantly attenuated 5-HT-evoked scratching in vivo. Using calcium imaging in cultured primary murine dorsal root ganglion neurons, the response of neurons after 5-HT application, but not other pruritogens, was significantly lower in <span class=\"highlight\">TRPV4<\/span> knockout compared with wild-type mice. A <span class=\"highlight\">TRPV4<\/span> antagonist significantly suppressed 5-HT-evoked responses in dorsal root ganglion cells from wild-type mice. Approximately 90% of 5-HT-sensitive dorsal root ganglion neurons were immunoreactive for an antibody to <span class=\"highlight\">TRPV4<\/span>, as assessed by calcium imaging. These results indicate that 5-HT-induced itch is linked to <span class=\"highlight\">TRPV4<\/span>.<\/p>\n<p><a href=\"http:\/\/misterx95.myds.me\/wordpress\/wp-content\/uploads\/2017\/10\/10.20.-Involvement-of-TRPV4-in-serotonin-evoked-scratching.pdf\">10.20. Involvement of TRPV4 in serotonin-evoked scratching<\/a><\/p>\n<\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Involvement of TRPV4 in Serotonin-Evoked Scratching. Akiyama T1, Ivanov M2, Nagamine M2, Davoodi A2, Carstens MI2, Ikoma A3, Cevikbas F3, Kempkes C3, Buddenkotte J4, Steinhoff M5, Carstens E6. Abstract Several thermosensitive transient receptor potential channels (transient receptor potential vanilloid type-1, -3; transient receptor potential cation channel, subfamily A, member 1) have been implicated in itch. 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