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Vasoactive Intestinal peptide modulates c-Fos activity in the trigeminal nucleus and dura mater mast cells in sympathectomized rats
Neurogenic inflammation in the dura mater caused by trigeminal nociceptive activation has been implicated in the pathophysiology of migraine. Vasoactive intestinal polypeptide (VIP) is a powerful neuroprotective neuropeptide that can modulate mast cell behavior. Migraine is also associated with symp...
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Published in: | Journal of neuroscience research 2015-04, Vol.93 (4), p.644-650 |
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description | Neurogenic inflammation in the dura mater caused by trigeminal nociceptive activation has been implicated in the pathophysiology of migraine. Vasoactive intestinal polypeptide (VIP) is a powerful neuroprotective neuropeptide that can modulate mast cell behavior. Migraine is also associated with sympathetic insufficiency. This study investigates the effects of VIP on the number of mast cells in the dura mater and on c‐Fos expression in the trigeminal nucleus of sympathectomized rats. Experiments were carried out with 32 Sprague‐Dawley male rats with body weights of 200–250 g. In the sympathectomized group, the left superior cervical sympathetic ganglion was removed. In the sympathectomized + VIP group, postoperative VIP 25 ng/kg/day (0.2 ml) was administered for 5 days. In the sham group, the ganglion and nerves were exposed but not dissected. Dura maters were stained with toluidine blue, and brainstems were labeled by indirect immunohistochemistry for c‐Fos. Sympathectomy significantly increased the number of mast cells in both the ipsilateral and the contralateral dura mater (P |
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Vasoactive intestinal polypeptide (VIP) is a powerful neuroprotective neuropeptide that can modulate mast cell behavior. Migraine is also associated with sympathetic insufficiency. This study investigates the effects of VIP on the number of mast cells in the dura mater and on c‐Fos expression in the trigeminal nucleus of sympathectomized rats. Experiments were carried out with 32 Sprague‐Dawley male rats with body weights of 200–250 g. In the sympathectomized group, the left superior cervical sympathetic ganglion was removed. In the sympathectomized + VIP group, postoperative VIP 25 ng/kg/day (0.2 ml) was administered for 5 days. In the sham group, the ganglion and nerves were exposed but not dissected. Dura maters were stained with toluidine blue, and brainstems were labeled by indirect immunohistochemistry for c‐Fos. Sympathectomy significantly increased the number of mast cells in both the ipsilateral and the contralateral dura mater (P < 0.001). VIP decreased the number of mast cells in both sides of the dura mater in sympathectomized rats. VIP also decreased c‐Fos expression in the ipsilateral trigeminal nucleus of sympathectomized rats (P < 0.001). In the context of an experimental superior cervical ganglionectomy model of migraine, VIP is an efficient modulator of neurogenic inflammation of the dura. © 2014 Wiley Periodicals, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.23523</identifier><identifier>PMID: 25476208</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>and inflammation ; Animals ; Dura Mater - cytology ; Male ; mast cell ; Mast Cells - drug effects ; migraine ; Oncogene Proteins v-fos - metabolism ; Rats ; Rats, Sprague-Dawley ; Statistics, Nonparametric ; Sympathectomy ; Trigeminal Nuclei - drug effects ; Trigeminal Nuclei - metabolism ; Vasoactive Intestinal Peptide - pharmacology ; VIP</subject><ispartof>Journal of neuroscience research, 2015-04, Vol.93 (4), p.644-650</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4603-9affd24a9128a371e1c2125afaeea31b12dad3c41c585a8661eaa18cb2181df73</citedby></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/25476208$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kilinc, Erkan</creatorcontrib><creatorcontrib>Firat, Tülin</creatorcontrib><creatorcontrib>Tore, Fatma</creatorcontrib><creatorcontrib>Kiyan, Aysu</creatorcontrib><creatorcontrib>Kukner, Aysel</creatorcontrib><creatorcontrib>Tunçel, Nese</creatorcontrib><title>Vasoactive Intestinal peptide modulates c-Fos activity in the trigeminal nucleus and dura mater mast cells in sympathectomized rats</title><title>Journal of neuroscience research</title><addtitle>Journal of Neuroscience Research</addtitle><description>Neurogenic inflammation in the dura mater caused by trigeminal nociceptive activation has been implicated in the pathophysiology of migraine. Vasoactive intestinal polypeptide (VIP) is a powerful neuroprotective neuropeptide that can modulate mast cell behavior. Migraine is also associated with sympathetic insufficiency. This study investigates the effects of VIP on the number of mast cells in the dura mater and on c‐Fos expression in the trigeminal nucleus of sympathectomized rats. Experiments were carried out with 32 Sprague‐Dawley male rats with body weights of 200–250 g. In the sympathectomized group, the left superior cervical sympathetic ganglion was removed. In the sympathectomized + VIP group, postoperative VIP 25 ng/kg/day (0.2 ml) was administered for 5 days. In the sham group, the ganglion and nerves were exposed but not dissected. Dura maters were stained with toluidine blue, and brainstems were labeled by indirect immunohistochemistry for c‐Fos. Sympathectomy significantly increased the number of mast cells in both the ipsilateral and the contralateral dura mater (P < 0.001). VIP decreased the number of mast cells in both sides of the dura mater in sympathectomized rats. VIP also decreased c‐Fos expression in the ipsilateral trigeminal nucleus of sympathectomized rats (P < 0.001). In the context of an experimental superior cervical ganglionectomy model of migraine, VIP is an efficient modulator of neurogenic inflammation of the dura. © 2014 Wiley Periodicals, Inc.</description><subject>and inflammation</subject><subject>Animals</subject><subject>Dura Mater - cytology</subject><subject>Male</subject><subject>mast cell</subject><subject>Mast Cells - drug effects</subject><subject>migraine</subject><subject>Oncogene Proteins v-fos - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Statistics, Nonparametric</subject><subject>Sympathectomy</subject><subject>Trigeminal Nuclei - drug effects</subject><subject>Trigeminal Nuclei - metabolism</subject><subject>Vasoactive Intestinal Peptide - pharmacology</subject><subject>VIP</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkc9vFCEUx4nR2LV68B8wJF68TMuDgZk5amNrTbOmRuuRvAVGWeeXwKjr1X9cdrb24MkLkPc-H8LjS8hTYCfAGD_dDuGEC8nFPbIC1lRFKcvqPlkxoVhRMuBH5FGMW8ZY00jxkBzx3Fec1Svy-wbjiCb5745eDsnF5Afs6OSm5K2j_WjnDnOZmuJ8jHQhfdpRP9D0xdEU_GfXL8owm87NGRkstXNA2mcv5DUmalzXxb0Td_2EWTRp7P0vZ2nAFB-TBy120T253Y_Jx_PXH87eFFfvLi7PXl4VplRMFA22reUlNsBrFBU4MBy4xBadQwEb4BatMCUYWUuslQKHCLXZcKjBtpU4Ji8O905h_DbnUXXv4_5pOLhxjhqUYiVUXDX_gUopOWeyzOjzf9DtOIf8IwtVVgKY2lPPbql50zurp-B7DDv9N4kMnB6AH75zu7s-ML2PWOeI9RKxfrt-vxyyURwMH5P7eWdg-KpVJSqpP60v9PoVVDfs-lqD-AO-Xqj2</recordid><startdate>201504</startdate><enddate>201504</enddate><creator>Kilinc, Erkan</creator><creator>Firat, Tülin</creator><creator>Tore, Fatma</creator><creator>Kiyan, Aysu</creator><creator>Kukner, Aysel</creator><creator>Tunçel, Nese</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201504</creationdate><title>Vasoactive Intestinal peptide modulates c-Fos activity in the trigeminal nucleus and dura mater mast cells in sympathectomized rats</title><author>Kilinc, Erkan ; Firat, Tülin ; Tore, Fatma ; Kiyan, Aysu ; Kukner, Aysel ; Tunçel, Nese</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4603-9affd24a9128a371e1c2125afaeea31b12dad3c41c585a8661eaa18cb2181df73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>and inflammation</topic><topic>Animals</topic><topic>Dura Mater - cytology</topic><topic>Male</topic><topic>mast cell</topic><topic>Mast Cells - drug effects</topic><topic>migraine</topic><topic>Oncogene Proteins v-fos - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Statistics, Nonparametric</topic><topic>Sympathectomy</topic><topic>Trigeminal Nuclei - drug effects</topic><topic>Trigeminal Nuclei - metabolism</topic><topic>Vasoactive Intestinal Peptide - pharmacology</topic><topic>VIP</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kilinc, Erkan</creatorcontrib><creatorcontrib>Firat, Tülin</creatorcontrib><creatorcontrib>Tore, Fatma</creatorcontrib><creatorcontrib>Kiyan, Aysu</creatorcontrib><creatorcontrib>Kukner, Aysel</creatorcontrib><creatorcontrib>Tunçel, Nese</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kilinc, Erkan</au><au>Firat, Tülin</au><au>Tore, Fatma</au><au>Kiyan, Aysu</au><au>Kukner, Aysel</au><au>Tunçel, Nese</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vasoactive Intestinal peptide modulates c-Fos activity in the trigeminal nucleus and dura mater mast cells in sympathectomized rats</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>Journal of Neuroscience Research</addtitle><date>2015-04</date><risdate>2015</risdate><volume>93</volume><issue>4</issue><spage>644</spage><epage>650</epage><pages>644-650</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Neurogenic inflammation in the dura mater caused by trigeminal nociceptive activation has been implicated in the pathophysiology of migraine. Vasoactive intestinal polypeptide (VIP) is a powerful neuroprotective neuropeptide that can modulate mast cell behavior. Migraine is also associated with sympathetic insufficiency. This study investigates the effects of VIP on the number of mast cells in the dura mater and on c‐Fos expression in the trigeminal nucleus of sympathectomized rats. Experiments were carried out with 32 Sprague‐Dawley male rats with body weights of 200–250 g. In the sympathectomized group, the left superior cervical sympathetic ganglion was removed. In the sympathectomized + VIP group, postoperative VIP 25 ng/kg/day (0.2 ml) was administered for 5 days. In the sham group, the ganglion and nerves were exposed but not dissected. Dura maters were stained with toluidine blue, and brainstems were labeled by indirect immunohistochemistry for c‐Fos. Sympathectomy significantly increased the number of mast cells in both the ipsilateral and the contralateral dura mater (P < 0.001). VIP decreased the number of mast cells in both sides of the dura mater in sympathectomized rats. VIP also decreased c‐Fos expression in the ipsilateral trigeminal nucleus of sympathectomized rats (P < 0.001). In the context of an experimental superior cervical ganglionectomy model of migraine, VIP is an efficient modulator of neurogenic inflammation of the dura. © 2014 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25476208</pmid><doi>10.1002/jnr.23523</doi><tpages>7</tpages></addata></record> |
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subjects | and inflammation Animals Dura Mater - cytology Male mast cell Mast Cells - drug effects migraine Oncogene Proteins v-fos - metabolism Rats Rats, Sprague-Dawley Statistics, Nonparametric Sympathectomy Trigeminal Nuclei - drug effects Trigeminal Nuclei - metabolism Vasoactive Intestinal Peptide - pharmacology VIP |
title | Vasoactive Intestinal peptide modulates c-Fos activity in the trigeminal nucleus and dura mater mast cells in sympathectomized rats |
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