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Changes in expression of growth-associated protein-43 in trigeminal ganglion neurons and of the jaw opening reflex following inferior alveolar nerve transection in rats
The aim of the present study was to clarify an involvement of growth‐associated protein‐43 (GAP‐43) in the regeneration of primary afferent trigeminal ganglion (TG) neurons following inferior alveolar nerve transection (IANX). A larger number of GAP‐43 immunoreactive (GAP‐43 IR) TG neurons was obser...
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Published in: | European journal of oral sciences 2013-04, Vol.121 (2), p.86-91 |
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creator | Teramoto, Kohei Tsuboi, Yoshiyuki Shinoda, Masamichi Hitomi, Suzuro Abe, Kimiko Kaji, Kaori Tamagawa, Takaaki Suzuki, Azumi Noma, Noboru Kobayashi, Masayuki Komiyama, Osamu Urata, Kentaro Iwata, Koichi |
description | The aim of the present study was to clarify an involvement of growth‐associated protein‐43 (GAP‐43) in the regeneration of primary afferent trigeminal ganglion (TG) neurons following inferior alveolar nerve transection (IANX). A larger number of GAP‐43 immunoreactive (GAP‐43 IR) TG neurons was observed in rats 3 d after IANX compared with sham rats. Growth‐associated protein‐43 IR TG neurons were also detected for 30 d after IANX, and the number of GAP‐43 IR TG neurons was significantly higher in the IANX model until day 30. The relative number of large (>600 μm2) GAP‐43 IR TG neurons was significantly lower, whereas the relative number of small ( |
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A larger number of GAP‐43 immunoreactive (GAP‐43 IR) TG neurons was observed in rats 3 d after IANX compared with sham rats. Growth‐associated protein‐43 IR TG neurons were also detected for 30 d after IANX, and the number of GAP‐43 IR TG neurons was significantly higher in the IANX model until day 30. The relative number of large (>600 μm2) GAP‐43 IR TG neurons was significantly lower, whereas the relative number of small (<400 μm2) GAP‐43 IR TG neurons was significantly higher than that at day 0 until 30 d after IANX. To evaluate the functional recovery of damaged IAN, the jaw opening reflex (JOR), elicited by the electrical stimulation of the IAN, was measured before and after IANX. Jaw opening reflex occurrence was gradually increased and the relative threshold of electrical stimulation eliciting JOR was gradually decreased over the 30‐d duration of the study. On day 30 after IANX, the JOR occurrence and relative JOR threshold were similar to those in sham rats. The present findings suggest that changes in the expression of GAP‐43 in TG neurons after IANX are involved in regeneration and functional recovery of the transected IAN.</description><identifier>ISSN: 0909-8836</identifier><identifier>EISSN: 1600-0722</identifier><identifier>DOI: 10.1111/eos.12021</identifier><identifier>PMID: 23489897</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Analysis of Variance ; Animals ; Dentistry ; GAP-43 Protein - metabolism ; growth-associated protein-43 ; Immunohistochemistry ; inferior alveolar nerve transection ; jaw opening reflex ; Nerve Regeneration - physiology ; Neurons, Afferent - metabolism ; Rats ; Rats, Sprague-Dawley ; Recovery of Function - physiology ; Reflex, Abnormal - physiology ; trigeminal ganglion ; Trigeminal Ganglion - metabolism ; Trigeminal Nerve Injuries - metabolism</subject><ispartof>European journal of oral sciences, 2013-04, Vol.121 (2), p.86-91</ispartof><rights>2013 Eur J Oral Sci</rights><rights>2013 Eur J Oral Sci.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4291-1e4e0fe797f8b7073786a0cdcbe7c16f3c7f42f83089f5084f94ea41443be93c3</citedby><cites>FETCH-LOGICAL-c4291-1e4e0fe797f8b7073786a0cdcbe7c16f3c7f42f83089f5084f94ea41443be93c3</cites></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/23489897$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Teramoto, Kohei</creatorcontrib><creatorcontrib>Tsuboi, Yoshiyuki</creatorcontrib><creatorcontrib>Shinoda, Masamichi</creatorcontrib><creatorcontrib>Hitomi, Suzuro</creatorcontrib><creatorcontrib>Abe, Kimiko</creatorcontrib><creatorcontrib>Kaji, Kaori</creatorcontrib><creatorcontrib>Tamagawa, Takaaki</creatorcontrib><creatorcontrib>Suzuki, Azumi</creatorcontrib><creatorcontrib>Noma, Noboru</creatorcontrib><creatorcontrib>Kobayashi, Masayuki</creatorcontrib><creatorcontrib>Komiyama, Osamu</creatorcontrib><creatorcontrib>Urata, Kentaro</creatorcontrib><creatorcontrib>Iwata, Koichi</creatorcontrib><title>Changes in expression of growth-associated protein-43 in trigeminal ganglion neurons and of the jaw opening reflex following inferior alveolar nerve transection in rats</title><title>European journal of oral sciences</title><addtitle>Eur J Oral Sci</addtitle><description>The aim of the present study was to clarify an involvement of growth‐associated protein‐43 (GAP‐43) in the regeneration of primary afferent trigeminal ganglion (TG) neurons following inferior alveolar nerve transection (IANX). A larger number of GAP‐43 immunoreactive (GAP‐43 IR) TG neurons was observed in rats 3 d after IANX compared with sham rats. Growth‐associated protein‐43 IR TG neurons were also detected for 30 d after IANX, and the number of GAP‐43 IR TG neurons was significantly higher in the IANX model until day 30. The relative number of large (>600 μm2) GAP‐43 IR TG neurons was significantly lower, whereas the relative number of small (<400 μm2) GAP‐43 IR TG neurons was significantly higher than that at day 0 until 30 d after IANX. To evaluate the functional recovery of damaged IAN, the jaw opening reflex (JOR), elicited by the electrical stimulation of the IAN, was measured before and after IANX. Jaw opening reflex occurrence was gradually increased and the relative threshold of electrical stimulation eliciting JOR was gradually decreased over the 30‐d duration of the study. On day 30 after IANX, the JOR occurrence and relative JOR threshold were similar to those in sham rats. The present findings suggest that changes in the expression of GAP‐43 in TG neurons after IANX are involved in regeneration and functional recovery of the transected IAN.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Dentistry</subject><subject>GAP-43 Protein - metabolism</subject><subject>growth-associated protein-43</subject><subject>Immunohistochemistry</subject><subject>inferior alveolar nerve transection</subject><subject>jaw opening reflex</subject><subject>Nerve Regeneration - physiology</subject><subject>Neurons, Afferent - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Recovery of Function - physiology</subject><subject>Reflex, Abnormal - physiology</subject><subject>trigeminal ganglion</subject><subject>Trigeminal Ganglion - metabolism</subject><subject>Trigeminal Nerve Injuries - metabolism</subject><issn>0909-8836</issn><issn>1600-0722</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kcFuGyEURVHVqnHTLvoDFct2MQkMeIBlZSVplaiRUlddIowfY1IMLoxj54_6mWXiJLuwQULnHXTfRegjJSe0nlNI5YS2pKWv0IR2hDREtO1rNCGKqEZK1h2hd6XcEkIZVeItOmoZl0oqMUH_ZisTeyjYRwz7TYZSfIo4OdzntBtWjSklWW8GWOJNTgP42HA20kP2Pax9NAH3VRHGsQjbnGLBJi5HxbACfGt2OG0g-tjjDC7AHrsUQtqNDz46yD5lbMIdpGByNeQ7qG4TC9hhdNavshnKe_TGmVDgw-N9jH6dn81n35qr64vvs69XjeWtog0FDsSBUMLJhSCCCdkZYpd2AcLSzjErHG-dZEQqNyWSO8XBcMo5W4Bilh2jzwdvTft3C2XQa18shGAipG3RdYVCMso6WtEvB9TmVEoNpzfZr02-15TosRhdi9EPxVT206N2u1jD8pl8aqICpwdg5wPcv2zSZ9c_n5TNYcKXAfbPEyb_0V3NPdW_f1zoeXdzKaZzriX7D5liqoE</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Teramoto, Kohei</creator><creator>Tsuboi, Yoshiyuki</creator><creator>Shinoda, Masamichi</creator><creator>Hitomi, Suzuro</creator><creator>Abe, Kimiko</creator><creator>Kaji, Kaori</creator><creator>Tamagawa, Takaaki</creator><creator>Suzuki, Azumi</creator><creator>Noma, Noboru</creator><creator>Kobayashi, Masayuki</creator><creator>Komiyama, Osamu</creator><creator>Urata, Kentaro</creator><creator>Iwata, Koichi</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>7X8</scope></search><sort><creationdate>201304</creationdate><title>Changes in expression of growth-associated protein-43 in trigeminal ganglion neurons and of the jaw opening reflex following inferior alveolar nerve transection in rats</title><author>Teramoto, Kohei ; Tsuboi, Yoshiyuki ; Shinoda, Masamichi ; Hitomi, Suzuro ; Abe, Kimiko ; Kaji, Kaori ; Tamagawa, Takaaki ; Suzuki, Azumi ; Noma, Noboru ; Kobayashi, Masayuki ; Komiyama, Osamu ; Urata, Kentaro ; Iwata, Koichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4291-1e4e0fe797f8b7073786a0cdcbe7c16f3c7f42f83089f5084f94ea41443be93c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Dentistry</topic><topic>GAP-43 Protein - metabolism</topic><topic>growth-associated protein-43</topic><topic>Immunohistochemistry</topic><topic>inferior alveolar nerve transection</topic><topic>jaw opening reflex</topic><topic>Nerve Regeneration - physiology</topic><topic>Neurons, Afferent - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Recovery of Function - physiology</topic><topic>Reflex, Abnormal - physiology</topic><topic>trigeminal ganglion</topic><topic>Trigeminal Ganglion - metabolism</topic><topic>Trigeminal Nerve Injuries - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Teramoto, Kohei</creatorcontrib><creatorcontrib>Tsuboi, Yoshiyuki</creatorcontrib><creatorcontrib>Shinoda, Masamichi</creatorcontrib><creatorcontrib>Hitomi, Suzuro</creatorcontrib><creatorcontrib>Abe, Kimiko</creatorcontrib><creatorcontrib>Kaji, Kaori</creatorcontrib><creatorcontrib>Tamagawa, Takaaki</creatorcontrib><creatorcontrib>Suzuki, Azumi</creatorcontrib><creatorcontrib>Noma, Noboru</creatorcontrib><creatorcontrib>Kobayashi, Masayuki</creatorcontrib><creatorcontrib>Komiyama, Osamu</creatorcontrib><creatorcontrib>Urata, Kentaro</creatorcontrib><creatorcontrib>Iwata, Koichi</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>MEDLINE - Academic</collection><jtitle>European journal of oral sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teramoto, Kohei</au><au>Tsuboi, Yoshiyuki</au><au>Shinoda, Masamichi</au><au>Hitomi, Suzuro</au><au>Abe, Kimiko</au><au>Kaji, Kaori</au><au>Tamagawa, Takaaki</au><au>Suzuki, Azumi</au><au>Noma, Noboru</au><au>Kobayashi, Masayuki</au><au>Komiyama, Osamu</au><au>Urata, Kentaro</au><au>Iwata, Koichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Changes in expression of growth-associated protein-43 in trigeminal ganglion neurons and of the jaw opening reflex following inferior alveolar nerve transection in rats</atitle><jtitle>European journal of oral sciences</jtitle><addtitle>Eur J Oral Sci</addtitle><date>2013-04</date><risdate>2013</risdate><volume>121</volume><issue>2</issue><spage>86</spage><epage>91</epage><pages>86-91</pages><issn>0909-8836</issn><eissn>1600-0722</eissn><abstract>The aim of the present study was to clarify an involvement of growth‐associated protein‐43 (GAP‐43) in the regeneration of primary afferent trigeminal ganglion (TG) neurons following inferior alveolar nerve transection (IANX). A larger number of GAP‐43 immunoreactive (GAP‐43 IR) TG neurons was observed in rats 3 d after IANX compared with sham rats. Growth‐associated protein‐43 IR TG neurons were also detected for 30 d after IANX, and the number of GAP‐43 IR TG neurons was significantly higher in the IANX model until day 30. The relative number of large (>600 μm2) GAP‐43 IR TG neurons was significantly lower, whereas the relative number of small (<400 μm2) GAP‐43 IR TG neurons was significantly higher than that at day 0 until 30 d after IANX. To evaluate the functional recovery of damaged IAN, the jaw opening reflex (JOR), elicited by the electrical stimulation of the IAN, was measured before and after IANX. Jaw opening reflex occurrence was gradually increased and the relative threshold of electrical stimulation eliciting JOR was gradually decreased over the 30‐d duration of the study. On day 30 after IANX, the JOR occurrence and relative JOR threshold were similar to those in sham rats. The present findings suggest that changes in the expression of GAP‐43 in TG neurons after IANX are involved in regeneration and functional recovery of the transected IAN.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>23489897</pmid><doi>10.1111/eos.12021</doi><tpages>6</tpages></addata></record> |
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subjects | Analysis of Variance Animals Dentistry GAP-43 Protein - metabolism growth-associated protein-43 Immunohistochemistry inferior alveolar nerve transection jaw opening reflex Nerve Regeneration - physiology Neurons, Afferent - metabolism Rats Rats, Sprague-Dawley Recovery of Function - physiology Reflex, Abnormal - physiology trigeminal ganglion Trigeminal Ganglion - metabolism Trigeminal Nerve Injuries - metabolism |
title | Changes in expression of growth-associated protein-43 in trigeminal ganglion neurons and of the jaw opening reflex following inferior alveolar nerve transection in rats |
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