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Latexin expression in smaller diameter primary sensory neurons in the rat
Most of the smaller diameter neurons of dorsal root and trigeminal ganglia in adult rats expressed latexin, which has the inhibitor activity of carboxypeptidase A. Most of the dorsal root ganglion (DRG) neurons containing either calcitonin gene-related peptide (CGRP), substance P (SP) or somatostati...
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Published in: | Brain research 1998-08, Vol.801 (1), p.9-20 |
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description | Most of the smaller diameter neurons of dorsal root and trigeminal ganglia in adult rats expressed latexin, which has the inhibitor activity of carboxypeptidase A. Most of the dorsal root ganglion (DRG) neurons containing either calcitonin gene-related peptide (CGRP), substance P (SP) or somatostatin (SST) coexpressed latexin. Latexin was widely distributed in the cytoplasm of the cell body and in axonal fibers of cultured DRG neurons which were sensitive to capsaicin. In addition, latexin-immunoreactivity was observed throughout lamina II of the spinal cord in normal animals, but was lost following sciatic nerve-axotomy, suggesting the presence of latexin-immunoreactive axonal fibers and/or terminals from DRG neurons. Immunoelectron microscopy indeed revealed latexin-immunoreactive axonal terminals and thinly myelinated and unmyelinated axonal fibers within the dorsal horn. These observations suggest that latexin may be involved in nociceptive information transmission or its modulation. |
doi_str_mv | 10.1016/S0006-8993(98)00496-X |
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Most of the dorsal root ganglion (DRG) neurons containing either calcitonin gene-related peptide (CGRP), substance P (SP) or somatostatin (SST) coexpressed latexin. Latexin was widely distributed in the cytoplasm of the cell body and in axonal fibers of cultured DRG neurons which were sensitive to capsaicin. In addition, latexin-immunoreactivity was observed throughout lamina II of the spinal cord in normal animals, but was lost following sciatic nerve-axotomy, suggesting the presence of latexin-immunoreactive axonal fibers and/or terminals from DRG neurons. Immunoelectron microscopy indeed revealed latexin-immunoreactive axonal terminals and thinly myelinated and unmyelinated axonal fibers within the dorsal horn. These observations suggest that latexin may be involved in nociceptive information transmission or its modulation.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/S0006-8993(98)00496-X</identifier><identifier>PMID: 9729242</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Animals ; Antigens - analysis ; Antigens - biosynthesis ; Biological and medical sciences ; Blotting, Western ; Capsaicin - pharmacology ; Cells, Cultured ; Dorsal root ganglion ; Fundamental and applied biological sciences. Psychology ; Ganglia, Spinal - chemistry ; Ganglia, Spinal - cytology ; Ganglia, Spinal - drug effects ; Immunohistochemistry ; Microscopy, Immunoelectron ; Nerve Tissue Proteins ; Neurons, Afferent - chemistry ; Neurons, Afferent - cytology ; Neurons, Afferent - ultrastructure ; Nociceptors - chemistry ; Nociceptors - cytology ; Pain ; Rats ; Rats, Wistar ; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors ; Spinal cord ; Spinal Cord - cytology ; Spinal Cord - ultrastructure ; Trigeminal ganglion ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research, 1998-08, Vol.801 (1), p.9-20</ispartof><rights>1998 Elsevier Science B.V.</rights><rights>1998 INIST-CNRS</rights><rights>Copyright 1998 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-e61a6e3670b95477cfbc52be1d459eb34718746bfe2810d1bf569cc22eb6e3b63</citedby><cites>FETCH-LOGICAL-c420t-e61a6e3670b95477cfbc52be1d459eb34718746bfe2810d1bf569cc22eb6e3b63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2338390$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9729242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takiguchi-Hayashi, Keiko</creatorcontrib><creatorcontrib>Sato, Michio</creatorcontrib><creatorcontrib>Sugo, Noriyuki</creatorcontrib><creatorcontrib>Ishida, Mami</creatorcontrib><creatorcontrib>Sato, Kazuki</creatorcontrib><creatorcontrib>Uratani, Yoshihiko</creatorcontrib><creatorcontrib>Arimatsu, Yasuyoshi</creatorcontrib><title>Latexin expression in smaller diameter primary sensory neurons in the rat</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Most of the smaller diameter neurons of dorsal root and trigeminal ganglia in adult rats expressed latexin, which has the inhibitor activity of carboxypeptidase A. Most of the dorsal root ganglion (DRG) neurons containing either calcitonin gene-related peptide (CGRP), substance P (SP) or somatostatin (SST) coexpressed latexin. Latexin was widely distributed in the cytoplasm of the cell body and in axonal fibers of cultured DRG neurons which were sensitive to capsaicin. In addition, latexin-immunoreactivity was observed throughout lamina II of the spinal cord in normal animals, but was lost following sciatic nerve-axotomy, suggesting the presence of latexin-immunoreactive axonal fibers and/or terminals from DRG neurons. Immunoelectron microscopy indeed revealed latexin-immunoreactive axonal terminals and thinly myelinated and unmyelinated axonal fibers within the dorsal horn. These observations suggest that latexin may be involved in nociceptive information transmission or its modulation.</description><subject>Animals</subject><subject>Antigens - analysis</subject><subject>Antigens - biosynthesis</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Capsaicin - pharmacology</subject><subject>Cells, Cultured</subject><subject>Dorsal root ganglion</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Ganglia, Spinal - chemistry</subject><subject>Ganglia, Spinal - cytology</subject><subject>Ganglia, Spinal - drug effects</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Immunoelectron</subject><subject>Nerve Tissue Proteins</subject><subject>Neurons, Afferent - chemistry</subject><subject>Neurons, Afferent - cytology</subject><subject>Neurons, Afferent - ultrastructure</subject><subject>Nociceptors - chemistry</subject><subject>Nociceptors - cytology</subject><subject>Pain</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</subject><subject>Spinal cord</subject><subject>Spinal Cord - cytology</subject><subject>Spinal Cord - ultrastructure</subject><subject>Trigeminal ganglion</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkUtLxDAQgIMouj5-gtCDiB6qeTVtTiLiCxY8qOAtJOkUI32sma7ovzfrlr16mgzzTSbzhZBjRi8YZerymVKq8kprcaarc0qlVvnbFpmxquS54pJuk9kG2SP7iB8pFULTXbKrS6655DPyOLcjfIc-g-9FBMQw9FnKsLNtCzGrg-1gTIdFDJ2NPxlCj0OKPSzj0OOKHd8hi3Y8JDuNbRGOpnhAXu9uX24e8vnT_ePN9Tz3ktMxB8WsAqFK6nQhy9I3zhfcAatlocEJWaYFpHIN8IrRmrmmUNp7zsGlNqfEATld37uIw-cScDRdQA9ta3sYlmhKUWmmOf0XZErqRIoEFmvQxwExQmOmbQ2jZuXa_Lk2K5FGV-bPtXlLfcfTgKXroN50TXJT_WSqW_S2baLtfcANxoWo0m8k7GqNQbL2FSAa9AF6D3WI4EdTD-Gfh_wCSbGbpA</recordid><startdate>19980810</startdate><enddate>19980810</enddate><creator>Takiguchi-Hayashi, Keiko</creator><creator>Sato, Michio</creator><creator>Sugo, Noriyuki</creator><creator>Ishida, Mami</creator><creator>Sato, Kazuki</creator><creator>Uratani, Yoshihiko</creator><creator>Arimatsu, Yasuyoshi</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</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>19980810</creationdate><title>Latexin expression in smaller diameter primary sensory neurons in the rat</title><author>Takiguchi-Hayashi, Keiko ; Sato, Michio ; Sugo, Noriyuki ; Ishida, Mami ; Sato, Kazuki ; Uratani, Yoshihiko ; Arimatsu, Yasuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-e61a6e3670b95477cfbc52be1d459eb34718746bfe2810d1bf569cc22eb6e3b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antigens - analysis</topic><topic>Antigens - biosynthesis</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Capsaicin - pharmacology</topic><topic>Cells, Cultured</topic><topic>Dorsal root ganglion</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Spinal - chemistry</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - drug effects</topic><topic>Immunohistochemistry</topic><topic>Microscopy, Immunoelectron</topic><topic>Nerve Tissue Proteins</topic><topic>Neurons, Afferent - chemistry</topic><topic>Neurons, Afferent - cytology</topic><topic>Neurons, Afferent - ultrastructure</topic><topic>Nociceptors - chemistry</topic><topic>Nociceptors - cytology</topic><topic>Pain</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</topic><topic>Spinal cord</topic><topic>Spinal Cord - cytology</topic><topic>Spinal Cord - ultrastructure</topic><topic>Trigeminal ganglion</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takiguchi-Hayashi, Keiko</creatorcontrib><creatorcontrib>Sato, Michio</creatorcontrib><creatorcontrib>Sugo, Noriyuki</creatorcontrib><creatorcontrib>Ishida, Mami</creatorcontrib><creatorcontrib>Sato, Kazuki</creatorcontrib><creatorcontrib>Uratani, Yoshihiko</creatorcontrib><creatorcontrib>Arimatsu, Yasuyoshi</creatorcontrib><collection>Pascal-Francis</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>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takiguchi-Hayashi, Keiko</au><au>Sato, Michio</au><au>Sugo, Noriyuki</au><au>Ishida, Mami</au><au>Sato, Kazuki</au><au>Uratani, Yoshihiko</au><au>Arimatsu, Yasuyoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Latexin expression in smaller diameter primary sensory neurons in the rat</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1998-08-10</date><risdate>1998</risdate><volume>801</volume><issue>1</issue><spage>9</spage><epage>20</epage><pages>9-20</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Most of the smaller diameter neurons of dorsal root and trigeminal ganglia in adult rats expressed latexin, which has the inhibitor activity of carboxypeptidase A. Most of the dorsal root ganglion (DRG) neurons containing either calcitonin gene-related peptide (CGRP), substance P (SP) or somatostatin (SST) coexpressed latexin. Latexin was widely distributed in the cytoplasm of the cell body and in axonal fibers of cultured DRG neurons which were sensitive to capsaicin. In addition, latexin-immunoreactivity was observed throughout lamina II of the spinal cord in normal animals, but was lost following sciatic nerve-axotomy, suggesting the presence of latexin-immunoreactive axonal fibers and/or terminals from DRG neurons. Immunoelectron microscopy indeed revealed latexin-immunoreactive axonal terminals and thinly myelinated and unmyelinated axonal fibers within the dorsal horn. These observations suggest that latexin may be involved in nociceptive information transmission or its modulation.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>9729242</pmid><doi>10.1016/S0006-8993(98)00496-X</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Antigens - analysis Antigens - biosynthesis Biological and medical sciences Blotting, Western Capsaicin - pharmacology Cells, Cultured Dorsal root ganglion Fundamental and applied biological sciences. Psychology Ganglia, Spinal - chemistry Ganglia, Spinal - cytology Ganglia, Spinal - drug effects Immunohistochemistry Microscopy, Immunoelectron Nerve Tissue Proteins Neurons, Afferent - chemistry Neurons, Afferent - cytology Neurons, Afferent - ultrastructure Nociceptors - chemistry Nociceptors - cytology Pain Rats Rats, Wistar Somesthesis and somesthetic pathways (proprioception, exteroception, nociception) interoception electrolocation. Sensory receptors Spinal cord Spinal Cord - cytology Spinal Cord - ultrastructure Trigeminal ganglion Vertebrates: nervous system and sense organs |
title | Latexin expression in smaller diameter primary sensory neurons in the rat |
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