Parvalbumin, calretinin and carbonic anhydrase in the trigeminal and spinal primary neurons of the rat

The cell-body size of parvalbumin-immunoreactive (-ir) primary neurons was measured in the trigeminal (TG) and lumber dorsal root ganglia (DRG). In the DRG, parvalbumin-ir was mostly detected in large cells (94% in the range of 600–2800 μm 2). Parvalbumin-ir TG cells were smaller than similar DRG ce...

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Veröffentlicht in:Brain research 1994-08, Vol.655 (1), p.241-245
Hauptverfasser: Ichikawa, Hiroyuki, Deguchi, Toru, Nakago, Tadao, Jacobowitz, David M., Sugimoto, Tomosada
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container_issue 1
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container_title Brain research
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creator Ichikawa, Hiroyuki
Deguchi, Toru
Nakago, Tadao
Jacobowitz, David M.
Sugimoto, Tomosada
description The cell-body size of parvalbumin-immunoreactive (-ir) primary neurons was measured in the trigeminal (TG) and lumber dorsal root ganglia (DRG). In the DRG, parvalbumin-ir was mostly detected in large cells (94% in the range of 600–2800 μm 2). Parvalbumin-ir TG cells were smaller than similar DRG cells and yet parvalbumin-ir TG cells of < 400 μm 2 (2.86%) were rare. Trichrome stains for parvalbumin, calretinin (CR) and carbonic anhydrase (CA), and for parvalbumin, calcitonin gene-related peptide (CGRP) and CA were performed to estimate possible overlap of these substances. Virtually all parvalbumin-ir DRG cells contained CA activity while a small subpopulation (28.5%) of CR-ir DRG cells lacked CA activity. All the CR-ir DRG cells that exhibited CA were also ir for parvalbumin. 31.1% of parvalbumin-ir DRG cells exhibited CR-ir while 71.5% of CR-ir DRG cells showed parvalbumin-ir. All the CR-ir DRG cells of < 400 μm 2 lacked CA activity and parvalbumin-ir while all those of > 800 μm 2 exhibited both activities. ∼30% of CR-ir DRG cells in the size range of 400–800 μm 2 co-expressed CA. DRG cel co-expressing parvalbumin and CGRP were rare (∼1%). As was the case for the DRG, most of parvalbumin-ir TG cells exhibited CA activity (89.24%) and lacked CGRP-ir (96.6%). CR-ir TG cells were also subdivided into two groups; one with and the other without co-expression of CA. Unlike in the DRG, however, co-expression of parvalbumin and CR could never be detected in the TG.
doi_str_mv 10.1016/0006-8993(94)91620-9
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In the DRG, parvalbumin-ir was mostly detected in large cells (94% in the range of 600–2800 μm 2). Parvalbumin-ir TG cells were smaller than similar DRG cells and yet parvalbumin-ir TG cells of &lt; 400 μm 2 (2.86%) were rare. Trichrome stains for parvalbumin, calretinin (CR) and carbonic anhydrase (CA), and for parvalbumin, calcitonin gene-related peptide (CGRP) and CA were performed to estimate possible overlap of these substances. Virtually all parvalbumin-ir DRG cells contained CA activity while a small subpopulation (28.5%) of CR-ir DRG cells lacked CA activity. All the CR-ir DRG cells that exhibited CA were also ir for parvalbumin. 31.1% of parvalbumin-ir DRG cells exhibited CR-ir while 71.5% of CR-ir DRG cells showed parvalbumin-ir. All the CR-ir DRG cells of &lt; 400 μm 2 lacked CA activity and parvalbumin-ir while all those of &gt; 800 μm 2 exhibited both activities. ∼30% of CR-ir DRG cells in the size range of 400–800 μm 2 co-expressed CA. DRG cel co-expressing parvalbumin and CGRP were rare (∼1%). As was the case for the DRG, most of parvalbumin-ir TG cells exhibited CA activity (89.24%) and lacked CGRP-ir (96.6%). CR-ir TG cells were also subdivided into two groups; one with and the other without co-expression of CA. Unlike in the DRG, however, co-expression of parvalbumin and CR could never be detected in the TG.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/0006-8993(94)91620-9</identifier><identifier>PMID: 7812779</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; Calbindin 2 ; Calcitonin Gene-Related Peptide - metabolism ; Calretinin ; Carbonic anhydrase ; Carbonic Anhydrases - metabolism ; Cell Size ; Dorsal root ganglion ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; Ganglia, Spinal - cytology ; Ganglia, Spinal - metabolism ; Ganglia, Spinal - ultrastructure ; General aspects. Models. Methods ; Immunohistochemistry ; Male ; Neurons - enzymology ; Neurons - metabolism ; Neurons - ultrastructure ; Parvalbumin ; Parvalbumins - metabolism ; Rat ; Rats ; Rats, Sprague-Dawley ; S100 Calcium Binding Protein G - metabolism ; Trigeminal ganglion ; Trigeminal Ganglion - cytology ; Trigeminal Ganglion - metabolism ; Trigeminal Ganglion - ultrastructure ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research, 1994-08, Vol.655 (1), p.241-245</ispartof><rights>1994</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c483t-2221987d7d1cbf4128ab7d0459d0f70524e840f3b86f4913bd0d1d5e4901b7e03</citedby><cites>FETCH-LOGICAL-c483t-2221987d7d1cbf4128ab7d0459d0f70524e840f3b86f4913bd0d1d5e4901b7e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0006-8993(94)91620-9$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4190546$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7812779$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ichikawa, Hiroyuki</creatorcontrib><creatorcontrib>Deguchi, Toru</creatorcontrib><creatorcontrib>Nakago, Tadao</creatorcontrib><creatorcontrib>Jacobowitz, David M.</creatorcontrib><creatorcontrib>Sugimoto, Tomosada</creatorcontrib><title>Parvalbumin, calretinin and carbonic anhydrase in the trigeminal and spinal primary neurons of the rat</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>The cell-body size of parvalbumin-immunoreactive (-ir) primary neurons was measured in the trigeminal (TG) and lumber dorsal root ganglia (DRG). In the DRG, parvalbumin-ir was mostly detected in large cells (94% in the range of 600–2800 μm 2). Parvalbumin-ir TG cells were smaller than similar DRG cells and yet parvalbumin-ir TG cells of &lt; 400 μm 2 (2.86%) were rare. Trichrome stains for parvalbumin, calretinin (CR) and carbonic anhydrase (CA), and for parvalbumin, calcitonin gene-related peptide (CGRP) and CA were performed to estimate possible overlap of these substances. Virtually all parvalbumin-ir DRG cells contained CA activity while a small subpopulation (28.5%) of CR-ir DRG cells lacked CA activity. All the CR-ir DRG cells that exhibited CA were also ir for parvalbumin. 31.1% of parvalbumin-ir DRG cells exhibited CR-ir while 71.5% of CR-ir DRG cells showed parvalbumin-ir. All the CR-ir DRG cells of &lt; 400 μm 2 lacked CA activity and parvalbumin-ir while all those of &gt; 800 μm 2 exhibited both activities. ∼30% of CR-ir DRG cells in the size range of 400–800 μm 2 co-expressed CA. DRG cel co-expressing parvalbumin and CGRP were rare (∼1%). As was the case for the DRG, most of parvalbumin-ir TG cells exhibited CA activity (89.24%) and lacked CGRP-ir (96.6%). CR-ir TG cells were also subdivided into two groups; one with and the other without co-expression of CA. Unlike in the DRG, however, co-expression of parvalbumin and CR could never be detected in the TG.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calbindin 2</subject><subject>Calcitonin Gene-Related Peptide - metabolism</subject><subject>Calretinin</subject><subject>Carbonic anhydrase</subject><subject>Carbonic Anhydrases - metabolism</subject><subject>Cell Size</subject><subject>Dorsal root ganglion</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. 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Methods</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Neurons - enzymology</subject><subject>Neurons - metabolism</subject><subject>Neurons - ultrastructure</subject><subject>Parvalbumin</subject><subject>Parvalbumins - metabolism</subject><subject>Rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>S100 Calcium Binding Protein G - metabolism</subject><subject>Trigeminal ganglion</subject><subject>Trigeminal Ganglion - cytology</subject><subject>Trigeminal Ganglion - metabolism</subject><subject>Trigeminal Ganglion - ultrastructure</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV9rFDEUxYModa1-A4V5EFHo6E0mkz8vBSlqhUL7oM8hk9zYyGxmTWYK_fZmd4d91Kfkcn7nkJxLyGsKHylQ8QkARKu07t5r_kFTwaDVT8iGKslawTg8JZsT8py8KOV3HbtOwxk5k4oyKfWGhDubH-w4LNuYLhpnx4xzTDE1Nvk65mFK0dXh_tFnW7CpynyPzZzjL6wWOx7AsjtcdzlubX5sEi55SqWZwgHOdn5JngU7Fny1nufk59cvP66u25vbb9-vPt-0jqtubhljVCvppaduCJwyZQfpgffaQ5DQM46KQ-gGJQLXtBs8eOp75BroIBG6c_LumLvL058Fy2y2sTgcR5twWoqRQrNeCP5fkAqpFfB9Ij-CLk-lZAxm_aWhYPZ7MPuSzb5ko7k57MHoanuz5i_DFv3JtBZf9berbkttPWSbXCwnjFMNPRcVuzxiWEt7iJhNcRGTQx8zutn4Kf77HX8BpGaj2A</recordid><startdate>19940829</startdate><enddate>19940829</enddate><creator>Ichikawa, Hiroyuki</creator><creator>Deguchi, Toru</creator><creator>Nakago, Tadao</creator><creator>Jacobowitz, David M.</creator><creator>Sugimoto, Tomosada</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>7QP</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19940829</creationdate><title>Parvalbumin, calretinin and carbonic anhydrase in the trigeminal and spinal primary neurons of the rat</title><author>Ichikawa, Hiroyuki ; Deguchi, Toru ; Nakago, Tadao ; Jacobowitz, David M. ; Sugimoto, Tomosada</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c483t-2221987d7d1cbf4128ab7d0459d0f70524e840f3b86f4913bd0d1d5e4901b7e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calbindin 2</topic><topic>Calcitonin Gene-Related Peptide - metabolism</topic><topic>Calretinin</topic><topic>Carbonic anhydrase</topic><topic>Carbonic Anhydrases - metabolism</topic><topic>Cell Size</topic><topic>Dorsal root ganglion</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Ganglia, Spinal - cytology</topic><topic>Ganglia, Spinal - metabolism</topic><topic>Ganglia, Spinal - ultrastructure</topic><topic>General aspects. Models. Methods</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Neurons - enzymology</topic><topic>Neurons - metabolism</topic><topic>Neurons - ultrastructure</topic><topic>Parvalbumin</topic><topic>Parvalbumins - metabolism</topic><topic>Rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>S100 Calcium Binding Protein G - metabolism</topic><topic>Trigeminal ganglion</topic><topic>Trigeminal Ganglion - cytology</topic><topic>Trigeminal Ganglion - metabolism</topic><topic>Trigeminal Ganglion - ultrastructure</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ichikawa, Hiroyuki</creatorcontrib><creatorcontrib>Deguchi, Toru</creatorcontrib><creatorcontrib>Nakago, Tadao</creatorcontrib><creatorcontrib>Jacobowitz, David M.</creatorcontrib><creatorcontrib>Sugimoto, Tomosada</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>Calcium &amp; Calcified Tissue Abstracts</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>Ichikawa, Hiroyuki</au><au>Deguchi, Toru</au><au>Nakago, Tadao</au><au>Jacobowitz, David M.</au><au>Sugimoto, Tomosada</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parvalbumin, calretinin and carbonic anhydrase in the trigeminal and spinal primary neurons of the rat</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1994-08-29</date><risdate>1994</risdate><volume>655</volume><issue>1</issue><spage>241</spage><epage>245</epage><pages>241-245</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>The cell-body size of parvalbumin-immunoreactive (-ir) primary neurons was measured in the trigeminal (TG) and lumber dorsal root ganglia (DRG). In the DRG, parvalbumin-ir was mostly detected in large cells (94% in the range of 600–2800 μm 2). Parvalbumin-ir TG cells were smaller than similar DRG cells and yet parvalbumin-ir TG cells of &lt; 400 μm 2 (2.86%) were rare. Trichrome stains for parvalbumin, calretinin (CR) and carbonic anhydrase (CA), and for parvalbumin, calcitonin gene-related peptide (CGRP) and CA were performed to estimate possible overlap of these substances. Virtually all parvalbumin-ir DRG cells contained CA activity while a small subpopulation (28.5%) of CR-ir DRG cells lacked CA activity. All the CR-ir DRG cells that exhibited CA were also ir for parvalbumin. 31.1% of parvalbumin-ir DRG cells exhibited CR-ir while 71.5% of CR-ir DRG cells showed parvalbumin-ir. All the CR-ir DRG cells of &lt; 400 μm 2 lacked CA activity and parvalbumin-ir while all those of &gt; 800 μm 2 exhibited both activities. ∼30% of CR-ir DRG cells in the size range of 400–800 μm 2 co-expressed CA. DRG cel co-expressing parvalbumin and CGRP were rare (∼1%). As was the case for the DRG, most of parvalbumin-ir TG cells exhibited CA activity (89.24%) and lacked CGRP-ir (96.6%). CR-ir TG cells were also subdivided into two groups; one with and the other without co-expression of CA. Unlike in the DRG, however, co-expression of parvalbumin and CR could never be detected in the TG.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>7812779</pmid><doi>10.1016/0006-8993(94)91620-9</doi><tpages>5</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Calbindin 2
Calcitonin Gene-Related Peptide - metabolism
Calretinin
Carbonic anhydrase
Carbonic Anhydrases - metabolism
Cell Size
Dorsal root ganglion
Fluorescent Antibody Technique
Fundamental and applied biological sciences. Psychology
Ganglia, Spinal - cytology
Ganglia, Spinal - metabolism
Ganglia, Spinal - ultrastructure
General aspects. Models. Methods
Immunohistochemistry
Male
Neurons - enzymology
Neurons - metabolism
Neurons - ultrastructure
Parvalbumin
Parvalbumins - metabolism
Rat
Rats
Rats, Sprague-Dawley
S100 Calcium Binding Protein G - metabolism
Trigeminal ganglion
Trigeminal Ganglion - cytology
Trigeminal Ganglion - metabolism
Trigeminal Ganglion - ultrastructure
Vertebrates: nervous system and sense organs
title Parvalbumin, calretinin and carbonic anhydrase in the trigeminal and spinal primary neurons of the rat
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