Distribution of nitric oxide synthase and nitric oxide-receptive, cyclic GMP-producing structures in the rat brain
The structures capable of synthesizing cyclic GMP in response to nitric oxide in the rat brain were compared relative to the anatomical localization of neuronal nitric oxide synthase. In order to do this, we used brain slices incubated in vitro, where cyclic GMP-synthesis was stimulated using sodium...
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Veröffentlicht in: | Neuroscience 1998-11, Vol.87 (1), p.207-241 |
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description | The structures capable of synthesizing cyclic GMP in response to nitric oxide in the rat brain were compared relative to the anatomical localization of neuronal nitric oxide synthase. In order to do this, we used brain slices incubated
in vitro, where cyclic GMP-synthesis was stimulated using sodium nitroprusside as a nitric oxide-donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine. Nitric oxide-stimulated cyclic GMP synthesis was found in cells and fibers, but was especially prominent in varicose fibers throughout the rat brain. Fibers containing the nitric oxide-stimulated cyclic GMP production were present in virtually every area of the rat brain although there were large regional variations in the density of the fiber networks. When compared with the localization of nitric oxide synthase, it was observed that although nitric oxide-responsive and the nitric oxide-producing structures were found in similar locations in general this distribution was complementary. Only occasionally was nitric oxide-mediated cyclic GMP synthesis observed in structures which also contained nitric oxide synthase.
We conclude that the nitric oxide-responsive soluble guanylyl cyclase and nitric oxide synthase are usually juxtaposed at very short distances in the rat brain. These findings very strongly support the proposed role of nitric oxide as an endogenous activator of the soluble guanylyl cyclase in the central nervous system and convincingly demonstrate the presence of the nitric oxide–cyclic GMP signal transduction pathway in virtually every area of the rat brain. |
doi_str_mv | 10.1016/S0306-4522(98)00171-7 |
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in vitro, where cyclic GMP-synthesis was stimulated using sodium nitroprusside as a nitric oxide-donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine. Nitric oxide-stimulated cyclic GMP synthesis was found in cells and fibers, but was especially prominent in varicose fibers throughout the rat brain. Fibers containing the nitric oxide-stimulated cyclic GMP production were present in virtually every area of the rat brain although there were large regional variations in the density of the fiber networks. When compared with the localization of nitric oxide synthase, it was observed that although nitric oxide-responsive and the nitric oxide-producing structures were found in similar locations in general this distribution was complementary. Only occasionally was nitric oxide-mediated cyclic GMP synthesis observed in structures which also contained nitric oxide synthase.
We conclude that the nitric oxide-responsive soluble guanylyl cyclase and nitric oxide synthase are usually juxtaposed at very short distances in the rat brain. These findings very strongly support the proposed role of nitric oxide as an endogenous activator of the soluble guanylyl cyclase in the central nervous system and convincingly demonstrate the presence of the nitric oxide–cyclic GMP signal transduction pathway in virtually every area of the rat brain.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/S0306-4522(98)00171-7</identifier><identifier>PMID: 9722153</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>1-Methyl-3-isobutylxanthine - pharmacology ; Anatomy ; Animals ; Biological and medical sciences ; Brain - anatomy & histology ; Brain - enzymology ; Brain - metabolism ; brain slices ; Central nervous system ; co-localization ; cyclic GMP ; Cyclic GMP - biosynthesis ; Fundamental and applied biological sciences. Psychology ; Guanylate Cyclase - metabolism ; immunocytochemistry ; Immunohistochemistry ; In Vitro Techniques ; Male ; Neurons - enzymology ; Nitric Oxide - metabolism ; nitric oxide synthase ; Nitric Oxide Synthase - metabolism ; Nitroprusside - pharmacology ; Phosphodiesterase Inhibitors - pharmacology ; rat ; Rats ; Rats, Inbred Lew ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 1998-11, Vol.87 (1), p.207-241</ispartof><rights>1998 IBRO</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-7912d47231a199316669db80a37cc58c00f2e5b55be7fbc030278ad34885809f3</citedby><cites>FETCH-LOGICAL-c389t-7912d47231a199316669db80a37cc58c00f2e5b55be7fbc030278ad34885809f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0306452298001717$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2349303$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9722153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Vente, J</creatorcontrib><creatorcontrib>Hopkins, D.A</creatorcontrib><creatorcontrib>Markerink-van Ittersum, M</creatorcontrib><creatorcontrib>Emson, P.C</creatorcontrib><creatorcontrib>Schmidt, H.H.H.W</creatorcontrib><creatorcontrib>Steinbusch, H.W.M</creatorcontrib><title>Distribution of nitric oxide synthase and nitric oxide-receptive, cyclic GMP-producing structures in the rat brain</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>The structures capable of synthesizing cyclic GMP in response to nitric oxide in the rat brain were compared relative to the anatomical localization of neuronal nitric oxide synthase. In order to do this, we used brain slices incubated
in vitro, where cyclic GMP-synthesis was stimulated using sodium nitroprusside as a nitric oxide-donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine. Nitric oxide-stimulated cyclic GMP synthesis was found in cells and fibers, but was especially prominent in varicose fibers throughout the rat brain. Fibers containing the nitric oxide-stimulated cyclic GMP production were present in virtually every area of the rat brain although there were large regional variations in the density of the fiber networks. When compared with the localization of nitric oxide synthase, it was observed that although nitric oxide-responsive and the nitric oxide-producing structures were found in similar locations in general this distribution was complementary. Only occasionally was nitric oxide-mediated cyclic GMP synthesis observed in structures which also contained nitric oxide synthase.
We conclude that the nitric oxide-responsive soluble guanylyl cyclase and nitric oxide synthase are usually juxtaposed at very short distances in the rat brain. These findings very strongly support the proposed role of nitric oxide as an endogenous activator of the soluble guanylyl cyclase in the central nervous system and convincingly demonstrate the presence of the nitric oxide–cyclic GMP signal transduction pathway in virtually every area of the rat brain.</description><subject>1-Methyl-3-isobutylxanthine - pharmacology</subject><subject>Anatomy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain - anatomy & histology</subject><subject>Brain - enzymology</subject><subject>Brain - metabolism</subject><subject>brain slices</subject><subject>Central nervous system</subject><subject>co-localization</subject><subject>cyclic GMP</subject><subject>Cyclic GMP - biosynthesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guanylate Cyclase - metabolism</subject><subject>immunocytochemistry</subject><subject>Immunohistochemistry</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Neurons - enzymology</subject><subject>Nitric Oxide - metabolism</subject><subject>nitric oxide synthase</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Nitroprusside - pharmacology</subject><subject>Phosphodiesterase Inhibitors - pharmacology</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1vFCEUhonR1O3qT2jCRdPYpKN8DANcNaZfmtRool4TBs5YzCyzBaZx_71sd7OJV3JD4H3O4fAgdELJe0po9-E74aRrWsHYO63OCaGSNvIFWlAleSNF275EiwPyGh3n_JvUJVp-hI60ZIwKvkDpOuSSQj-XMEU8DTiGenR4-hM84LyJ5cFmwDb6f5ImgYN1CU9wgd3GjfX-7su3Zp0mP7sQf-HadHZlTpBxiLg8AE624D7ZEN-gV4MdM7zd70v08_bmx9Wn5v7r3eerj_eN40qXRmrKfCsZp5ZqzWnXddr3ilgunRPKETIwEL0QPcihd_WrTCrreauUUEQPfInOdn3rVI8z5GJWITsYRxthmrORXAkhWlZBsQNdmnJOMJh1CiubNoYSs3Vtnl2brUijlXl2XcuX6GT_wNyvwB-q9nJrfrrPbXZ2HJKNLuQDxnirOdlilzsMqoynAMlkFyA68KFaLsZP4T-D_AWodJtp</recordid><startdate>19981101</startdate><enddate>19981101</enddate><creator>de Vente, J</creator><creator>Hopkins, D.A</creator><creator>Markerink-van Ittersum, M</creator><creator>Emson, P.C</creator><creator>Schmidt, H.H.H.W</creator><creator>Steinbusch, H.W.M</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>19981101</creationdate><title>Distribution of nitric oxide synthase and nitric oxide-receptive, cyclic GMP-producing structures in the rat brain</title><author>de Vente, J ; Hopkins, D.A ; Markerink-van Ittersum, M ; Emson, P.C ; Schmidt, H.H.H.W ; Steinbusch, H.W.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-7912d47231a199316669db80a37cc58c00f2e5b55be7fbc030278ad34885809f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>1-Methyl-3-isobutylxanthine - pharmacology</topic><topic>Anatomy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain - anatomy & histology</topic><topic>Brain - enzymology</topic><topic>Brain - metabolism</topic><topic>brain slices</topic><topic>Central nervous system</topic><topic>co-localization</topic><topic>cyclic GMP</topic><topic>Cyclic GMP - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guanylate Cyclase - metabolism</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Neurons - enzymology</topic><topic>Nitric Oxide - metabolism</topic><topic>nitric oxide synthase</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Nitroprusside - pharmacology</topic><topic>Phosphodiesterase Inhibitors - pharmacology</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Vente, J</creatorcontrib><creatorcontrib>Hopkins, D.A</creatorcontrib><creatorcontrib>Markerink-van Ittersum, M</creatorcontrib><creatorcontrib>Emson, P.C</creatorcontrib><creatorcontrib>Schmidt, H.H.H.W</creatorcontrib><creatorcontrib>Steinbusch, H.W.M</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>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Vente, J</au><au>Hopkins, D.A</au><au>Markerink-van Ittersum, M</au><au>Emson, P.C</au><au>Schmidt, H.H.H.W</au><au>Steinbusch, H.W.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of nitric oxide synthase and nitric oxide-receptive, cyclic GMP-producing structures in the rat brain</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>1998-11-01</date><risdate>1998</risdate><volume>87</volume><issue>1</issue><spage>207</spage><epage>241</epage><pages>207-241</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>The structures capable of synthesizing cyclic GMP in response to nitric oxide in the rat brain were compared relative to the anatomical localization of neuronal nitric oxide synthase. In order to do this, we used brain slices incubated
in vitro, where cyclic GMP-synthesis was stimulated using sodium nitroprusside as a nitric oxide-donor compound, in the presence of the phosphodiesterase inhibitor isobutylmethylxanthine. Nitric oxide-stimulated cyclic GMP synthesis was found in cells and fibers, but was especially prominent in varicose fibers throughout the rat brain. Fibers containing the nitric oxide-stimulated cyclic GMP production were present in virtually every area of the rat brain although there were large regional variations in the density of the fiber networks. When compared with the localization of nitric oxide synthase, it was observed that although nitric oxide-responsive and the nitric oxide-producing structures were found in similar locations in general this distribution was complementary. Only occasionally was nitric oxide-mediated cyclic GMP synthesis observed in structures which also contained nitric oxide synthase.
We conclude that the nitric oxide-responsive soluble guanylyl cyclase and nitric oxide synthase are usually juxtaposed at very short distances in the rat brain. These findings very strongly support the proposed role of nitric oxide as an endogenous activator of the soluble guanylyl cyclase in the central nervous system and convincingly demonstrate the presence of the nitric oxide–cyclic GMP signal transduction pathway in virtually every area of the rat brain.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>9722153</pmid><doi>10.1016/S0306-4522(98)00171-7</doi><tpages>35</tpages></addata></record> |
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subjects | 1-Methyl-3-isobutylxanthine - pharmacology Anatomy Animals Biological and medical sciences Brain - anatomy & histology Brain - enzymology Brain - metabolism brain slices Central nervous system co-localization cyclic GMP Cyclic GMP - biosynthesis Fundamental and applied biological sciences. Psychology Guanylate Cyclase - metabolism immunocytochemistry Immunohistochemistry In Vitro Techniques Male Neurons - enzymology Nitric Oxide - metabolism nitric oxide synthase Nitric Oxide Synthase - metabolism Nitroprusside - pharmacology Phosphodiesterase Inhibitors - pharmacology rat Rats Rats, Inbred Lew Vertebrates: nervous system and sense organs |
title | Distribution of nitric oxide synthase and nitric oxide-receptive, cyclic GMP-producing structures in the rat brain |
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