Distribution of prepro-nociceptin/ orphanin FQ mRNA and its receptor mRNA in developing and adult mouse central nervous systems
Nociceptin/orphanin FQ (N/OFQ) and its receptor share similarities to opioids and their receptors in terms of the molecular structure and signaling pathway, but the two systems exhibit different actions in vivo. To understand the mechanism of N/OFQ‐system actions, we examined, by in situ hybridizati...
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container_title | Journal of comparative neurology (1911) |
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creator | Ikeda, Kazutaka Watanabe, Masahiko Ichikawa, Tomio Kobayashi, Toru Yano, Ryoji Kumanishi, Toshiro |
description | Nociceptin/orphanin FQ (N/OFQ) and its receptor share similarities to opioids and their receptors in terms of the molecular structure and signaling pathway, but the two systems exhibit different actions in vivo. To understand the mechanism of N/OFQ‐system actions, we examined, by in situ hybridization analysis, the distribution of preproN/OFQ and N/OFQ receptor mRNAs in the developing and adult mouse central nervous systems (CNS). In most neural regions, preproN/OFQ mRNA was mainly expressed in a small population of middle‐sized neurons. These neurons were scattered between large projection‐type neurons or within the neuropil, suggestive of interneurons. In some other nuclei (lateral septum, bed nucleus of the stria terminalis, reticular thalamic nucleus, inferior colliculus, and rostral periolivery nucleus), preproN/OFQ mRNA was expressed in a number of large projection‐type neurons. By contrast, N/OFQ receptor mRNA was evenly expressed in most neurons of the adult CNS. Considering the inhibitory actions of N/OFQ, the distinct cellular expression pattern of the N/OFQ system suggests that the release of N/OFQ from interneurons may lower neuronal and synaptic activities of neighboring neurons, leading to integration or modulation of local circuits. Furthermore, the cellular expression pattern, distinct from that of the opioid system, may provide a possible molecular/cellular basis for the different in vivo actions of N/OFQ and opioids. In embryonic stages, both preproN/OFQ and N/OFQ receptor mRNAs were highly and widely expressed in the mantle zone, suggesting the possible importance of N/OFQ signaling in CNS development. J. Comp. Neurol. 399:139–151, 1998. © 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1096-9861(19980914)399:1<139::AID-CNE11>3.0.CO;2-C |
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To understand the mechanism of N/OFQ‐system actions, we examined, by in situ hybridization analysis, the distribution of preproN/OFQ and N/OFQ receptor mRNAs in the developing and adult mouse central nervous systems (CNS). In most neural regions, preproN/OFQ mRNA was mainly expressed in a small population of middle‐sized neurons. These neurons were scattered between large projection‐type neurons or within the neuropil, suggestive of interneurons. In some other nuclei (lateral septum, bed nucleus of the stria terminalis, reticular thalamic nucleus, inferior colliculus, and rostral periolivery nucleus), preproN/OFQ mRNA was expressed in a number of large projection‐type neurons. By contrast, N/OFQ receptor mRNA was evenly expressed in most neurons of the adult CNS. Considering the inhibitory actions of N/OFQ, the distinct cellular expression pattern of the N/OFQ system suggests that the release of N/OFQ from interneurons may lower neuronal and synaptic activities of neighboring neurons, leading to integration or modulation of local circuits. Furthermore, the cellular expression pattern, distinct from that of the opioid system, may provide a possible molecular/cellular basis for the different in vivo actions of N/OFQ and opioids. In embryonic stages, both preproN/OFQ and N/OFQ receptor mRNAs were highly and widely expressed in the mantle zone, suggesting the possible importance of N/OFQ signaling in CNS development. J. Comp. Neurol. 399:139–151, 1998. © 1998 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/(SICI)1096-9861(19980914)399:1<139::AID-CNE11>3.0.CO;2-C</identifier><identifier>PMID: 9725707</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Age Factors ; analgesia ; Animals ; Central Nervous System - chemistry ; Central Nervous System - cytology ; Central Nervous System - embryology ; Fetus - chemistry ; Gene Expression Regulation, Developmental ; in situ hybridization ; interneuron ; Interneurons - chemistry ; Interneurons - physiology ; Mice ; Mice, Inbred C57BL - embryology ; N/OFQ ; Nociceptin ; Nociceptin Receptor ; opioid ; Opioid Peptides - genetics ; Receptors, Opioid - genetics ; RNA, Messenger - analysis</subject><ispartof>Journal of comparative neurology (1911), 1998-09, Vol.399 (1), p.139-151</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4381-1c66e00e23727e8084c00a84e27a2a58bfed6f03279dcd8086f5ab1c1ef0dc183</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291096-9861%2819980914%29399%3A1%3C139%3A%3AAID-CNE11%3E3.0.CO%3B2-C$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291096-9861%2819980914%29399%3A1%3C139%3A%3AAID-CNE11%3E3.0.CO%3B2-C$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9725707$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikeda, Kazutaka</creatorcontrib><creatorcontrib>Watanabe, Masahiko</creatorcontrib><creatorcontrib>Ichikawa, Tomio</creatorcontrib><creatorcontrib>Kobayashi, Toru</creatorcontrib><creatorcontrib>Yano, Ryoji</creatorcontrib><creatorcontrib>Kumanishi, Toshiro</creatorcontrib><title>Distribution of prepro-nociceptin/ orphanin FQ mRNA and its receptor mRNA in developing and adult mouse central nervous systems</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Nociceptin/orphanin FQ (N/OFQ) and its receptor share similarities to opioids and their receptors in terms of the molecular structure and signaling pathway, but the two systems exhibit different actions in vivo. To understand the mechanism of N/OFQ‐system actions, we examined, by in situ hybridization analysis, the distribution of preproN/OFQ and N/OFQ receptor mRNAs in the developing and adult mouse central nervous systems (CNS). In most neural regions, preproN/OFQ mRNA was mainly expressed in a small population of middle‐sized neurons. These neurons were scattered between large projection‐type neurons or within the neuropil, suggestive of interneurons. In some other nuclei (lateral septum, bed nucleus of the stria terminalis, reticular thalamic nucleus, inferior colliculus, and rostral periolivery nucleus), preproN/OFQ mRNA was expressed in a number of large projection‐type neurons. By contrast, N/OFQ receptor mRNA was evenly expressed in most neurons of the adult CNS. Considering the inhibitory actions of N/OFQ, the distinct cellular expression pattern of the N/OFQ system suggests that the release of N/OFQ from interneurons may lower neuronal and synaptic activities of neighboring neurons, leading to integration or modulation of local circuits. Furthermore, the cellular expression pattern, distinct from that of the opioid system, may provide a possible molecular/cellular basis for the different in vivo actions of N/OFQ and opioids. In embryonic stages, both preproN/OFQ and N/OFQ receptor mRNAs were highly and widely expressed in the mantle zone, suggesting the possible importance of N/OFQ signaling in CNS development. J. Comp. Neurol. 399:139–151, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Age Factors</subject><subject>analgesia</subject><subject>Animals</subject><subject>Central Nervous System - chemistry</subject><subject>Central Nervous System - cytology</subject><subject>Central Nervous System - embryology</subject><subject>Fetus - chemistry</subject><subject>Gene Expression Regulation, Developmental</subject><subject>in situ hybridization</subject><subject>interneuron</subject><subject>Interneurons - chemistry</subject><subject>Interneurons - physiology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL - embryology</subject><subject>N/OFQ</subject><subject>Nociceptin</subject><subject>Nociceptin Receptor</subject><subject>opioid</subject><subject>Opioid Peptides - genetics</subject><subject>Receptors, Opioid - genetics</subject><subject>RNA, Messenger - analysis</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkl1v0zAUhiMEGt3gJyD5Cm0X6ey4ie2CEFW6lUpTK9jQBjdHbnICHvmanQ56xV_HXUpvQNqV5XNeP8fW4yB4z-iQURqdHl_O0_kJoyoJlUzYMVNKUsVGJ1ypMXvLuBqPJ_NpmC7OGHvHh3SYLt9EYfokGOwPPQ0GHsVCpRLxPDh07pZSqhSXB8GBElEsqBgEv6fGddas1p1patIUpLXY2iasm8xk2HamPiWNbb_r2tTk_COpPi0mRNc5MZ0jFreRxvZVH8jxHsumNfW3h4zO12VHqmbtkGRYd1aXpEZ77wvEbVyHlXsRPCt06fDlbj0KPp-fXaUfwovlbJ5OLsJsxCULWZYkSClGXEQCJZWjjFItRxgJHelYrgrMk4LySKg8y30_KWK9YhnDguYZk_woeN1z_ePu1ug6qIzLsCx1jf46ILgUTEbxo0EmGB0lQvngTR_MbOOcxQJaayptN8AobCUCbCXC1gdsfcBfieAlgt9yBeAlwoNE4EAhXUIEqUe_2t1hvaow34N31nz_S9__aUrc_DP38bH_m9oXPDvs2f5f4K89W9sfkAguYrhezODr1fT6JrmcQcz_AFC-yMw</recordid><startdate>19980914</startdate><enddate>19980914</enddate><creator>Ikeda, Kazutaka</creator><creator>Watanabe, Masahiko</creator><creator>Ichikawa, Tomio</creator><creator>Kobayashi, Toru</creator><creator>Yano, Ryoji</creator><creator>Kumanishi, Toshiro</creator><general>John Wiley & Sons, Inc</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>19980914</creationdate><title>Distribution of prepro-nociceptin/ orphanin FQ mRNA and its receptor mRNA in developing and adult mouse central nervous systems</title><author>Ikeda, Kazutaka ; Watanabe, Masahiko ; Ichikawa, Tomio ; Kobayashi, Toru ; Yano, Ryoji ; Kumanishi, Toshiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4381-1c66e00e23727e8084c00a84e27a2a58bfed6f03279dcd8086f5ab1c1ef0dc183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Age Factors</topic><topic>analgesia</topic><topic>Animals</topic><topic>Central Nervous System - chemistry</topic><topic>Central Nervous System - cytology</topic><topic>Central Nervous System - embryology</topic><topic>Fetus - chemistry</topic><topic>Gene Expression Regulation, Developmental</topic><topic>in situ hybridization</topic><topic>interneuron</topic><topic>Interneurons - chemistry</topic><topic>Interneurons - physiology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL - embryology</topic><topic>N/OFQ</topic><topic>Nociceptin</topic><topic>Nociceptin Receptor</topic><topic>opioid</topic><topic>Opioid Peptides - genetics</topic><topic>Receptors, Opioid - genetics</topic><topic>RNA, Messenger - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikeda, Kazutaka</creatorcontrib><creatorcontrib>Watanabe, Masahiko</creatorcontrib><creatorcontrib>Ichikawa, Tomio</creatorcontrib><creatorcontrib>Kobayashi, Toru</creatorcontrib><creatorcontrib>Yano, Ryoji</creatorcontrib><creatorcontrib>Kumanishi, Toshiro</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikeda, Kazutaka</au><au>Watanabe, Masahiko</au><au>Ichikawa, Tomio</au><au>Kobayashi, Toru</au><au>Yano, Ryoji</au><au>Kumanishi, Toshiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of prepro-nociceptin/ orphanin FQ mRNA and its receptor mRNA in developing and adult mouse central nervous systems</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1998-09-14</date><risdate>1998</risdate><volume>399</volume><issue>1</issue><spage>139</spage><epage>151</epage><pages>139-151</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Nociceptin/orphanin FQ (N/OFQ) and its receptor share similarities to opioids and their receptors in terms of the molecular structure and signaling pathway, but the two systems exhibit different actions in vivo. To understand the mechanism of N/OFQ‐system actions, we examined, by in situ hybridization analysis, the distribution of preproN/OFQ and N/OFQ receptor mRNAs in the developing and adult mouse central nervous systems (CNS). In most neural regions, preproN/OFQ mRNA was mainly expressed in a small population of middle‐sized neurons. These neurons were scattered between large projection‐type neurons or within the neuropil, suggestive of interneurons. In some other nuclei (lateral septum, bed nucleus of the stria terminalis, reticular thalamic nucleus, inferior colliculus, and rostral periolivery nucleus), preproN/OFQ mRNA was expressed in a number of large projection‐type neurons. By contrast, N/OFQ receptor mRNA was evenly expressed in most neurons of the adult CNS. Considering the inhibitory actions of N/OFQ, the distinct cellular expression pattern of the N/OFQ system suggests that the release of N/OFQ from interneurons may lower neuronal and synaptic activities of neighboring neurons, leading to integration or modulation of local circuits. Furthermore, the cellular expression pattern, distinct from that of the opioid system, may provide a possible molecular/cellular basis for the different in vivo actions of N/OFQ and opioids. In embryonic stages, both preproN/OFQ and N/OFQ receptor mRNAs were highly and widely expressed in the mantle zone, suggesting the possible importance of N/OFQ signaling in CNS development. J. Comp. Neurol. 399:139–151, 1998. © 1998 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>9725707</pmid><doi>10.1002/(SICI)1096-9861(19980914)399:1<139::AID-CNE11>3.0.CO;2-C</doi><tpages>13</tpages></addata></record> |
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subjects | Age Factors analgesia Animals Central Nervous System - chemistry Central Nervous System - cytology Central Nervous System - embryology Fetus - chemistry Gene Expression Regulation, Developmental in situ hybridization interneuron Interneurons - chemistry Interneurons - physiology Mice Mice, Inbred C57BL - embryology N/OFQ Nociceptin Nociceptin Receptor opioid Opioid Peptides - genetics Receptors, Opioid - genetics RNA, Messenger - analysis |
title | Distribution of prepro-nociceptin/ orphanin FQ mRNA and its receptor mRNA in developing and adult mouse central nervous systems |
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