Orphan neuropeptide NocII, a putative pronociceptin maturation product, stimulates locomotion in mice
NOCII is a heptadecapeptide whose sequence lies immediately downstream of nociceptin, the newly discovered natural agonist of the ORL1 receptor, in pronociceptin, nociceptinʼs precursor polypeptide. Since the sequence of NocII is framed by putative convertase excision sites and it totally conserved...
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Veröffentlicht in: | Neuroreport 1997-02, Vol.8 (3), p.705-707 |
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description | NOCII is a heptadecapeptide whose sequence lies immediately downstream of nociceptin, the newly discovered natural agonist of the ORL1 receptor, in pronociceptin, nociceptinʼs precursor polypeptide. Since the sequence of NocII is framed by putative convertase excision sites and it totally conserved across murine and human species, we have sought to determine whether this orphan neuropeptide might by physiologically significant, i.e. endowed with central biological activity in vivo. Intracerebroventricular administration of 10 and 100 ng of NocII increased locomotion in mice. However, unlike nociceptin, which stimulates both the horizontal and vertical (rearing) components of locomotion, NocII affected only the horizontal component. The motor stimulant action of NocII appears to depend largely on dopamine transmission since it is totally reversed by the D1 or the D2 dopamine receptor antagonists SCH 23390 and haloperidol. NocII does not modify the number of explored holes in the hole board test, indicating that, unlike nociceptin, the orphan peptide does not affect exploratory behavior in mice. |
doi_str_mv | 10.1097/00001756-199702100-00025 |
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Since the sequence of NocII is framed by putative convertase excision sites and it totally conserved across murine and human species, we have sought to determine whether this orphan neuropeptide might by physiologically significant, i.e. endowed with central biological activity in vivo. Intracerebroventricular administration of 10 and 100 ng of NocII increased locomotion in mice. However, unlike nociceptin, which stimulates both the horizontal and vertical (rearing) components of locomotion, NocII affected only the horizontal component. The motor stimulant action of NocII appears to depend largely on dopamine transmission since it is totally reversed by the D1 or the D2 dopamine receptor antagonists SCH 23390 and haloperidol. NocII does not modify the number of explored holes in the hole board test, indicating that, unlike nociceptin, the orphan peptide does not affect exploratory behavior in mice.</description><identifier>ISSN: 0959-4965</identifier><identifier>EISSN: 1473-558X</identifier><identifier>DOI: 10.1097/00001756-199702100-00025</identifier><identifier>PMID: 9106751</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Amino Acid Sequence ; Animals ; Behavioral psychophysiology ; Benzazepines - pharmacology ; Biological and medical sciences ; Conserved Sequence ; Dopamine Antagonists - pharmacology ; Dose-Response Relationship, Drug ; Exploratory Behavior - drug effects ; Fundamental and applied biological sciences. Psychology ; Haloperidol - pharmacology ; Humans ; Male ; Mice ; Molecular Sequence Data ; Motor Activity - drug effects ; Neuropeptides - chemistry ; Neuropeptides - pharmacology ; Neurotransmission and behavior ; Nociceptin ; Opioid Peptides - pharmacology ; Psychology. Psychoanalysis. Psychiatry ; Psychology. Psychophysiology ; Receptors, Dopamine D1 - physiology ; Receptors, Dopamine D2 - physiology ; Receptors, Opioid - agonists</subject><ispartof>Neuroreport, 1997-02, Vol.8 (3), p.705-707</ispartof><rights>Lippincott-Raven Publishers.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4155-7ea7032f66c122559dbc8d4bf8672755ae3a984e9f38dc7482733d32bd5a16b23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2598394$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9106751$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Florin, Sébastien</creatorcontrib><creatorcontrib>Suaudeau, Charles</creatorcontrib><creatorcontrib>Meunier, Jean-Claude</creatorcontrib><creatorcontrib>Costentin, Jean</creatorcontrib><title>Orphan neuropeptide NocII, a putative pronociceptin maturation product, stimulates locomotion in mice</title><title>Neuroreport</title><addtitle>Neuroreport</addtitle><description>NOCII is a heptadecapeptide whose sequence lies immediately downstream of nociceptin, the newly discovered natural agonist of the ORL1 receptor, in pronociceptin, nociceptinʼs precursor polypeptide. Since the sequence of NocII is framed by putative convertase excision sites and it totally conserved across murine and human species, we have sought to determine whether this orphan neuropeptide might by physiologically significant, i.e. endowed with central biological activity in vivo. Intracerebroventricular administration of 10 and 100 ng of NocII increased locomotion in mice. However, unlike nociceptin, which stimulates both the horizontal and vertical (rearing) components of locomotion, NocII affected only the horizontal component. The motor stimulant action of NocII appears to depend largely on dopamine transmission since it is totally reversed by the D1 or the D2 dopamine receptor antagonists SCH 23390 and haloperidol. NocII does not modify the number of explored holes in the hole board test, indicating that, unlike nociceptin, the orphan peptide does not affect exploratory behavior in mice.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Behavioral psychophysiology</subject><subject>Benzazepines - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Conserved Sequence</subject><subject>Dopamine Antagonists - pharmacology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Exploratory Behavior - drug effects</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Haloperidol - pharmacology</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Motor Activity - drug effects</subject><subject>Neuropeptides - chemistry</subject><subject>Neuropeptides - pharmacology</subject><subject>Neurotransmission and behavior</subject><subject>Nociceptin</subject><subject>Opioid Peptides - pharmacology</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychology. Psychophysiology</subject><subject>Receptors, Dopamine D1 - physiology</subject><subject>Receptors, Dopamine D2 - physiology</subject><subject>Receptors, Opioid - agonists</subject><issn>0959-4965</issn><issn>1473-558X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAUhS0EKtPCIyB5gVg11D9xbC9RVWCkqt1QqTvLcW40AScO_mnF2-PpDLPDG0v-vuNrHSOEKflMiZZXpC4qRddQrSVhlJCmnjDxCm1oK3kjhHp8jTZEC920uhNv0XlKP6uiCVVn6ExT0klBNwju47qzC16gxLDCmqcB8F1w2-0ltngt2ebpCfAawxLc5PbCgmebS6wgLHswFJcvccrTXLzNkLAPLszhBe_lmnqH3ozWJ3h_3C_Qw9ebH9ffm9v7b9vrL7eNa6kQjQQrCWdj1znKmBB66J0a2n5UnWRSCAvcatWCHrkanGwVk5wPnPWDsLTrGb9Anw731mf9LpCymafkwHu7QCjJ0I5wSomoojqILoaUIoxmjdNs4x9Didk3bP41bE4Nm5eGa_TDcUbpZxhOwWOllX88cpuc9WO0i5vSSWNCK67bqrUH7Tn4DDH98uUZotmB9Xln_ve__C-8bJPV</recordid><startdate>19970210</startdate><enddate>19970210</enddate><creator>Florin, Sébastien</creator><creator>Suaudeau, Charles</creator><creator>Meunier, Jean-Claude</creator><creator>Costentin, Jean</creator><general>Lippincott-Raven Publishers</general><general>Lippincott Williams and Wilkins</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>7QG</scope><scope>7TK</scope></search><sort><creationdate>19970210</creationdate><title>Orphan neuropeptide NocII, a putative pronociceptin maturation product, stimulates locomotion in mice</title><author>Florin, Sébastien ; Suaudeau, Charles ; Meunier, Jean-Claude ; Costentin, Jean</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4155-7ea7032f66c122559dbc8d4bf8672755ae3a984e9f38dc7482733d32bd5a16b23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Behavioral psychophysiology</topic><topic>Benzazepines - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Conserved Sequence</topic><topic>Dopamine Antagonists - pharmacology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Exploratory Behavior - drug effects</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Haloperidol - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Motor Activity - drug effects</topic><topic>Neuropeptides - chemistry</topic><topic>Neuropeptides - pharmacology</topic><topic>Neurotransmission and behavior</topic><topic>Nociceptin</topic><topic>Opioid Peptides - pharmacology</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychology. Psychophysiology</topic><topic>Receptors, Dopamine D1 - physiology</topic><topic>Receptors, Dopamine D2 - physiology</topic><topic>Receptors, Opioid - agonists</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Florin, Sébastien</creatorcontrib><creatorcontrib>Suaudeau, Charles</creatorcontrib><creatorcontrib>Meunier, Jean-Claude</creatorcontrib><creatorcontrib>Costentin, Jean</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>Animal Behavior Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroreport</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Florin, Sébastien</au><au>Suaudeau, Charles</au><au>Meunier, Jean-Claude</au><au>Costentin, Jean</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Orphan neuropeptide NocII, a putative pronociceptin maturation product, stimulates locomotion in mice</atitle><jtitle>Neuroreport</jtitle><addtitle>Neuroreport</addtitle><date>1997-02-10</date><risdate>1997</risdate><volume>8</volume><issue>3</issue><spage>705</spage><epage>707</epage><pages>705-707</pages><issn>0959-4965</issn><eissn>1473-558X</eissn><abstract>NOCII is a heptadecapeptide whose sequence lies immediately downstream of nociceptin, the newly discovered natural agonist of the ORL1 receptor, in pronociceptin, nociceptinʼs precursor polypeptide. Since the sequence of NocII is framed by putative convertase excision sites and it totally conserved across murine and human species, we have sought to determine whether this orphan neuropeptide might by physiologically significant, i.e. endowed with central biological activity in vivo. Intracerebroventricular administration of 10 and 100 ng of NocII increased locomotion in mice. However, unlike nociceptin, which stimulates both the horizontal and vertical (rearing) components of locomotion, NocII affected only the horizontal component. The motor stimulant action of NocII appears to depend largely on dopamine transmission since it is totally reversed by the D1 or the D2 dopamine receptor antagonists SCH 23390 and haloperidol. NocII does not modify the number of explored holes in the hole board test, indicating that, unlike nociceptin, the orphan peptide does not affect exploratory behavior in mice.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>9106751</pmid><doi>10.1097/00001756-199702100-00025</doi><tpages>3</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Behavioral psychophysiology Benzazepines - pharmacology Biological and medical sciences Conserved Sequence Dopamine Antagonists - pharmacology Dose-Response Relationship, Drug Exploratory Behavior - drug effects Fundamental and applied biological sciences. Psychology Haloperidol - pharmacology Humans Male Mice Molecular Sequence Data Motor Activity - drug effects Neuropeptides - chemistry Neuropeptides - pharmacology Neurotransmission and behavior Nociceptin Opioid Peptides - pharmacology Psychology. Psychoanalysis. Psychiatry Psychology. Psychophysiology Receptors, Dopamine D1 - physiology Receptors, Dopamine D2 - physiology Receptors, Opioid - agonists |
title | Orphan neuropeptide NocII, a putative pronociceptin maturation product, stimulates locomotion in mice |
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