Peptidergic innervation of guinea-pig brain vessels: comparison with immunohistochemistry and in vitro pharmacology in rostrally and caudally located arteries
The peptidergic innervation of the guinea-pig basilar artery and the posterior, middle and anterior cerebral arteries were studied by means of immunohistochemical and image analysis techniques using whole mount preparations. An in vitro pharmacological study was performed to correlate the distributi...
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Veröffentlicht in: | Journal of the autonomic nervous system 1995-11, Vol.55 (3), p.179-188 |
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description | The peptidergic innervation of the guinea-pig basilar artery and the posterior, middle and anterior cerebral arteries were studied by means of immunohistochemical and image analysis techniques using whole mount preparations. An in vitro pharmacological study was performed to correlate the distribution of peptide-containing nerves and the action of neuropeptides on vessel segments from the same vascular regions. The overall distribution of perivascular nerve fibres was demonstrated using an antiserum to the general neuronal marker protein gene product 9.5 (PGP 9.5) and the percentage immunostained area of total vessel wall area occupied by PGP-containing nerves, in each of the basilar, posterior and middle cerebral arteries, was set at 100% and used to determine the relative density of specific populations of autonomic and sensory nerve fibres. In all four cerebral arteries, the majority of nerve fibres possessed neuropeptide Y (NPY) and tyrosine hydroxylase (TH) immunoreactivity, occupying 6.2–13.3% and 5.8–7.5% of the total vessel wall area, respectively. Vasoactive intestinal peptide (VIP), substance P (SP) and calcitonin-gene-related peptide (CGRP) were detected at lower densities. The pharmacological study performed on small circular segments with an intact endothelium revealed that, in all four cerebral arteries, NPY was a more potent constrictor than noradrenaline (NA). The rank order of potency for relaxant agents was CGRP = SP > VIP > ACh in the PCA and MCA, and SP = CGRP > VIP > ACh in the BA and ACA. The correlation between immunostained nerve area and the agonist potency suggested that the denser the peptidergic nerve-supply, the lower the sensitivity to the agonist. |
doi_str_mv | 10.1016/0165-1838(95)00045-Y |
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An in vitro pharmacological study was performed to correlate the distribution of peptide-containing nerves and the action of neuropeptides on vessel segments from the same vascular regions. The overall distribution of perivascular nerve fibres was demonstrated using an antiserum to the general neuronal marker protein gene product 9.5 (PGP 9.5) and the percentage immunostained area of total vessel wall area occupied by PGP-containing nerves, in each of the basilar, posterior and middle cerebral arteries, was set at 100% and used to determine the relative density of specific populations of autonomic and sensory nerve fibres. In all four cerebral arteries, the majority of nerve fibres possessed neuropeptide Y (NPY) and tyrosine hydroxylase (TH) immunoreactivity, occupying 6.2–13.3% and 5.8–7.5% of the total vessel wall area, respectively. Vasoactive intestinal peptide (VIP), substance P (SP) and calcitonin-gene-related peptide (CGRP) were detected at lower densities. The pharmacological study performed on small circular segments with an intact endothelium revealed that, in all four cerebral arteries, NPY was a more potent constrictor than noradrenaline (NA). The rank order of potency for relaxant agents was CGRP = SP > VIP > ACh in the PCA and MCA, and SP = CGRP > VIP > ACh in the BA and ACA. The correlation between immunostained nerve area and the agonist potency suggested that the denser the peptidergic nerve-supply, the lower the sensitivity to the agonist.</description><identifier>ISSN: 0165-1838</identifier><identifier>EISSN: 1872-7476</identifier><identifier>DOI: 10.1016/0165-1838(95)00045-Y</identifier><identifier>PMID: 8801268</identifier><identifier>CODEN: JASYDS</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Basilar Artery - chemistry ; Basilar Artery - drug effects ; Basilar Artery - innervation ; Biological and medical sciences ; Brain vessel ; Cerebral Arteries - chemistry ; Cerebral Arteries - drug effects ; Cerebral Arteries - innervation ; Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges ; Comparative aspect ; Fluorescent Antibody Technique, Indirect ; Fundamental and applied biological sciences. Psychology ; Guinea pig ; Guinea Pigs ; Immunohistochemistry ; In vitro pharmacology ; In Vitro Techniques ; Male ; Muscle Contraction - drug effects ; Muscle Contraction - physiology ; Muscle Relaxation - drug effects ; Muscle, Smooth, Vascular - chemistry ; Muscle, Smooth, Vascular - drug effects ; Muscle, Smooth, Vascular - innervation ; Muscle, Smooth, Vascular - physiology ; Nerve Tissue Proteins - analysis ; Neuropeptides - analysis ; Neuropeptides - pharmacology ; Neuropeptides - physiology ; Norepinephrine - pharmacology ; Peptidergic mechanism ; Thiolester Hydrolases - analysis ; Ubiquitin Thiolesterase ; Vasoconstrictor Agents - pharmacology ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of the autonomic nervous system, 1995-11, Vol.55 (3), p.179-188</ispartof><rights>1995</rights><rights>1996 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-cd8d99ba9007f2ce08abd1ab658efadb9b7fce9b0f53e6180a65cf31f43ca27c3</citedby><cites>FETCH-LOGICAL-c386t-cd8d99ba9007f2ce08abd1ab658efadb9b7fce9b0f53e6180a65cf31f43ca27c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2903760$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8801268$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>You, Junping</creatorcontrib><creatorcontrib>Gulbenkian, Sergio</creatorcontrib><creatorcontrib>Olesen, Inger Jansen</creatorcontrib><creatorcontrib>Marron, Kevin</creatorcontrib><creatorcontrib>Wharton, John</creatorcontrib><creatorcontrib>Barroso, Carla P.</creatorcontrib><creatorcontrib>Polak, Julia M.</creatorcontrib><creatorcontrib>Edvinsson, Lars</creatorcontrib><title>Peptidergic innervation of guinea-pig brain vessels: comparison with immunohistochemistry and in vitro pharmacology in rostrally and caudally located arteries</title><title>Journal of the autonomic nervous system</title><addtitle>J Auton Nerv Syst</addtitle><description>The peptidergic innervation of the guinea-pig basilar artery and the posterior, middle and anterior cerebral arteries were studied by means of immunohistochemical and image analysis techniques using whole mount preparations. An in vitro pharmacological study was performed to correlate the distribution of peptide-containing nerves and the action of neuropeptides on vessel segments from the same vascular regions. The overall distribution of perivascular nerve fibres was demonstrated using an antiserum to the general neuronal marker protein gene product 9.5 (PGP 9.5) and the percentage immunostained area of total vessel wall area occupied by PGP-containing nerves, in each of the basilar, posterior and middle cerebral arteries, was set at 100% and used to determine the relative density of specific populations of autonomic and sensory nerve fibres. In all four cerebral arteries, the majority of nerve fibres possessed neuropeptide Y (NPY) and tyrosine hydroxylase (TH) immunoreactivity, occupying 6.2–13.3% and 5.8–7.5% of the total vessel wall area, respectively. Vasoactive intestinal peptide (VIP), substance P (SP) and calcitonin-gene-related peptide (CGRP) were detected at lower densities. The pharmacological study performed on small circular segments with an intact endothelium revealed that, in all four cerebral arteries, NPY was a more potent constrictor than noradrenaline (NA). The rank order of potency for relaxant agents was CGRP = SP > VIP > ACh in the PCA and MCA, and SP = CGRP > VIP > ACh in the BA and ACA. The correlation between immunostained nerve area and the agonist potency suggested that the denser the peptidergic nerve-supply, the lower the sensitivity to the agonist.</description><subject>Animals</subject><subject>Basilar Artery - chemistry</subject><subject>Basilar Artery - drug effects</subject><subject>Basilar Artery - innervation</subject><subject>Biological and medical sciences</subject><subject>Brain vessel</subject><subject>Cerebral Arteries - chemistry</subject><subject>Cerebral Arteries - drug effects</subject><subject>Cerebral Arteries - innervation</subject><subject>Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges</subject><subject>Comparative aspect</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guinea pig</subject><subject>Guinea Pigs</subject><subject>Immunohistochemistry</subject><subject>In vitro pharmacology</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Muscle Contraction - drug effects</subject><subject>Muscle Contraction - physiology</subject><subject>Muscle Relaxation - drug effects</subject><subject>Muscle, Smooth, Vascular - chemistry</subject><subject>Muscle, Smooth, Vascular - drug effects</subject><subject>Muscle, Smooth, Vascular - innervation</subject><subject>Muscle, Smooth, Vascular - physiology</subject><subject>Nerve Tissue Proteins - analysis</subject><subject>Neuropeptides - analysis</subject><subject>Neuropeptides - pharmacology</subject><subject>Neuropeptides - physiology</subject><subject>Norepinephrine - pharmacology</subject><subject>Peptidergic mechanism</subject><subject>Thiolester Hydrolases - analysis</subject><subject>Ubiquitin Thiolesterase</subject><subject>Vasoconstrictor Agents - pharmacology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0165-1838</issn><issn>1872-7476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc-KFDEQxoMo6-zqGyjkILIeWpPp6e5kD4Is_oMFPehhT6E6qcxEupM2SY_My_ispneGOXoIRVK_r0h9HyEvOHvLGW_fldNUXNTiWjZvGGObprp_RFZcdOuq23TtY7I6I0_JZUq_GOMdk-KCXAjB-LoVK_L3O07ZGYxbp6nzHuMesgueBku3s_MI1eS2tI_gPN1jSjikG6rDOEF0qXB_XN5RN46zDzuXctA7HEuNBwre0EXkcgx02kEcQYchbA_LawyFgWE4Yhpm83AZgoaMhkLMGB2mZ-SJhSHh81O9Ij8_ffxx-6W6-_b56-2Hu0rXos2VNsJI2YNkrLNrjUxAbzj0bSPQgull31mNsme2qbHlgkHbaFtzu6k1rDtdX5HXx7lTDL9nTFmVJTQOA3gMc1JdVxyTsing5gjqskGKaNUU3QjxoDhTSyxq8VwtnivZqIdY1H2RvTzNn_sRzVl0yqH0X536kDQMNoLXLp2xtWR117KCvT9iJQXcO4wqaYdeo3ERdVYmuP__4x95Lq-f</recordid><startdate>19951106</startdate><enddate>19951106</enddate><creator>You, Junping</creator><creator>Gulbenkian, Sergio</creator><creator>Olesen, Inger Jansen</creator><creator>Marron, Kevin</creator><creator>Wharton, John</creator><creator>Barroso, Carla P.</creator><creator>Polak, Julia M.</creator><creator>Edvinsson, Lars</creator><general>Elsevier B.V</general><general>Elsevier Science</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>19951106</creationdate><title>Peptidergic innervation of guinea-pig brain vessels: comparison with immunohistochemistry and in vitro pharmacology in rostrally and caudally located arteries</title><author>You, Junping ; Gulbenkian, Sergio ; Olesen, Inger Jansen ; Marron, Kevin ; Wharton, John ; Barroso, Carla P. ; Polak, Julia M. ; Edvinsson, Lars</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-cd8d99ba9007f2ce08abd1ab658efadb9b7fce9b0f53e6180a65cf31f43ca27c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Basilar Artery - chemistry</topic><topic>Basilar Artery - drug effects</topic><topic>Basilar Artery - innervation</topic><topic>Biological and medical sciences</topic><topic>Brain vessel</topic><topic>Cerebral Arteries - chemistry</topic><topic>Cerebral Arteries - drug effects</topic><topic>Cerebral Arteries - innervation</topic><topic>Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges</topic><topic>Comparative aspect</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guinea pig</topic><topic>Guinea Pigs</topic><topic>Immunohistochemistry</topic><topic>In vitro pharmacology</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Muscle Contraction - drug effects</topic><topic>Muscle Contraction - physiology</topic><topic>Muscle Relaxation - drug effects</topic><topic>Muscle, Smooth, Vascular - chemistry</topic><topic>Muscle, Smooth, Vascular - drug effects</topic><topic>Muscle, Smooth, Vascular - innervation</topic><topic>Muscle, Smooth, Vascular - physiology</topic><topic>Nerve Tissue Proteins - analysis</topic><topic>Neuropeptides - analysis</topic><topic>Neuropeptides - pharmacology</topic><topic>Neuropeptides - physiology</topic><topic>Norepinephrine - pharmacology</topic><topic>Peptidergic mechanism</topic><topic>Thiolester Hydrolases - analysis</topic><topic>Ubiquitin Thiolesterase</topic><topic>Vasoconstrictor Agents - pharmacology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>online_resources</toplevel><creatorcontrib>You, Junping</creatorcontrib><creatorcontrib>Gulbenkian, Sergio</creatorcontrib><creatorcontrib>Olesen, Inger Jansen</creatorcontrib><creatorcontrib>Marron, Kevin</creatorcontrib><creatorcontrib>Wharton, John</creatorcontrib><creatorcontrib>Barroso, Carla P.</creatorcontrib><creatorcontrib>Polak, Julia M.</creatorcontrib><creatorcontrib>Edvinsson, Lars</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>Journal of the autonomic nervous system</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>You, Junping</au><au>Gulbenkian, Sergio</au><au>Olesen, Inger Jansen</au><au>Marron, Kevin</au><au>Wharton, John</au><au>Barroso, Carla P.</au><au>Polak, Julia M.</au><au>Edvinsson, Lars</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peptidergic innervation of guinea-pig brain vessels: comparison with immunohistochemistry and in vitro pharmacology in rostrally and caudally located arteries</atitle><jtitle>Journal of the autonomic nervous system</jtitle><addtitle>J Auton Nerv Syst</addtitle><date>1995-11-06</date><risdate>1995</risdate><volume>55</volume><issue>3</issue><spage>179</spage><epage>188</epage><pages>179-188</pages><issn>0165-1838</issn><eissn>1872-7476</eissn><coden>JASYDS</coden><abstract>The peptidergic innervation of the guinea-pig basilar artery and the posterior, middle and anterior cerebral arteries were studied by means of immunohistochemical and image analysis techniques using whole mount preparations. An in vitro pharmacological study was performed to correlate the distribution of peptide-containing nerves and the action of neuropeptides on vessel segments from the same vascular regions. The overall distribution of perivascular nerve fibres was demonstrated using an antiserum to the general neuronal marker protein gene product 9.5 (PGP 9.5) and the percentage immunostained area of total vessel wall area occupied by PGP-containing nerves, in each of the basilar, posterior and middle cerebral arteries, was set at 100% and used to determine the relative density of specific populations of autonomic and sensory nerve fibres. In all four cerebral arteries, the majority of nerve fibres possessed neuropeptide Y (NPY) and tyrosine hydroxylase (TH) immunoreactivity, occupying 6.2–13.3% and 5.8–7.5% of the total vessel wall area, respectively. Vasoactive intestinal peptide (VIP), substance P (SP) and calcitonin-gene-related peptide (CGRP) were detected at lower densities. The pharmacological study performed on small circular segments with an intact endothelium revealed that, in all four cerebral arteries, NPY was a more potent constrictor than noradrenaline (NA). The rank order of potency for relaxant agents was CGRP = SP > VIP > ACh in the PCA and MCA, and SP = CGRP > VIP > ACh in the BA and ACA. The correlation between immunostained nerve area and the agonist potency suggested that the denser the peptidergic nerve-supply, the lower the sensitivity to the agonist.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>8801268</pmid><doi>10.1016/0165-1838(95)00045-Y</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Basilar Artery - chemistry Basilar Artery - drug effects Basilar Artery - innervation Biological and medical sciences Brain vessel Cerebral Arteries - chemistry Cerebral Arteries - drug effects Cerebral Arteries - innervation Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges Comparative aspect Fluorescent Antibody Technique, Indirect Fundamental and applied biological sciences. Psychology Guinea pig Guinea Pigs Immunohistochemistry In vitro pharmacology In Vitro Techniques Male Muscle Contraction - drug effects Muscle Contraction - physiology Muscle Relaxation - drug effects Muscle, Smooth, Vascular - chemistry Muscle, Smooth, Vascular - drug effects Muscle, Smooth, Vascular - innervation Muscle, Smooth, Vascular - physiology Nerve Tissue Proteins - analysis Neuropeptides - analysis Neuropeptides - pharmacology Neuropeptides - physiology Norepinephrine - pharmacology Peptidergic mechanism Thiolester Hydrolases - analysis Ubiquitin Thiolesterase Vasoconstrictor Agents - pharmacology Vertebrates: nervous system and sense organs |
title | Peptidergic innervation of guinea-pig brain vessels: comparison with immunohistochemistry and in vitro pharmacology in rostrally and caudally located arteries |
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