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Immunolocalization of CB 1 receptor in rat striatal neurons: A confocal microscopy study
Several lines of evidence indicate that cannabinoids, among other functions, are involved in motor control. Although cannabinoid receptors (CB 1 ) mRNA has been observed in medium‐sized spiny neurons of the striatum, a description of the precise localization of CB 1 at a protein level among striatal...
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Published in: | Synapse (New York, N.Y.) N.Y.), 2004-09, Vol.53 (3), p.159-167 |
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container_title | Synapse (New York, N.Y.) |
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creator | Fusco, F.R. Martorana, A. Giampà, C. De March, Z. Farini, D. D'Angelo, V. Sancesario, G. Bernardi, G. |
description | Several lines of evidence indicate that cannabinoids, among other functions, are involved in motor control. Although cannabinoid receptors (CB
1
) mRNA has been observed in medium‐sized spiny neurons of the striatum, a description of the precise localization of CB
1
at a protein level among striatal cells is still lacking. Therefore, we performed immunohistochemical studies with light and confocal microscopy to identify neuronal subpopulations that express CB
1
and to assess the distribution of the receptor within these neurons. In our single label light microscopy study, CB
1
was observed in most medium‐sized neurons of the caudate‐putamen. However, CB
1
was also present in large‐sized neurons scattered throughout the striatum. Our dual‐label study showed that 89.3% of projection neurons in matrix contain CB
1
, and that 56.4% of projection neurons in patch are labeled for CB
1
. To investigate the presence of CB
1
among the different subclasses of striatal interneurons we performed a double‐labeling study matching CB
1
and each of the striatal interneuron markers, namely, choline acetyl‐transferase, parvalbumin, calretinin, and nitric oxide synthase. Our double‐label study showed that most parvalbumin immunoreactive interneurons (86.5%), more than one‐third (39.2%) of cholinergic interneurons, and about one‐third (30.4%) of the NOS‐positive neurons are labeled for CB
1
. Calretinin‐immunolabeled neurons were devoid of CB
1
. Synapse 53:159–167, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/syn.20047 |
format | article |
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1
) mRNA has been observed in medium‐sized spiny neurons of the striatum, a description of the precise localization of CB
1
at a protein level among striatal cells is still lacking. Therefore, we performed immunohistochemical studies with light and confocal microscopy to identify neuronal subpopulations that express CB
1
and to assess the distribution of the receptor within these neurons. In our single label light microscopy study, CB
1
was observed in most medium‐sized neurons of the caudate‐putamen. However, CB
1
was also present in large‐sized neurons scattered throughout the striatum. Our dual‐label study showed that 89.3% of projection neurons in matrix contain CB
1
, and that 56.4% of projection neurons in patch are labeled for CB
1
. To investigate the presence of CB
1
among the different subclasses of striatal interneurons we performed a double‐labeling study matching CB
1
and each of the striatal interneuron markers, namely, choline acetyl‐transferase, parvalbumin, calretinin, and nitric oxide synthase. Our double‐label study showed that most parvalbumin immunoreactive interneurons (86.5%), more than one‐third (39.2%) of cholinergic interneurons, and about one‐third (30.4%) of the NOS‐positive neurons are labeled for CB
1
. Calretinin‐immunolabeled neurons were devoid of CB
1
. Synapse 53:159–167, 2004. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0887-4476</identifier><identifier>EISSN: 1098-2396</identifier><identifier>DOI: 10.1002/syn.20047</identifier><language>eng</language><ispartof>Synapse (New York, N.Y.), 2004-09, Vol.53 (3), p.159-167</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c747-db13f92ebd5e986f96911dbd3424e8fa84bb57a7650a7d349f4e6c7f3bf931a83</citedby><cites>FETCH-LOGICAL-c747-db13f92ebd5e986f96911dbd3424e8fa84bb57a7650a7d349f4e6c7f3bf931a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Fusco, F.R.</creatorcontrib><creatorcontrib>Martorana, A.</creatorcontrib><creatorcontrib>Giampà, C.</creatorcontrib><creatorcontrib>De March, Z.</creatorcontrib><creatorcontrib>Farini, D.</creatorcontrib><creatorcontrib>D'Angelo, V.</creatorcontrib><creatorcontrib>Sancesario, G.</creatorcontrib><creatorcontrib>Bernardi, G.</creatorcontrib><title>Immunolocalization of CB 1 receptor in rat striatal neurons: A confocal microscopy study</title><title>Synapse (New York, N.Y.)</title><description>Several lines of evidence indicate that cannabinoids, among other functions, are involved in motor control. Although cannabinoid receptors (CB
1
) mRNA has been observed in medium‐sized spiny neurons of the striatum, a description of the precise localization of CB
1
at a protein level among striatal cells is still lacking. Therefore, we performed immunohistochemical studies with light and confocal microscopy to identify neuronal subpopulations that express CB
1
and to assess the distribution of the receptor within these neurons. In our single label light microscopy study, CB
1
was observed in most medium‐sized neurons of the caudate‐putamen. However, CB
1
was also present in large‐sized neurons scattered throughout the striatum. Our dual‐label study showed that 89.3% of projection neurons in matrix contain CB
1
, and that 56.4% of projection neurons in patch are labeled for CB
1
. To investigate the presence of CB
1
among the different subclasses of striatal interneurons we performed a double‐labeling study matching CB
1
and each of the striatal interneuron markers, namely, choline acetyl‐transferase, parvalbumin, calretinin, and nitric oxide synthase. Our double‐label study showed that most parvalbumin immunoreactive interneurons (86.5%), more than one‐third (39.2%) of cholinergic interneurons, and about one‐third (30.4%) of the NOS‐positive neurons are labeled for CB
1
. Calretinin‐immunolabeled neurons were devoid of CB
1
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1
) mRNA has been observed in medium‐sized spiny neurons of the striatum, a description of the precise localization of CB
1
at a protein level among striatal cells is still lacking. Therefore, we performed immunohistochemical studies with light and confocal microscopy to identify neuronal subpopulations that express CB
1
and to assess the distribution of the receptor within these neurons. In our single label light microscopy study, CB
1
was observed in most medium‐sized neurons of the caudate‐putamen. However, CB
1
was also present in large‐sized neurons scattered throughout the striatum. Our dual‐label study showed that 89.3% of projection neurons in matrix contain CB
1
, and that 56.4% of projection neurons in patch are labeled for CB
1
. To investigate the presence of CB
1
among the different subclasses of striatal interneurons we performed a double‐labeling study matching CB
1
and each of the striatal interneuron markers, namely, choline acetyl‐transferase, parvalbumin, calretinin, and nitric oxide synthase. Our double‐label study showed that most parvalbumin immunoreactive interneurons (86.5%), more than one‐third (39.2%) of cholinergic interneurons, and about one‐third (30.4%) of the NOS‐positive neurons are labeled for CB
1
. Calretinin‐immunolabeled neurons were devoid of CB
1
. Synapse 53:159–167, 2004. © 2004 Wiley‐Liss, Inc.</abstract><doi>10.1002/syn.20047</doi><tpages>9</tpages></addata></record> |
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title | Immunolocalization of CB 1 receptor in rat striatal neurons: A confocal microscopy study |
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