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Distribution of type 1 cannabinoid receptor-expressing neurons in the septal-hypothalamic region of the mouse: Colocalization with GABAergic and glutamatergic markers
Type 1 cannabinoid receptor (CB1) is the principal mediator of retrograde endocannabinoid signaling in the brain. In this study, we addressed the topographic distribution and amino acid neurotransmitter phenotype of endocannabinoid‐sensitive hypothalamic neurons in mice. The in situ hybridization de...
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Published in: | Journal of comparative neurology (1911) 2012-04, Vol.520 (5), p.1005-1020 |
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container_title | Journal of comparative neurology (1911) |
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description | Type 1 cannabinoid receptor (CB1) is the principal mediator of retrograde endocannabinoid signaling in the brain. In this study, we addressed the topographic distribution and amino acid neurotransmitter phenotype of endocannabinoid‐sensitive hypothalamic neurons in mice. The in situ hybridization detection of CB1 mRNA revealed high levels of expression in the medial septum (MS) and the diagonal band of Broca (DBB), moderate levels in the preoptic area and the hypothalamic lateroanterior (LA), paraventricular (Pa), ventromedial (VMH), lateral mammillary (LM), and ventral premammillary (PMV) nuclei, and low levels in many other hypothalamic regions including the suprachiasmatic (SCh) and arcuate (Arc) nuclei. This regional distribution pattern was compared with location of γ‐aminobutyric acid (GABA)ergic and glutamatergic cell groups, as identified by the expression of glutamic acid decarboxylase 65 (GAD65) and type 2 vesicular glutamate transporter (VGLUT2) mRNAs, respectively. The MS, DBB, and preoptic area showed overlaps between GABAergic and CB1‐expressing neurons, whereas hypothalamic sites with moderate CB1 signals, including the LA, Pa, VMH, LM, and PMV, were dominated by glutamatergic neurons. Low CB1 mRNA levels were also present in other glutamatergic and GABAergic regions. Dual‐label in situ hybridization experiments confirmed the cellular co‐expression of CB1 with both glutamatergic and GABAergic markers. In this report we provide a detailed anatomical map of hypothalamic glutamatergic and GABAergic systems whose neurotransmitter release is controlled by retrograde endocannabinoid signaling from hypothalamic and extrahypothalamic target neurons. This neuroanatomical information contributes to an understanding of the role that the endocannabinoid system plays in the regulation of endocrine and metabolic functions. J. Comp. Neurol. 520:1005–1020, 2012. © 2011 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/cne.22766 |
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In this study, we addressed the topographic distribution and amino acid neurotransmitter phenotype of endocannabinoid‐sensitive hypothalamic neurons in mice. The in situ hybridization detection of CB1 mRNA revealed high levels of expression in the medial septum (MS) and the diagonal band of Broca (DBB), moderate levels in the preoptic area and the hypothalamic lateroanterior (LA), paraventricular (Pa), ventromedial (VMH), lateral mammillary (LM), and ventral premammillary (PMV) nuclei, and low levels in many other hypothalamic regions including the suprachiasmatic (SCh) and arcuate (Arc) nuclei. This regional distribution pattern was compared with location of γ‐aminobutyric acid (GABA)ergic and glutamatergic cell groups, as identified by the expression of glutamic acid decarboxylase 65 (GAD65) and type 2 vesicular glutamate transporter (VGLUT2) mRNAs, respectively. The MS, DBB, and preoptic area showed overlaps between GABAergic and CB1‐expressing neurons, whereas hypothalamic sites with moderate CB1 signals, including the LA, Pa, VMH, LM, and PMV, were dominated by glutamatergic neurons. Low CB1 mRNA levels were also present in other glutamatergic and GABAergic regions. Dual‐label in situ hybridization experiments confirmed the cellular co‐expression of CB1 with both glutamatergic and GABAergic markers. In this report we provide a detailed anatomical map of hypothalamic glutamatergic and GABAergic systems whose neurotransmitter release is controlled by retrograde endocannabinoid signaling from hypothalamic and extrahypothalamic target neurons. This neuroanatomical information contributes to an understanding of the role that the endocannabinoid system plays in the regulation of endocrine and metabolic functions. J. Comp. Neurol. 520:1005–1020, 2012. © 2011 Wiley Periodicals, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.22766</identifier><identifier>PMID: 21935941</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Biomarkers - metabolism ; endocannabinoid ; gamma-Aminobutyric Acid - metabolism ; gamma-Aminobutyric Acid - physiology ; Glutamic Acid - metabolism ; Glutamic Acid - physiology ; glutamic acid decarboxylase (GAD) ; Hypothalamus - chemistry ; Hypothalamus - cytology ; Hypothalamus - metabolism ; in situ hybridization ; Male ; Mice ; Neural Pathways - chemistry ; Neural Pathways - metabolism ; Neural Pathways - physiology ; Neurons - chemistry ; Neurons - metabolism ; Neurons - physiology ; Receptor, Cannabinoid, CB1 - biosynthesis ; Receptor, Cannabinoid, CB1 - metabolism ; Septum of Brain - chemistry ; Septum of Brain - metabolism ; type 1 cannabinoid receptor (CB1) ; vesicular glutamate transporter 2 (VGLUT2) ; γ-aminobutyric acid (GABA)</subject><ispartof>Journal of comparative neurology (1911), 2012-04, Vol.520 (5), p.1005-1020</ispartof><rights>Copyright © 2011 Wiley‐Liss, Inc.</rights><rights>Copyright © 2011 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4586-4085ca3ed28f54fc7f4f670efdcbb392721951c7b0f38ddc2bb0ebb76c78bd13</citedby><cites>FETCH-LOGICAL-c4586-4085ca3ed28f54fc7f4f670efdcbb392721951c7b0f38ddc2bb0ebb76c78bd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21935941$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hrabovszky, Erik</creatorcontrib><creatorcontrib>Wittmann, Gábor</creatorcontrib><creatorcontrib>Kalló, Imre</creatorcontrib><creatorcontrib>Füzesi, Tamás</creatorcontrib><creatorcontrib>Fekete, Csaba</creatorcontrib><creatorcontrib>Liposits, Zsolt</creatorcontrib><title>Distribution of type 1 cannabinoid receptor-expressing neurons in the septal-hypothalamic region of the mouse: Colocalization with GABAergic and glutamatergic markers</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Type 1 cannabinoid receptor (CB1) is the principal mediator of retrograde endocannabinoid signaling in the brain. In this study, we addressed the topographic distribution and amino acid neurotransmitter phenotype of endocannabinoid‐sensitive hypothalamic neurons in mice. The in situ hybridization detection of CB1 mRNA revealed high levels of expression in the medial septum (MS) and the diagonal band of Broca (DBB), moderate levels in the preoptic area and the hypothalamic lateroanterior (LA), paraventricular (Pa), ventromedial (VMH), lateral mammillary (LM), and ventral premammillary (PMV) nuclei, and low levels in many other hypothalamic regions including the suprachiasmatic (SCh) and arcuate (Arc) nuclei. This regional distribution pattern was compared with location of γ‐aminobutyric acid (GABA)ergic and glutamatergic cell groups, as identified by the expression of glutamic acid decarboxylase 65 (GAD65) and type 2 vesicular glutamate transporter (VGLUT2) mRNAs, respectively. The MS, DBB, and preoptic area showed overlaps between GABAergic and CB1‐expressing neurons, whereas hypothalamic sites with moderate CB1 signals, including the LA, Pa, VMH, LM, and PMV, were dominated by glutamatergic neurons. Low CB1 mRNA levels were also present in other glutamatergic and GABAergic regions. Dual‐label in situ hybridization experiments confirmed the cellular co‐expression of CB1 with both glutamatergic and GABAergic markers. In this report we provide a detailed anatomical map of hypothalamic glutamatergic and GABAergic systems whose neurotransmitter release is controlled by retrograde endocannabinoid signaling from hypothalamic and extrahypothalamic target neurons. This neuroanatomical information contributes to an understanding of the role that the endocannabinoid system plays in the regulation of endocrine and metabolic functions. J. Comp. 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Wittmann, Gábor ; Kalló, Imre ; Füzesi, Tamás ; Fekete, Csaba ; Liposits, Zsolt</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4586-4085ca3ed28f54fc7f4f670efdcbb392721951c7b0f38ddc2bb0ebb76c78bd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biomarkers - metabolism</topic><topic>endocannabinoid</topic><topic>gamma-Aminobutyric Acid - metabolism</topic><topic>gamma-Aminobutyric Acid - physiology</topic><topic>Glutamic Acid - metabolism</topic><topic>Glutamic Acid - physiology</topic><topic>glutamic acid decarboxylase (GAD)</topic><topic>Hypothalamus - chemistry</topic><topic>Hypothalamus - cytology</topic><topic>Hypothalamus - metabolism</topic><topic>in situ hybridization</topic><topic>Male</topic><topic>Mice</topic><topic>Neural Pathways - chemistry</topic><topic>Neural Pathways - metabolism</topic><topic>Neural Pathways - physiology</topic><topic>Neurons - chemistry</topic><topic>Neurons - metabolism</topic><topic>Neurons - physiology</topic><topic>Receptor, Cannabinoid, CB1 - biosynthesis</topic><topic>Receptor, Cannabinoid, CB1 - metabolism</topic><topic>Septum of Brain - chemistry</topic><topic>Septum of Brain - metabolism</topic><topic>type 1 cannabinoid receptor (CB1)</topic><topic>vesicular glutamate transporter 2 (VGLUT2)</topic><topic>γ-aminobutyric acid (GABA)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hrabovszky, Erik</creatorcontrib><creatorcontrib>Wittmann, Gábor</creatorcontrib><creatorcontrib>Kalló, Imre</creatorcontrib><creatorcontrib>Füzesi, Tamás</creatorcontrib><creatorcontrib>Fekete, Csaba</creatorcontrib><creatorcontrib>Liposits, Zsolt</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>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering 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>Hrabovszky, Erik</au><au>Wittmann, Gábor</au><au>Kalló, Imre</au><au>Füzesi, Tamás</au><au>Fekete, Csaba</au><au>Liposits, Zsolt</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distribution of type 1 cannabinoid receptor-expressing neurons in the septal-hypothalamic region of the mouse: Colocalization with GABAergic and glutamatergic markers</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2012-04-01</date><risdate>2012</risdate><volume>520</volume><issue>5</issue><spage>1005</spage><epage>1020</epage><pages>1005-1020</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Type 1 cannabinoid receptor (CB1) is the principal mediator of retrograde endocannabinoid signaling in the brain. In this study, we addressed the topographic distribution and amino acid neurotransmitter phenotype of endocannabinoid‐sensitive hypothalamic neurons in mice. The in situ hybridization detection of CB1 mRNA revealed high levels of expression in the medial septum (MS) and the diagonal band of Broca (DBB), moderate levels in the preoptic area and the hypothalamic lateroanterior (LA), paraventricular (Pa), ventromedial (VMH), lateral mammillary (LM), and ventral premammillary (PMV) nuclei, and low levels in many other hypothalamic regions including the suprachiasmatic (SCh) and arcuate (Arc) nuclei. This regional distribution pattern was compared with location of γ‐aminobutyric acid (GABA)ergic and glutamatergic cell groups, as identified by the expression of glutamic acid decarboxylase 65 (GAD65) and type 2 vesicular glutamate transporter (VGLUT2) mRNAs, respectively. The MS, DBB, and preoptic area showed overlaps between GABAergic and CB1‐expressing neurons, whereas hypothalamic sites with moderate CB1 signals, including the LA, Pa, VMH, LM, and PMV, were dominated by glutamatergic neurons. Low CB1 mRNA levels were also present in other glutamatergic and GABAergic regions. Dual‐label in situ hybridization experiments confirmed the cellular co‐expression of CB1 with both glutamatergic and GABAergic markers. In this report we provide a detailed anatomical map of hypothalamic glutamatergic and GABAergic systems whose neurotransmitter release is controlled by retrograde endocannabinoid signaling from hypothalamic and extrahypothalamic target neurons. This neuroanatomical information contributes to an understanding of the role that the endocannabinoid system plays in the regulation of endocrine and metabolic functions. J. Comp. Neurol. 520:1005–1020, 2012. © 2011 Wiley Periodicals, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21935941</pmid><doi>10.1002/cne.22766</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomarkers - metabolism endocannabinoid gamma-Aminobutyric Acid - metabolism gamma-Aminobutyric Acid - physiology Glutamic Acid - metabolism Glutamic Acid - physiology glutamic acid decarboxylase (GAD) Hypothalamus - chemistry Hypothalamus - cytology Hypothalamus - metabolism in situ hybridization Male Mice Neural Pathways - chemistry Neural Pathways - metabolism Neural Pathways - physiology Neurons - chemistry Neurons - metabolism Neurons - physiology Receptor, Cannabinoid, CB1 - biosynthesis Receptor, Cannabinoid, CB1 - metabolism Septum of Brain - chemistry Septum of Brain - metabolism type 1 cannabinoid receptor (CB1) vesicular glutamate transporter 2 (VGLUT2) γ-aminobutyric acid (GABA) |
title | Distribution of type 1 cannabinoid receptor-expressing neurons in the septal-hypothalamic region of the mouse: Colocalization with GABAergic and glutamatergic markers |
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