Loading…
Cannabinoid CB1 receptor and serotonin 3 receptor subunit A (5-HT3A) are co-expressed in GABA neurons in the rat telencephalon
Among all described serotonin (5‐HT) receptors in mammals, the type three (5‐HT3) is the only ligand‐gated ion channel receptor for serotonin. By using double in situ hybridization histochemistry, we found co‐expression of the functional 5‐HT3A subunit of the 5‐HT3 receptor and the central CB1 canna...
Saved in:
Published in: | Journal of comparative neurology (1911) 2004-01, Vol.468 (2), p.205-216 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873 |
---|---|
cites | cdi_FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873 |
container_end_page | 216 |
container_issue | 2 |
container_start_page | 205 |
container_title | Journal of comparative neurology (1911) |
container_volume | 468 |
creator | Morales, Marisela Wang, Shwun-De Diaz-Ruiz, Oscar Hyun-Jin Jho, Diana |
description | Among all described serotonin (5‐HT) receptors in mammals, the type three (5‐HT3) is the only ligand‐gated ion channel receptor for serotonin. By using double in situ hybridization histochemistry, we found co‐expression of the functional 5‐HT3A subunit of the 5‐HT3 receptor and the central CB1 cannabinoid receptor in neurons of the rat telencephalon. Double‐labeled 5‐HT3A/CB1 neurons were found in the anterior olfactory nucleus, superficial and deep layers of the cortex, hippocampal formation (hippocampus, dentate gyrus, subiculum, and entorhinal cortex) and amygdala. Analysis of the proportion of neurons co‐expressing 5‐HT3A and CB1 receptors in the cortex and amygdala showed that, depending on the brain region, 37–53% of all neurons expressing the 5‐HT3A subunit also expressed CB1 transcripts; 16–72% of the total population of neurons expressing CB1 mRNA co‐expressed the 5‐HT3A subunit. By using a combination of double in situ hybridization and immunohistochemistry, we demonstrated that 5‐HT3A/CB1‐expressing neurons contained the inhibitory neurotransmitter γ‐aminobutyric acid (GABA). These results imply that in distinct regions of the telencephalon, GABA neurons that react to cannabinoids may also be responsive to serotonin through 5‐HT3 receptors. Cellular coexistence of 5‐HT3A and CB1 transcripts in interneurons of the cortex, hippocampal formation, and amygdala suggest possible interactions between the cannabinoid and serotonergic systems at the level of GABA neurotransmission in brain areas involved in cognition, memory, and emotion. J. Comp. Neurol. 468:205–216, 2004. Published 2003 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cne.10968 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71554962</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71554962</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873</originalsourceid><addsrcrecordid>eNqFkcFO3DAQhq2qFWy3HPoClU8VHFLsOLbjY4hgoUWgSrRIvViOPREpWXuxEwGXPjvZ7racEKeZ0Xz_d_kR-kjJF0pIfmg9TIsS5Rs0W89MlYK-RbPpRzOlhNxF71P6TQhRipU7aJcWoihFSWboT228N03nQ-dwfURxBAurIURsvMMJYhiC7zxmz480NqPvBlzhfZ6dXrHqAJsI2IYMHlYRUgKHp8SiOqqwhzEGn9b3cAM4mgEP0IOfVDemD_4DeteaPsHeds7Rj5Pjq_o0O79cnNXVeWaZImXmWiMK2gDhzBQ0bwhI6bhwlhrpJPBW2pzT3FFVtMQ1jnPG2sI6IbkUrJRsjj5vvKsY7kZIg152yULfGw9hTFpSzgsl8ldBqnIiyOSfo4MNaGNIKUKrV7FbmvioKdHrVvTUiv7bysR-2krHZgnumdzWMAGHG-C-6-HxZZOuL47_KbNNoksDPPxPmHirhWSS6-uLhb7--v3Xt58nVHP2BCqopGA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19206055</pqid></control><display><type>article</type><title>Cannabinoid CB1 receptor and serotonin 3 receptor subunit A (5-HT3A) are co-expressed in GABA neurons in the rat telencephalon</title><source>Wiley</source><creator>Morales, Marisela ; Wang, Shwun-De ; Diaz-Ruiz, Oscar ; Hyun-Jin Jho, Diana</creator><creatorcontrib>Morales, Marisela ; Wang, Shwun-De ; Diaz-Ruiz, Oscar ; Hyun-Jin Jho, Diana</creatorcontrib><description>Among all described serotonin (5‐HT) receptors in mammals, the type three (5‐HT3) is the only ligand‐gated ion channel receptor for serotonin. By using double in situ hybridization histochemistry, we found co‐expression of the functional 5‐HT3A subunit of the 5‐HT3 receptor and the central CB1 cannabinoid receptor in neurons of the rat telencephalon. Double‐labeled 5‐HT3A/CB1 neurons were found in the anterior olfactory nucleus, superficial and deep layers of the cortex, hippocampal formation (hippocampus, dentate gyrus, subiculum, and entorhinal cortex) and amygdala. Analysis of the proportion of neurons co‐expressing 5‐HT3A and CB1 receptors in the cortex and amygdala showed that, depending on the brain region, 37–53% of all neurons expressing the 5‐HT3A subunit also expressed CB1 transcripts; 16–72% of the total population of neurons expressing CB1 mRNA co‐expressed the 5‐HT3A subunit. By using a combination of double in situ hybridization and immunohistochemistry, we demonstrated that 5‐HT3A/CB1‐expressing neurons contained the inhibitory neurotransmitter γ‐aminobutyric acid (GABA). These results imply that in distinct regions of the telencephalon, GABA neurons that react to cannabinoids may also be responsive to serotonin through 5‐HT3 receptors. Cellular coexistence of 5‐HT3A and CB1 transcripts in interneurons of the cortex, hippocampal formation, and amygdala suggest possible interactions between the cannabinoid and serotonergic systems at the level of GABA neurotransmission in brain areas involved in cognition, memory, and emotion. J. Comp. Neurol. 468:205–216, 2004. Published 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.10968</identifier><identifier>PMID: 14648680</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>amygdala ; Animals ; Cannabinoids - analysis ; Cannabinoids - biosynthesis ; Cannabinoids - genetics ; CCK ; cortex ; gamma-Aminobutyric Acid - analysis ; gamma-Aminobutyric Acid - biosynthesis ; gamma-Aminobutyric Acid - genetics ; Gene Expression Regulation - physiology ; Male ; Neurons - chemistry ; Neurons - metabolism ; Rats ; Rats, Sprague-Dawley ; Receptor, Cannabinoid, CB1 - analysis ; Receptor, Cannabinoid, CB1 - biosynthesis ; Receptor, Cannabinoid, CB1 - genetics ; Receptors, Serotonin, 5-HT3 - analysis ; Receptors, Serotonin, 5-HT3 - biosynthesis ; Receptors, Serotonin, 5-HT3 - genetics ; Telencephalon - chemistry ; Telencephalon - metabolism</subject><ispartof>Journal of comparative neurology (1911), 2004-01, Vol.468 (2), p.205-216</ispartof><rights>Published 2003 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873</citedby><cites>FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873</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/14648680$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morales, Marisela</creatorcontrib><creatorcontrib>Wang, Shwun-De</creatorcontrib><creatorcontrib>Diaz-Ruiz, Oscar</creatorcontrib><creatorcontrib>Hyun-Jin Jho, Diana</creatorcontrib><title>Cannabinoid CB1 receptor and serotonin 3 receptor subunit A (5-HT3A) are co-expressed in GABA neurons in the rat telencephalon</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Among all described serotonin (5‐HT) receptors in mammals, the type three (5‐HT3) is the only ligand‐gated ion channel receptor for serotonin. By using double in situ hybridization histochemistry, we found co‐expression of the functional 5‐HT3A subunit of the 5‐HT3 receptor and the central CB1 cannabinoid receptor in neurons of the rat telencephalon. Double‐labeled 5‐HT3A/CB1 neurons were found in the anterior olfactory nucleus, superficial and deep layers of the cortex, hippocampal formation (hippocampus, dentate gyrus, subiculum, and entorhinal cortex) and amygdala. Analysis of the proportion of neurons co‐expressing 5‐HT3A and CB1 receptors in the cortex and amygdala showed that, depending on the brain region, 37–53% of all neurons expressing the 5‐HT3A subunit also expressed CB1 transcripts; 16–72% of the total population of neurons expressing CB1 mRNA co‐expressed the 5‐HT3A subunit. By using a combination of double in situ hybridization and immunohistochemistry, we demonstrated that 5‐HT3A/CB1‐expressing neurons contained the inhibitory neurotransmitter γ‐aminobutyric acid (GABA). These results imply that in distinct regions of the telencephalon, GABA neurons that react to cannabinoids may also be responsive to serotonin through 5‐HT3 receptors. Cellular coexistence of 5‐HT3A and CB1 transcripts in interneurons of the cortex, hippocampal formation, and amygdala suggest possible interactions between the cannabinoid and serotonergic systems at the level of GABA neurotransmission in brain areas involved in cognition, memory, and emotion. J. Comp. Neurol. 468:205–216, 2004. Published 2003 Wiley‐Liss, Inc.</description><subject>amygdala</subject><subject>Animals</subject><subject>Cannabinoids - analysis</subject><subject>Cannabinoids - biosynthesis</subject><subject>Cannabinoids - genetics</subject><subject>CCK</subject><subject>cortex</subject><subject>gamma-Aminobutyric Acid - analysis</subject><subject>gamma-Aminobutyric Acid - biosynthesis</subject><subject>gamma-Aminobutyric Acid - genetics</subject><subject>Gene Expression Regulation - physiology</subject><subject>Male</subject><subject>Neurons - chemistry</subject><subject>Neurons - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, Cannabinoid, CB1 - analysis</subject><subject>Receptor, Cannabinoid, CB1 - biosynthesis</subject><subject>Receptor, Cannabinoid, CB1 - genetics</subject><subject>Receptors, Serotonin, 5-HT3 - analysis</subject><subject>Receptors, Serotonin, 5-HT3 - biosynthesis</subject><subject>Receptors, Serotonin, 5-HT3 - genetics</subject><subject>Telencephalon - chemistry</subject><subject>Telencephalon - metabolism</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkcFO3DAQhq2qFWy3HPoClU8VHFLsOLbjY4hgoUWgSrRIvViOPREpWXuxEwGXPjvZ7racEKeZ0Xz_d_kR-kjJF0pIfmg9TIsS5Rs0W89MlYK-RbPpRzOlhNxF71P6TQhRipU7aJcWoihFSWboT228N03nQ-dwfURxBAurIURsvMMJYhiC7zxmz480NqPvBlzhfZ6dXrHqAJsI2IYMHlYRUgKHp8SiOqqwhzEGn9b3cAM4mgEP0IOfVDemD_4DeteaPsHeds7Rj5Pjq_o0O79cnNXVeWaZImXmWiMK2gDhzBQ0bwhI6bhwlhrpJPBW2pzT3FFVtMQ1jnPG2sI6IbkUrJRsjj5vvKsY7kZIg152yULfGw9hTFpSzgsl8ldBqnIiyOSfo4MNaGNIKUKrV7FbmvioKdHrVvTUiv7bysR-2krHZgnumdzWMAGHG-C-6-HxZZOuL47_KbNNoksDPPxPmHirhWSS6-uLhb7--v3Xt58nVHP2BCqopGA</recordid><startdate>20040106</startdate><enddate>20040106</enddate><creator>Morales, Marisela</creator><creator>Wang, Shwun-De</creator><creator>Diaz-Ruiz, Oscar</creator><creator>Hyun-Jin Jho, Diana</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>20040106</creationdate><title>Cannabinoid CB1 receptor and serotonin 3 receptor subunit A (5-HT3A) are co-expressed in GABA neurons in the rat telencephalon</title><author>Morales, Marisela ; Wang, Shwun-De ; Diaz-Ruiz, Oscar ; Hyun-Jin Jho, Diana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>amygdala</topic><topic>Animals</topic><topic>Cannabinoids - analysis</topic><topic>Cannabinoids - biosynthesis</topic><topic>Cannabinoids - genetics</topic><topic>CCK</topic><topic>cortex</topic><topic>gamma-Aminobutyric Acid - analysis</topic><topic>gamma-Aminobutyric Acid - biosynthesis</topic><topic>gamma-Aminobutyric Acid - genetics</topic><topic>Gene Expression Regulation - physiology</topic><topic>Male</topic><topic>Neurons - chemistry</topic><topic>Neurons - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, Cannabinoid, CB1 - analysis</topic><topic>Receptor, Cannabinoid, CB1 - biosynthesis</topic><topic>Receptor, Cannabinoid, CB1 - genetics</topic><topic>Receptors, Serotonin, 5-HT3 - analysis</topic><topic>Receptors, Serotonin, 5-HT3 - biosynthesis</topic><topic>Receptors, Serotonin, 5-HT3 - genetics</topic><topic>Telencephalon - chemistry</topic><topic>Telencephalon - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morales, Marisela</creatorcontrib><creatorcontrib>Wang, Shwun-De</creatorcontrib><creatorcontrib>Diaz-Ruiz, Oscar</creatorcontrib><creatorcontrib>Hyun-Jin Jho, Diana</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>Morales, Marisela</au><au>Wang, Shwun-De</au><au>Diaz-Ruiz, Oscar</au><au>Hyun-Jin Jho, Diana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cannabinoid CB1 receptor and serotonin 3 receptor subunit A (5-HT3A) are co-expressed in GABA neurons in the rat telencephalon</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2004-01-06</date><risdate>2004</risdate><volume>468</volume><issue>2</issue><spage>205</spage><epage>216</epage><pages>205-216</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Among all described serotonin (5‐HT) receptors in mammals, the type three (5‐HT3) is the only ligand‐gated ion channel receptor for serotonin. By using double in situ hybridization histochemistry, we found co‐expression of the functional 5‐HT3A subunit of the 5‐HT3 receptor and the central CB1 cannabinoid receptor in neurons of the rat telencephalon. Double‐labeled 5‐HT3A/CB1 neurons were found in the anterior olfactory nucleus, superficial and deep layers of the cortex, hippocampal formation (hippocampus, dentate gyrus, subiculum, and entorhinal cortex) and amygdala. Analysis of the proportion of neurons co‐expressing 5‐HT3A and CB1 receptors in the cortex and amygdala showed that, depending on the brain region, 37–53% of all neurons expressing the 5‐HT3A subunit also expressed CB1 transcripts; 16–72% of the total population of neurons expressing CB1 mRNA co‐expressed the 5‐HT3A subunit. By using a combination of double in situ hybridization and immunohistochemistry, we demonstrated that 5‐HT3A/CB1‐expressing neurons contained the inhibitory neurotransmitter γ‐aminobutyric acid (GABA). These results imply that in distinct regions of the telencephalon, GABA neurons that react to cannabinoids may also be responsive to serotonin through 5‐HT3 receptors. Cellular coexistence of 5‐HT3A and CB1 transcripts in interneurons of the cortex, hippocampal formation, and amygdala suggest possible interactions between the cannabinoid and serotonergic systems at the level of GABA neurotransmission in brain areas involved in cognition, memory, and emotion. J. Comp. Neurol. 468:205–216, 2004. Published 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14648680</pmid><doi>10.1002/cne.10968</doi><tpages>12</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9967 |
ispartof | Journal of comparative neurology (1911), 2004-01, Vol.468 (2), p.205-216 |
issn | 0021-9967 1096-9861 |
language | eng |
recordid | cdi_proquest_miscellaneous_71554962 |
source | Wiley |
subjects | amygdala Animals Cannabinoids - analysis Cannabinoids - biosynthesis Cannabinoids - genetics CCK cortex gamma-Aminobutyric Acid - analysis gamma-Aminobutyric Acid - biosynthesis gamma-Aminobutyric Acid - genetics Gene Expression Regulation - physiology Male Neurons - chemistry Neurons - metabolism Rats Rats, Sprague-Dawley Receptor, Cannabinoid, CB1 - analysis Receptor, Cannabinoid, CB1 - biosynthesis Receptor, Cannabinoid, CB1 - genetics Receptors, Serotonin, 5-HT3 - analysis Receptors, Serotonin, 5-HT3 - biosynthesis Receptors, Serotonin, 5-HT3 - genetics Telencephalon - chemistry Telencephalon - metabolism |
title | Cannabinoid CB1 receptor and serotonin 3 receptor subunit A (5-HT3A) are co-expressed in GABA neurons in the rat telencephalon |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T02%3A20%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cannabinoid%20CB1%20receptor%20and%20serotonin%203%20receptor%20subunit%20A%20(5-HT3A)%20are%20co-expressed%20in%20GABA%20neurons%20in%20the%20rat%20telencephalon&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Morales,%20Marisela&rft.date=2004-01-06&rft.volume=468&rft.issue=2&rft.spage=205&rft.epage=216&rft.pages=205-216&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/cne.10968&rft_dat=%3Cproquest_cross%3E71554962%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3908-dfa641be053a412b0e77d56dc1a7d7e5f7c2512d194f0dbd5533f4cd675763873%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=19206055&rft_id=info:pmid/14648680&rfr_iscdi=true |