Investigating the Influence of GABA Neurons on Dopamine Neurons in the Ventral Tegmental Area Using Optogenetic Techniques
Dopamine (DA) is the key regulator of reward behavior. The DA neurons in the ventral tegmental area (VTA) and their projection areas, which include the prefrontal cortex (PFC), nucleus accumbens (NAc), and amygdala, play a primary role in the process of reward-driven behavior induced by the drugs of...
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Veröffentlicht in: | International journal of molecular sciences 2022-01, Vol.23 (3), p.1114 |
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creator | Ohta, Yasumi Murakami, Takaaki E Kawahara, Mamiko Haruta, Makito Takehara, Hironari Tashiro, Hiroyuki Sasagawa, Kiyotaka Ohta, Jun Akay, Metin Akay, Yasemin M |
description | Dopamine (DA) is the key regulator of reward behavior. The DA neurons in the ventral tegmental area (VTA) and their projection areas, which include the prefrontal cortex (PFC), nucleus accumbens (NAc), and amygdala, play a primary role in the process of reward-driven behavior induced by the drugs of addiction, including nicotine and alcohol. In our previous study, we developed a novel platform consisting of micro-LED array devices to stimulate a large area of the brain of rats and monkeys with photo-stimulation and a microdialysis probe to estimate the DA release in the PFC. Our results suggested that the platform was able to detect the increased level of dopamine in the PFC in response to the photo-stimulation of both the PFC and VTA. In this study, we used this platform to photo-stimulate the VTA neurons in both ChrimsonR-expressing (non-specific) wild and dopamine transporter (DAT)-Cre (dopamine specific) mice, and measured the dopamine release in the nucleus accumbens shell (NAcShell). We measured the DA release in the NAcShell in response to optogenetic stimulation of the VTA neurons and investigated the effect of GABAergic neurons on dopaminergic neurons by histochemical studies. Comparing the photo-stimulation frequency of 2 Hz with that of 20 Hz, the change in DA concentration at the NAcShell was greater at 20 Hz in both cases. When ChrimsonR was expressed specifically for DA, the release of DA at the NAcShell increased in response to photo-stimulation of the VTA. In contrast, when ChrimsonR was expressed non-specifically, the amount of DA released was almost unchanged upon photo-stimulation. However, for nonspecifically expressed ChrimsonR, intraperitoneal injection of bicuculline, a competitive antagonist at the GABA-binding site of the GABA
receptor, also significantly increased the release of DA at the NAcShell in response to photo-stimulation of the VTA. The results of immunochemical staining confirm that GABAergic neurons in the VTA suppress DA activation, and also indicate that alterations in GABAergic neurons may have serious downstream effects on DA activity, NAcShell release, and neural adaptation of the VTA. This study also confirms that optogenetics technology is crucial to study the relationship between the mesolimbic dopaminergic and GABAergic neurons in a neural-specific manner. |
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receptor, also significantly increased the release of DA at the NAcShell in response to photo-stimulation of the VTA. The results of immunochemical staining confirm that GABAergic neurons in the VTA suppress DA activation, and also indicate that alterations in GABAergic neurons may have serious downstream effects on DA activity, NAcShell release, and neural adaptation of the VTA. This study also confirms that optogenetics technology is crucial to study the relationship between the mesolimbic dopaminergic and GABAergic neurons in a neural-specific manner.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23031114</identifier><identifier>PMID: 35163036</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Addictions ; Alcohol ; Amygdala ; Animals ; Bicuculline ; Bicuculline - pharmacology ; Binding sites ; Channelrhodopsins - genetics ; Dopamine ; Dopamine - metabolism ; Dopamine Plasma Membrane Transport Proteins - genetics ; Dopamine Plasma Membrane Transport Proteins - metabolism ; Dopamine receptors ; Dopamine transporter ; Dopaminergic Neurons - metabolism ; Drug addiction ; Experiments ; GABAergic Neurons - metabolism ; Genetics ; Information processing ; Male ; Mesolimbic system ; Mice ; Microdialysis ; Microscopy ; Neurons ; Nicotine ; Nucleus accumbens ; Nucleus Accumbens - metabolism ; Optical Imaging ; Optogenetics - methods ; Prefrontal cortex ; Reinforcement ; Stimulation ; Transgenic animals ; Ventral Tegmental Area - metabolism ; Ventral tegmentum ; γ-Aminobutyric acid A receptors</subject><ispartof>International journal of molecular sciences, 2022-01, Vol.23 (3), p.1114</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-527668c54a9a6205f08aad66741808ee3c2302edb654a94e80f26fb55e334aec3</citedby><cites>FETCH-LOGICAL-c522t-527668c54a9a6205f08aad66741808ee3c2302edb654a94e80f26fb55e334aec3</cites><orcidid>0000-0001-8194-9020</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834722/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8834722/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35163036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ohta, Yasumi</creatorcontrib><creatorcontrib>Murakami, Takaaki E</creatorcontrib><creatorcontrib>Kawahara, Mamiko</creatorcontrib><creatorcontrib>Haruta, Makito</creatorcontrib><creatorcontrib>Takehara, Hironari</creatorcontrib><creatorcontrib>Tashiro, Hiroyuki</creatorcontrib><creatorcontrib>Sasagawa, Kiyotaka</creatorcontrib><creatorcontrib>Ohta, Jun</creatorcontrib><creatorcontrib>Akay, Metin</creatorcontrib><creatorcontrib>Akay, Yasemin M</creatorcontrib><title>Investigating the Influence of GABA Neurons on Dopamine Neurons in the Ventral Tegmental Area Using Optogenetic Techniques</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Dopamine (DA) is the key regulator of reward behavior. The DA neurons in the ventral tegmental area (VTA) and their projection areas, which include the prefrontal cortex (PFC), nucleus accumbens (NAc), and amygdala, play a primary role in the process of reward-driven behavior induced by the drugs of addiction, including nicotine and alcohol. In our previous study, we developed a novel platform consisting of micro-LED array devices to stimulate a large area of the brain of rats and monkeys with photo-stimulation and a microdialysis probe to estimate the DA release in the PFC. Our results suggested that the platform was able to detect the increased level of dopamine in the PFC in response to the photo-stimulation of both the PFC and VTA. In this study, we used this platform to photo-stimulate the VTA neurons in both ChrimsonR-expressing (non-specific) wild and dopamine transporter (DAT)-Cre (dopamine specific) mice, and measured the dopamine release in the nucleus accumbens shell (NAcShell). We measured the DA release in the NAcShell in response to optogenetic stimulation of the VTA neurons and investigated the effect of GABAergic neurons on dopaminergic neurons by histochemical studies. Comparing the photo-stimulation frequency of 2 Hz with that of 20 Hz, the change in DA concentration at the NAcShell was greater at 20 Hz in both cases. When ChrimsonR was expressed specifically for DA, the release of DA at the NAcShell increased in response to photo-stimulation of the VTA. In contrast, when ChrimsonR was expressed non-specifically, the amount of DA released was almost unchanged upon photo-stimulation. However, for nonspecifically expressed ChrimsonR, intraperitoneal injection of bicuculline, a competitive antagonist at the GABA-binding site of the GABA
receptor, also significantly increased the release of DA at the NAcShell in response to photo-stimulation of the VTA. The results of immunochemical staining confirm that GABAergic neurons in the VTA suppress DA activation, and also indicate that alterations in GABAergic neurons may have serious downstream effects on DA activity, NAcShell release, and neural adaptation of the VTA. This study also confirms that optogenetics technology is crucial to study the relationship between the mesolimbic dopaminergic and GABAergic neurons in a neural-specific manner.</description><subject>Addictions</subject><subject>Alcohol</subject><subject>Amygdala</subject><subject>Animals</subject><subject>Bicuculline</subject><subject>Bicuculline - pharmacology</subject><subject>Binding sites</subject><subject>Channelrhodopsins - genetics</subject><subject>Dopamine</subject><subject>Dopamine - metabolism</subject><subject>Dopamine Plasma Membrane Transport Proteins - genetics</subject><subject>Dopamine Plasma Membrane Transport Proteins - metabolism</subject><subject>Dopamine receptors</subject><subject>Dopamine transporter</subject><subject>Dopaminergic Neurons - metabolism</subject><subject>Drug addiction</subject><subject>Experiments</subject><subject>GABAergic Neurons - metabolism</subject><subject>Genetics</subject><subject>Information processing</subject><subject>Male</subject><subject>Mesolimbic system</subject><subject>Mice</subject><subject>Microdialysis</subject><subject>Microscopy</subject><subject>Neurons</subject><subject>Nicotine</subject><subject>Nucleus accumbens</subject><subject>Nucleus Accumbens - metabolism</subject><subject>Optical Imaging</subject><subject>Optogenetics - methods</subject><subject>Prefrontal cortex</subject><subject>Reinforcement</subject><subject>Stimulation</subject><subject>Transgenic animals</subject><subject>Ventral Tegmental Area - metabolism</subject><subject>Ventral tegmentum</subject><subject>γ-Aminobutyric acid A receptors</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdkUtP4zAUhS3EiPeONbLEhgWd8SN2kg1SeU4lNGyAreW6N6mrxC52Umnm1-NQqMqsfOT73aN7dBA6peQn5yX5ZRdtZJxwSmm2gw5oxtiIEJnvbul9dBjjghDGmSj30D4XVKYVeYD-TdwKYmdr3VlX424OeOKqpgdnAPsKP4yvx_gP9MG7iL3Dt36pW-tg82fdx9IruC7oBj9D3SaZ1DiAxi9xcH1adr4GB501CTBzZ996iMfoR6WbCCef7xF6ub97vvk9enx6mNyMH0dGMNaNBMulLIzIdKklI6IihdYzKfOMFqQA4CalZzCbygHJoCAVk9VUCOA802D4Ebpa-y77aQszs75ULYNtdfirvLbq-8TZuar9ShUFz3LGksHFp0Hww-Gdam000DTage-jYpKVROSU5wk9_w9d-D64FG-gUpCSZTJRl2vKBB9jgGpzDCVqKFVtl5rws-0AG_irRf4OIb6eVQ</recordid><startdate>20220120</startdate><enddate>20220120</enddate><creator>Ohta, Yasumi</creator><creator>Murakami, Takaaki E</creator><creator>Kawahara, Mamiko</creator><creator>Haruta, Makito</creator><creator>Takehara, Hironari</creator><creator>Tashiro, Hiroyuki</creator><creator>Sasagawa, Kiyotaka</creator><creator>Ohta, Jun</creator><creator>Akay, Metin</creator><creator>Akay, Yasemin M</creator><general>MDPI AG</general><general>MDPI</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-8194-9020</orcidid></search><sort><creationdate>20220120</creationdate><title>Investigating the Influence of GABA Neurons on Dopamine Neurons in the Ventral Tegmental Area Using Optogenetic Techniques</title><author>Ohta, Yasumi ; Murakami, Takaaki E ; Kawahara, Mamiko ; Haruta, Makito ; Takehara, Hironari ; Tashiro, Hiroyuki ; Sasagawa, Kiyotaka ; Ohta, Jun ; Akay, Metin ; Akay, Yasemin M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c522t-527668c54a9a6205f08aad66741808ee3c2302edb654a94e80f26fb55e334aec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Addictions</topic><topic>Alcohol</topic><topic>Amygdala</topic><topic>Animals</topic><topic>Bicuculline</topic><topic>Bicuculline - pharmacology</topic><topic>Binding sites</topic><topic>Channelrhodopsins - genetics</topic><topic>Dopamine</topic><topic>Dopamine - metabolism</topic><topic>Dopamine Plasma Membrane Transport Proteins - genetics</topic><topic>Dopamine Plasma Membrane Transport Proteins - metabolism</topic><topic>Dopamine receptors</topic><topic>Dopamine transporter</topic><topic>Dopaminergic Neurons - metabolism</topic><topic>Drug addiction</topic><topic>Experiments</topic><topic>GABAergic Neurons - metabolism</topic><topic>Genetics</topic><topic>Information processing</topic><topic>Male</topic><topic>Mesolimbic system</topic><topic>Mice</topic><topic>Microdialysis</topic><topic>Microscopy</topic><topic>Neurons</topic><topic>Nicotine</topic><topic>Nucleus accumbens</topic><topic>Nucleus Accumbens - metabolism</topic><topic>Optical Imaging</topic><topic>Optogenetics - methods</topic><topic>Prefrontal cortex</topic><topic>Reinforcement</topic><topic>Stimulation</topic><topic>Transgenic animals</topic><topic>Ventral Tegmental Area - metabolism</topic><topic>Ventral tegmentum</topic><topic>γ-Aminobutyric acid A receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohta, Yasumi</creatorcontrib><creatorcontrib>Murakami, Takaaki E</creatorcontrib><creatorcontrib>Kawahara, Mamiko</creatorcontrib><creatorcontrib>Haruta, Makito</creatorcontrib><creatorcontrib>Takehara, Hironari</creatorcontrib><creatorcontrib>Tashiro, Hiroyuki</creatorcontrib><creatorcontrib>Sasagawa, Kiyotaka</creatorcontrib><creatorcontrib>Ohta, Jun</creatorcontrib><creatorcontrib>Akay, Metin</creatorcontrib><creatorcontrib>Akay, Yasemin M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohta, Yasumi</au><au>Murakami, Takaaki E</au><au>Kawahara, Mamiko</au><au>Haruta, Makito</au><au>Takehara, Hironari</au><au>Tashiro, Hiroyuki</au><au>Sasagawa, Kiyotaka</au><au>Ohta, Jun</au><au>Akay, Metin</au><au>Akay, Yasemin M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigating the Influence of GABA Neurons on Dopamine Neurons in the Ventral Tegmental Area Using Optogenetic Techniques</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2022-01-20</date><risdate>2022</risdate><volume>23</volume><issue>3</issue><spage>1114</spage><pages>1114-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Dopamine (DA) is the key regulator of reward behavior. The DA neurons in the ventral tegmental area (VTA) and their projection areas, which include the prefrontal cortex (PFC), nucleus accumbens (NAc), and amygdala, play a primary role in the process of reward-driven behavior induced by the drugs of addiction, including nicotine and alcohol. In our previous study, we developed a novel platform consisting of micro-LED array devices to stimulate a large area of the brain of rats and monkeys with photo-stimulation and a microdialysis probe to estimate the DA release in the PFC. Our results suggested that the platform was able to detect the increased level of dopamine in the PFC in response to the photo-stimulation of both the PFC and VTA. In this study, we used this platform to photo-stimulate the VTA neurons in both ChrimsonR-expressing (non-specific) wild and dopamine transporter (DAT)-Cre (dopamine specific) mice, and measured the dopamine release in the nucleus accumbens shell (NAcShell). We measured the DA release in the NAcShell in response to optogenetic stimulation of the VTA neurons and investigated the effect of GABAergic neurons on dopaminergic neurons by histochemical studies. Comparing the photo-stimulation frequency of 2 Hz with that of 20 Hz, the change in DA concentration at the NAcShell was greater at 20 Hz in both cases. When ChrimsonR was expressed specifically for DA, the release of DA at the NAcShell increased in response to photo-stimulation of the VTA. In contrast, when ChrimsonR was expressed non-specifically, the amount of DA released was almost unchanged upon photo-stimulation. However, for nonspecifically expressed ChrimsonR, intraperitoneal injection of bicuculline, a competitive antagonist at the GABA-binding site of the GABA
receptor, also significantly increased the release of DA at the NAcShell in response to photo-stimulation of the VTA. The results of immunochemical staining confirm that GABAergic neurons in the VTA suppress DA activation, and also indicate that alterations in GABAergic neurons may have serious downstream effects on DA activity, NAcShell release, and neural adaptation of the VTA. This study also confirms that optogenetics technology is crucial to study the relationship between the mesolimbic dopaminergic and GABAergic neurons in a neural-specific manner.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35163036</pmid><doi>10.3390/ijms23031114</doi><orcidid>https://orcid.org/0000-0001-8194-9020</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Addictions Alcohol Amygdala Animals Bicuculline Bicuculline - pharmacology Binding sites Channelrhodopsins - genetics Dopamine Dopamine - metabolism Dopamine Plasma Membrane Transport Proteins - genetics Dopamine Plasma Membrane Transport Proteins - metabolism Dopamine receptors Dopamine transporter Dopaminergic Neurons - metabolism Drug addiction Experiments GABAergic Neurons - metabolism Genetics Information processing Male Mesolimbic system Mice Microdialysis Microscopy Neurons Nicotine Nucleus accumbens Nucleus Accumbens - metabolism Optical Imaging Optogenetics - methods Prefrontal cortex Reinforcement Stimulation Transgenic animals Ventral Tegmental Area - metabolism Ventral tegmentum γ-Aminobutyric acid A receptors |
title | Investigating the Influence of GABA Neurons on Dopamine Neurons in the Ventral Tegmental Area Using Optogenetic Techniques |
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