Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta
Despite the importance of somatodendritic dopamine (DA) release in the Substantia Nigra pars compacta (SNc), its mechanism remains poorly understood. Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mecha...
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description | Despite the importance of somatodendritic dopamine (DA) release in the Substantia Nigra pars compacta (SNc), its mechanism remains poorly understood. Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+.
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The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological ac |
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Open science badges
This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.
The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological activity of SNc neurons. We show that basal [DA]out is largely independent of action potentials, but is strongly regulated by intracellular Ca2+. These data shed new light on differences between somatodendritic DA release and axon terminal release, indicating that release from these sites can be controlled independently.
Open Science: This manuscript was awarded with the Open Materials Badge.
For more information see: https://cos.io/our-services/open-science-badges/</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/jnc.14587</identifier><identifier>PMID: 30203851</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Action potential ; Adenosine triphosphatase ; Amphetamines ; Brain ; Brain slice preparation ; Ca2+ imaging ; Ca2+-transporting ATPase ; Calcium ; Calcium (extracellular) ; Calcium (intracellular) ; Calcium (reticular) ; Calcium channels ; Calcium channels (voltage-gated) ; Calcium influx ; Calcium ions ; Cell membranes ; Cocaine ; Dependence ; Dihydroxyphenylalanine ; Dopamine ; Dopamine D2 receptors ; electrochemistry ; Electrophysiology ; Endoplasmic reticulum ; Ethyl carbamate ; Firing rate ; FSCAV ; Hyperpolarization ; Inhibition ; Intracellular ; Levodopa ; Pharmacology ; Quinpirole ; rat brain ; Reduction ; Substantia nigra ; Tetrodotoxin</subject><ispartof>Journal of neurochemistry, 2019-02, Vol.148 (4), p.462-479</ispartof><rights>2018 International Society for Neurochemistry</rights><rights>2018 International Society for Neurochemistry.</rights><rights>Copyright © 2019 International Society for Neurochemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3887-284626d6c4cee0537597c73c145320d2593c921ef74a6561c52a2d3185915c433</citedby><cites>FETCH-LOGICAL-c3887-284626d6c4cee0537597c73c145320d2593c921ef74a6561c52a2d3185915c433</cites><orcidid>0000-0002-0981-6634 ; 0000-0001-6109-8724</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjnc.14587$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjnc.14587$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30203851$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yee, Andrew G.</creatorcontrib><creatorcontrib>Forbes, Blaze</creatorcontrib><creatorcontrib>Cheung, Pang‐Ying</creatorcontrib><creatorcontrib>Martini, Alessandro</creatorcontrib><creatorcontrib>Burrell, Mark H.</creatorcontrib><creatorcontrib>Freestone, Peter S.</creatorcontrib><creatorcontrib>Lipski, Janusz</creatorcontrib><title>Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>Despite the importance of somatodendritic dopamine (DA) release in the Substantia Nigra pars compacta (SNc), its mechanism remains poorly understood. Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+.
Open science badges
This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.
The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological activity of SNc neurons. We show that basal [DA]out is largely independent of action potentials, but is strongly regulated by intracellular Ca2+. These data shed new light on differences between somatodendritic DA release and axon terminal release, indicating that release from these sites can be controlled independently.
Open Science: This manuscript was awarded with the Open Materials Badge.
For more information see: https://cos.io/our-services/open-science-badges/</description><subject>Action potential</subject><subject>Adenosine triphosphatase</subject><subject>Amphetamines</subject><subject>Brain</subject><subject>Brain slice preparation</subject><subject>Ca2+ imaging</subject><subject>Ca2+-transporting ATPase</subject><subject>Calcium</subject><subject>Calcium (extracellular)</subject><subject>Calcium (intracellular)</subject><subject>Calcium (reticular)</subject><subject>Calcium channels</subject><subject>Calcium channels (voltage-gated)</subject><subject>Calcium influx</subject><subject>Calcium ions</subject><subject>Cell membranes</subject><subject>Cocaine</subject><subject>Dependence</subject><subject>Dihydroxyphenylalanine</subject><subject>Dopamine</subject><subject>Dopamine D2 receptors</subject><subject>electrochemistry</subject><subject>Electrophysiology</subject><subject>Endoplasmic reticulum</subject><subject>Ethyl carbamate</subject><subject>Firing rate</subject><subject>FSCAV</subject><subject>Hyperpolarization</subject><subject>Inhibition</subject><subject>Intracellular</subject><subject>Levodopa</subject><subject>Pharmacology</subject><subject>Quinpirole</subject><subject>rat brain</subject><subject>Reduction</subject><subject>Substantia nigra</subject><subject>Tetrodotoxin</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1kT1PHDEQhq0oKBwkBX8gspSGFMv5cz9KdIJAhI4CUq_MeA582rU3tlcn_n1MDigixcVYHj16NOOXkBPOzng5y62HM65023wgC64aXimuu49kwZgQlWRKHJKjlLaM8VrV_BM5lEww2Wq-ILtzyC54OoWMPjszUOMtBTOAm0dqcUJv0QPSsKE5eAc0hdHkUJo2ulzeNkxmdB5pxAFNQuo8zU9I7-aHlM2Lk67dYzR0MjFRCONkIJvP5GBjhoRfXu9j8uvy4n51Vd3c_rhend9UINu2qUSralHbGhQgMi0b3TXQSCjbSsGs0J2ETnDcNMrUuuaghRFW8lZ3XIOS8pic7r1TDL9nTLkfXQIcBuMxzKkXnAlZSi0K-u0fdBvm6Mt0hWqFbKUSXaG-7ymIIaWIm36KbjTxueesf0mjL2n0f9Mo7NdX4_wwon0n376_AMs9sHMDPv_f1P9cr_bKP8JsksY</recordid><startdate>201902</startdate><enddate>201902</enddate><creator>Yee, Andrew G.</creator><creator>Forbes, Blaze</creator><creator>Cheung, Pang‐Ying</creator><creator>Martini, Alessandro</creator><creator>Burrell, Mark H.</creator><creator>Freestone, Peter S.</creator><creator>Lipski, Janusz</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0981-6634</orcidid><orcidid>https://orcid.org/0000-0001-6109-8724</orcidid></search><sort><creationdate>201902</creationdate><title>Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta</title><author>Yee, Andrew G. ; Forbes, Blaze ; Cheung, Pang‐Ying ; Martini, Alessandro ; Burrell, Mark H. ; Freestone, Peter S. ; Lipski, Janusz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3887-284626d6c4cee0537597c73c145320d2593c921ef74a6561c52a2d3185915c433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Action potential</topic><topic>Adenosine triphosphatase</topic><topic>Amphetamines</topic><topic>Brain</topic><topic>Brain slice preparation</topic><topic>Ca2+ imaging</topic><topic>Ca2+-transporting ATPase</topic><topic>Calcium</topic><topic>Calcium (extracellular)</topic><topic>Calcium (intracellular)</topic><topic>Calcium (reticular)</topic><topic>Calcium channels</topic><topic>Calcium channels (voltage-gated)</topic><topic>Calcium influx</topic><topic>Calcium ions</topic><topic>Cell membranes</topic><topic>Cocaine</topic><topic>Dependence</topic><topic>Dihydroxyphenylalanine</topic><topic>Dopamine</topic><topic>Dopamine D2 receptors</topic><topic>electrochemistry</topic><topic>Electrophysiology</topic><topic>Endoplasmic reticulum</topic><topic>Ethyl carbamate</topic><topic>Firing rate</topic><topic>FSCAV</topic><topic>Hyperpolarization</topic><topic>Inhibition</topic><topic>Intracellular</topic><topic>Levodopa</topic><topic>Pharmacology</topic><topic>Quinpirole</topic><topic>rat brain</topic><topic>Reduction</topic><topic>Substantia nigra</topic><topic>Tetrodotoxin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yee, Andrew G.</creatorcontrib><creatorcontrib>Forbes, Blaze</creatorcontrib><creatorcontrib>Cheung, Pang‐Ying</creatorcontrib><creatorcontrib>Martini, Alessandro</creatorcontrib><creatorcontrib>Burrell, Mark H.</creatorcontrib><creatorcontrib>Freestone, Peter S.</creatorcontrib><creatorcontrib>Lipski, Janusz</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yee, Andrew G.</au><au>Forbes, Blaze</au><au>Cheung, Pang‐Ying</au><au>Martini, Alessandro</au><au>Burrell, Mark H.</au><au>Freestone, Peter S.</au><au>Lipski, Janusz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>2019-02</date><risdate>2019</risdate><volume>148</volume><issue>4</issue><spage>462</spage><epage>479</epage><pages>462-479</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><abstract>Despite the importance of somatodendritic dopamine (DA) release in the Substantia Nigra pars compacta (SNc), its mechanism remains poorly understood. Using a novel approach combining fast‐scan controlled‐adsorption voltammetry (FSCAV) and single‐unit electrophysiology, we have investigated the mechanism of somatodendritic release by directly correlating basal (non‐stimulated) extracellular DA concentration ([DA]out), with pharmacologically‐induced changes of firing of nigral dopaminergic neurons in rat brain slices. FSCAV measurements indicated that basal [DA]out in the SNc was 40.7 ± 2.0 nM (at 34 ± 0.5°C), which was enhanced by amphetamine, cocaine, and L‐DOPA, and reduced by VMAT2 inhibitor, Ro4‐1284. Complete inhibition of firing by TTX decreased basal [DA]out, but this reduction was smaller than the effect of D2 receptor agonist, quinpirole. Despite similar effects on neuronal firing, the larger decrease in [DA]out evoked by quinpirole was attributed to cell membrane hyperpolarization and greater reduction in cytosolic free Ca2+ ([Ca2+]in). Decreasing extracellular Ca2+ also reduced basal [DA]out, despite increasing firing frequency. Furthermore, inhibiting L‐type Ca2+ channels decreased basal [DA]out, although specific Cav1.3 channel inhibition did not affect firing rate. Inhibition of sarcoplasmic/endoplasmic reticulum Ca2+‐ATPase (SERCA) also decreased [DA]out, demonstrating the importance of intracellular Ca2+ stores for somatodendritic release. Finally, in vivo FSCAV measurements showed that basal [DA]out in the SNc was 79.8 ± 10.9 nM in urethane‐anesthetized rats, which was enhanced by amphetamine. Overall, our findings indicate that although tonic somatodendritic DA release is largely independent of action potentials, basal [DA]out is strongly regulated by voltage‐dependent Ca2+ influx and release of intracellular Ca2+.
Open science badges
This article has received a badge for *Open Materials* because it provided all relevant information to reproduce the study in the manuscript. The complete Open Science Disclosure form for this article can be found at the end of the article. More information about the Open Practices badges can be found at https://cos.io/our-services/open-science-badges/.
The mechanism underlying tonic dopamine (DA) release from somata and dendrites of Substantia Nigra pars compacta (SNc) neurons remains poorly understood. We have directly correlated absolute extracellular DA concentration ([DA]out) with electrophysiological activity of SNc neurons. We show that basal [DA]out is largely independent of action potentials, but is strongly regulated by intracellular Ca2+. These data shed new light on differences between somatodendritic DA release and axon terminal release, indicating that release from these sites can be controlled independently.
Open Science: This manuscript was awarded with the Open Materials Badge.
For more information see: https://cos.io/our-services/open-science-badges/</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>30203851</pmid><doi>10.1111/jnc.14587</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-0981-6634</orcidid><orcidid>https://orcid.org/0000-0001-6109-8724</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Action potential Adenosine triphosphatase Amphetamines Brain Brain slice preparation Ca2+ imaging Ca2+-transporting ATPase Calcium Calcium (extracellular) Calcium (intracellular) Calcium (reticular) Calcium channels Calcium channels (voltage-gated) Calcium influx Calcium ions Cell membranes Cocaine Dependence Dihydroxyphenylalanine Dopamine Dopamine D2 receptors electrochemistry Electrophysiology Endoplasmic reticulum Ethyl carbamate Firing rate FSCAV Hyperpolarization Inhibition Intracellular Levodopa Pharmacology Quinpirole rat brain Reduction Substantia nigra Tetrodotoxin |
title | Action potential and calcium dependence of tonic somatodendritic dopamine release in the Substantia Nigra pars compacta |
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