Regulation of psychomotor functions by dopamine: integration of various approaches
(1)The basal ganglia circuitry mediates a wide rage of brain functions such as motor control, behavioral planning, and reward prediction. Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons...
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Veröffentlicht in: | Folia Pharmacologica Japonica 2003, Vol.122(3), pp.215-225 |
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creator | SASA, Masashi NISHI, Akinori KOBAYASHI, Kazuto SANO, Hiromi MOMIYAMA, Toshihiko URAMURA, Kazuhide YADA, Toshihiko MORI, Norio SUZUKI, Katsuaki MINABE, Yoshio |
description | (1)The basal ganglia circuitry mediates a wide rage of brain functions such as motor control, behavioral planning, and reward prediction. Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons but also is involved in the pattern formation of their firing. The striatopallidal neurons containing dopamine D2 receptor plays a dual role in motor coordination dependent on DA transmission. (2)Activation of presynaptic D2-like receptors on GABAergic terminals onto striatal cholinergic interneurons selectively blocks N-type Ca2+ channels, thereby inhibiting GABA release. In addition, contribution of N-type channels and D2-like receptor-mediated presynaptic inhibition decreases in parallel with development, implying some relationship between basal ganglia-related function or dysfunction and age. (3)As an approach to determine dopamine neuronal activity, we monitored neuronal activities by measuring cytosolic Ca2+ concentration in VTA dopamine neurons. The present study indicates that VTA dopamine neurons are the direct targets of orexin-A and psychostimulants, and the [Ca2+]i signaling is thought to play a significant role in the regulation of dopamine neuronal activity. (4)The excitability of neostriatal neurons is regulated by a balance of glutamatergic and dopaminergic inputs. Glutamate has been shown to modulate dopaminergic signaling. Studies on the regulation of DARPP-32 phosphorylation by glutamate provide a molecular basis for both the synergistic and antagonistic effects of glutamate on dopaminergic signaling. (5) Impairment of function of stem/progenitor cells may be implicated in the pathogenesis of schizophrenia. To test this hypothesis, several experiments are currently ongoing in our laboratory, and the preliminary results obtained are described here. |
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Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons but also is involved in the pattern formation of their firing. The striatopallidal neurons containing dopamine D2 receptor plays a dual role in motor coordination dependent on DA transmission. (2)Activation of presynaptic D2-like receptors on GABAergic terminals onto striatal cholinergic interneurons selectively blocks N-type Ca2+ channels, thereby inhibiting GABA release. In addition, contribution of N-type channels and D2-like receptor-mediated presynaptic inhibition decreases in parallel with development, implying some relationship between basal ganglia-related function or dysfunction and age. (3)As an approach to determine dopamine neuronal activity, we monitored neuronal activities by measuring cytosolic Ca2+ concentration in VTA dopamine neurons. The present study indicates that VTA dopamine neurons are the direct targets of orexin-A and psychostimulants, and the [Ca2+]i signaling is thought to play a significant role in the regulation of dopamine neuronal activity. (4)The excitability of neostriatal neurons is regulated by a balance of glutamatergic and dopaminergic inputs. Glutamate has been shown to modulate dopaminergic signaling. Studies on the regulation of DARPP-32 phosphorylation by glutamate provide a molecular basis for both the synergistic and antagonistic effects of glutamate on dopaminergic signaling. (5) Impairment of function of stem/progenitor cells may be implicated in the pathogenesis of schizophrenia. To test this hypothesis, several experiments are currently ongoing in our laboratory, and the preliminary results obtained are described here.</description><identifier>ISSN: 0015-5691</identifier><identifier>EISSN: 1347-8397</identifier><identifier>DOI: 10.1254/fpj.122.215</identifier><identifier>PMID: 12939539</identifier><language>jpn</language><publisher>Japan: The Japanese Pharmacological Society</publisher><subject>Animals ; Brain - physiology ; Calcium - metabolism ; Calcium Channels, N-Type - physiology ; Calcium Signaling - physiology ; DARPP-32 ; Dopamine - physiology ; Dopamine and cAMP-Regulated Phosphoprotein 32 ; dopamine neuron ; dopamine receptor ; Glutamates - physiology ; Humans ; Nerve Tissue Proteins ; Phosphoproteins - physiology ; Psychomotor Performance - physiology ; Receptors, Dopamine D2 - physiology ; Receptors, Glutamate - physiology ; schizophrenia ; Schizophrenia - etiology ; striatal neuron ; Synaptic Transmission - physiology</subject><ispartof>Folia Pharmacologica Japonica, 2003, Vol.122(3), pp.215-225</ispartof><rights>2003 by The Japanese Pharmacological Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2955-549c25a2571ec76c0e52db05ba3a91735d39ad3d6f7800d56be2701bdbcd5fb93</citedby><cites>FETCH-LOGICAL-c2955-549c25a2571ec76c0e52db05ba3a91735d39ad3d6f7800d56be2701bdbcd5fb93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4014,27914,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12939539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SASA, Masashi</creatorcontrib><creatorcontrib>NISHI, Akinori</creatorcontrib><creatorcontrib>KOBAYASHI, Kazuto</creatorcontrib><creatorcontrib>SANO, Hiromi</creatorcontrib><creatorcontrib>MOMIYAMA, Toshihiko</creatorcontrib><creatorcontrib>URAMURA, Kazuhide</creatorcontrib><creatorcontrib>YADA, Toshihiko</creatorcontrib><creatorcontrib>MORI, Norio</creatorcontrib><creatorcontrib>SUZUKI, Katsuaki</creatorcontrib><creatorcontrib>MINABE, Yoshio</creatorcontrib><title>Regulation of psychomotor functions by dopamine: integration of various approaches</title><title>Folia Pharmacologica Japonica</title><addtitle>Nihon Yakurigaku Zasshi</addtitle><description>(1)The basal ganglia circuitry mediates a wide rage of brain functions such as motor control, behavioral planning, and reward prediction. Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons but also is involved in the pattern formation of their firing. The striatopallidal neurons containing dopamine D2 receptor plays a dual role in motor coordination dependent on DA transmission. (2)Activation of presynaptic D2-like receptors on GABAergic terminals onto striatal cholinergic interneurons selectively blocks N-type Ca2+ channels, thereby inhibiting GABA release. In addition, contribution of N-type channels and D2-like receptor-mediated presynaptic inhibition decreases in parallel with development, implying some relationship between basal ganglia-related function or dysfunction and age. (3)As an approach to determine dopamine neuronal activity, we monitored neuronal activities by measuring cytosolic Ca2+ concentration in VTA dopamine neurons. The present study indicates that VTA dopamine neurons are the direct targets of orexin-A and psychostimulants, and the [Ca2+]i signaling is thought to play a significant role in the regulation of dopamine neuronal activity. (4)The excitability of neostriatal neurons is regulated by a balance of glutamatergic and dopaminergic inputs. Glutamate has been shown to modulate dopaminergic signaling. Studies on the regulation of DARPP-32 phosphorylation by glutamate provide a molecular basis for both the synergistic and antagonistic effects of glutamate on dopaminergic signaling. (5) Impairment of function of stem/progenitor cells may be implicated in the pathogenesis of schizophrenia. To test this hypothesis, several experiments are currently ongoing in our laboratory, and the preliminary results obtained are described here.</description><subject>Animals</subject><subject>Brain - physiology</subject><subject>Calcium - metabolism</subject><subject>Calcium Channels, N-Type - physiology</subject><subject>Calcium Signaling - physiology</subject><subject>DARPP-32</subject><subject>Dopamine - physiology</subject><subject>Dopamine and cAMP-Regulated Phosphoprotein 32</subject><subject>dopamine neuron</subject><subject>dopamine receptor</subject><subject>Glutamates - physiology</subject><subject>Humans</subject><subject>Nerve Tissue Proteins</subject><subject>Phosphoproteins - physiology</subject><subject>Psychomotor Performance - physiology</subject><subject>Receptors, Dopamine D2 - physiology</subject><subject>Receptors, Glutamate - physiology</subject><subject>schizophrenia</subject><subject>Schizophrenia - etiology</subject><subject>striatal neuron</subject><subject>Synaptic Transmission - physiology</subject><issn>0015-5691</issn><issn>1347-8397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkMtrwzAMxs3YWEvX0-4jp11GOj_quN6tjL2gMCjb2fiV1iWJMzsZ9L-fS0N2kYT00yfxAXCL4AJhunws20Mq8AIjegGmiCxZviKcXYIphIjmtOBoAuYxOgUhZZgVBF2DCcKccEr4FGy3dtdXsnO-yXyZtfGo9772nQ9Z2Tf61I-ZOmbGt7J2jX3KXNPZXRg3fmVwvo-ZbNvgpd7beAOuSllFOx_yDHy_vnw9v-ebz7eP5_Um15jT9NqSa0wlpgxZzQoNLcVGQaokkRwxQg3h0hBTlGwFoaGFsphBpIzShpaKkxm4P-umwz-9jZ2oXdS2qmRj00eCkYIRgooEPpxBHXyMwZaiDa6W4SgQFCcXRXIxFVgkFxN9N8j2qrbmnx08S8D6DBxiJ3d2BGTonK7sKEaGmETHmd7LIGxD_gBtnoYC</recordid><startdate>2003</startdate><enddate>2003</enddate><creator>SASA, Masashi</creator><creator>NISHI, Akinori</creator><creator>KOBAYASHI, Kazuto</creator><creator>SANO, Hiromi</creator><creator>MOMIYAMA, Toshihiko</creator><creator>URAMURA, Kazuhide</creator><creator>YADA, Toshihiko</creator><creator>MORI, Norio</creator><creator>SUZUKI, Katsuaki</creator><creator>MINABE, Yoshio</creator><general>The Japanese Pharmacological Society</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>7X8</scope></search><sort><creationdate>2003</creationdate><title>Regulation of psychomotor functions by dopamine: integration of various approaches</title><author>SASA, Masashi ; NISHI, Akinori ; KOBAYASHI, Kazuto ; SANO, Hiromi ; MOMIYAMA, Toshihiko ; URAMURA, Kazuhide ; YADA, Toshihiko ; MORI, Norio ; SUZUKI, Katsuaki ; MINABE, Yoshio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2955-549c25a2571ec76c0e52db05ba3a91735d39ad3d6f7800d56be2701bdbcd5fb93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Brain - physiology</topic><topic>Calcium - metabolism</topic><topic>Calcium Channels, N-Type - physiology</topic><topic>Calcium Signaling - physiology</topic><topic>DARPP-32</topic><topic>Dopamine - physiology</topic><topic>Dopamine and cAMP-Regulated Phosphoprotein 32</topic><topic>dopamine neuron</topic><topic>dopamine receptor</topic><topic>Glutamates - physiology</topic><topic>Humans</topic><topic>Nerve Tissue Proteins</topic><topic>Phosphoproteins - physiology</topic><topic>Psychomotor Performance - physiology</topic><topic>Receptors, Dopamine D2 - physiology</topic><topic>Receptors, Glutamate - physiology</topic><topic>schizophrenia</topic><topic>Schizophrenia - etiology</topic><topic>striatal neuron</topic><topic>Synaptic Transmission - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SASA, Masashi</creatorcontrib><creatorcontrib>NISHI, Akinori</creatorcontrib><creatorcontrib>KOBAYASHI, Kazuto</creatorcontrib><creatorcontrib>SANO, Hiromi</creatorcontrib><creatorcontrib>MOMIYAMA, Toshihiko</creatorcontrib><creatorcontrib>URAMURA, Kazuhide</creatorcontrib><creatorcontrib>YADA, Toshihiko</creatorcontrib><creatorcontrib>MORI, Norio</creatorcontrib><creatorcontrib>SUZUKI, Katsuaki</creatorcontrib><creatorcontrib>MINABE, Yoshio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Folia Pharmacologica Japonica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SASA, Masashi</au><au>NISHI, Akinori</au><au>KOBAYASHI, Kazuto</au><au>SANO, Hiromi</au><au>MOMIYAMA, Toshihiko</au><au>URAMURA, Kazuhide</au><au>YADA, Toshihiko</au><au>MORI, Norio</au><au>SUZUKI, Katsuaki</au><au>MINABE, Yoshio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of psychomotor functions by dopamine: integration of various approaches</atitle><jtitle>Folia Pharmacologica Japonica</jtitle><addtitle>Nihon Yakurigaku Zasshi</addtitle><date>2003</date><risdate>2003</risdate><volume>122</volume><issue>3</issue><spage>215</spage><epage>225</epage><pages>215-225</pages><issn>0015-5691</issn><eissn>1347-8397</eissn><abstract>(1)The basal ganglia circuitry mediates a wide rage of brain functions such as motor control, behavioral planning, and reward prediction. Dopamine (DA) transmission plays an essential role in the regulation of these brain functions. DA action not only regulates the firing activity of target neurons but also is involved in the pattern formation of their firing. The striatopallidal neurons containing dopamine D2 receptor plays a dual role in motor coordination dependent on DA transmission. (2)Activation of presynaptic D2-like receptors on GABAergic terminals onto striatal cholinergic interneurons selectively blocks N-type Ca2+ channels, thereby inhibiting GABA release. In addition, contribution of N-type channels and D2-like receptor-mediated presynaptic inhibition decreases in parallel with development, implying some relationship between basal ganglia-related function or dysfunction and age. (3)As an approach to determine dopamine neuronal activity, we monitored neuronal activities by measuring cytosolic Ca2+ concentration in VTA dopamine neurons. The present study indicates that VTA dopamine neurons are the direct targets of orexin-A and psychostimulants, and the [Ca2+]i signaling is thought to play a significant role in the regulation of dopamine neuronal activity. (4)The excitability of neostriatal neurons is regulated by a balance of glutamatergic and dopaminergic inputs. Glutamate has been shown to modulate dopaminergic signaling. Studies on the regulation of DARPP-32 phosphorylation by glutamate provide a molecular basis for both the synergistic and antagonistic effects of glutamate on dopaminergic signaling. (5) Impairment of function of stem/progenitor cells may be implicated in the pathogenesis of schizophrenia. To test this hypothesis, several experiments are currently ongoing in our laboratory, and the preliminary results obtained are described here.</abstract><cop>Japan</cop><pub>The Japanese Pharmacological Society</pub><pmid>12939539</pmid><doi>10.1254/fpj.122.215</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Brain - physiology Calcium - metabolism Calcium Channels, N-Type - physiology Calcium Signaling - physiology DARPP-32 Dopamine - physiology Dopamine and cAMP-Regulated Phosphoprotein 32 dopamine neuron dopamine receptor Glutamates - physiology Humans Nerve Tissue Proteins Phosphoproteins - physiology Psychomotor Performance - physiology Receptors, Dopamine D2 - physiology Receptors, Glutamate - physiology schizophrenia Schizophrenia - etiology striatal neuron Synaptic Transmission - physiology |
title | Regulation of psychomotor functions by dopamine: integration of various approaches |
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