In vitro and in vivo physiology of low nanomolar concentrations of Zn2+ in artificial cerebrospinal fluid
Artificial cerebrospinal fluid (ACSF), i.e., brain extracellular medium, which includes Ca 2+ and Mg 2+ , but not other divalent cations such as Zn 2+ , has been used for in vitro and in vivo experiments. The present study deals with the physiological significance of extracellular Zn 2+ in ACSF. Spo...
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description | Artificial cerebrospinal fluid (ACSF), i.e., brain extracellular medium, which includes Ca
2+
and Mg
2+
, but not other divalent cations such as Zn
2+
, has been used for
in vitro
and
in vivo
experiments. The present study deals with the physiological significance of extracellular Zn
2+
in ACSF. Spontaneous presynaptic activity is suppressed in the stratum lucidum of brain slices from young rats bathed in ACSF containing 10 nM ZnCl
2
, indicating that extracellular Zn
2+
modifies hippocampal presynaptic activity. To examine the
in vivo
action of 10 nM ZnCl
2
on long-term potentiation (LTP), the recording region was perfused using a recording electrode attached to a microdialysis probe. The magnitude of LTP was not modified in young rats by perfusion with ACSF containing 10 nM ZnCl
2
, compared to perfusion with ACSF without Zn
2+
, but attenuated by perfusion with ACSF containing 100 nM ZnCl
2
. Interestingly, the magnitude of LTP was not modified in aged rats even by perfusion with ACSF containing 100 nM ZnCl
2
, but enhanced by perfusion with ACSF containing 10 mM CaEDTA, an extracellular Zn
2+
chelator. The present study indicates that the basal levels of extracellular Zn
2+
, which are in the range of low nanomolar concentrations, are critical for synaptic activity and perhaps increased age-dependently. |
doi_str_mv | 10.1038/srep42897 |
format | Article |
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2+
and Mg
2+
, but not other divalent cations such as Zn
2+
, has been used for
in vitro
and
in vivo
experiments. The present study deals with the physiological significance of extracellular Zn
2+
in ACSF. Spontaneous presynaptic activity is suppressed in the stratum lucidum of brain slices from young rats bathed in ACSF containing 10 nM ZnCl
2
, indicating that extracellular Zn
2+
modifies hippocampal presynaptic activity. To examine the
in vivo
action of 10 nM ZnCl
2
on long-term potentiation (LTP), the recording region was perfused using a recording electrode attached to a microdialysis probe. The magnitude of LTP was not modified in young rats by perfusion with ACSF containing 10 nM ZnCl
2
, compared to perfusion with ACSF without Zn
2+
, but attenuated by perfusion with ACSF containing 100 nM ZnCl
2
. Interestingly, the magnitude of LTP was not modified in aged rats even by perfusion with ACSF containing 100 nM ZnCl
2
, but enhanced by perfusion with ACSF containing 10 mM CaEDTA, an extracellular Zn
2+
chelator. The present study indicates that the basal levels of extracellular Zn
2+
, which are in the range of low nanomolar concentrations, are critical for synaptic activity and perhaps increased age-dependently.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep42897</identifier><identifier>PMID: 28211543</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14 ; 14/19 ; 631/378/548/2589 ; 631/443/376 ; Age ; Brain slice preparation ; Calcium (extracellular) ; Cations ; Cerebrospinal fluid ; Hippocampus ; Humanities and Social Sciences ; Long-term potentiation ; Magnesium ; Microdialysis ; multidisciplinary ; Perfusion ; Physiology ; Rodents ; Science ; Zinc</subject><ispartof>Scientific reports, 2017-02, Vol.7 (1), p.42897-42897, Article 42897</ispartof><rights>The Author(s) 2017</rights><rights>Copyright Nature Publishing Group Feb 2017</rights><rights>Copyright © 2017, The Author(s) 2017 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c411t-3330d1bc52235bfac50727c33db3689c22e08fcbe4eddba42b1cb2e40ba035c73</citedby><cites>FETCH-LOGICAL-c411t-3330d1bc52235bfac50727c33db3689c22e08fcbe4eddba42b1cb2e40ba035c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314341/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314341/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,27905,27906,41101,42170,51557,53772,53774</link.rule.ids></links><search><creatorcontrib>Tamano, Haruna</creatorcontrib><creatorcontrib>Nishio, Ryusuke</creatorcontrib><creatorcontrib>Shakushi, Yukina</creatorcontrib><creatorcontrib>Sasaki, Miku</creatorcontrib><creatorcontrib>koike, Yuta</creatorcontrib><creatorcontrib>Osawa, Misa</creatorcontrib><creatorcontrib>Takeda, Atsushi</creatorcontrib><title>In vitro and in vivo physiology of low nanomolar concentrations of Zn2+ in artificial cerebrospinal fluid</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><description>Artificial cerebrospinal fluid (ACSF), i.e., brain extracellular medium, which includes Ca
2+
and Mg
2+
, but not other divalent cations such as Zn
2+
, has been used for
in vitro
and
in vivo
experiments. The present study deals with the physiological significance of extracellular Zn
2+
in ACSF. Spontaneous presynaptic activity is suppressed in the stratum lucidum of brain slices from young rats bathed in ACSF containing 10 nM ZnCl
2
, indicating that extracellular Zn
2+
modifies hippocampal presynaptic activity. To examine the
in vivo
action of 10 nM ZnCl
2
on long-term potentiation (LTP), the recording region was perfused using a recording electrode attached to a microdialysis probe. The magnitude of LTP was not modified in young rats by perfusion with ACSF containing 10 nM ZnCl
2
, compared to perfusion with ACSF without Zn
2+
, but attenuated by perfusion with ACSF containing 100 nM ZnCl
2
. Interestingly, the magnitude of LTP was not modified in aged rats even by perfusion with ACSF containing 100 nM ZnCl
2
, but enhanced by perfusion with ACSF containing 10 mM CaEDTA, an extracellular Zn
2+
chelator. The present study indicates that the basal levels of extracellular Zn
2+
, which are in the range of low nanomolar concentrations, are critical for synaptic activity and perhaps increased age-dependently.</description><subject>14</subject><subject>14/19</subject><subject>631/378/548/2589</subject><subject>631/443/376</subject><subject>Age</subject><subject>Brain slice preparation</subject><subject>Calcium (extracellular)</subject><subject>Cations</subject><subject>Cerebrospinal fluid</subject><subject>Hippocampus</subject><subject>Humanities and Social Sciences</subject><subject>Long-term potentiation</subject><subject>Magnesium</subject><subject>Microdialysis</subject><subject>multidisciplinary</subject><subject>Perfusion</subject><subject>Physiology</subject><subject>Rodents</subject><subject>Science</subject><subject>Zinc</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkcFLIzEUxoMoq1QP-x8EvKwr1eQl6cxcBJFdVyh40YuXkGQybUqazCYzXfrfm1IRV98l7_F--fiSD6HvlFxRwurrnGzPoW6qA3QChIspMIDDD_0xOst5RUoJaDhtvqFjqIFSwdkJcg8Bb9yQIlahxW43bCLul9vsoo-LLY4d9vEfDirEdfQqYRODsWFIanAx5N3-JcDl7qpKg-ucccpjY5PVKebehTJ1fnTtKTrqlM_27O2coOffv57u_kznj_cPd7fzqeGUDlPGGGmpNgKACd0pI0gFlWGs1WxWNwbAkroz2nLbtlpx0NRosJxoRZgwFZugm71uP-q1bfdeveyTW6u0lVE5-f8muKVcxI0UjHLGaRH48SaQ4t_R5kGuXTbWexVsHLOk9axpZlxAXdDzT-gqjqk8uVANoRXQmjaFuthTpvxIiat7N0OJ3GUo3zMs7M89mwsTFjZ9UPwCvwI2EJ3F</recordid><startdate>20170217</startdate><enddate>20170217</enddate><creator>Tamano, Haruna</creator><creator>Nishio, Ryusuke</creator><creator>Shakushi, Yukina</creator><creator>Sasaki, Miku</creator><creator>koike, Yuta</creator><creator>Osawa, Misa</creator><creator>Takeda, Atsushi</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170217</creationdate><title>In vitro and in vivo physiology of low nanomolar concentrations of Zn2+ in artificial cerebrospinal fluid</title><author>Tamano, Haruna ; Nishio, Ryusuke ; Shakushi, Yukina ; Sasaki, Miku ; koike, Yuta ; Osawa, Misa ; Takeda, Atsushi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c411t-3330d1bc52235bfac50727c33db3689c22e08fcbe4eddba42b1cb2e40ba035c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>14</topic><topic>14/19</topic><topic>631/378/548/2589</topic><topic>631/443/376</topic><topic>Age</topic><topic>Brain slice preparation</topic><topic>Calcium (extracellular)</topic><topic>Cations</topic><topic>Cerebrospinal fluid</topic><topic>Hippocampus</topic><topic>Humanities and Social Sciences</topic><topic>Long-term potentiation</topic><topic>Magnesium</topic><topic>Microdialysis</topic><topic>multidisciplinary</topic><topic>Perfusion</topic><topic>Physiology</topic><topic>Rodents</topic><topic>Science</topic><topic>Zinc</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamano, Haruna</creatorcontrib><creatorcontrib>Nishio, Ryusuke</creatorcontrib><creatorcontrib>Shakushi, Yukina</creatorcontrib><creatorcontrib>Sasaki, Miku</creatorcontrib><creatorcontrib>koike, Yuta</creatorcontrib><creatorcontrib>Osawa, Misa</creatorcontrib><creatorcontrib>Takeda, Atsushi</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</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>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamano, Haruna</au><au>Nishio, Ryusuke</au><au>Shakushi, Yukina</au><au>Sasaki, Miku</au><au>koike, Yuta</au><au>Osawa, Misa</au><au>Takeda, Atsushi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro and in vivo physiology of low nanomolar concentrations of Zn2+ in artificial cerebrospinal fluid</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><date>2017-02-17</date><risdate>2017</risdate><volume>7</volume><issue>1</issue><spage>42897</spage><epage>42897</epage><pages>42897-42897</pages><artnum>42897</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Artificial cerebrospinal fluid (ACSF), i.e., brain extracellular medium, which includes Ca
2+
and Mg
2+
, but not other divalent cations such as Zn
2+
, has been used for
in vitro
and
in vivo
experiments. The present study deals with the physiological significance of extracellular Zn
2+
in ACSF. Spontaneous presynaptic activity is suppressed in the stratum lucidum of brain slices from young rats bathed in ACSF containing 10 nM ZnCl
2
, indicating that extracellular Zn
2+
modifies hippocampal presynaptic activity. To examine the
in vivo
action of 10 nM ZnCl
2
on long-term potentiation (LTP), the recording region was perfused using a recording electrode attached to a microdialysis probe. The magnitude of LTP was not modified in young rats by perfusion with ACSF containing 10 nM ZnCl
2
, compared to perfusion with ACSF without Zn
2+
, but attenuated by perfusion with ACSF containing 100 nM ZnCl
2
. Interestingly, the magnitude of LTP was not modified in aged rats even by perfusion with ACSF containing 100 nM ZnCl
2
, but enhanced by perfusion with ACSF containing 10 mM CaEDTA, an extracellular Zn
2+
chelator. The present study indicates that the basal levels of extracellular Zn
2+
, which are in the range of low nanomolar concentrations, are critical for synaptic activity and perhaps increased age-dependently.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>28211543</pmid><doi>10.1038/srep42897</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Springer Nature OA Free Journals; Nature Free; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | 14 14/19 631/378/548/2589 631/443/376 Age Brain slice preparation Calcium (extracellular) Cations Cerebrospinal fluid Hippocampus Humanities and Social Sciences Long-term potentiation Magnesium Microdialysis multidisciplinary Perfusion Physiology Rodents Science Zinc |
title | In vitro and in vivo physiology of low nanomolar concentrations of Zn2+ in artificial cerebrospinal fluid |
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