Modification of hippocampal excitability in brain slices pretreated with a low nanomolar concentration of Zn super(2+)
Synaptic Zn super(2+) homeostasis may be changed during brain slice preparation. However, much less attention has been paid to Zn super(2+) in artificial cerebrospinal fluid (ACSF) used for slice experiments than has been paid to Ca super(2+). The present study assesses addition of Zn super(2+) to A...
Gespeichert in:
Veröffentlicht in: | Journal of neuroscience research 2015-11, Vol.93 (11), p.1641-1647 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1647 |
---|---|
container_issue | 11 |
container_start_page | 1641 |
container_title | Journal of neuroscience research |
container_volume | 93 |
creator | Takeda, Atsushi Shakushi, Yukina Tamano, Haruna |
description | Synaptic Zn super(2+) homeostasis may be changed during brain slice preparation. However, much less attention has been paid to Zn super(2+) in artificial cerebrospinal fluid (ACSF) used for slice experiments than has been paid to Ca super(2+). The present study assesses addition of Zn super(2+) to ACSF, focused on hippocampal excitability after acute brain slice preparation. When the static levels of intracellular Zn super(2+) and Ca super(2+) were compared between brain slices prepared with conventional ACSF without Zn super(2+) and those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr, both levels were almost the same. On the other hand, intracellular Ca super(2+) levels were significantly increased in the stratum lucidum of the control brain slices after stimulation with high K super(+), although the increase was significantly suppressed by the pretreatment with ACSF containing Zn super(2+), suggesting that neuronal excitation is enhanced in brain slices prepared with ACSF without Zn super(2+). The increase in extracellular Zn super(2+) level, an index of glutamate release, after stimulation with high K super(+) was also significantly suppressed by pretreatment with ACSF containing Zn super(2+). When mossy fiber excitation was assessed in brain slices with FM4-64, an indicator of presynaptic activity, attenuation of FM 4-64 fluorescence based on presynaptic activity was suppressed in the stratum lucidum of brain slices pretreated with ACSF containing Zn super(2+). The present study indicates that hippocampal excitability is enhanced in brain slices prepared with ACSF without Zn super(2+). It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF. Hippocampal excitability is more enhanced in brain slices prepared with conventional artificial cerebrospinal fluid (ACSF) without Zn super(2+) than in those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr. It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF. |
doi_str_mv | 10.1002/jnr.23629 |
format | Article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1722175409</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1722175409</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_17221754093</originalsourceid><addsrcrecordid>eNqVjL1OwzAURi0EEuFn4A3uWIRSrp2kUWYEYunGxFLdujfqrRzb2A6Ft6cDYmf5znLOp9SdxqVGNI8Hn5amWZnhTFUah75uu7Y_VxU2K6xb1OZSXeV8QMRh6JpKfa7DTkaxVCR4CCPsJcZgaYrkgL-sFNqKk_IN4mGb6LTZieUMMXFJTIV3cJSyBwIXjuDJhyk4SmCDt-xL-nt-P6Vz5LQwD_c36mIkl_n2l9dq8fL89vRaxxQ-Zs5lM0m27Bx5DnPe6N4Y3XctDs0_1B_gO1aN</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1722175409</pqid></control><display><type>article</type><title>Modification of hippocampal excitability in brain slices pretreated with a low nanomolar concentration of Zn super(2+)</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Takeda, Atsushi ; Shakushi, Yukina ; Tamano, Haruna</creator><creatorcontrib>Takeda, Atsushi ; Shakushi, Yukina ; Tamano, Haruna</creatorcontrib><description>Synaptic Zn super(2+) homeostasis may be changed during brain slice preparation. However, much less attention has been paid to Zn super(2+) in artificial cerebrospinal fluid (ACSF) used for slice experiments than has been paid to Ca super(2+). The present study assesses addition of Zn super(2+) to ACSF, focused on hippocampal excitability after acute brain slice preparation. When the static levels of intracellular Zn super(2+) and Ca super(2+) were compared between brain slices prepared with conventional ACSF without Zn super(2+) and those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr, both levels were almost the same. On the other hand, intracellular Ca super(2+) levels were significantly increased in the stratum lucidum of the control brain slices after stimulation with high K super(+), although the increase was significantly suppressed by the pretreatment with ACSF containing Zn super(2+), suggesting that neuronal excitation is enhanced in brain slices prepared with ACSF without Zn super(2+). The increase in extracellular Zn super(2+) level, an index of glutamate release, after stimulation with high K super(+) was also significantly suppressed by pretreatment with ACSF containing Zn super(2+). When mossy fiber excitation was assessed in brain slices with FM4-64, an indicator of presynaptic activity, attenuation of FM 4-64 fluorescence based on presynaptic activity was suppressed in the stratum lucidum of brain slices pretreated with ACSF containing Zn super(2+). The present study indicates that hippocampal excitability is enhanced in brain slices prepared with ACSF without Zn super(2+). It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF. Hippocampal excitability is more enhanced in brain slices prepared with conventional artificial cerebrospinal fluid (ACSF) without Zn super(2+) than in those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr. It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.23629</identifier><language>eng</language><ispartof>Journal of neuroscience research, 2015-11, Vol.93 (11), p.1641-1647</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Takeda, Atsushi</creatorcontrib><creatorcontrib>Shakushi, Yukina</creatorcontrib><creatorcontrib>Tamano, Haruna</creatorcontrib><title>Modification of hippocampal excitability in brain slices pretreated with a low nanomolar concentration of Zn super(2+)</title><title>Journal of neuroscience research</title><description>Synaptic Zn super(2+) homeostasis may be changed during brain slice preparation. However, much less attention has been paid to Zn super(2+) in artificial cerebrospinal fluid (ACSF) used for slice experiments than has been paid to Ca super(2+). The present study assesses addition of Zn super(2+) to ACSF, focused on hippocampal excitability after acute brain slice preparation. When the static levels of intracellular Zn super(2+) and Ca super(2+) were compared between brain slices prepared with conventional ACSF without Zn super(2+) and those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr, both levels were almost the same. On the other hand, intracellular Ca super(2+) levels were significantly increased in the stratum lucidum of the control brain slices after stimulation with high K super(+), although the increase was significantly suppressed by the pretreatment with ACSF containing Zn super(2+), suggesting that neuronal excitation is enhanced in brain slices prepared with ACSF without Zn super(2+). The increase in extracellular Zn super(2+) level, an index of glutamate release, after stimulation with high K super(+) was also significantly suppressed by pretreatment with ACSF containing Zn super(2+). When mossy fiber excitation was assessed in brain slices with FM4-64, an indicator of presynaptic activity, attenuation of FM 4-64 fluorescence based on presynaptic activity was suppressed in the stratum lucidum of brain slices pretreated with ACSF containing Zn super(2+). The present study indicates that hippocampal excitability is enhanced in brain slices prepared with ACSF without Zn super(2+). It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF. Hippocampal excitability is more enhanced in brain slices prepared with conventional artificial cerebrospinal fluid (ACSF) without Zn super(2+) than in those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr. It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF.</description><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqVjL1OwzAURi0EEuFn4A3uWIRSrp2kUWYEYunGxFLdujfqrRzb2A6Ft6cDYmf5znLOp9SdxqVGNI8Hn5amWZnhTFUah75uu7Y_VxU2K6xb1OZSXeV8QMRh6JpKfa7DTkaxVCR4CCPsJcZgaYrkgL-sFNqKk_IN4mGb6LTZieUMMXFJTIV3cJSyBwIXjuDJhyk4SmCDt-xL-nt-P6Vz5LQwD_c36mIkl_n2l9dq8fL89vRaxxQ-Zs5lM0m27Bx5DnPe6N4Y3XctDs0_1B_gO1aN</recordid><startdate>20151101</startdate><enddate>20151101</enddate><creator>Takeda, Atsushi</creator><creator>Shakushi, Yukina</creator><creator>Tamano, Haruna</creator><scope>7TK</scope></search><sort><creationdate>20151101</creationdate><title>Modification of hippocampal excitability in brain slices pretreated with a low nanomolar concentration of Zn super(2+)</title><author>Takeda, Atsushi ; Shakushi, Yukina ; Tamano, Haruna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_17221754093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeda, Atsushi</creatorcontrib><creatorcontrib>Shakushi, Yukina</creatorcontrib><creatorcontrib>Tamano, Haruna</creatorcontrib><collection>Neurosciences Abstracts</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeda, Atsushi</au><au>Shakushi, Yukina</au><au>Tamano, Haruna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modification of hippocampal excitability in brain slices pretreated with a low nanomolar concentration of Zn super(2+)</atitle><jtitle>Journal of neuroscience research</jtitle><date>2015-11-01</date><risdate>2015</risdate><volume>93</volume><issue>11</issue><spage>1641</spage><epage>1647</epage><pages>1641-1647</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Synaptic Zn super(2+) homeostasis may be changed during brain slice preparation. However, much less attention has been paid to Zn super(2+) in artificial cerebrospinal fluid (ACSF) used for slice experiments than has been paid to Ca super(2+). The present study assesses addition of Zn super(2+) to ACSF, focused on hippocampal excitability after acute brain slice preparation. When the static levels of intracellular Zn super(2+) and Ca super(2+) were compared between brain slices prepared with conventional ACSF without Zn super(2+) and those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr, both levels were almost the same. On the other hand, intracellular Ca super(2+) levels were significantly increased in the stratum lucidum of the control brain slices after stimulation with high K super(+), although the increase was significantly suppressed by the pretreatment with ACSF containing Zn super(2+), suggesting that neuronal excitation is enhanced in brain slices prepared with ACSF without Zn super(2+). The increase in extracellular Zn super(2+) level, an index of glutamate release, after stimulation with high K super(+) was also significantly suppressed by pretreatment with ACSF containing Zn super(2+). When mossy fiber excitation was assessed in brain slices with FM4-64, an indicator of presynaptic activity, attenuation of FM 4-64 fluorescence based on presynaptic activity was suppressed in the stratum lucidum of brain slices pretreated with ACSF containing Zn super(2+). The present study indicates that hippocampal excitability is enhanced in brain slices prepared with ACSF without Zn super(2+). It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF. Hippocampal excitability is more enhanced in brain slices prepared with conventional artificial cerebrospinal fluid (ACSF) without Zn super(2+) than in those pretreated with ACSF containing 20 nM ZnCl sub(2) for 1 hr. It is likely that a low nanomolar concentration of Zn super(2+) is necessary for ACSF.</abstract><doi>10.1002/jnr.23629</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0360-4012 |
ispartof | Journal of neuroscience research, 2015-11, Vol.93 (11), p.1641-1647 |
issn | 0360-4012 1097-4547 |
language | eng |
recordid | cdi_proquest_miscellaneous_1722175409 |
source | Wiley Online Library Journals Frontfile Complete |
title | Modification of hippocampal excitability in brain slices pretreated with a low nanomolar concentration of Zn super(2+) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T01%3A38%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Modification%20of%20hippocampal%20excitability%20in%20brain%20slices%20pretreated%20with%20a%20low%20nanomolar%20concentration%20of%20Zn%20super(2+)&rft.jtitle=Journal%20of%20neuroscience%20research&rft.au=Takeda,%20Atsushi&rft.date=2015-11-01&rft.volume=93&rft.issue=11&rft.spage=1641&rft.epage=1647&rft.pages=1641-1647&rft.issn=0360-4012&rft.eissn=1097-4547&rft_id=info:doi/10.1002/jnr.23629&rft_dat=%3Cproquest%3E1722175409%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1722175409&rft_id=info:pmid/&rfr_iscdi=true |