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Quinolinate-induced Rat Striatal Excitotoxicity Impairs Endoplasmic Reticulum Ca2+-ATPase Function
Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca 2+ homeostasis may be lethal (excitotoxic) to neurons. Such excitotoxicity can be induced in vivo by intrastriatal infusion of quinolinate, as this substance selectively activates NMDA receptors. The aim of t...
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Published in: | Neurochemical research 2008-09, Vol.33 (9), p.1749-1758 |
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container_title | Neurochemical research |
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creator | Fernandes, Anna M. A. P. Landeira-Fernandez, Ana M. Souza-Santos, Patrícia Carvalho-Alves, Paulo C. Castilho, Roger F. |
description | Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca
2+
homeostasis may be lethal (excitotoxic) to neurons. Such excitotoxicity can be induced in vivo by intrastriatal infusion of quinolinate, as this substance selectively activates NMDA receptors. The aim of the present research was to investigate whether the in vivo treatment of striatal tissue with quinolinate would lead to an early impairment of sarco/endoplasmic reticulum Ca
2+
-ATPase (SERCA) activity or mitochondrial Ca
2+
sequestration, two intracellular mechanisms involved in Ca
2+
homeostasis and signaling. Sodium quinolinate was infused intrastriatally into adult rats, and 6 h later the brains were removed and the
corpora striata
dissected. At this time point, striatal sections stained with Fluoro-Jade, a cellular marker of cell death, showed initial signs of neuronal degeneration. In addition, SERCA activity decreased 39% in relation to the activity observed in the control striata. A corresponding decrease of the same magnitude in
45
Ca
2+
uptake by striatal microsomes was also found in the treated striata. Western blot analysis did not indicate any decrease in SERCA levels in striatal tissue after quinolinate infusion. Mitochondrial Ca
2+
sequestration was still preserved in quinolinate-treated striatal tissue when the assay was carried out in the presence of physiological concentrations of ATP and Mg
2+
. These results suggest that impairment of the SERCA function may be an early event in excitotoxicity. |
doi_str_mv | 10.1007/s11064-008-9619-7 |
format | article |
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2+
homeostasis may be lethal (excitotoxic) to neurons. Such excitotoxicity can be induced in vivo by intrastriatal infusion of quinolinate, as this substance selectively activates NMDA receptors. The aim of the present research was to investigate whether the in vivo treatment of striatal tissue with quinolinate would lead to an early impairment of sarco/endoplasmic reticulum Ca
2+
-ATPase (SERCA) activity or mitochondrial Ca
2+
sequestration, two intracellular mechanisms involved in Ca
2+
homeostasis and signaling. Sodium quinolinate was infused intrastriatally into adult rats, and 6 h later the brains were removed and the
corpora striata
dissected. At this time point, striatal sections stained with Fluoro-Jade, a cellular marker of cell death, showed initial signs of neuronal degeneration. In addition, SERCA activity decreased 39% in relation to the activity observed in the control striata. A corresponding decrease of the same magnitude in
45
Ca
2+
uptake by striatal microsomes was also found in the treated striata. Western blot analysis did not indicate any decrease in SERCA levels in striatal tissue after quinolinate infusion. Mitochondrial Ca
2+
sequestration was still preserved in quinolinate-treated striatal tissue when the assay was carried out in the presence of physiological concentrations of ATP and Mg
2+
. These results suggest that impairment of the SERCA function may be an early event in excitotoxicity.</description><identifier>ISSN: 0364-3190</identifier><identifier>EISSN: 1573-6903</identifier><identifier>DOI: 10.1007/s11064-008-9619-7</identifier><identifier>PMID: 18307036</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Animals ; Biochemistry ; Biomedical and Life Sciences ; Biomedicine ; Calcium - metabolism ; Cell Biology ; Corpus Striatum - drug effects ; Endoplasmic Reticulum - enzymology ; Excitatory Amino Acid Agonists - pharmacology ; Female ; Homeostasis ; Mitochondria - metabolism ; Neurochemistry ; Neurology ; Neurosciences ; Neurotoxins - pharmacology ; Original Paper ; Quinolinic Acid - pharmacology ; Rats ; Rats, Wistar ; Receptors, N-Methyl-D-Aspartate - metabolism ; Sarcoplasmic Reticulum Calcium-Transporting ATPases - metabolism</subject><ispartof>Neurochemical research, 2008-09, Vol.33 (9), p.1749-1758</ispartof><rights>Springer Science+Business Media, LLC 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c299t-dbb65c7d1736821ff7af83af93be501b1f9db50a29f3240b7e5257bf8db785f23</citedby><cites>FETCH-LOGICAL-c299t-dbb65c7d1736821ff7af83af93be501b1f9db50a29f3240b7e5257bf8db785f23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18307036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fernandes, Anna M. A. P.</creatorcontrib><creatorcontrib>Landeira-Fernandez, Ana M.</creatorcontrib><creatorcontrib>Souza-Santos, Patrícia</creatorcontrib><creatorcontrib>Carvalho-Alves, Paulo C.</creatorcontrib><creatorcontrib>Castilho, Roger F.</creatorcontrib><title>Quinolinate-induced Rat Striatal Excitotoxicity Impairs Endoplasmic Reticulum Ca2+-ATPase Function</title><title>Neurochemical research</title><addtitle>Neurochem Res</addtitle><addtitle>Neurochem Res</addtitle><description>Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca
2+
homeostasis may be lethal (excitotoxic) to neurons. Such excitotoxicity can be induced in vivo by intrastriatal infusion of quinolinate, as this substance selectively activates NMDA receptors. The aim of the present research was to investigate whether the in vivo treatment of striatal tissue with quinolinate would lead to an early impairment of sarco/endoplasmic reticulum Ca
2+
-ATPase (SERCA) activity or mitochondrial Ca
2+
sequestration, two intracellular mechanisms involved in Ca
2+
homeostasis and signaling. Sodium quinolinate was infused intrastriatally into adult rats, and 6 h later the brains were removed and the
corpora striata
dissected. At this time point, striatal sections stained with Fluoro-Jade, a cellular marker of cell death, showed initial signs of neuronal degeneration. In addition, SERCA activity decreased 39% in relation to the activity observed in the control striata. A corresponding decrease of the same magnitude in
45
Ca
2+
uptake by striatal microsomes was also found in the treated striata. Western blot analysis did not indicate any decrease in SERCA levels in striatal tissue after quinolinate infusion. Mitochondrial Ca
2+
sequestration was still preserved in quinolinate-treated striatal tissue when the assay was carried out in the presence of physiological concentrations of ATP and Mg
2+
. These results suggest that impairment of the SERCA function may be an early event in excitotoxicity.</description><subject>Animals</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Calcium - metabolism</subject><subject>Cell Biology</subject><subject>Corpus Striatum - drug effects</subject><subject>Endoplasmic Reticulum - enzymology</subject><subject>Excitatory Amino Acid Agonists - pharmacology</subject><subject>Female</subject><subject>Homeostasis</subject><subject>Mitochondria - metabolism</subject><subject>Neurochemistry</subject><subject>Neurology</subject><subject>Neurosciences</subject><subject>Neurotoxins - pharmacology</subject><subject>Original Paper</subject><subject>Quinolinic Acid - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, N-Methyl-D-Aspartate - metabolism</subject><subject>Sarcoplasmic Reticulum Calcium-Transporting ATPases - metabolism</subject><issn>0364-3190</issn><issn>1573-6903</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LwzAcxoMoOqcfwIsUrxL9J2mb5ihjU0FQp55D0iYS6ctMUpjf3owOPHl6Ds8b_BC6IHBDAPhtIATKHANUWJREYH6AZqTgDJcC2CGaAUsuIwJO0GkIXwCpRckxOiEVA57cGdKvo-uH1vUqGuz6ZqxNk61VzN6idyqqNltuaxeHOGxd0p_ssdso50O27Jth06rQuTpbm-jqsR27bKHoNb57f1HBZKuxr6Mb-jN0ZFUbzPle5-hjtXxfPOCn5_vHxd0TrqkQETdal0XNG8JZWVFiLVe2YsoKpk0BRBMrGl2AosIymoPmpqAF17ZqNK8KS9kcXU27Gz98jyZE-TWMvk-XklLCyzxnkEJkCtV-CMEbKzfedcr_SAJyB1VOUGWCKndQJU-dy_3wqDvT_DX2FFOAToGQrP7T-L_n_1d_AWHGgpE</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Fernandes, Anna M. 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P.</creator><creator>Landeira-Fernandez, Ana M.</creator><creator>Souza-Santos, Patrícia</creator><creator>Carvalho-Alves, Paulo C.</creator><creator>Castilho, Roger F.</creator><general>Springer US</general><general>Springer Nature B.V</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>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</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>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20080901</creationdate><title>Quinolinate-induced Rat Striatal Excitotoxicity Impairs Endoplasmic Reticulum Ca2+-ATPase Function</title><author>Fernandes, Anna M. 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P.</creatorcontrib><creatorcontrib>Landeira-Fernandez, Ana M.</creatorcontrib><creatorcontrib>Souza-Santos, Patrícia</creatorcontrib><creatorcontrib>Carvalho-Alves, Paulo C.</creatorcontrib><creatorcontrib>Castilho, Roger F.</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>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</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>PML(ProQuest Medical Library)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</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 China</collection><jtitle>Neurochemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fernandes, Anna M. A. P.</au><au>Landeira-Fernandez, Ana M.</au><au>Souza-Santos, Patrícia</au><au>Carvalho-Alves, Paulo C.</au><au>Castilho, Roger F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quinolinate-induced Rat Striatal Excitotoxicity Impairs Endoplasmic Reticulum Ca2+-ATPase Function</atitle><jtitle>Neurochemical research</jtitle><stitle>Neurochem Res</stitle><addtitle>Neurochem Res</addtitle><date>2008-09-01</date><risdate>2008</risdate><volume>33</volume><issue>9</issue><spage>1749</spage><epage>1758</epage><pages>1749-1758</pages><issn>0364-3190</issn><eissn>1573-6903</eissn><abstract>Excessive activation of NMDA glutamate receptors and the resulting loss of intracellular Ca
2+
homeostasis may be lethal (excitotoxic) to neurons. Such excitotoxicity can be induced in vivo by intrastriatal infusion of quinolinate, as this substance selectively activates NMDA receptors. The aim of the present research was to investigate whether the in vivo treatment of striatal tissue with quinolinate would lead to an early impairment of sarco/endoplasmic reticulum Ca
2+
-ATPase (SERCA) activity or mitochondrial Ca
2+
sequestration, two intracellular mechanisms involved in Ca
2+
homeostasis and signaling. Sodium quinolinate was infused intrastriatally into adult rats, and 6 h later the brains were removed and the
corpora striata
dissected. At this time point, striatal sections stained with Fluoro-Jade, a cellular marker of cell death, showed initial signs of neuronal degeneration. In addition, SERCA activity decreased 39% in relation to the activity observed in the control striata. A corresponding decrease of the same magnitude in
45
Ca
2+
uptake by striatal microsomes was also found in the treated striata. Western blot analysis did not indicate any decrease in SERCA levels in striatal tissue after quinolinate infusion. Mitochondrial Ca
2+
sequestration was still preserved in quinolinate-treated striatal tissue when the assay was carried out in the presence of physiological concentrations of ATP and Mg
2+
. These results suggest that impairment of the SERCA function may be an early event in excitotoxicity.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>18307036</pmid><doi>10.1007/s11064-008-9619-7</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Biochemistry Biomedical and Life Sciences Biomedicine Calcium - metabolism Cell Biology Corpus Striatum - drug effects Endoplasmic Reticulum - enzymology Excitatory Amino Acid Agonists - pharmacology Female Homeostasis Mitochondria - metabolism Neurochemistry Neurology Neurosciences Neurotoxins - pharmacology Original Paper Quinolinic Acid - pharmacology Rats Rats, Wistar Receptors, N-Methyl-D-Aspartate - metabolism Sarcoplasmic Reticulum Calcium-Transporting ATPases - metabolism |
title | Quinolinate-induced Rat Striatal Excitotoxicity Impairs Endoplasmic Reticulum Ca2+-ATPase Function |
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