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Manganese accumulates in iron-deficient rat brain regions in a heterogeneous fashion and is associated with neurochemical alterations
Previous studies have shown that iron deficiency (ID) increases brain manganese (Mn), but specific regional changes have not been addressed. Weanling rats were fed one of three semipurified diets: control (CN), iron deficient (ID), or iron deficient/manganese fortified (IDMn+). Seven brain regions w...
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Published in: | Biological trace element research 2002, Vol.87 (1-3), p.143-156 |
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description | Previous studies have shown that iron deficiency (ID) increases brain manganese (Mn), but specific regional changes have not been addressed. Weanling rats were fed one of three semipurified diets: control (CN), iron deficient (ID), or iron deficient/manganese fortified (IDMn+). Seven brain regions were analyzed for Mn concentration and amino acid (glutamate, glutamine, taurine, gamma-aminobutyric acid) concentrations. Both ID and IDMn+ diets caused significant (p |
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Weanling rats were fed one of three semipurified diets: control (CN), iron deficient (ID), or iron deficient/manganese fortified (IDMn+). Seven brain regions were analyzed for Mn concentration and amino acid (glutamate, glutamine, taurine, gamma-aminobutyric acid) concentrations. Both ID and IDMn+ diets caused significant (p<0.05) increases in Mn concentration across brain regions compared to CN. The hippocampus was the only brain region in which the IDMn+ group accumulated significantly more Mn than both the CN and ID groups. ID significantly decreased GABA concentration in hippocampus, caudate putamen, and globus pallidus compared to CN rats. Taurine was significantly increased in the substantia nigra of the IDMn+ group compared to both ID and CN. ID also altered glutamate and glutamine concentrations in cortex, caudate putamen, and thalamus compared to CN. In the substantia nigra, Mn concentration positively correlated with increased taurine concentration, whereas in caudate putamen, Mn concentration negatively correlated with decreased GABA. These data show that ID is a significant risk factor for central nervous system Mn accumulation and that some of the neurochemical alterations associated with ID are specifically attributable to Mn accumulation.</description><identifier>ISSN: 0163-4984</identifier><identifier>EISSN: 0163-4984</identifier><identifier>EISSN: 1559-0720</identifier><identifier>DOI: 10.1385/BTER:87:1-3:143</identifier><identifier>PMID: 12117224</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Amino acids ; Amino Acids - metabolism ; Animals ; Body Weight ; Brain ; Brain - metabolism ; Central nervous system ; Deficiency Diseases - metabolism ; Iron ; Iron - deficiency ; Male ; Manganese ; Manganese - metabolism ; Manganese compounds ; Neurochemistry ; Nutrient deficiency ; Organ Size ; Parkinson's disease ; Rats ; Rats, Sprague-Dawley ; Risk factors</subject><ispartof>Biological trace element research, 2002, Vol.87 (1-3), p.143-156</ispartof><rights>Humana Press Inc. 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-610f26e0deb1aa3bb845a49e3338136a98d591760e9ee1124f603045623d13853</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12117224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Erikson, Keith M</creatorcontrib><creatorcontrib>Shihabi, Zakariya K</creatorcontrib><creatorcontrib>Aschner, Judy L</creatorcontrib><creatorcontrib>Aschner, Michael</creatorcontrib><title>Manganese accumulates in iron-deficient rat brain regions in a heterogeneous fashion and is associated with neurochemical alterations</title><title>Biological trace element research</title><addtitle>Biol Trace Elem Res</addtitle><description>Previous studies have shown that iron deficiency (ID) increases brain manganese (Mn), but specific regional changes have not been addressed. Weanling rats were fed one of three semipurified diets: control (CN), iron deficient (ID), or iron deficient/manganese fortified (IDMn+). Seven brain regions were analyzed for Mn concentration and amino acid (glutamate, glutamine, taurine, gamma-aminobutyric acid) concentrations. Both ID and IDMn+ diets caused significant (p<0.05) increases in Mn concentration across brain regions compared to CN. The hippocampus was the only brain region in which the IDMn+ group accumulated significantly more Mn than both the CN and ID groups. ID significantly decreased GABA concentration in hippocampus, caudate putamen, and globus pallidus compared to CN rats. Taurine was significantly increased in the substantia nigra of the IDMn+ group compared to both ID and CN. ID also altered glutamate and glutamine concentrations in cortex, caudate putamen, and thalamus compared to CN. In the substantia nigra, Mn concentration positively correlated with increased taurine concentration, whereas in caudate putamen, Mn concentration negatively correlated with decreased GABA. These data show that ID is a significant risk factor for central nervous system Mn accumulation and that some of the neurochemical alterations associated with ID are specifically attributable to Mn accumulation.</description><subject>Amino acids</subject><subject>Amino Acids - metabolism</subject><subject>Animals</subject><subject>Body Weight</subject><subject>Brain</subject><subject>Brain - metabolism</subject><subject>Central nervous system</subject><subject>Deficiency Diseases - metabolism</subject><subject>Iron</subject><subject>Iron - deficiency</subject><subject>Male</subject><subject>Manganese</subject><subject>Manganese - metabolism</subject><subject>Manganese compounds</subject><subject>Neurochemistry</subject><subject>Nutrient deficiency</subject><subject>Organ Size</subject><subject>Parkinson's disease</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Risk factors</subject><issn>0163-4984</issn><issn>0163-4984</issn><issn>1559-0720</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp9kUFv1DAQhSNERUvhzA1ZHOCU1mM7ib03qApUKkJC5WxNnMmuq8QudiLED-B_421XAnHoaZ403zzNzKuqV8DPQOrm_MPN5beN7jZQyw0o-aQ64dDKWhmtnv6jj6vnOd9yDp0w8ll1DAKKFOqk-v0FwxYDZWLo3DqvEy6UmQ_MpxjqgUbvPIWFJVxYn7A0Em19DPcMsh0tlOKWAsU1sxHzrvQYhoH5zDDn6HwxHNhPv-xYoDVFt6PZO5wYTmUUl73Xi-poxCnTy0M9rb5_vLy5-Fxff_10dfH-unayEUvdAh9FS3ygHhBl32vVoDIkpdQgWzR6aAx0LSdDBCDU2HLJVdMKOezfJU-rdw--dyn-WCkvdvbZ0TTh_f5W805ogNYU8u2jZAfayMZ0BXzzH3gb1xTKFVaAVgIU6AKdP0AuxZwTjfYu-RnTLwvc7jez-yCt7ixYaUuQZeL1wXbtZxr-8ofk5B-VT5oI</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Erikson, Keith M</creator><creator>Shihabi, Zakariya K</creator><creator>Aschner, Judy L</creator><creator>Aschner, Michael</creator><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>7QH</scope><scope>7QP</scope><scope>7TN</scope><scope>7U7</scope><scope>7UA</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</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>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>F1W</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H97</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L.G</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PCBAR</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7TK</scope></search><sort><creationdate>2002</creationdate><title>Manganese accumulates in iron-deficient rat brain regions in a heterogeneous fashion and is associated with neurochemical alterations</title><author>Erikson, Keith M ; Shihabi, Zakariya K ; Aschner, Judy L ; Aschner, Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-610f26e0deb1aa3bb845a49e3338136a98d591760e9ee1124f603045623d13853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino acids</topic><topic>Amino Acids - metabolism</topic><topic>Animals</topic><topic>Body Weight</topic><topic>Brain</topic><topic>Brain - metabolism</topic><topic>Central nervous system</topic><topic>Deficiency Diseases - metabolism</topic><topic>Iron</topic><topic>Iron - deficiency</topic><topic>Male</topic><topic>Manganese</topic><topic>Manganese - metabolism</topic><topic>Manganese compounds</topic><topic>Neurochemistry</topic><topic>Nutrient deficiency</topic><topic>Organ Size</topic><topic>Parkinson's disease</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Risk factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Erikson, Keith M</creatorcontrib><creatorcontrib>Shihabi, Zakariya K</creatorcontrib><creatorcontrib>Aschner, Judy L</creatorcontrib><creatorcontrib>Aschner, Michael</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>Aqualine</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Oceanic Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Water Resources Abstracts</collection><collection>ProQuest 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 Pharma Collection</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 One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Biological Science Database</collection><collection>Earth, Atmospheric & Aquatic Science 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>Neurosciences Abstracts</collection><jtitle>Biological trace element research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Erikson, Keith M</au><au>Shihabi, Zakariya K</au><au>Aschner, Judy L</au><au>Aschner, Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Manganese accumulates in iron-deficient rat brain regions in a heterogeneous fashion and is associated with neurochemical alterations</atitle><jtitle>Biological trace element research</jtitle><addtitle>Biol Trace Elem Res</addtitle><date>2002</date><risdate>2002</risdate><volume>87</volume><issue>1-3</issue><spage>143</spage><epage>156</epage><pages>143-156</pages><issn>0163-4984</issn><eissn>0163-4984</eissn><eissn>1559-0720</eissn><abstract>Previous studies have shown that iron deficiency (ID) increases brain manganese (Mn), but specific regional changes have not been addressed. Weanling rats were fed one of three semipurified diets: control (CN), iron deficient (ID), or iron deficient/manganese fortified (IDMn+). Seven brain regions were analyzed for Mn concentration and amino acid (glutamate, glutamine, taurine, gamma-aminobutyric acid) concentrations. Both ID and IDMn+ diets caused significant (p<0.05) increases in Mn concentration across brain regions compared to CN. The hippocampus was the only brain region in which the IDMn+ group accumulated significantly more Mn than both the CN and ID groups. ID significantly decreased GABA concentration in hippocampus, caudate putamen, and globus pallidus compared to CN rats. Taurine was significantly increased in the substantia nigra of the IDMn+ group compared to both ID and CN. ID also altered glutamate and glutamine concentrations in cortex, caudate putamen, and thalamus compared to CN. In the substantia nigra, Mn concentration positively correlated with increased taurine concentration, whereas in caudate putamen, Mn concentration negatively correlated with decreased GABA. These data show that ID is a significant risk factor for central nervous system Mn accumulation and that some of the neurochemical alterations associated with ID are specifically attributable to Mn accumulation.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>12117224</pmid><doi>10.1385/BTER:87:1-3:143</doi><tpages>14</tpages></addata></record> |
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subjects | Amino acids Amino Acids - metabolism Animals Body Weight Brain Brain - metabolism Central nervous system Deficiency Diseases - metabolism Iron Iron - deficiency Male Manganese Manganese - metabolism Manganese compounds Neurochemistry Nutrient deficiency Organ Size Parkinson's disease Rats Rats, Sprague-Dawley Risk factors |
title | Manganese accumulates in iron-deficient rat brain regions in a heterogeneous fashion and is associated with neurochemical alterations |
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