Gallium‐67 as a Potential Marker for Aluminium Transport in Rat Brain: Implications for Alzheimer's Disease
: Evidence of a link between aluminium and Alzheimer's disease, parkinsonism‐dementia of Guam, and dialysis encephalopathy raises questions regarding the role of this element in the pathogenesis of these conditions. Therefore, we have investigated the use of gallium‐67 (67Ga) as a marker for br...
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Veröffentlicht in: | Journal of neurochemistry 1990-07, Vol.55 (1), p.251-259 |
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creator | Pullen, R. G. L. Candy, J. M. Morris, C. M. Taylor, G. Keith, A. B. Edwardson, J. A. |
description | : Evidence of a link between aluminium and Alzheimer's disease, parkinsonism‐dementia of Guam, and dialysis encephalopathy raises questions regarding the role of this element in the pathogenesis of these conditions. Therefore, we have investigated the use of gallium‐67 (67Ga) as a marker for brain uptake of aluminium. The binding of 67Ga to plasma proteins has been studied, and the blood‐brain barrier permeability and autoradiographic distribution of this isotope in rat brain determined in vivo. The autoradiographic distribution of 125I‐Fe‐transferrin receptors in rat brain has also been determined in vitro. Results show that 67Ga was bound to plasma transferrin, entered the brain with a blood‐brain barrier permeability of 2.48 X 10‐6 ml/min/g, and showed a marked regional distribution that was very similar to that of 125I‐Fe‐transferrin receptors. Our data suggest that the vulnerability of the hippocampus, amygdala, and cerebral cortex in conditions such as those mentioned above may be partly due to an increased uptake and deposition of aluminium in these regions by the iron transport system. |
doi_str_mv | 10.1111/j.1471-4159.1990.tb08846.x |
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G. L. ; Candy, J. M. ; Morris, C. M. ; Taylor, G. ; Keith, A. B. ; Edwardson, J. A.</creator><creatorcontrib>Pullen, R. G. L. ; Candy, J. M. ; Morris, C. M. ; Taylor, G. ; Keith, A. B. ; Edwardson, J. A.</creatorcontrib><description>: Evidence of a link between aluminium and Alzheimer's disease, parkinsonism‐dementia of Guam, and dialysis encephalopathy raises questions regarding the role of this element in the pathogenesis of these conditions. Therefore, we have investigated the use of gallium‐67 (67Ga) as a marker for brain uptake of aluminium. The binding of 67Ga to plasma proteins has been studied, and the blood‐brain barrier permeability and autoradiographic distribution of this isotope in rat brain determined in vivo. The autoradiographic distribution of 125I‐Fe‐transferrin receptors in rat brain has also been determined in vitro. Results show that 67Ga was bound to plasma transferrin, entered the brain with a blood‐brain barrier permeability of 2.48 X 10‐6 ml/min/g, and showed a marked regional distribution that was very similar to that of 125I‐Fe‐transferrin receptors. Our data suggest that the vulnerability of the hippocampus, amygdala, and cerebral cortex in conditions such as those mentioned above may be partly due to an increased uptake and deposition of aluminium in these regions by the iron transport system.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.1990.tb08846.x</identifier><identifier>PMID: 2355220</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Aluminium ; Aluminum - metabolism ; Alzheimer Disease - metabolism ; Alzheimer's disease ; Animals ; Autoradiography ; Blood-Brain Barrier ; Brain - metabolism ; Capillary Permeability ; Gallium - blood ; Gallium - metabolism ; Gallium Radioisotopes ; Gallium‐67 ; Iron ; Male ; Proteins - metabolism ; Rats ; Rats, Inbred Strains ; Tissue Distribution ; Transferrin ; Transferrin - metabolism</subject><ispartof>Journal of neurochemistry, 1990-07, Vol.55 (1), p.251-259</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3151-14493935bb09489c9e1db401fbafcf270feef0dcaee75cbb751844c38e0fe6193</citedby><cites>FETCH-LOGICAL-c3151-14493935bb09489c9e1db401fbafcf270feef0dcaee75cbb751844c38e0fe6193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.1990.tb08846.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.1990.tb08846.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2355220$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pullen, R. G. L.</creatorcontrib><creatorcontrib>Candy, J. M.</creatorcontrib><creatorcontrib>Morris, C. M.</creatorcontrib><creatorcontrib>Taylor, G.</creatorcontrib><creatorcontrib>Keith, A. B.</creatorcontrib><creatorcontrib>Edwardson, J. A.</creatorcontrib><title>Gallium‐67 as a Potential Marker for Aluminium Transport in Rat Brain: Implications for Alzheimer's Disease</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>: Evidence of a link between aluminium and Alzheimer's disease, parkinsonism‐dementia of Guam, and dialysis encephalopathy raises questions regarding the role of this element in the pathogenesis of these conditions. Therefore, we have investigated the use of gallium‐67 (67Ga) as a marker for brain uptake of aluminium. The binding of 67Ga to plasma proteins has been studied, and the blood‐brain barrier permeability and autoradiographic distribution of this isotope in rat brain determined in vivo. The autoradiographic distribution of 125I‐Fe‐transferrin receptors in rat brain has also been determined in vitro. Results show that 67Ga was bound to plasma transferrin, entered the brain with a blood‐brain barrier permeability of 2.48 X 10‐6 ml/min/g, and showed a marked regional distribution that was very similar to that of 125I‐Fe‐transferrin receptors. Our data suggest that the vulnerability of the hippocampus, amygdala, and cerebral cortex in conditions such as those mentioned above may be partly due to an increased uptake and deposition of aluminium in these regions by the iron transport system.</description><subject>Aluminium</subject><subject>Aluminum - metabolism</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer's disease</subject><subject>Animals</subject><subject>Autoradiography</subject><subject>Blood-Brain Barrier</subject><subject>Brain - metabolism</subject><subject>Capillary Permeability</subject><subject>Gallium - blood</subject><subject>Gallium - metabolism</subject><subject>Gallium Radioisotopes</subject><subject>Gallium‐67</subject><subject>Iron</subject><subject>Male</subject><subject>Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Tissue Distribution</subject><subject>Transferrin</subject><subject>Transferrin - metabolism</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUc1O3DAQthAVbCmPgGRxgFNST2wnMQck2LaUihaE4Gw53onw4iSLnajQUx-hz9gnabYbca060mgO389I30fIIbAUxnm_TEEUkAiQKgWlWNpXrCxFnj5vkdkrtE1mjGVZwpnIdsnbGJeMQS5y2CE7GZcyy9iMNBfGezc0v3_-ygtqIjX0puux7Z3x9KsJjxho3QV65ofGtSOR3gXTxlUXeupaemt6eh6Ma0_oZbPyzpredW2cJD8e0DUYjiP94CKaiO_Im9r4iPvT3SP3nz7ezT8nV9cXl_Ozq8RykJCAEIorLquKKVEqqxAWlWBQV6a2dVawGrFmC2sQC2mrqpBQCmF5iSOSg-J75Gjjuwrd04Cx142LFr03LXZD1IUq-bjFP4kgc1HIv8STDdGGLsaAtV4F15jwooHpdSl6qdfJ63Xyel2KnkrRz6P4YPoyVA0uXqVTCyN-usG_O48v_-Gsv3ybZxL4H46encg</recordid><startdate>199007</startdate><enddate>199007</enddate><creator>Pullen, R. G. L.</creator><creator>Candy, J. M.</creator><creator>Morris, C. M.</creator><creator>Taylor, G.</creator><creator>Keith, A. B.</creator><creator>Edwardson, J. A.</creator><general>Blackwell Publishing Ltd</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>199007</creationdate><title>Gallium‐67 as a Potential Marker for Aluminium Transport in Rat Brain: Implications for Alzheimer's Disease</title><author>Pullen, R. G. L. ; Candy, J. M. ; Morris, C. M. ; Taylor, G. ; Keith, A. B. ; Edwardson, J. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3151-14493935bb09489c9e1db401fbafcf270feef0dcaee75cbb751844c38e0fe6193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Aluminium</topic><topic>Aluminum - metabolism</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer's disease</topic><topic>Animals</topic><topic>Autoradiography</topic><topic>Blood-Brain Barrier</topic><topic>Brain - metabolism</topic><topic>Capillary Permeability</topic><topic>Gallium - blood</topic><topic>Gallium - metabolism</topic><topic>Gallium Radioisotopes</topic><topic>Gallium‐67</topic><topic>Iron</topic><topic>Male</topic><topic>Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Tissue Distribution</topic><topic>Transferrin</topic><topic>Transferrin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pullen, R. G. L.</creatorcontrib><creatorcontrib>Candy, J. M.</creatorcontrib><creatorcontrib>Morris, C. M.</creatorcontrib><creatorcontrib>Taylor, G.</creatorcontrib><creatorcontrib>Keith, A. B.</creatorcontrib><creatorcontrib>Edwardson, J. A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pullen, R. G. L.</au><au>Candy, J. M.</au><au>Morris, C. M.</au><au>Taylor, G.</au><au>Keith, A. B.</au><au>Edwardson, J. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gallium‐67 as a Potential Marker for Aluminium Transport in Rat Brain: Implications for Alzheimer's Disease</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1990-07</date><risdate>1990</risdate><volume>55</volume><issue>1</issue><spage>251</spage><epage>259</epage><pages>251-259</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><abstract>: Evidence of a link between aluminium and Alzheimer's disease, parkinsonism‐dementia of Guam, and dialysis encephalopathy raises questions regarding the role of this element in the pathogenesis of these conditions. Therefore, we have investigated the use of gallium‐67 (67Ga) as a marker for brain uptake of aluminium. The binding of 67Ga to plasma proteins has been studied, and the blood‐brain barrier permeability and autoradiographic distribution of this isotope in rat brain determined in vivo. The autoradiographic distribution of 125I‐Fe‐transferrin receptors in rat brain has also been determined in vitro. Results show that 67Ga was bound to plasma transferrin, entered the brain with a blood‐brain barrier permeability of 2.48 X 10‐6 ml/min/g, and showed a marked regional distribution that was very similar to that of 125I‐Fe‐transferrin receptors. Our data suggest that the vulnerability of the hippocampus, amygdala, and cerebral cortex in conditions such as those mentioned above may be partly due to an increased uptake and deposition of aluminium in these regions by the iron transport system.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>2355220</pmid><doi>10.1111/j.1471-4159.1990.tb08846.x</doi><tpages>9</tpages></addata></record> |
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subjects | Aluminium Aluminum - metabolism Alzheimer Disease - metabolism Alzheimer's disease Animals Autoradiography Blood-Brain Barrier Brain - metabolism Capillary Permeability Gallium - blood Gallium - metabolism Gallium Radioisotopes Gallium‐67 Iron Male Proteins - metabolism Rats Rats, Inbred Strains Tissue Distribution Transferrin Transferrin - metabolism |
title | Gallium‐67 as a Potential Marker for Aluminium Transport in Rat Brain: Implications for Alzheimer's Disease |
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