Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit
Few studies have investigated physiologic and cognitive effects of "long-term" electromagnetic field (EMF) exposure in humans or animals. Our recent studies have provided initial insight into the long-term impact of adulthood EMF exposure (GSM, pulsed/modulated, 918 MHz, 0.25-1.05 W/kg) by...
Gespeichert in:
Veröffentlicht in: | PloS one 2012, Vol.7 (4), p.e35751-e35751 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | e35751 |
---|---|
container_issue | 4 |
container_start_page | e35751 |
container_title | PloS one |
container_volume | 7 |
creator | Arendash, Gary W Mori, Takashi Dorsey, Maggie Gonzalez, Rich Tajiri, Naoki Borlongan, Cesar |
description | Few studies have investigated physiologic and cognitive effects of "long-term" electromagnetic field (EMF) exposure in humans or animals. Our recent studies have provided initial insight into the long-term impact of adulthood EMF exposure (GSM, pulsed/modulated, 918 MHz, 0.25-1.05 W/kg) by showing 6+ months of daily EMF treatment protects against or reverses cognitive impairment in Alzheimer's transgenic (Tg) mice, while even having cognitive benefit to normal mice. Mechanistically, EMF-induced cognitive benefits involve suppression of brain β-amyloid (Aβ) aggregation/deposition in Tg mice and brain mitochondrial enhancement in both Tg and normal mice. The present study extends this work by showing that daily EMF treatment given to very old (21-27 month) Tg mice over a 2-month period reverses their very advanced brain Aβ aggregation/deposition. These very old Tg mice and their normal littermates together showed an increase in general memory function in the Y-maze task, although not in more complex tasks. Measurement of both body and brain temperature at intervals during the 2-month EMF treatment, as well as in a separate group of Tg mice during a 12-day treatment period, revealed no appreciable increases in brain temperature (and no/slight increases in body temperature) during EMF "ON" periods. Thus, the neuropathologic/cognitive benefits of EMF treatment occur without brain hyperthermia. Finally, regional cerebral blood flow in cerebral cortex was determined to be reduced in both Tg and normal mice after 2 months of EMF treatment, most probably through cerebrovascular constriction induced by freed/disaggregated Aβ (Tg mice) and slight body hyperthermia during "ON" periods. These results demonstrate that long-term EMF treatment can provide general cognitive benefit to very old Alzheimer's Tg mice and normal mice, as well as reversal of advanced Aβ neuropathology in Tg mice without brain heating. Results further underscore the potential for EMF treatment against AD. |
doi_str_mv | 10.1371/journal.pone.0035751 |
format | Article |
fullrecord | <record><control><sourceid>proquest_plos_</sourceid><recordid>TN_cdi_plos_journals_1324595785</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_2d20de50fc93457093b27fcd310bd8fe</doaj_id><sourcerecordid>2939346051</sourcerecordid><originalsourceid>FETCH-LOGICAL-c526t-e00f026f3cc22ccfd6e22fb6a7811e8a997148db321c24fefe4b1a18eddd69fb3</originalsourceid><addsrcrecordid>eNptUstuFDEQHCEQCYE_QGCJQzhkFz_GM54LUhQFiBSJC5wtj93eeOWZXuzZjcKP8B_5EL4JL7uJEsTJLXdVdXepquo1o3MmWvZhies0mjhf4QhzSoVsJXtSHbJO8FnDqXj6oD6oXuS8pFQK1TTPqwPOpVScNYfVr_MIdko4mMUIU7BkSmCmAcaJTEgwOnIaf15BGCAdZzIECyTBBlKGTH7fzsxwEzE44mCFOUwBxxMyoAs-lL6FBH0ykfQR0REf8fqEmNGRVcJNcAWRYTsdHLG4GAt9A6SHEXyYXlbPvIkZXu3fo-r7p_NvZ19ml18_X5ydXs6s5M00A0o95Y0X1nJurXcNcO77xrSKMVCm61pWK9cLziyvPXioe2aYAudc0_leHFVvd7qriFnvPc2aCV7LTrZKFsTFDuHQLPUqhcGkG40m6L8fmBbapOJcBM0dpw4k9bYTtWxpJ3reeusEo71THorWx_20dT-As8Xm4s8j0cedMVzpBW60EELVDS8C7_cCCX-sIU96CNlCjGYEXJe9KWOsk1SpAn33D_T_19U7lE2YcwJ_vwyjepuzO5be5kzvc1Zobx4eck-6C5b4Aw6C1ns</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1324595785</pqid></control><display><type>article</type><title>Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit</title><source>MEDLINE</source><source>DOAJ Directory of Open Access Journals</source><source>Public Library of Science (PLoS) Journals Open Access</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Free Full-Text Journals in Chemistry</source><creator>Arendash, Gary W ; Mori, Takashi ; Dorsey, Maggie ; Gonzalez, Rich ; Tajiri, Naoki ; Borlongan, Cesar</creator><contributor>Skoulakis, Efthimios M. C.</contributor><creatorcontrib>Arendash, Gary W ; Mori, Takashi ; Dorsey, Maggie ; Gonzalez, Rich ; Tajiri, Naoki ; Borlongan, Cesar ; Skoulakis, Efthimios M. C.</creatorcontrib><description>Few studies have investigated physiologic and cognitive effects of "long-term" electromagnetic field (EMF) exposure in humans or animals. Our recent studies have provided initial insight into the long-term impact of adulthood EMF exposure (GSM, pulsed/modulated, 918 MHz, 0.25-1.05 W/kg) by showing 6+ months of daily EMF treatment protects against or reverses cognitive impairment in Alzheimer's transgenic (Tg) mice, while even having cognitive benefit to normal mice. Mechanistically, EMF-induced cognitive benefits involve suppression of brain β-amyloid (Aβ) aggregation/deposition in Tg mice and brain mitochondrial enhancement in both Tg and normal mice. The present study extends this work by showing that daily EMF treatment given to very old (21-27 month) Tg mice over a 2-month period reverses their very advanced brain Aβ aggregation/deposition. These very old Tg mice and their normal littermates together showed an increase in general memory function in the Y-maze task, although not in more complex tasks. Measurement of both body and brain temperature at intervals during the 2-month EMF treatment, as well as in a separate group of Tg mice during a 12-day treatment period, revealed no appreciable increases in brain temperature (and no/slight increases in body temperature) during EMF "ON" periods. Thus, the neuropathologic/cognitive benefits of EMF treatment occur without brain hyperthermia. Finally, regional cerebral blood flow in cerebral cortex was determined to be reduced in both Tg and normal mice after 2 months of EMF treatment, most probably through cerebrovascular constriction induced by freed/disaggregated Aβ (Tg mice) and slight body hyperthermia during "ON" periods. These results demonstrate that long-term EMF treatment can provide general cognitive benefit to very old Alzheimer's Tg mice and normal mice, as well as reversal of advanced Aβ neuropathology in Tg mice without brain heating. Results further underscore the potential for EMF treatment against AD.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0035751</identifier><identifier>PMID: 22558216</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Agglomeration ; Alzheimer Disease - metabolism ; Alzheimer Disease - pathology ; Alzheimer Disease - radiotherapy ; Alzheimer's disease ; Amyloid beta-Peptides - metabolism ; Animals ; Biology ; Blood ; Blood flow ; Blood-brain barrier ; Body temperature ; Body Temperature - radiation effects ; Bone marrow ; Brain ; Caffeine ; Cellular telephones ; Cerebral blood flow ; Cerebral cortex ; Cerebrovascular Circulation - radiation effects ; Cerebrovascular system ; Cognition - radiation effects ; Cognitive ability ; Deposition ; Disease Models, Animal ; Edema ; Electromagnetic Fields ; Exposure ; Fatty acids ; Humans ; Hyperthermia ; Ischemia ; Low frequency ; Magnetic Field Therapy - methods ; Maze Learning - radiation effects ; Medicine ; Memory ; Memory - radiation effects ; Metabolism ; Mice ; Mice, Transgenic ; Mitochondria ; Mitochondria - radiation effects ; Neurodegenerative diseases ; Neurosciences ; Neurosurgery ; Nitric oxide ; Pathology ; Pharmaceutical industry ; Psychomotor Performance - radiation effects ; Rodents ; Spectrum analysis ; Studies ; Task complexity ; Temperature ; Temperature effects ; Transgenic animals ; Transgenic mice ; β-Amyloid</subject><ispartof>PloS one, 2012, Vol.7 (4), p.e35751-e35751</ispartof><rights>2012 Arendash et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Arendash et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-e00f026f3cc22ccfd6e22fb6a7811e8a997148db321c24fefe4b1a18eddd69fb3</citedby><cites>FETCH-LOGICAL-c526t-e00f026f3cc22ccfd6e22fb6a7811e8a997148db321c24fefe4b1a18eddd69fb3</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/PMC3338462/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338462/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,4024,23866,27923,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22558216$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Skoulakis, Efthimios M. C.</contributor><creatorcontrib>Arendash, Gary W</creatorcontrib><creatorcontrib>Mori, Takashi</creatorcontrib><creatorcontrib>Dorsey, Maggie</creatorcontrib><creatorcontrib>Gonzalez, Rich</creatorcontrib><creatorcontrib>Tajiri, Naoki</creatorcontrib><creatorcontrib>Borlongan, Cesar</creatorcontrib><title>Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Few studies have investigated physiologic and cognitive effects of "long-term" electromagnetic field (EMF) exposure in humans or animals. Our recent studies have provided initial insight into the long-term impact of adulthood EMF exposure (GSM, pulsed/modulated, 918 MHz, 0.25-1.05 W/kg) by showing 6+ months of daily EMF treatment protects against or reverses cognitive impairment in Alzheimer's transgenic (Tg) mice, while even having cognitive benefit to normal mice. Mechanistically, EMF-induced cognitive benefits involve suppression of brain β-amyloid (Aβ) aggregation/deposition in Tg mice and brain mitochondrial enhancement in both Tg and normal mice. The present study extends this work by showing that daily EMF treatment given to very old (21-27 month) Tg mice over a 2-month period reverses their very advanced brain Aβ aggregation/deposition. These very old Tg mice and their normal littermates together showed an increase in general memory function in the Y-maze task, although not in more complex tasks. Measurement of both body and brain temperature at intervals during the 2-month EMF treatment, as well as in a separate group of Tg mice during a 12-day treatment period, revealed no appreciable increases in brain temperature (and no/slight increases in body temperature) during EMF "ON" periods. Thus, the neuropathologic/cognitive benefits of EMF treatment occur without brain hyperthermia. Finally, regional cerebral blood flow in cerebral cortex was determined to be reduced in both Tg and normal mice after 2 months of EMF treatment, most probably through cerebrovascular constriction induced by freed/disaggregated Aβ (Tg mice) and slight body hyperthermia during "ON" periods. These results demonstrate that long-term EMF treatment can provide general cognitive benefit to very old Alzheimer's Tg mice and normal mice, as well as reversal of advanced Aβ neuropathology in Tg mice without brain heating. Results further underscore the potential for EMF treatment against AD.</description><subject>Agglomeration</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer Disease - pathology</subject><subject>Alzheimer Disease - radiotherapy</subject><subject>Alzheimer's disease</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Animals</subject><subject>Biology</subject><subject>Blood</subject><subject>Blood flow</subject><subject>Blood-brain barrier</subject><subject>Body temperature</subject><subject>Body Temperature - radiation effects</subject><subject>Bone marrow</subject><subject>Brain</subject><subject>Caffeine</subject><subject>Cellular telephones</subject><subject>Cerebral blood flow</subject><subject>Cerebral cortex</subject><subject>Cerebrovascular Circulation - radiation effects</subject><subject>Cerebrovascular system</subject><subject>Cognition - radiation effects</subject><subject>Cognitive ability</subject><subject>Deposition</subject><subject>Disease Models, Animal</subject><subject>Edema</subject><subject>Electromagnetic Fields</subject><subject>Exposure</subject><subject>Fatty acids</subject><subject>Humans</subject><subject>Hyperthermia</subject><subject>Ischemia</subject><subject>Low frequency</subject><subject>Magnetic Field Therapy - methods</subject><subject>Maze Learning - radiation effects</subject><subject>Medicine</subject><subject>Memory</subject><subject>Memory - radiation effects</subject><subject>Metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mitochondria</subject><subject>Mitochondria - radiation effects</subject><subject>Neurodegenerative diseases</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Nitric oxide</subject><subject>Pathology</subject><subject>Pharmaceutical industry</subject><subject>Psychomotor Performance - radiation effects</subject><subject>Rodents</subject><subject>Spectrum analysis</subject><subject>Studies</subject><subject>Task complexity</subject><subject>Temperature</subject><subject>Temperature effects</subject><subject>Transgenic animals</subject><subject>Transgenic mice</subject><subject>β-Amyloid</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNptUstuFDEQHCEQCYE_QGCJQzhkFz_GM54LUhQFiBSJC5wtj93eeOWZXuzZjcKP8B_5EL4JL7uJEsTJLXdVdXepquo1o3MmWvZhies0mjhf4QhzSoVsJXtSHbJO8FnDqXj6oD6oXuS8pFQK1TTPqwPOpVScNYfVr_MIdko4mMUIU7BkSmCmAcaJTEgwOnIaf15BGCAdZzIECyTBBlKGTH7fzsxwEzE44mCFOUwBxxMyoAs-lL6FBH0ykfQR0REf8fqEmNGRVcJNcAWRYTsdHLG4GAt9A6SHEXyYXlbPvIkZXu3fo-r7p_NvZ19ml18_X5ydXs6s5M00A0o95Y0X1nJurXcNcO77xrSKMVCm61pWK9cLziyvPXioe2aYAudc0_leHFVvd7qriFnvPc2aCV7LTrZKFsTFDuHQLPUqhcGkG40m6L8fmBbapOJcBM0dpw4k9bYTtWxpJ3reeusEo71THorWx_20dT-As8Xm4s8j0cedMVzpBW60EELVDS8C7_cCCX-sIU96CNlCjGYEXJe9KWOsk1SpAn33D_T_19U7lE2YcwJ_vwyjepuzO5be5kzvc1Zobx4eck-6C5b4Aw6C1ns</recordid><startdate>2012</startdate><enddate>2012</enddate><creator>Arendash, Gary W</creator><creator>Mori, Takashi</creator><creator>Dorsey, Maggie</creator><creator>Gonzalez, Rich</creator><creator>Tajiri, Naoki</creator><creator>Borlongan, Cesar</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>2012</creationdate><title>Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit</title><author>Arendash, Gary W ; Mori, Takashi ; Dorsey, Maggie ; Gonzalez, Rich ; Tajiri, Naoki ; Borlongan, Cesar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-e00f026f3cc22ccfd6e22fb6a7811e8a997148db321c24fefe4b1a18eddd69fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Agglomeration</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer Disease - pathology</topic><topic>Alzheimer Disease - radiotherapy</topic><topic>Alzheimer's disease</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Animals</topic><topic>Biology</topic><topic>Blood</topic><topic>Blood flow</topic><topic>Blood-brain barrier</topic><topic>Body temperature</topic><topic>Body Temperature - radiation effects</topic><topic>Bone marrow</topic><topic>Brain</topic><topic>Caffeine</topic><topic>Cellular telephones</topic><topic>Cerebral blood flow</topic><topic>Cerebral cortex</topic><topic>Cerebrovascular Circulation - radiation effects</topic><topic>Cerebrovascular system</topic><topic>Cognition - radiation effects</topic><topic>Cognitive ability</topic><topic>Deposition</topic><topic>Disease Models, Animal</topic><topic>Edema</topic><topic>Electromagnetic Fields</topic><topic>Exposure</topic><topic>Fatty acids</topic><topic>Humans</topic><topic>Hyperthermia</topic><topic>Ischemia</topic><topic>Low frequency</topic><topic>Magnetic Field Therapy - methods</topic><topic>Maze Learning - radiation effects</topic><topic>Medicine</topic><topic>Memory</topic><topic>Memory - radiation effects</topic><topic>Metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Mitochondria</topic><topic>Mitochondria - radiation effects</topic><topic>Neurodegenerative diseases</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Nitric oxide</topic><topic>Pathology</topic><topic>Pharmaceutical industry</topic><topic>Psychomotor Performance - radiation effects</topic><topic>Rodents</topic><topic>Spectrum analysis</topic><topic>Studies</topic><topic>Task complexity</topic><topic>Temperature</topic><topic>Temperature effects</topic><topic>Transgenic animals</topic><topic>Transgenic mice</topic><topic>β-Amyloid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arendash, Gary W</creatorcontrib><creatorcontrib>Mori, Takashi</creatorcontrib><creatorcontrib>Dorsey, Maggie</creatorcontrib><creatorcontrib>Gonzalez, Rich</creatorcontrib><creatorcontrib>Tajiri, Naoki</creatorcontrib><creatorcontrib>Borlongan, Cesar</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>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Materials Science Collection</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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arendash, Gary W</au><au>Mori, Takashi</au><au>Dorsey, Maggie</au><au>Gonzalez, Rich</au><au>Tajiri, Naoki</au><au>Borlongan, Cesar</au><au>Skoulakis, Efthimios M. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2012</date><risdate>2012</risdate><volume>7</volume><issue>4</issue><spage>e35751</spage><epage>e35751</epage><pages>e35751-e35751</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Few studies have investigated physiologic and cognitive effects of "long-term" electromagnetic field (EMF) exposure in humans or animals. Our recent studies have provided initial insight into the long-term impact of adulthood EMF exposure (GSM, pulsed/modulated, 918 MHz, 0.25-1.05 W/kg) by showing 6+ months of daily EMF treatment protects against or reverses cognitive impairment in Alzheimer's transgenic (Tg) mice, while even having cognitive benefit to normal mice. Mechanistically, EMF-induced cognitive benefits involve suppression of brain β-amyloid (Aβ) aggregation/deposition in Tg mice and brain mitochondrial enhancement in both Tg and normal mice. The present study extends this work by showing that daily EMF treatment given to very old (21-27 month) Tg mice over a 2-month period reverses their very advanced brain Aβ aggregation/deposition. These very old Tg mice and their normal littermates together showed an increase in general memory function in the Y-maze task, although not in more complex tasks. Measurement of both body and brain temperature at intervals during the 2-month EMF treatment, as well as in a separate group of Tg mice during a 12-day treatment period, revealed no appreciable increases in brain temperature (and no/slight increases in body temperature) during EMF "ON" periods. Thus, the neuropathologic/cognitive benefits of EMF treatment occur without brain hyperthermia. Finally, regional cerebral blood flow in cerebral cortex was determined to be reduced in both Tg and normal mice after 2 months of EMF treatment, most probably through cerebrovascular constriction induced by freed/disaggregated Aβ (Tg mice) and slight body hyperthermia during "ON" periods. These results demonstrate that long-term EMF treatment can provide general cognitive benefit to very old Alzheimer's Tg mice and normal mice, as well as reversal of advanced Aβ neuropathology in Tg mice without brain heating. Results further underscore the potential for EMF treatment against AD.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>22558216</pmid><doi>10.1371/journal.pone.0035751</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2012, Vol.7 (4), p.e35751-e35751 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1324595785 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Public Library of Science (PLoS) Journals Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Agglomeration Alzheimer Disease - metabolism Alzheimer Disease - pathology Alzheimer Disease - radiotherapy Alzheimer's disease Amyloid beta-Peptides - metabolism Animals Biology Blood Blood flow Blood-brain barrier Body temperature Body Temperature - radiation effects Bone marrow Brain Caffeine Cellular telephones Cerebral blood flow Cerebral cortex Cerebrovascular Circulation - radiation effects Cerebrovascular system Cognition - radiation effects Cognitive ability Deposition Disease Models, Animal Edema Electromagnetic Fields Exposure Fatty acids Humans Hyperthermia Ischemia Low frequency Magnetic Field Therapy - methods Maze Learning - radiation effects Medicine Memory Memory - radiation effects Metabolism Mice Mice, Transgenic Mitochondria Mitochondria - radiation effects Neurodegenerative diseases Neurosciences Neurosurgery Nitric oxide Pathology Pharmaceutical industry Psychomotor Performance - radiation effects Rodents Spectrum analysis Studies Task complexity Temperature Temperature effects Transgenic animals Transgenic mice β-Amyloid |
title | Electromagnetic treatment to old Alzheimer's mice reverses β-amyloid deposition, modifies cerebral blood flow, and provides selected cognitive benefit |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T15%3A40%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Electromagnetic%20treatment%20to%20old%20Alzheimer's%20mice%20reverses%20%CE%B2-amyloid%20deposition,%20modifies%20cerebral%20blood%20flow,%20and%20provides%20selected%20cognitive%20benefit&rft.jtitle=PloS%20one&rft.au=Arendash,%20Gary%20W&rft.date=2012&rft.volume=7&rft.issue=4&rft.spage=e35751&rft.epage=e35751&rft.pages=e35751-e35751&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0035751&rft_dat=%3Cproquest_plos_%3E2939346051%3C/proquest_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1324595785&rft_id=info:pmid/22558216&rft_doaj_id=oai_doaj_org_article_2d20de50fc93457093b27fcd310bd8fe&rfr_iscdi=true |