Cerebral mapping of glutamate using chemical exchange saturation transfer imaging in a rat model of stress‐induced sleep disturbance at 7.0T
Background Glutamate chemical exchange saturation transfer (GluCEST) imaging has been widely used in brain psychiatric disorders. Glutamate signal changes may help to evaluate the sleep‐related disorders, and could be useful in diagnosis. Purpose To evaluate signal changes in the hippocampus and cor...
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creator | Lee, Dong‐Hoon Woo, Chul‐Woong Kwon, Jae‐Im Chae, Yeon Ji Ham, Su Jung Suh, Ji‐Yeon Kim, Sang‐Tae Kim, Jeong Kon Kim, Kyung Won Woo, Dong‐Cheol Lee, Do‐Wan |
description | Background
Glutamate chemical exchange saturation transfer (GluCEST) imaging has been widely used in brain psychiatric disorders. Glutamate signal changes may help to evaluate the sleep‐related disorders, and could be useful in diagnosis.
Purpose
To evaluate signal changes in the hippocampus and cortex of a rat model of stress‐induced sleep disturbance using GluCEST.
Study Type
Prospective animal study.
Animal Model
Fourteen male Sprague–Dawley rats.
Field Strength/Sequence
7.0T small bore MRI / fat‐suppressed, turbo‐rapid acquisition with relaxation enhancement (RARE) for CEST, and spin‐echo, point‐resolved proton MR spectroscopy (1H MRS).
Assessment
Rats were divided into two groups: the stress‐induced sleep‐disturbance group (SSD, n = 7) and the control group (CTRL, n = 7), to evaluate and compare the cerebral glutamate signal changes. GluCEST data were quantified using a conventional magnetization transfer ratio asymmetry in the left‐ and right‐side hippocampus and cortex. The correlation between GluCEST signal and glutamate concentrations, derived from 1H MRS, was evaluated.
Statistical Analysis
Wilcoxon rank‐sum test between CEST signals and multiparametric MR signals, Wilcoxon signed‐rank test between CEST signals on the left and right hemispheres, and a correlation test between CEST signals and glutamate concentrations derived from 1H MRS.
Results
Measured GluCEST signals showed significant differences between the two groups (left hippocampus; 4.23 ± 0.27% / 5.27 ± 0.42% [SSD / CTRL, P = 0.002], right hippocampus; 4.50 ± 0.44% / 5.04 ± 0.34% [P = 0.035], left cortex; 2.81 ± 0.38% / 3.56 ± 0.41% [P = 0.004], and right cortex; 2.95 ± 0.47% / 3.82 ± 0.26% [P = 0.003]). GluCEST signals showed positive correlation with glutamate concentrations (R2 = 0.312; P = 0.038).
Data Conclusion
GluCEST allowed the visualization of cerebral glutamate changes in rats subjected to sleep disturbance, and may yield valuable insights for interpreting alterations in cerebral biochemical information.
Level of Evidence: 2
Technical Efficacy: Stage 2
J. Magn. Reson. Imaging 2019;50:1866–1872. |
doi_str_mv | 10.1002/jmri.26769 |
format | Article |
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Glutamate chemical exchange saturation transfer (GluCEST) imaging has been widely used in brain psychiatric disorders. Glutamate signal changes may help to evaluate the sleep‐related disorders, and could be useful in diagnosis.
Purpose
To evaluate signal changes in the hippocampus and cortex of a rat model of stress‐induced sleep disturbance using GluCEST.
Study Type
Prospective animal study.
Animal Model
Fourteen male Sprague–Dawley rats.
Field Strength/Sequence
7.0T small bore MRI / fat‐suppressed, turbo‐rapid acquisition with relaxation enhancement (RARE) for CEST, and spin‐echo, point‐resolved proton MR spectroscopy (1H MRS).
Assessment
Rats were divided into two groups: the stress‐induced sleep‐disturbance group (SSD, n = 7) and the control group (CTRL, n = 7), to evaluate and compare the cerebral glutamate signal changes. GluCEST data were quantified using a conventional magnetization transfer ratio asymmetry in the left‐ and right‐side hippocampus and cortex. The correlation between GluCEST signal and glutamate concentrations, derived from 1H MRS, was evaluated.
Statistical Analysis
Wilcoxon rank‐sum test between CEST signals and multiparametric MR signals, Wilcoxon signed‐rank test between CEST signals on the left and right hemispheres, and a correlation test between CEST signals and glutamate concentrations derived from 1H MRS.
Results
Measured GluCEST signals showed significant differences between the two groups (left hippocampus; 4.23 ± 0.27% / 5.27 ± 0.42% [SSD / CTRL, P = 0.002], right hippocampus; 4.50 ± 0.44% / 5.04 ± 0.34% [P = 0.035], left cortex; 2.81 ± 0.38% / 3.56 ± 0.41% [P = 0.004], and right cortex; 2.95 ± 0.47% / 3.82 ± 0.26% [P = 0.003]). GluCEST signals showed positive correlation with glutamate concentrations (R2 = 0.312; P = 0.038).
Data Conclusion
GluCEST allowed the visualization of cerebral glutamate changes in rats subjected to sleep disturbance, and may yield valuable insights for interpreting alterations in cerebral biochemical information.
Level of Evidence: 2
Technical Efficacy: Stage 2
J. Magn. Reson. Imaging 2019;50:1866–1872.</description><identifier>ISSN: 1053-1807</identifier><identifier>EISSN: 1522-2586</identifier><identifier>DOI: 10.1002/jmri.26769</identifier><identifier>PMID: 31033089</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Animal models ; chemical exchange saturation transfer ; Correlation ; Disorders ; Disturbance ; Evaluation ; Exchanging ; Field strength ; glutamate ; Hemispheres ; Hemispheric laterality ; Hippocampus ; Magnetic resonance imaging ; Magnetic resonance spectroscopy ; Mapping ; Medical imaging ; Mental disorders ; Neuroimaging ; Organic chemistry ; proton magnetic resonance spectroscopy ; Rank tests ; Saturation ; Sleep ; sleep disturbance ; Statistical analysis ; Stress</subject><ispartof>Journal of magnetic resonance imaging, 2019-12, Vol.50 (6), p.1866-1872</ispartof><rights>2019 International Society for Magnetic Resonance in Medicine</rights><rights>2019 International Society for Magnetic Resonance in Medicine.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3579-5c9e81f1df68a127228d148468e7f5af824c40bfb1d5853d4377d1be6610598b3</citedby><cites>FETCH-LOGICAL-c3579-5c9e81f1df68a127228d148468e7f5af824c40bfb1d5853d4377d1be6610598b3</cites><orcidid>0000-0001-7925-0333 ; 0000-0002-5013-4440</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmri.26769$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmri.26769$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31033089$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Dong‐Hoon</creatorcontrib><creatorcontrib>Woo, Chul‐Woong</creatorcontrib><creatorcontrib>Kwon, Jae‐Im</creatorcontrib><creatorcontrib>Chae, Yeon Ji</creatorcontrib><creatorcontrib>Ham, Su Jung</creatorcontrib><creatorcontrib>Suh, Ji‐Yeon</creatorcontrib><creatorcontrib>Kim, Sang‐Tae</creatorcontrib><creatorcontrib>Kim, Jeong Kon</creatorcontrib><creatorcontrib>Kim, Kyung Won</creatorcontrib><creatorcontrib>Woo, Dong‐Cheol</creatorcontrib><creatorcontrib>Lee, Do‐Wan</creatorcontrib><title>Cerebral mapping of glutamate using chemical exchange saturation transfer imaging in a rat model of stress‐induced sleep disturbance at 7.0T</title><title>Journal of magnetic resonance imaging</title><addtitle>J Magn Reson Imaging</addtitle><description>Background
Glutamate chemical exchange saturation transfer (GluCEST) imaging has been widely used in brain psychiatric disorders. Glutamate signal changes may help to evaluate the sleep‐related disorders, and could be useful in diagnosis.
Purpose
To evaluate signal changes in the hippocampus and cortex of a rat model of stress‐induced sleep disturbance using GluCEST.
Study Type
Prospective animal study.
Animal Model
Fourteen male Sprague–Dawley rats.
Field Strength/Sequence
7.0T small bore MRI / fat‐suppressed, turbo‐rapid acquisition with relaxation enhancement (RARE) for CEST, and spin‐echo, point‐resolved proton MR spectroscopy (1H MRS).
Assessment
Rats were divided into two groups: the stress‐induced sleep‐disturbance group (SSD, n = 7) and the control group (CTRL, n = 7), to evaluate and compare the cerebral glutamate signal changes. GluCEST data were quantified using a conventional magnetization transfer ratio asymmetry in the left‐ and right‐side hippocampus and cortex. The correlation between GluCEST signal and glutamate concentrations, derived from 1H MRS, was evaluated.
Statistical Analysis
Wilcoxon rank‐sum test between CEST signals and multiparametric MR signals, Wilcoxon signed‐rank test between CEST signals on the left and right hemispheres, and a correlation test between CEST signals and glutamate concentrations derived from 1H MRS.
Results
Measured GluCEST signals showed significant differences between the two groups (left hippocampus; 4.23 ± 0.27% / 5.27 ± 0.42% [SSD / CTRL, P = 0.002], right hippocampus; 4.50 ± 0.44% / 5.04 ± 0.34% [P = 0.035], left cortex; 2.81 ± 0.38% / 3.56 ± 0.41% [P = 0.004], and right cortex; 2.95 ± 0.47% / 3.82 ± 0.26% [P = 0.003]). GluCEST signals showed positive correlation with glutamate concentrations (R2 = 0.312; P = 0.038).
Data Conclusion
GluCEST allowed the visualization of cerebral glutamate changes in rats subjected to sleep disturbance, and may yield valuable insights for interpreting alterations in cerebral biochemical information.
Level of Evidence: 2
Technical Efficacy: Stage 2
J. Magn. Reson. Imaging 2019;50:1866–1872.</description><subject>Animal models</subject><subject>chemical exchange saturation transfer</subject><subject>Correlation</subject><subject>Disorders</subject><subject>Disturbance</subject><subject>Evaluation</subject><subject>Exchanging</subject><subject>Field strength</subject><subject>glutamate</subject><subject>Hemispheres</subject><subject>Hemispheric laterality</subject><subject>Hippocampus</subject><subject>Magnetic resonance imaging</subject><subject>Magnetic resonance spectroscopy</subject><subject>Mapping</subject><subject>Medical imaging</subject><subject>Mental disorders</subject><subject>Neuroimaging</subject><subject>Organic chemistry</subject><subject>proton magnetic resonance spectroscopy</subject><subject>Rank tests</subject><subject>Saturation</subject><subject>Sleep</subject><subject>sleep disturbance</subject><subject>Statistical analysis</subject><subject>Stress</subject><issn>1053-1807</issn><issn>1522-2586</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kc9qFTEUh4NYbK1ufAAJuCnCXPNnksks5VK1UhGkrkMmObnNZSYzJjNodz6B-Ix9kma8rQsXrnLI-fg4_H4IvaBkQwlhb_ZDChsmG9k-QidUMFYxoeTjMhPBK6pIc4ye5rwnhLRtLZ6gY04J50S1J-jXFhJ0yfR4MNMU4g6PHu_6ZTaDmQEvef2y1zAEWxj4Ya9N3AHOZl6SmcMY8ZxMzB4SDoPZrXSI2OCyxMPooF99eU6Q8-3P3yG6xYLDuQeYsAu5WDoTLeCCNxty9QwdedNneH7_nqKv786vth-qy8_vL7ZvLyvLRdNWwragqKfOS2UoaxhTjtaqlgoaL4xXrLY16XxHnVCCu5o3jaMdSFkiaVXHT9HZwTul8dsCedZDyBb63kQYl6wZo2ueXJKCvvoH3Y9LiuU6zTita9VKKgr1-kDZNOacwOsplUDSjaZEry3ptSX9p6UCv7xXLt0A7i_6UEsB6AH4Hnq4-Y9Kf_z05eIgvQNUO56d</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Lee, Dong‐Hoon</creator><creator>Woo, Chul‐Woong</creator><creator>Kwon, Jae‐Im</creator><creator>Chae, Yeon Ji</creator><creator>Ham, Su Jung</creator><creator>Suh, Ji‐Yeon</creator><creator>Kim, Sang‐Tae</creator><creator>Kim, Jeong Kon</creator><creator>Kim, Kyung Won</creator><creator>Woo, Dong‐Cheol</creator><creator>Lee, Do‐Wan</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7925-0333</orcidid><orcidid>https://orcid.org/0000-0002-5013-4440</orcidid></search><sort><creationdate>201912</creationdate><title>Cerebral mapping of glutamate using chemical exchange saturation transfer imaging in a rat model of stress‐induced sleep disturbance at 7.0T</title><author>Lee, Dong‐Hoon ; Woo, Chul‐Woong ; Kwon, Jae‐Im ; Chae, Yeon Ji ; Ham, Su Jung ; Suh, Ji‐Yeon ; Kim, Sang‐Tae ; Kim, Jeong Kon ; Kim, Kyung Won ; Woo, Dong‐Cheol ; Lee, Do‐Wan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3579-5c9e81f1df68a127228d148468e7f5af824c40bfb1d5853d4377d1be6610598b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animal models</topic><topic>chemical exchange saturation transfer</topic><topic>Correlation</topic><topic>Disorders</topic><topic>Disturbance</topic><topic>Evaluation</topic><topic>Exchanging</topic><topic>Field strength</topic><topic>glutamate</topic><topic>Hemispheres</topic><topic>Hemispheric laterality</topic><topic>Hippocampus</topic><topic>Magnetic resonance imaging</topic><topic>Magnetic resonance spectroscopy</topic><topic>Mapping</topic><topic>Medical imaging</topic><topic>Mental disorders</topic><topic>Neuroimaging</topic><topic>Organic chemistry</topic><topic>proton magnetic resonance spectroscopy</topic><topic>Rank tests</topic><topic>Saturation</topic><topic>Sleep</topic><topic>sleep disturbance</topic><topic>Statistical analysis</topic><topic>Stress</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Dong‐Hoon</creatorcontrib><creatorcontrib>Woo, Chul‐Woong</creatorcontrib><creatorcontrib>Kwon, Jae‐Im</creatorcontrib><creatorcontrib>Chae, Yeon Ji</creatorcontrib><creatorcontrib>Ham, Su Jung</creatorcontrib><creatorcontrib>Suh, Ji‐Yeon</creatorcontrib><creatorcontrib>Kim, Sang‐Tae</creatorcontrib><creatorcontrib>Kim, Jeong Kon</creatorcontrib><creatorcontrib>Kim, Kyung Won</creatorcontrib><creatorcontrib>Woo, Dong‐Cheol</creatorcontrib><creatorcontrib>Lee, Do‐Wan</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Dong‐Hoon</au><au>Woo, Chul‐Woong</au><au>Kwon, Jae‐Im</au><au>Chae, Yeon Ji</au><au>Ham, Su Jung</au><au>Suh, Ji‐Yeon</au><au>Kim, Sang‐Tae</au><au>Kim, Jeong Kon</au><au>Kim, Kyung Won</au><au>Woo, Dong‐Cheol</au><au>Lee, Do‐Wan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebral mapping of glutamate using chemical exchange saturation transfer imaging in a rat model of stress‐induced sleep disturbance at 7.0T</atitle><jtitle>Journal of magnetic resonance imaging</jtitle><addtitle>J Magn Reson Imaging</addtitle><date>2019-12</date><risdate>2019</risdate><volume>50</volume><issue>6</issue><spage>1866</spage><epage>1872</epage><pages>1866-1872</pages><issn>1053-1807</issn><eissn>1522-2586</eissn><abstract>Background
Glutamate chemical exchange saturation transfer (GluCEST) imaging has been widely used in brain psychiatric disorders. Glutamate signal changes may help to evaluate the sleep‐related disorders, and could be useful in diagnosis.
Purpose
To evaluate signal changes in the hippocampus and cortex of a rat model of stress‐induced sleep disturbance using GluCEST.
Study Type
Prospective animal study.
Animal Model
Fourteen male Sprague–Dawley rats.
Field Strength/Sequence
7.0T small bore MRI / fat‐suppressed, turbo‐rapid acquisition with relaxation enhancement (RARE) for CEST, and spin‐echo, point‐resolved proton MR spectroscopy (1H MRS).
Assessment
Rats were divided into two groups: the stress‐induced sleep‐disturbance group (SSD, n = 7) and the control group (CTRL, n = 7), to evaluate and compare the cerebral glutamate signal changes. GluCEST data were quantified using a conventional magnetization transfer ratio asymmetry in the left‐ and right‐side hippocampus and cortex. The correlation between GluCEST signal and glutamate concentrations, derived from 1H MRS, was evaluated.
Statistical Analysis
Wilcoxon rank‐sum test between CEST signals and multiparametric MR signals, Wilcoxon signed‐rank test between CEST signals on the left and right hemispheres, and a correlation test between CEST signals and glutamate concentrations derived from 1H MRS.
Results
Measured GluCEST signals showed significant differences between the two groups (left hippocampus; 4.23 ± 0.27% / 5.27 ± 0.42% [SSD / CTRL, P = 0.002], right hippocampus; 4.50 ± 0.44% / 5.04 ± 0.34% [P = 0.035], left cortex; 2.81 ± 0.38% / 3.56 ± 0.41% [P = 0.004], and right cortex; 2.95 ± 0.47% / 3.82 ± 0.26% [P = 0.003]). GluCEST signals showed positive correlation with glutamate concentrations (R2 = 0.312; P = 0.038).
Data Conclusion
GluCEST allowed the visualization of cerebral glutamate changes in rats subjected to sleep disturbance, and may yield valuable insights for interpreting alterations in cerebral biochemical information.
Level of Evidence: 2
Technical Efficacy: Stage 2
J. Magn. Reson. Imaging 2019;50:1866–1872.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>31033089</pmid><doi>10.1002/jmri.26769</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7925-0333</orcidid><orcidid>https://orcid.org/0000-0002-5013-4440</orcidid></addata></record> |
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subjects | Animal models chemical exchange saturation transfer Correlation Disorders Disturbance Evaluation Exchanging Field strength glutamate Hemispheres Hemispheric laterality Hippocampus Magnetic resonance imaging Magnetic resonance spectroscopy Mapping Medical imaging Mental disorders Neuroimaging Organic chemistry proton magnetic resonance spectroscopy Rank tests Saturation Sleep sleep disturbance Statistical analysis Stress |
title | Cerebral mapping of glutamate using chemical exchange saturation transfer imaging in a rat model of stress‐induced sleep disturbance at 7.0T |
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