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MR properties of excised neural tissue following experimentally induced inflammation
Changes in the MR parameters of inflamed neural tissue were measured in vitro. Tumor necrosis factor‐alpha (TNF‐α) was injected into rat sciatic nerves to induce inflammation with negligible axonal loss and demyelination. The MR parameters, such as T1/T2 relaxation and magnetization transfer (MT), w...
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Published in: | Magnetic resonance in medicine 2004-03, Vol.51 (3), p.473-479 |
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container_title | Magnetic resonance in medicine |
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creator | Stanisz, Greg J. Webb, Stephanie Munro, Catherine A. Pun, Teresa Midha, Rajiv |
description | Changes in the MR parameters of inflamed neural tissue were measured in vitro. Tumor necrosis factor‐alpha (TNF‐α) was injected into rat sciatic nerves to induce inflammation with negligible axonal loss and demyelination. The MR parameters, such as T1/T2 relaxation and magnetization transfer (MT), were measured 2 days after TNF‐α injection and were found to be substantially different from those of normal nerves. The average T1/T2 relaxation times increased, whereas the MT ratio (MTR) and the quantitative MT parameter M0B (which describes the semisolid pool of protons) decreased. The MR parameters correlated very well with the extracellular volume fraction (EM) of neural tissue evaluated by quantitative histopathology. The multicomponent T2 relaxation was shown to provide the best quantitative assessment of changes in neural tissue microstructure, and allowed us to distinguish between the processes of inflammation and demyelination. In comparison, the MT measurements were less successful due to competing contributions of demyelination and pH‐sensitive changes in the MT effect. Magn Reson Med 51:473–479, 2004. © 2004 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/mrm.20008 |
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Tumor necrosis factor‐alpha (TNF‐α) was injected into rat sciatic nerves to induce inflammation with negligible axonal loss and demyelination. The MR parameters, such as T1/T2 relaxation and magnetization transfer (MT), were measured 2 days after TNF‐α injection and were found to be substantially different from those of normal nerves. The average T1/T2 relaxation times increased, whereas the MT ratio (MTR) and the quantitative MT parameter M0B (which describes the semisolid pool of protons) decreased. The MR parameters correlated very well with the extracellular volume fraction (EM) of neural tissue evaluated by quantitative histopathology. The multicomponent T2 relaxation was shown to provide the best quantitative assessment of changes in neural tissue microstructure, and allowed us to distinguish between the processes of inflammation and demyelination. In comparison, the MT measurements were less successful due to competing contributions of demyelination and pH‐sensitive changes in the MT effect. 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Reson. Med</addtitle><description>Changes in the MR parameters of inflamed neural tissue were measured in vitro. Tumor necrosis factor‐alpha (TNF‐α) was injected into rat sciatic nerves to induce inflammation with negligible axonal loss and demyelination. The MR parameters, such as T1/T2 relaxation and magnetization transfer (MT), were measured 2 days after TNF‐α injection and were found to be substantially different from those of normal nerves. The average T1/T2 relaxation times increased, whereas the MT ratio (MTR) and the quantitative MT parameter M0B (which describes the semisolid pool of protons) decreased. The MR parameters correlated very well with the extracellular volume fraction (EM) of neural tissue evaluated by quantitative histopathology. The multicomponent T2 relaxation was shown to provide the best quantitative assessment of changes in neural tissue microstructure, and allowed us to distinguish between the processes of inflammation and demyelination. In comparison, the MT measurements were less successful due to competing contributions of demyelination and pH‐sensitive changes in the MT effect. Magn Reson Med 51:473–479, 2004. © 2004 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Axons - ultrastructure</subject><subject>Coloring Agents</subject><subject>Demyelinating Diseases - pathology</subject><subject>Disease Models, Animal</subject><subject>Extracellular Fluid</subject><subject>Hydrogen-Ion Concentration</subject><subject>Image Processing, Computer-Assisted</subject><subject>inflammation</subject><subject>Lewis rat</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>magnetization transfer</subject><subject>Male</subject><subject>MRI</subject><subject>MTR</subject><subject>Myelin Sheath - pathology</subject><subject>Nerve Degeneration - pathology</subject><subject>rat sciatic nerve</subject><subject>Rats</subject><subject>Rats, Inbred Lew</subject><subject>Sciatic Nerve - drug effects</subject><subject>Sciatic Nerve - pathology</subject><subject>Sciatic Neuropathy - chemically induced</subject><subject>Sciatic Neuropathy - pathology</subject><subject>TNF-α</subject><subject>Tolonium Chloride</subject><subject>Tumor Necrosis Factor-alpha - adverse effects</subject><issn>0740-3194</issn><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNp10E9PwyAYBnBiNG5OD34B05OJh25AYZSjMTo1m8Zl_rkRWsCgtJ2lzbZvL9qpJ08c3t_7hPcB4BjBIYIQj4q6GGIIYboD-ohiHGPKyS7oQ0ZgnCBOeuDA-7cgOGdkH_QQhZCwlPXBYjaPlnW11HVjtY8qE-l1br1WUanbWrqosd63OjKVc9XKlq9hHrAtdNlI5zaRLVWbB25L42RRyMZW5SHYM9J5fbR9B-Dx6nJxcR1P7yc3F-fTOCd0nMaUQ54xpU2WEzhGkhmVEJWmHEqlVKZQniOcGqXGhCLEFEWpVAxiLjE2MOXJAJx2ueGCj1b7RhTW59o5Weqq9QKxhBFCcIBnHczryvtaG7EMJ8h6IxAUXxWKUKH4rjDYk21omxVa_cltZwGMOrCyTm_-TxKz-ewnMu42rG_0-ndD1u9iHL5IxfPdRDzNGZ2-3D4ImnwCOjqLpQ</recordid><startdate>200403</startdate><enddate>200403</enddate><creator>Stanisz, Greg J.</creator><creator>Webb, Stephanie</creator><creator>Munro, Catherine A.</creator><creator>Pun, Teresa</creator><creator>Midha, Rajiv</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>200403</creationdate><title>MR properties of excised neural tissue following experimentally induced inflammation</title><author>Stanisz, Greg J. ; Webb, Stephanie ; Munro, Catherine A. ; Pun, Teresa ; Midha, Rajiv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4568-5909b7defbc4061a7fd34d8890adddbd1cc128fdd645117d518ad7029a22f0893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Axons - ultrastructure</topic><topic>Coloring Agents</topic><topic>Demyelinating Diseases - pathology</topic><topic>Disease Models, Animal</topic><topic>Extracellular Fluid</topic><topic>Hydrogen-Ion Concentration</topic><topic>Image Processing, Computer-Assisted</topic><topic>inflammation</topic><topic>Lewis rat</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>magnetization transfer</topic><topic>Male</topic><topic>MRI</topic><topic>MTR</topic><topic>Myelin Sheath - pathology</topic><topic>Nerve Degeneration - pathology</topic><topic>rat sciatic nerve</topic><topic>Rats</topic><topic>Rats, Inbred Lew</topic><topic>Sciatic Nerve - drug effects</topic><topic>Sciatic Nerve - pathology</topic><topic>Sciatic Neuropathy - chemically induced</topic><topic>Sciatic Neuropathy - pathology</topic><topic>TNF-α</topic><topic>Tolonium Chloride</topic><topic>Tumor Necrosis Factor-alpha - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stanisz, Greg J.</creatorcontrib><creatorcontrib>Webb, Stephanie</creatorcontrib><creatorcontrib>Munro, Catherine A.</creatorcontrib><creatorcontrib>Pun, Teresa</creatorcontrib><creatorcontrib>Midha, Rajiv</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stanisz, Greg J.</au><au>Webb, Stephanie</au><au>Munro, Catherine A.</au><au>Pun, Teresa</au><au>Midha, Rajiv</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MR properties of excised neural tissue following experimentally induced inflammation</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn. 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The multicomponent T2 relaxation was shown to provide the best quantitative assessment of changes in neural tissue microstructure, and allowed us to distinguish between the processes of inflammation and demyelination. In comparison, the MT measurements were less successful due to competing contributions of demyelination and pH‐sensitive changes in the MT effect. Magn Reson Med 51:473–479, 2004. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15004787</pmid><doi>10.1002/mrm.20008</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Axons - ultrastructure Coloring Agents Demyelinating Diseases - pathology Disease Models, Animal Extracellular Fluid Hydrogen-Ion Concentration Image Processing, Computer-Assisted inflammation Lewis rat Magnetic Resonance Spectroscopy magnetization transfer Male MRI MTR Myelin Sheath - pathology Nerve Degeneration - pathology rat sciatic nerve Rats Rats, Inbred Lew Sciatic Nerve - drug effects Sciatic Nerve - pathology Sciatic Neuropathy - chemically induced Sciatic Neuropathy - pathology TNF-α Tolonium Chloride Tumor Necrosis Factor-alpha - adverse effects |
title | MR properties of excised neural tissue following experimentally induced inflammation |
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