Bioactive anti-inflammatory coating for chronic neural electrodes
Chronic electrodes are widely used for brain degenerative and psychiatric daises such as Parkinson's diseases, major depression, and obsessive‐compulsive disorder, and for neuronal prosthesis. Brain immune reaction to electrodes in the form of glial scar encapsulates the electrode and reduces t...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2012-07, Vol.100A (7), p.1854-1858 |
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creator | Taub, Aryeh H. Hogri, Roni Magal, Ari Mintz, Matti Shacham-Diamand, Yosi |
description | Chronic electrodes are widely used for brain degenerative and psychiatric daises such as Parkinson's diseases, major depression, and obsessive‐compulsive disorder, and for neuronal prosthesis. Brain immune reaction to electrodes in the form of glial scar encapsulates the electrode and reduces the efficacy of deep brain stimulation and neuronal prosthesis. State‐of‐the‐art strategies for improving brain–electrode interface use passive protein coating to “camouflage” the electrode from the immune system. In this study, we actively reduced the brain immune reaction to the chronic electrodes using immune suppressing protein, that is, interleukin (IL)‐1 receptor antagonist. IL‐1 receptor antagonist‐coated electrodes and noncoated electrodes were chronically implanted in rats. An additional group of rats was chronically implanted with IL‐1 receptor antagonist‐ and laminin‐coated electrodes (as passive protein). Examination of glial scaring 1ne and 4 weeks after implantation indicated a significant reduction in the amount of glial scar in the vicinity of the IL‐1 receptor antagonist‐coated electrode in comparison to both noncoated electrode and laminin‐coated electrodes. The results strongly suggest that active immune suppressing protein reduces the level of immune reaction to chronic electrodes already after 1 week after implantation and generates less immune reaction then passive protein coating. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012. |
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Brain immune reaction to electrodes in the form of glial scar encapsulates the electrode and reduces the efficacy of deep brain stimulation and neuronal prosthesis. State‐of‐the‐art strategies for improving brain–electrode interface use passive protein coating to “camouflage” the electrode from the immune system. In this study, we actively reduced the brain immune reaction to the chronic electrodes using immune suppressing protein, that is, interleukin (IL)‐1 receptor antagonist. IL‐1 receptor antagonist‐coated electrodes and noncoated electrodes were chronically implanted in rats. An additional group of rats was chronically implanted with IL‐1 receptor antagonist‐ and laminin‐coated electrodes (as passive protein). Examination of glial scaring 1ne and 4 weeks after implantation indicated a significant reduction in the amount of glial scar in the vicinity of the IL‐1 receptor antagonist‐coated electrode in comparison to both noncoated electrode and laminin‐coated electrodes. The results strongly suggest that active immune suppressing protein reduces the level of immune reaction to chronic electrodes already after 1 week after implantation and generates less immune reaction then passive protein coating. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.34152</identifier><identifier>PMID: 22488754</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Anti-Inflammatory Agents - administration & dosage ; Anti-Inflammatory Agents - pharmacology ; Applied sciences ; Biological and medical sciences ; brain computer interface ; chronic electrode ; Computer science; control theory; systems ; Computer systems and distributed systems. User interface ; deep brain stimulation ; Electrodes ; Exact sciences and technology ; Glial Fibrillary Acidic Protein - metabolism ; glial scar ; Immunohistochemistry ; Interleukin 1 Receptor Antagonist Protein - administration & dosage ; Interleukin 1 Receptor Antagonist Protein - pharmacology ; interleukin-1 receptor antagonist ; Medical sciences ; Neurons - cytology ; Rats ; Rats, Sprague-Dawley ; Software ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Technology. Biomaterials. Equipments</subject><ispartof>Journal of biomedical materials research. 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Part A</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Chronic electrodes are widely used for brain degenerative and psychiatric daises such as Parkinson's diseases, major depression, and obsessive‐compulsive disorder, and for neuronal prosthesis. Brain immune reaction to electrodes in the form of glial scar encapsulates the electrode and reduces the efficacy of deep brain stimulation and neuronal prosthesis. State‐of‐the‐art strategies for improving brain–electrode interface use passive protein coating to “camouflage” the electrode from the immune system. In this study, we actively reduced the brain immune reaction to the chronic electrodes using immune suppressing protein, that is, interleukin (IL)‐1 receptor antagonist. IL‐1 receptor antagonist‐coated electrodes and noncoated electrodes were chronically implanted in rats. An additional group of rats was chronically implanted with IL‐1 receptor antagonist‐ and laminin‐coated electrodes (as passive protein). Examination of glial scaring 1ne and 4 weeks after implantation indicated a significant reduction in the amount of glial scar in the vicinity of the IL‐1 receptor antagonist‐coated electrode in comparison to both noncoated electrode and laminin‐coated electrodes. The results strongly suggest that active immune suppressing protein reduces the level of immune reaction to chronic electrodes already after 1 week after implantation and generates less immune reaction then passive protein coating. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - administration & dosage</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>brain computer interface</subject><subject>chronic electrode</subject><subject>Computer science; control theory; systems</subject><subject>Computer systems and distributed systems. User interface</subject><subject>deep brain stimulation</subject><subject>Electrodes</subject><subject>Exact sciences and technology</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>glial scar</subject><subject>Immunohistochemistry</subject><subject>Interleukin 1 Receptor Antagonist Protein - administration & dosage</subject><subject>Interleukin 1 Receptor Antagonist Protein - pharmacology</subject><subject>interleukin-1 receptor antagonist</subject><subject>Medical sciences</subject><subject>Neurons - cytology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Software</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Technology. Biomaterials. Equipments</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90M9P2zAUB3BrGoKOcdod5TJpEkrxj9iOj4BoGWphh63bzXpxHHBJYmang_73uGtht53eO3zeD30R-kTwmGBMT5dVN4YxKwin79CIcE7zQgn-ftMXKmdUiQP0IcZlwgJzuo8OKC3KUvJihM7OnQczuD82g35wueubFroOBh_WmfEwuP4ua3zIzH3wvTNZb1cB2sy21gzB1zZ-RHsNtNEe7eoh-jG5_H5xlc9up18vzma5YUrRvClrxqqGlIwWFSkxGFYyKYqKgzAS14ITXCpWCcOgqok1kjKbvsW2UTWhnB2iL9u9j8H_Xtk46M5FY9sWeutXURNMhJAFZTLRky01wccYbKMfg-sgrBPSm8x0ykyD_ptZ0se7xauqs_WbfQ0pgc87ANFA2wTojYv_XAoVK6mSI1v35Fq7_t9NfX0-fz2eb2dcHOzz2wyEBy0kk1z_vJnqq2-_yGS-4HrBXgDwg5Jc</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Taub, Aryeh H.</creator><creator>Hogri, Roni</creator><creator>Magal, Ari</creator><creator>Mintz, Matti</creator><creator>Shacham-Diamand, Yosi</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Blackwell</general><scope>BSCLL</scope><scope>IQODW</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>7X8</scope></search><sort><creationdate>201207</creationdate><title>Bioactive anti-inflammatory coating for chronic neural electrodes</title><author>Taub, Aryeh H. ; Hogri, Roni ; Magal, Ari ; Mintz, Matti ; Shacham-Diamand, Yosi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3992-f8d33bf18324b180ac383764b5a6c70d6510893b6c3abd1ec723e0520ef9d1253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - administration & dosage</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Applied sciences</topic><topic>Biological and medical sciences</topic><topic>brain computer interface</topic><topic>chronic electrode</topic><topic>Computer science; control theory; systems</topic><topic>Computer systems and distributed systems. User interface</topic><topic>deep brain stimulation</topic><topic>Electrodes</topic><topic>Exact sciences and technology</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>glial scar</topic><topic>Immunohistochemistry</topic><topic>Interleukin 1 Receptor Antagonist Protein - administration & dosage</topic><topic>Interleukin 1 Receptor Antagonist Protein - pharmacology</topic><topic>interleukin-1 receptor antagonist</topic><topic>Medical sciences</topic><topic>Neurons - cytology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Software</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Technology. Biomaterials. Equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Taub, Aryeh H.</creatorcontrib><creatorcontrib>Hogri, Roni</creatorcontrib><creatorcontrib>Magal, Ari</creatorcontrib><creatorcontrib>Mintz, Matti</creatorcontrib><creatorcontrib>Shacham-Diamand, Yosi</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomedical materials research. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Taub, Aryeh H.</au><au>Hogri, Roni</au><au>Magal, Ari</au><au>Mintz, Matti</au><au>Shacham-Diamand, Yosi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bioactive anti-inflammatory coating for chronic neural electrodes</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2012-07</date><risdate>2012</risdate><volume>100A</volume><issue>7</issue><spage>1854</spage><epage>1858</epage><pages>1854-1858</pages><issn>1549-3296</issn><eissn>1552-4965</eissn><abstract>Chronic electrodes are widely used for brain degenerative and psychiatric daises such as Parkinson's diseases, major depression, and obsessive‐compulsive disorder, and for neuronal prosthesis. Brain immune reaction to electrodes in the form of glial scar encapsulates the electrode and reduces the efficacy of deep brain stimulation and neuronal prosthesis. State‐of‐the‐art strategies for improving brain–electrode interface use passive protein coating to “camouflage” the electrode from the immune system. In this study, we actively reduced the brain immune reaction to the chronic electrodes using immune suppressing protein, that is, interleukin (IL)‐1 receptor antagonist. IL‐1 receptor antagonist‐coated electrodes and noncoated electrodes were chronically implanted in rats. An additional group of rats was chronically implanted with IL‐1 receptor antagonist‐ and laminin‐coated electrodes (as passive protein). Examination of glial scaring 1ne and 4 weeks after implantation indicated a significant reduction in the amount of glial scar in the vicinity of the IL‐1 receptor antagonist‐coated electrode in comparison to both noncoated electrode and laminin‐coated electrodes. The results strongly suggest that active immune suppressing protein reduces the level of immune reaction to chronic electrodes already after 1 week after implantation and generates less immune reaction then passive protein coating. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22488754</pmid><doi>10.1002/jbm.a.34152</doi><tpages>5</tpages></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - administration & dosage Anti-Inflammatory Agents - pharmacology Applied sciences Biological and medical sciences brain computer interface chronic electrode Computer science control theory systems Computer systems and distributed systems. User interface deep brain stimulation Electrodes Exact sciences and technology Glial Fibrillary Acidic Protein - metabolism glial scar Immunohistochemistry Interleukin 1 Receptor Antagonist Protein - administration & dosage Interleukin 1 Receptor Antagonist Protein - pharmacology interleukin-1 receptor antagonist Medical sciences Neurons - cytology Rats Rats, Sprague-Dawley Software Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Technology. Biomaterials. Equipments |
title | Bioactive anti-inflammatory coating for chronic neural electrodes |
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