(−)-Epigallocatechin-3-gallate protects cultured spiral ganglion cells from H2O2-induced oxidizing damage

Objective Oxidants play an important role in many diseases, including hearing loss. We hypothesized that (−)-epigallocatechin-3-gallate (EGCG) would protect spiral ganglion cells (SGCs) from H2O2-induced oxidizing damage. Material and Methods SGCs of postnatal day 1-3 mice were cultured in vitro. H2...

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Veröffentlicht in:Acta oto-laryngologica 2004-05, Vol.124 (4), p.464-470
Hauptverfasser: Xie, Dinghua, Liu, Guohui, Zhu, Ganghua, Wu, Weijing, Ge, Shenglei
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container_title Acta oto-laryngologica
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creator Xie, Dinghua
Liu, Guohui
Zhu, Ganghua
Wu, Weijing
Ge, Shenglei
description Objective Oxidants play an important role in many diseases, including hearing loss. We hypothesized that (−)-epigallocatechin-3-gallate (EGCG) would protect spiral ganglion cells (SGCs) from H2O2-induced oxidizing damage. Material and Methods SGCs of postnatal day 1-3 mice were cultured in vitro. H2O2 and EGCG were used at various concentrations. The apoptotic rate of SGCs was evaluated using Hoechst 33 258 staining, and cell viability was determined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide method. Semi-quantitative reverse transcriptase polymerase chain reaction was used to observe manganese superoxide dismutase (MnSOD) gene expression of SGCs treated with H2O2 and EGCG. Results The viability of cultured SGCs was significantly decreased, and the apoptotic rate of SGCs significantly increased, at H2O2 concentrations ≥50 μM compared with the control (p
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We hypothesized that (−)-epigallocatechin-3-gallate (EGCG) would protect spiral ganglion cells (SGCs) from H2O2-induced oxidizing damage. Material and Methods SGCs of postnatal day 1-3 mice were cultured in vitro. H2O2 and EGCG were used at various concentrations. The apoptotic rate of SGCs was evaluated using Hoechst 33 258 staining, and cell viability was determined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide method. Semi-quantitative reverse transcriptase polymerase chain reaction was used to observe manganese superoxide dismutase (MnSOD) gene expression of SGCs treated with H2O2 and EGCG. Results The viability of cultured SGCs was significantly decreased, and the apoptotic rate of SGCs significantly increased, at H2O2 concentrations ≥50 μM compared with the control (p&lt;0.05). MnSOD gene expression was upregulated with increasing H2O2 concentration in cultured SGCs, while this upregulation was suppressed by EGCG. Conclusion It is suggested that EGCG, as an antioxidant, significantly protects auditory neurons against H2O2-induced oxidative damage.</description><identifier>ISSN: 0001-6489</identifier><identifier>EISSN: 1651-2251</identifier><identifier>DOI: 10.1080/00016480410018278</identifier><identifier>PMID: 15224876</identifier><identifier>CODEN: AOLAAJ</identifier><language>eng</language><publisher>Stockholm: Informa UK Ltd</publisher><subject>(−)-epigallocatechin-3-gallate ; Animals ; antioxidant enzyme ; Antioxidants - pharmacology ; apoptosis ; Apoptosis - drug effects ; Biological and medical sciences ; Catechin - analogs &amp; derivatives ; Catechin - pharmacology ; Cell Survival - drug effects ; cell viability ; Cells, Cultured ; Gene Expression - drug effects ; H2O2 ; Hydrogen Peroxide - toxicity ; manganese superoxide dismutase gene ; Medical sciences ; Mice ; Otorhinolaryngology. Stomatology ; Oxidation-Reduction ; oxygen free radical ; Reverse Transcriptase Polymerase Chain Reaction ; semi-quantitative reverse transcriptase polymerase chain reaction ; Spiral Ganglion - cytology ; Spiral Ganglion - drug effects ; Spiral Ganglion - metabolism ; spiral ganglion cells ; Superoxide Dismutase - genetics ; Superoxide Dismutase - metabolism ; Up-Regulation</subject><ispartof>Acta oto-laryngologica, 2004-05, Vol.124 (4), p.464-470</ispartof><rights>2004 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2004</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00016480410018278$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00016480410018278$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,23909,23910,25118,27901,27902,59620,59726,60409,60515,61194,61229,61375,61410</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15773712$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15224876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xie, Dinghua</creatorcontrib><creatorcontrib>Liu, Guohui</creatorcontrib><creatorcontrib>Zhu, Ganghua</creatorcontrib><creatorcontrib>Wu, Weijing</creatorcontrib><creatorcontrib>Ge, Shenglei</creatorcontrib><title>(−)-Epigallocatechin-3-gallate protects cultured spiral ganglion cells from H2O2-induced oxidizing damage</title><title>Acta oto-laryngologica</title><addtitle>Acta Otolaryngol</addtitle><description>Objective Oxidants play an important role in many diseases, including hearing loss. We hypothesized that (−)-epigallocatechin-3-gallate (EGCG) would protect spiral ganglion cells (SGCs) from H2O2-induced oxidizing damage. Material and Methods SGCs of postnatal day 1-3 mice were cultured in vitro. H2O2 and EGCG were used at various concentrations. The apoptotic rate of SGCs was evaluated using Hoechst 33 258 staining, and cell viability was determined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide method. Semi-quantitative reverse transcriptase polymerase chain reaction was used to observe manganese superoxide dismutase (MnSOD) gene expression of SGCs treated with H2O2 and EGCG. Results The viability of cultured SGCs was significantly decreased, and the apoptotic rate of SGCs significantly increased, at H2O2 concentrations ≥50 μM compared with the control (p&lt;0.05). MnSOD gene expression was upregulated with increasing H2O2 concentration in cultured SGCs, while this upregulation was suppressed by EGCG. Conclusion It is suggested that EGCG, as an antioxidant, significantly protects auditory neurons against H2O2-induced oxidative damage.</description><subject>(−)-epigallocatechin-3-gallate</subject><subject>Animals</subject><subject>antioxidant enzyme</subject><subject>Antioxidants - pharmacology</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Biological and medical sciences</subject><subject>Catechin - analogs &amp; derivatives</subject><subject>Catechin - pharmacology</subject><subject>Cell Survival - drug effects</subject><subject>cell viability</subject><subject>Cells, Cultured</subject><subject>Gene Expression - drug effects</subject><subject>H2O2</subject><subject>Hydrogen Peroxide - toxicity</subject><subject>manganese superoxide dismutase gene</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Otorhinolaryngology. Stomatology</subject><subject>Oxidation-Reduction</subject><subject>oxygen free radical</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>semi-quantitative reverse transcriptase polymerase chain reaction</subject><subject>Spiral Ganglion - cytology</subject><subject>Spiral Ganglion - drug effects</subject><subject>Spiral Ganglion - metabolism</subject><subject>spiral ganglion cells</subject><subject>Superoxide Dismutase - genetics</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Up-Regulation</subject><issn>0001-6489</issn><issn>1651-2251</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1TAQhS0EopfCA7BB2YDowsV_SRzBBlWlRarUDawtx57kujj2xU4E5QlY9xH7JDjqrQRC1Sw8x_7OaDyD0EtKjimR5B0hhDZCEkFLIlkrH6ENbWqKGavpY7RZ33EBugP0LOerVXayfooOaM2YkG2zQd_e3v6-OcKnOzdq76PRM5itC5jjVRdV7VIsd3OuzOLnJYGt8s4l7atRh9G7GCoD3udqSHGqztklwy7YxRQu_nTW_XJhrKye9AjP0ZNB-wwv9uch-vrp9MvJOb64PPt88vECO8G7GQ-8RPkSlYLVrbBGCqJ7ADFw6E3HmGSDaXrBmewYEEOAgLGdsX3X8B4IP0Rv7uqW1r8vkGc1ubw2qQPEJStGuoY1jBbw1R5c-gms2iU36XSt7sdTgNd7QGej_ZB0MC7_xbUtbykr3Ic7zoUhpkn_iMlbNetrH9O9iVOi1q2p_7ZW7O__sW9B-3lrdAJ1FZcUyrDUw-4_eiybNQ</recordid><startdate>20040501</startdate><enddate>20040501</enddate><creator>Xie, Dinghua</creator><creator>Liu, Guohui</creator><creator>Zhu, Ganghua</creator><creator>Wu, Weijing</creator><creator>Ge, Shenglei</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><general>Taylor and Francis</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope></search><sort><creationdate>20040501</creationdate><title>(−)-Epigallocatechin-3-gallate protects cultured spiral ganglion cells from H2O2-induced oxidizing damage</title><author>Xie, Dinghua ; Liu, Guohui ; Zhu, Ganghua ; Wu, Weijing ; Ge, Shenglei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i439t-f3f3f4101842574dc840abee4f3ebc92282fc6b432892e0c0e0ecd9cdb963be03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>(−)-epigallocatechin-3-gallate</topic><topic>Animals</topic><topic>antioxidant enzyme</topic><topic>Antioxidants - pharmacology</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biological and medical sciences</topic><topic>Catechin - analogs &amp; derivatives</topic><topic>Catechin - pharmacology</topic><topic>Cell Survival - drug effects</topic><topic>cell viability</topic><topic>Cells, Cultured</topic><topic>Gene Expression - drug effects</topic><topic>H2O2</topic><topic>Hydrogen Peroxide - toxicity</topic><topic>manganese superoxide dismutase gene</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Otorhinolaryngology. Stomatology</topic><topic>Oxidation-Reduction</topic><topic>oxygen free radical</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>semi-quantitative reverse transcriptase polymerase chain reaction</topic><topic>Spiral Ganglion - cytology</topic><topic>Spiral Ganglion - drug effects</topic><topic>Spiral Ganglion - metabolism</topic><topic>spiral ganglion cells</topic><topic>Superoxide Dismutase - genetics</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xie, Dinghua</creatorcontrib><creatorcontrib>Liu, Guohui</creatorcontrib><creatorcontrib>Zhu, Ganghua</creatorcontrib><creatorcontrib>Wu, Weijing</creatorcontrib><creatorcontrib>Ge, Shenglei</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><jtitle>Acta oto-laryngologica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xie, Dinghua</au><au>Liu, Guohui</au><au>Zhu, Ganghua</au><au>Wu, Weijing</au><au>Ge, Shenglei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>(−)-Epigallocatechin-3-gallate protects cultured spiral ganglion cells from H2O2-induced oxidizing damage</atitle><jtitle>Acta oto-laryngologica</jtitle><addtitle>Acta Otolaryngol</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>124</volume><issue>4</issue><spage>464</spage><epage>470</epage><pages>464-470</pages><issn>0001-6489</issn><eissn>1651-2251</eissn><coden>AOLAAJ</coden><abstract>Objective Oxidants play an important role in many diseases, including hearing loss. We hypothesized that (−)-epigallocatechin-3-gallate (EGCG) would protect spiral ganglion cells (SGCs) from H2O2-induced oxidizing damage. Material and Methods SGCs of postnatal day 1-3 mice were cultured in vitro. H2O2 and EGCG were used at various concentrations. The apoptotic rate of SGCs was evaluated using Hoechst 33 258 staining, and cell viability was determined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide method. Semi-quantitative reverse transcriptase polymerase chain reaction was used to observe manganese superoxide dismutase (MnSOD) gene expression of SGCs treated with H2O2 and EGCG. Results The viability of cultured SGCs was significantly decreased, and the apoptotic rate of SGCs significantly increased, at H2O2 concentrations ≥50 μM compared with the control (p&lt;0.05). MnSOD gene expression was upregulated with increasing H2O2 concentration in cultured SGCs, while this upregulation was suppressed by EGCG. Conclusion It is suggested that EGCG, as an antioxidant, significantly protects auditory neurons against H2O2-induced oxidative damage.</abstract><cop>Stockholm</cop><pub>Informa UK Ltd</pub><pmid>15224876</pmid><doi>10.1080/00016480410018278</doi><tpages>7</tpages></addata></record>
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subjects (−)-epigallocatechin-3-gallate
Animals
antioxidant enzyme
Antioxidants - pharmacology
apoptosis
Apoptosis - drug effects
Biological and medical sciences
Catechin - analogs & derivatives
Catechin - pharmacology
Cell Survival - drug effects
cell viability
Cells, Cultured
Gene Expression - drug effects
H2O2
Hydrogen Peroxide - toxicity
manganese superoxide dismutase gene
Medical sciences
Mice
Otorhinolaryngology. Stomatology
Oxidation-Reduction
oxygen free radical
Reverse Transcriptase Polymerase Chain Reaction
semi-quantitative reverse transcriptase polymerase chain reaction
Spiral Ganglion - cytology
Spiral Ganglion - drug effects
Spiral Ganglion - metabolism
spiral ganglion cells
Superoxide Dismutase - genetics
Superoxide Dismutase - metabolism
Up-Regulation
title (−)-Epigallocatechin-3-gallate protects cultured spiral ganglion cells from H2O2-induced oxidizing damage
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