Curcumin protects retinal pigment epithelial cells against oxidative stress via induction of heme oxygenase-1 expression and reduction of reactive oxygen

To determine whether curcumin induces expression of the defensive enzyme heme oxygenase-1 (HO-1) and protects cells against oxidative stress in cultured human retinal pigment epithelial cells. Effective concentrations and toxicities of curcumin were determined after 3 h of curcumin treatment with th...

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Veröffentlicht in:Molecular vision 2012-04, Vol.18, p.901-908
Hauptverfasser: Woo, Je Moon, Shin, Da-Yong, Lee, Sung Ju, Joe, Yeonsoo, Zheng, Min, Yim, Jin Ho, Callaway, Zak, Chung, Hun Taeg
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container_issue
container_start_page 901
container_title Molecular vision
container_volume 18
creator Woo, Je Moon
Shin, Da-Yong
Lee, Sung Ju
Joe, Yeonsoo
Zheng, Min
Yim, Jin Ho
Callaway, Zak
Chung, Hun Taeg
description To determine whether curcumin induces expression of the defensive enzyme heme oxygenase-1 (HO-1) and protects cells against oxidative stress in cultured human retinal pigment epithelial cells. Effective concentrations and toxicities of curcumin were determined after 3 h of curcumin treatment with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Confluent human retinal pigment epithelium cell lines (ARPE-19) were preincubated with curcumin and oxidatively challenged with H(2)O(2). HO-1 expression was determined with western blot analysis. To confirm the protective role of HO-1 in oxidative stress, small interfering RNA (siRNA) against HO-1 or inhibitor of HO-1 was treated with curcumin in retinal pigment epithelium cells. Intracellular levels of reactive oxygen species (ROS) were measured with flow cytometry and confocal microscopy. Apoptosis was evaluated with Annexin V-fluoroscein isothiocyanate staining. Curcumin had little cytotoxicity at concentrations less than 30 μM, and HO-1 expression was the highest at the 15 μM concentration. At this concentration, curcumin also increased the cytoprotective effect against the oxidative stress of H(2)O(2) through the reduction of ROS levels in human retinal pigment epithelial cells. Curcumin's effect on the reduction of ROS was mediated by the increase in HO-1 expression. Curcumin upregulated the oxidative stress defense enzyme HO-1 and may protect human retinal pigment epithelial cells against oxidative stress by reducing ROS levels.
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Effective concentrations and toxicities of curcumin were determined after 3 h of curcumin treatment with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Confluent human retinal pigment epithelium cell lines (ARPE-19) were preincubated with curcumin and oxidatively challenged with H(2)O(2). HO-1 expression was determined with western blot analysis. To confirm the protective role of HO-1 in oxidative stress, small interfering RNA (siRNA) against HO-1 or inhibitor of HO-1 was treated with curcumin in retinal pigment epithelium cells. Intracellular levels of reactive oxygen species (ROS) were measured with flow cytometry and confocal microscopy. Apoptosis was evaluated with Annexin V-fluoroscein isothiocyanate staining. Curcumin had little cytotoxicity at concentrations less than 30 μM, and HO-1 expression was the highest at the 15 μM concentration. At this concentration, curcumin also increased the cytoprotective effect against the oxidative stress of H(2)O(2) through the reduction of ROS levels in human retinal pigment epithelial cells. Curcumin's effect on the reduction of ROS was mediated by the increase in HO-1 expression. Curcumin upregulated the oxidative stress defense enzyme HO-1 and may protect human retinal pigment epithelial cells against oxidative stress by reducing ROS levels.</description><identifier>ISSN: 1090-0535</identifier><identifier>EISSN: 1090-0535</identifier><identifier>PMID: 22539869</identifier><language>eng</language><publisher>United States: Molecular Vision</publisher><subject>Annexins ; Anti-Inflammatory Agents, Non-Steroidal - pharmacology ; Apoptosis ; Apoptosis - drug effects ; bromides ; Cell Line ; Cell Survival - drug effects ; Confocal microscopy ; Curcumin ; Curcumin - pharmacology ; Cytoprotection ; Cytotoxicity ; Enzymes ; Epithelial Cells - cytology ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Flow cytometry ; Gene Expression - drug effects ; Heme oxygenase (decyclizing) ; Heme Oxygenase-1 - antagonists &amp; inhibitors ; Heme Oxygenase-1 - genetics ; Heme Oxygenase-1 - metabolism ; Humans ; Hydrogen peroxide ; Hydrogen Peroxide - pharmacology ; Imidazoles - pharmacology ; Intracellular levels ; isothiocyanate ; Oxidative stress ; Oxidative Stress - drug effects ; Pyridines - pharmacology ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; Retina ; retinal pigment epithelium ; Retinal Pigment Epithelium - cytology ; Retinal Pigment Epithelium - drug effects ; Retinal Pigment Epithelium - metabolism ; RNA, Small Interfering - genetics ; RNA, Small Interfering - metabolism ; siRNA ; Toxicity ; Up-Regulation ; Western blotting</subject><ispartof>Molecular vision, 2012-04, Vol.18, p.901-908</ispartof><rights>Copyright © 2012 Molecular Vision. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335783/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335783/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22539869$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Woo, Je Moon</creatorcontrib><creatorcontrib>Shin, Da-Yong</creatorcontrib><creatorcontrib>Lee, Sung Ju</creatorcontrib><creatorcontrib>Joe, Yeonsoo</creatorcontrib><creatorcontrib>Zheng, Min</creatorcontrib><creatorcontrib>Yim, Jin Ho</creatorcontrib><creatorcontrib>Callaway, Zak</creatorcontrib><creatorcontrib>Chung, Hun Taeg</creatorcontrib><title>Curcumin protects retinal pigment epithelial cells against oxidative stress via induction of heme oxygenase-1 expression and reduction of reactive oxygen</title><title>Molecular vision</title><addtitle>Mol Vis</addtitle><description>To determine whether curcumin induces expression of the defensive enzyme heme oxygenase-1 (HO-1) and protects cells against oxidative stress in cultured human retinal pigment epithelial cells. Effective concentrations and toxicities of curcumin were determined after 3 h of curcumin treatment with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Confluent human retinal pigment epithelium cell lines (ARPE-19) were preincubated with curcumin and oxidatively challenged with H(2)O(2). HO-1 expression was determined with western blot analysis. To confirm the protective role of HO-1 in oxidative stress, small interfering RNA (siRNA) against HO-1 or inhibitor of HO-1 was treated with curcumin in retinal pigment epithelium cells. Intracellular levels of reactive oxygen species (ROS) were measured with flow cytometry and confocal microscopy. Apoptosis was evaluated with Annexin V-fluoroscein isothiocyanate staining. Curcumin had little cytotoxicity at concentrations less than 30 μM, and HO-1 expression was the highest at the 15 μM concentration. At this concentration, curcumin also increased the cytoprotective effect against the oxidative stress of H(2)O(2) through the reduction of ROS levels in human retinal pigment epithelial cells. Curcumin's effect on the reduction of ROS was mediated by the increase in HO-1 expression. Curcumin upregulated the oxidative stress defense enzyme HO-1 and may protect human retinal pigment epithelial cells against oxidative stress by reducing ROS levels.</description><subject>Annexins</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>bromides</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Confocal microscopy</subject><subject>Curcumin</subject><subject>Curcumin - pharmacology</subject><subject>Cytoprotection</subject><subject>Cytotoxicity</subject><subject>Enzymes</subject><subject>Epithelial Cells - cytology</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Flow cytometry</subject><subject>Gene Expression - drug effects</subject><subject>Heme oxygenase (decyclizing)</subject><subject>Heme Oxygenase-1 - antagonists &amp; inhibitors</subject><subject>Heme Oxygenase-1 - genetics</subject><subject>Heme Oxygenase-1 - metabolism</subject><subject>Humans</subject><subject>Hydrogen peroxide</subject><subject>Hydrogen Peroxide - pharmacology</subject><subject>Imidazoles - pharmacology</subject><subject>Intracellular levels</subject><subject>isothiocyanate</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Pyridines - pharmacology</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Retina</subject><subject>retinal pigment epithelium</subject><subject>Retinal Pigment Epithelium - cytology</subject><subject>Retinal Pigment Epithelium - drug effects</subject><subject>Retinal Pigment Epithelium - metabolism</subject><subject>RNA, Small Interfering - genetics</subject><subject>RNA, Small Interfering - metabolism</subject><subject>siRNA</subject><subject>Toxicity</subject><subject>Up-Regulation</subject><subject>Western blotting</subject><issn>1090-0535</issn><issn>1090-0535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkc9OwzAMxisEYmPwCihHLpXSpM2SCxKa-CdN4gLnKk3cLqhNSpJO26PwtrQw0DjZsj__Ptk-SeYZFjjFBS1Oj_JZchHCO8YkK_LleTIjpKCCMzFPPleDV0NnLOq9i6BiQB6isbJFvWk6sBFBb-IGWjOWFLRtQLKRxoaI3M5oGc0WUIgeQkBbI5GxelDROItcjTbQwSjbN2BlgDRDsOsn5dSWVo9WR2IPUn3TfgYuk7NatgGuDnGRvD3cv66e0vXL4_Pqbp32RIiY1gQTXPGaL3OpKypq0DpjRDDGag4852JZ1ZxxRUDoKgdeSM6UxnmuGR0FdJHc_nD7oepAq3FlL9uy96aTfl86acr_HWs2ZeO2JaW0WHI6Am4OAO8-Bgix7EyYLiUtuCGUGWYiE4KLyev62OvP5Pcf9At2EY4I</recordid><startdate>20120411</startdate><enddate>20120411</enddate><creator>Woo, Je Moon</creator><creator>Shin, Da-Yong</creator><creator>Lee, Sung Ju</creator><creator>Joe, Yeonsoo</creator><creator>Zheng, Min</creator><creator>Yim, Jin Ho</creator><creator>Callaway, Zak</creator><creator>Chung, Hun Taeg</creator><general>Molecular Vision</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20120411</creationdate><title>Curcumin protects retinal pigment epithelial cells against oxidative stress via induction of heme oxygenase-1 expression and reduction of reactive oxygen</title><author>Woo, Je Moon ; Shin, Da-Yong ; Lee, Sung Ju ; Joe, Yeonsoo ; Zheng, Min ; Yim, Jin Ho ; Callaway, Zak ; Chung, Hun Taeg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p299t-f2020b8f874adb39fedd1629666f8e84897bf868c2e9db4e85a86cd044d638e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Annexins</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>bromides</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Confocal microscopy</topic><topic>Curcumin</topic><topic>Curcumin - pharmacology</topic><topic>Cytoprotection</topic><topic>Cytotoxicity</topic><topic>Enzymes</topic><topic>Epithelial Cells - cytology</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Flow cytometry</topic><topic>Gene Expression - drug effects</topic><topic>Heme oxygenase (decyclizing)</topic><topic>Heme Oxygenase-1 - antagonists &amp; inhibitors</topic><topic>Heme Oxygenase-1 - genetics</topic><topic>Heme Oxygenase-1 - metabolism</topic><topic>Humans</topic><topic>Hydrogen peroxide</topic><topic>Hydrogen Peroxide - pharmacology</topic><topic>Imidazoles - pharmacology</topic><topic>Intracellular levels</topic><topic>isothiocyanate</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Pyridines - pharmacology</topic><topic>Reactive oxygen species</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Retina</topic><topic>retinal pigment epithelium</topic><topic>Retinal Pigment Epithelium - cytology</topic><topic>Retinal Pigment Epithelium - drug effects</topic><topic>Retinal Pigment Epithelium - metabolism</topic><topic>RNA, Small Interfering - genetics</topic><topic>RNA, Small Interfering - metabolism</topic><topic>siRNA</topic><topic>Toxicity</topic><topic>Up-Regulation</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Woo, Je Moon</creatorcontrib><creatorcontrib>Shin, Da-Yong</creatorcontrib><creatorcontrib>Lee, Sung Ju</creatorcontrib><creatorcontrib>Joe, Yeonsoo</creatorcontrib><creatorcontrib>Zheng, Min</creatorcontrib><creatorcontrib>Yim, Jin Ho</creatorcontrib><creatorcontrib>Callaway, Zak</creatorcontrib><creatorcontrib>Chung, Hun Taeg</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular vision</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Woo, Je Moon</au><au>Shin, Da-Yong</au><au>Lee, Sung Ju</au><au>Joe, Yeonsoo</au><au>Zheng, Min</au><au>Yim, Jin Ho</au><au>Callaway, Zak</au><au>Chung, Hun Taeg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Curcumin protects retinal pigment epithelial cells against oxidative stress via induction of heme oxygenase-1 expression and reduction of reactive oxygen</atitle><jtitle>Molecular vision</jtitle><addtitle>Mol Vis</addtitle><date>2012-04-11</date><risdate>2012</risdate><volume>18</volume><spage>901</spage><epage>908</epage><pages>901-908</pages><issn>1090-0535</issn><eissn>1090-0535</eissn><abstract>To determine whether curcumin induces expression of the defensive enzyme heme oxygenase-1 (HO-1) and protects cells against oxidative stress in cultured human retinal pigment epithelial cells. Effective concentrations and toxicities of curcumin were determined after 3 h of curcumin treatment with the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Confluent human retinal pigment epithelium cell lines (ARPE-19) were preincubated with curcumin and oxidatively challenged with H(2)O(2). HO-1 expression was determined with western blot analysis. To confirm the protective role of HO-1 in oxidative stress, small interfering RNA (siRNA) against HO-1 or inhibitor of HO-1 was treated with curcumin in retinal pigment epithelium cells. Intracellular levels of reactive oxygen species (ROS) were measured with flow cytometry and confocal microscopy. Apoptosis was evaluated with Annexin V-fluoroscein isothiocyanate staining. Curcumin had little cytotoxicity at concentrations less than 30 μM, and HO-1 expression was the highest at the 15 μM concentration. At this concentration, curcumin also increased the cytoprotective effect against the oxidative stress of H(2)O(2) through the reduction of ROS levels in human retinal pigment epithelial cells. Curcumin's effect on the reduction of ROS was mediated by the increase in HO-1 expression. Curcumin upregulated the oxidative stress defense enzyme HO-1 and may protect human retinal pigment epithelial cells against oxidative stress by reducing ROS levels.</abstract><cop>United States</cop><pub>Molecular Vision</pub><pmid>22539869</pmid><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Annexins
Anti-Inflammatory Agents, Non-Steroidal - pharmacology
Apoptosis
Apoptosis - drug effects
bromides
Cell Line
Cell Survival - drug effects
Confocal microscopy
Curcumin
Curcumin - pharmacology
Cytoprotection
Cytotoxicity
Enzymes
Epithelial Cells - cytology
Epithelial Cells - drug effects
Epithelial Cells - metabolism
Flow cytometry
Gene Expression - drug effects
Heme oxygenase (decyclizing)
Heme Oxygenase-1 - antagonists & inhibitors
Heme Oxygenase-1 - genetics
Heme Oxygenase-1 - metabolism
Humans
Hydrogen peroxide
Hydrogen Peroxide - pharmacology
Imidazoles - pharmacology
Intracellular levels
isothiocyanate
Oxidative stress
Oxidative Stress - drug effects
Pyridines - pharmacology
Reactive oxygen species
Reactive Oxygen Species - metabolism
Retina
retinal pigment epithelium
Retinal Pigment Epithelium - cytology
Retinal Pigment Epithelium - drug effects
Retinal Pigment Epithelium - metabolism
RNA, Small Interfering - genetics
RNA, Small Interfering - metabolism
siRNA
Toxicity
Up-Regulation
Western blotting
title Curcumin protects retinal pigment epithelial cells against oxidative stress via induction of heme oxygenase-1 expression and reduction of reactive oxygen
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