Modulation of adriamycin ® accumulation and efflux by flavonoids in HCT-15 colon cells : Activation of P-glycoprotein as a putative mechanism
Since P-glycoprotein (P-gp) in normal tissues may serve as a cellular defense mechanism against naturally occurring xenobiotics, we considered whether physiologically active components of commonly ingested plant foods could influence P-gp function. To examine this possibility, a series of flavonoids...
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Veröffentlicht in: | Biochemical pharmacology 1994-10, Vol.48 (7), p.1437-1445 |
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description | Since P-glycoprotein (P-gp) in normal tissues may serve as a cellular defense mechanism against naturally occurring xenobiotics, we considered whether physiologically active components of commonly ingested plant foods could influence P-gp function. To examine this possibility, a series of flavonoids commonly found in plant foods was tested for their ability to modulate [
14C]Adriamycin
® ([
14C]ADR) accumulation and efflux in P-gp-expressing HCT-15 colon cells. Many flavonoids, in the micromolar range, inhibited the accumulation of [
14C]ADR. Detailed experiments utilizing flavonoids with the greatest activity in reducing [
14C]ADR accumulation, i.e. galangin, kaempferol, and quercetin, revealed that the efflux of [
14C]ADR is increased markedly in the presence of these compounds. Flavonoid-induced stimulation of efflux was rapid and was blocked by the multidrug-resistant (MDR) reversal agents verapamil, vinblastine, and quinidine. The magnitude of flavonoid-stimulated efflux in sodium butyrate-treated cells with a 4-fold induction of P-gp protein was similar to that in uninduced cells. [
3H]Azidopine photoaffinity labeling of P-gp in crude membrane preparations revealed mild to no competition for binding by flavonoids possessing either activity or inactivity in reducing ADR accumulation. Although flavonoid hydrophobicity was found to be unrelated to flavonoid activity in altering [
14C]ADR accumulation, certain structural features were associated with enhancement or diminution of activity. Finally, the significance of flavonoid-related reduction of [
14C]ADR accumulation was underscored in cell growth studies, showing partial protection by quercetin against ADR-induced growth inhibition. It is concluded that certain naturally occuring plant flavonoids may acutely upregulate the apparent activity of P-gp. |
doi_str_mv | 10.1016/0006-2952(94)90568-1 |
format | Article |
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14C]Adriamycin
® ([
14C]ADR) accumulation and efflux in P-gp-expressing HCT-15 colon cells. Many flavonoids, in the micromolar range, inhibited the accumulation of [
14C]ADR. Detailed experiments utilizing flavonoids with the greatest activity in reducing [
14C]ADR accumulation, i.e. galangin, kaempferol, and quercetin, revealed that the efflux of [
14C]ADR is increased markedly in the presence of these compounds. Flavonoid-induced stimulation of efflux was rapid and was blocked by the multidrug-resistant (MDR) reversal agents verapamil, vinblastine, and quinidine. The magnitude of flavonoid-stimulated efflux in sodium butyrate-treated cells with a 4-fold induction of P-gp protein was similar to that in uninduced cells. [
3H]Azidopine photoaffinity labeling of P-gp in crude membrane preparations revealed mild to no competition for binding by flavonoids possessing either activity or inactivity in reducing ADR accumulation. Although flavonoid hydrophobicity was found to be unrelated to flavonoid activity in altering [
14C]ADR accumulation, certain structural features were associated with enhancement or diminution of activity. Finally, the significance of flavonoid-related reduction of [
14C]ADR accumulation was underscored in cell growth studies, showing partial protection by quercetin against ADR-induced growth inhibition. It is concluded that certain naturally occuring plant flavonoids may acutely upregulate the apparent activity of P-gp.</description><identifier>ISSN: 0006-2952</identifier><identifier>EISSN: 1873-2968</identifier><identifier>DOI: 10.1016/0006-2952(94)90568-1</identifier><identifier>PMID: 7945444</identifier><identifier>CODEN: BCPCA6</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adriamycin ; ATP Binding Cassette Transporter, Subfamily B, Member 1 - metabolism ; Biological and medical sciences ; Butyrates - pharmacology ; Butyric Acid ; Carcinogenesis, carcinogens and anticarcinogens ; Cell Division - drug effects ; Cell Line ; Cell Survival - drug effects ; Diet ; Dose-Response Relationship, Drug ; Doxorubicin - metabolism ; Doxorubicin - toxicity ; Drug Interactions ; flavonoids ; Flavonoids - pharmacology ; Foods and miscellaneous ; HCT-15 cells ; Humans ; Kaempferols ; Medical sciences ; P-glycoprotein ; quercetin ; Quercetin - analogs & derivatives ; Quercetin - pharmacology ; Structure-Activity Relationship ; Tumors ; Verapamil - pharmacology ; Vinblastine - pharmacology</subject><ispartof>Biochemical pharmacology, 1994-10, Vol.48 (7), p.1437-1445</ispartof><rights>1994</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0006-2952(94)90568-1$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3310855$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7945444$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Critchfield, James W.</creatorcontrib><creatorcontrib>Welsh, Clement J.</creatorcontrib><creatorcontrib>Phang, James M.</creatorcontrib><creatorcontrib>Chao Yeh, Grace</creatorcontrib><title>Modulation of adriamycin ® accumulation and efflux by flavonoids in HCT-15 colon cells : Activation of P-glycoprotein as a putative mechanism</title><title>Biochemical pharmacology</title><addtitle>Biochem Pharmacol</addtitle><description>Since P-glycoprotein (P-gp) in normal tissues may serve as a cellular defense mechanism against naturally occurring xenobiotics, we considered whether physiologically active components of commonly ingested plant foods could influence P-gp function. To examine this possibility, a series of flavonoids commonly found in plant foods was tested for their ability to modulate [
14C]Adriamycin
® ([
14C]ADR) accumulation and efflux in P-gp-expressing HCT-15 colon cells. Many flavonoids, in the micromolar range, inhibited the accumulation of [
14C]ADR. Detailed experiments utilizing flavonoids with the greatest activity in reducing [
14C]ADR accumulation, i.e. galangin, kaempferol, and quercetin, revealed that the efflux of [
14C]ADR is increased markedly in the presence of these compounds. Flavonoid-induced stimulation of efflux was rapid and was blocked by the multidrug-resistant (MDR) reversal agents verapamil, vinblastine, and quinidine. The magnitude of flavonoid-stimulated efflux in sodium butyrate-treated cells with a 4-fold induction of P-gp protein was similar to that in uninduced cells. [
3H]Azidopine photoaffinity labeling of P-gp in crude membrane preparations revealed mild to no competition for binding by flavonoids possessing either activity or inactivity in reducing ADR accumulation. Although flavonoid hydrophobicity was found to be unrelated to flavonoid activity in altering [
14C]ADR accumulation, certain structural features were associated with enhancement or diminution of activity. Finally, the significance of flavonoid-related reduction of [
14C]ADR accumulation was underscored in cell growth studies, showing partial protection by quercetin against ADR-induced growth inhibition. It is concluded that certain naturally occuring plant flavonoids may acutely upregulate the apparent activity of P-gp.</description><subject>Adriamycin</subject><subject>ATP Binding Cassette Transporter, Subfamily B, Member 1 - metabolism</subject><subject>Biological and medical sciences</subject><subject>Butyrates - pharmacology</subject><subject>Butyric Acid</subject><subject>Carcinogenesis, carcinogens and anticarcinogens</subject><subject>Cell Division - drug effects</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Diet</subject><subject>Dose-Response Relationship, Drug</subject><subject>Doxorubicin - metabolism</subject><subject>Doxorubicin - toxicity</subject><subject>Drug Interactions</subject><subject>flavonoids</subject><subject>Flavonoids - pharmacology</subject><subject>Foods and miscellaneous</subject><subject>HCT-15 cells</subject><subject>Humans</subject><subject>Kaempferols</subject><subject>Medical sciences</subject><subject>P-glycoprotein</subject><subject>quercetin</subject><subject>Quercetin - analogs & derivatives</subject><subject>Quercetin - pharmacology</subject><subject>Structure-Activity Relationship</subject><subject>Tumors</subject><subject>Verapamil - pharmacology</subject><subject>Vinblastine - pharmacology</subject><issn>0006-2952</issn><issn>1873-2968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kUGO1DAQRS0EGpqBG4DkBQtYBMqJ7U5YII1awCANgsWwtsp2GYycuBUnLfoSHIVDcDISpulVqeq_-irVZ-ypgFcChH4NALqqO1W_6OTLDpRuK3GPbUS7bZaxbu-zzRl5yB6V8mNtWy0u2MW2k0pKuWG_PmU_J5xiHngOHP0YsT-6OPA_vzk6N_f_VRw8pxDS_JPbIw8JD3nI0Re-sNe720oo7nJaQEcpFf6GX7kpHs7OX6pv6ejyfswTLRtYOPL9PC36gXhP7jsOsfSP2YOAqdCTU71kX9-_u91dVzefP3zcXd1UVHcwVV46GxqnRBAQqFFt0JqsBQVAwvquaWFbk7IEUjgPvsaahLYaQSLaWjWX7Nmd7362PXmzH2OP49Gc_rLoz086FocpjDi4WM5Y0who1Wrz9g6j5dZDpNEUF2lw5ONIbjI-RyPArHGZ9flmzcJ00vyLy4jmL0WciLQ</recordid><startdate>19941007</startdate><enddate>19941007</enddate><creator>Critchfield, James W.</creator><creator>Welsh, Clement J.</creator><creator>Phang, James M.</creator><creator>Chao Yeh, Grace</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19941007</creationdate><title>Modulation of adriamycin ® accumulation and efflux by flavonoids in HCT-15 colon cells : Activation of P-glycoprotein as a putative mechanism</title><author>Critchfield, James W. ; Welsh, Clement J. ; Phang, James M. ; Chao Yeh, Grace</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e290t-d4cbf3c51f10fe358f66ebb0500e1bd938072e5be041cd0d2a2e16b6a04aab253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Adriamycin</topic><topic>ATP Binding Cassette Transporter, Subfamily B, Member 1 - metabolism</topic><topic>Biological and medical sciences</topic><topic>Butyrates - pharmacology</topic><topic>Butyric Acid</topic><topic>Carcinogenesis, carcinogens and anticarcinogens</topic><topic>Cell Division - drug effects</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Diet</topic><topic>Dose-Response Relationship, Drug</topic><topic>Doxorubicin - metabolism</topic><topic>Doxorubicin - toxicity</topic><topic>Drug Interactions</topic><topic>flavonoids</topic><topic>Flavonoids - pharmacology</topic><topic>Foods and miscellaneous</topic><topic>HCT-15 cells</topic><topic>Humans</topic><topic>Kaempferols</topic><topic>Medical sciences</topic><topic>P-glycoprotein</topic><topic>quercetin</topic><topic>Quercetin - analogs & derivatives</topic><topic>Quercetin - pharmacology</topic><topic>Structure-Activity Relationship</topic><topic>Tumors</topic><topic>Verapamil - pharmacology</topic><topic>Vinblastine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Critchfield, James W.</creatorcontrib><creatorcontrib>Welsh, Clement J.</creatorcontrib><creatorcontrib>Phang, James M.</creatorcontrib><creatorcontrib>Chao Yeh, Grace</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Biochemical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Critchfield, James W.</au><au>Welsh, Clement J.</au><au>Phang, James M.</au><au>Chao Yeh, Grace</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of adriamycin ® accumulation and efflux by flavonoids in HCT-15 colon cells : Activation of P-glycoprotein as a putative mechanism</atitle><jtitle>Biochemical pharmacology</jtitle><addtitle>Biochem Pharmacol</addtitle><date>1994-10-07</date><risdate>1994</risdate><volume>48</volume><issue>7</issue><spage>1437</spage><epage>1445</epage><pages>1437-1445</pages><issn>0006-2952</issn><eissn>1873-2968</eissn><coden>BCPCA6</coden><abstract>Since P-glycoprotein (P-gp) in normal tissues may serve as a cellular defense mechanism against naturally occurring xenobiotics, we considered whether physiologically active components of commonly ingested plant foods could influence P-gp function. To examine this possibility, a series of flavonoids commonly found in plant foods was tested for their ability to modulate [
14C]Adriamycin
® ([
14C]ADR) accumulation and efflux in P-gp-expressing HCT-15 colon cells. Many flavonoids, in the micromolar range, inhibited the accumulation of [
14C]ADR. Detailed experiments utilizing flavonoids with the greatest activity in reducing [
14C]ADR accumulation, i.e. galangin, kaempferol, and quercetin, revealed that the efflux of [
14C]ADR is increased markedly in the presence of these compounds. Flavonoid-induced stimulation of efflux was rapid and was blocked by the multidrug-resistant (MDR) reversal agents verapamil, vinblastine, and quinidine. The magnitude of flavonoid-stimulated efflux in sodium butyrate-treated cells with a 4-fold induction of P-gp protein was similar to that in uninduced cells. [
3H]Azidopine photoaffinity labeling of P-gp in crude membrane preparations revealed mild to no competition for binding by flavonoids possessing either activity or inactivity in reducing ADR accumulation. Although flavonoid hydrophobicity was found to be unrelated to flavonoid activity in altering [
14C]ADR accumulation, certain structural features were associated with enhancement or diminution of activity. Finally, the significance of flavonoid-related reduction of [
14C]ADR accumulation was underscored in cell growth studies, showing partial protection by quercetin against ADR-induced growth inhibition. It is concluded that certain naturally occuring plant flavonoids may acutely upregulate the apparent activity of P-gp.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>7945444</pmid><doi>10.1016/0006-2952(94)90568-1</doi><tpages>9</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Adriamycin ATP Binding Cassette Transporter, Subfamily B, Member 1 - metabolism Biological and medical sciences Butyrates - pharmacology Butyric Acid Carcinogenesis, carcinogens and anticarcinogens Cell Division - drug effects Cell Line Cell Survival - drug effects Diet Dose-Response Relationship, Drug Doxorubicin - metabolism Doxorubicin - toxicity Drug Interactions flavonoids Flavonoids - pharmacology Foods and miscellaneous HCT-15 cells Humans Kaempferols Medical sciences P-glycoprotein quercetin Quercetin - analogs & derivatives Quercetin - pharmacology Structure-Activity Relationship Tumors Verapamil - pharmacology Vinblastine - pharmacology |
title | Modulation of adriamycin ® accumulation and efflux by flavonoids in HCT-15 colon cells : Activation of P-glycoprotein as a putative mechanism |
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