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Selective modulation of P-glycoprotein activity by steroidal saponines from Paris polyphylla
Bio-guided fractionation of the roots of Paris polyphylla (Trilliaceae), based on inhibition of P-glycoprotein-mediated daunorubicin efflux in K562/R7 cell line, led to isolation and identification of the three saponins 3- O-Rha(1 → 2)[Ara(1 → 4)]Glc-pennogenine, gracillin and polyphyllin D, and the...
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Published in: | Fitoterapia 2009, Vol.80 (1), p.39-42 |
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container_end_page | 42 |
container_issue | 1 |
container_start_page | 39 |
container_title | Fitoterapia |
container_volume | 80 |
creator | Nguyen, Van Thi Bao Darbour, Nicole Bayet, Christine Doreau, Agnès Raad, Imad Phung, Binh Hoa Dumontet, Charles Di Pietro, Attilio Dijoux-Franca, Marie-Geneviève Guilet, David |
description | Bio-guided fractionation of the roots of
Paris polyphylla (Trilliaceae), based on inhibition of P-glycoprotein-mediated daunorubicin efflux in K562/R7 cell line, led to isolation and identification of the three saponins 3-
O-Rha(1
→
2)[Ara(1
→
4)]Glc-pennogenine, gracillin and polyphyllin D, and the two ecdysteroids 20-hydroxyecdysone and pinnatasterone. These compounds were tested for multidrug reversion on P-glycoprotein (ABCB1) with both drug-selected and transfected cell lines, and also on Breast Cancer Resistance Protein (BCRP/ABCG2). By contrast to a weak efficiency on BCRP, the three saponins displayed significant effects as inhibitors of P-glycoprotein-mediated drug efflux. |
doi_str_mv | 10.1016/j.fitote.2008.09.010 |
format | article |
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Paris polyphylla (Trilliaceae), based on inhibition of P-glycoprotein-mediated daunorubicin efflux in K562/R7 cell line, led to isolation and identification of the three saponins 3-
O-Rha(1
→
2)[Ara(1
→
4)]Glc-pennogenine, gracillin and polyphyllin D, and the two ecdysteroids 20-hydroxyecdysone and pinnatasterone. These compounds were tested for multidrug reversion on P-glycoprotein (ABCB1) with both drug-selected and transfected cell lines, and also on Breast Cancer Resistance Protein (BCRP/ABCG2). By contrast to a weak efficiency on BCRP, the three saponins displayed significant effects as inhibitors of P-glycoprotein-mediated drug efflux.</description><identifier>ISSN: 0367-326X</identifier><identifier>EISSN: 1873-6971</identifier><identifier>DOI: 10.1016/j.fitote.2008.09.010</identifier><identifier>PMID: 18940238</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>ABCB1 ; Analytical chemistry ; BCRP (ABCG2) ; Biological and medical sciences ; Breast Cancer Resistance Protein ; Chemical Sciences ; Ecdysteroids ; General pharmacology ; Life Sciences ; MDR ; Medical sciences ; Multidrug resistance ; P-glycoprotein ; Paris polyphylla ; Pharmaceutical sciences ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. Drug treatments ; Saponins</subject><ispartof>Fitoterapia, 2009, Vol.80 (1), p.39-42</ispartof><rights>2008 Elsevier B.V.</rights><rights>2009 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c424t-489fe6682dd72f3a1b971cd5cd85a2bd191eb7821368576bc062c168dea9f4d63</citedby><cites>FETCH-LOGICAL-c424t-489fe6682dd72f3a1b971cd5cd85a2bd191eb7821368576bc062c168dea9f4d63</cites><orcidid>0000-0002-8035-214X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21657211$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-lyon1.hal.science/hal-02545047$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Nguyen, Van Thi Bao</creatorcontrib><creatorcontrib>Darbour, Nicole</creatorcontrib><creatorcontrib>Bayet, Christine</creatorcontrib><creatorcontrib>Doreau, Agnès</creatorcontrib><creatorcontrib>Raad, Imad</creatorcontrib><creatorcontrib>Phung, Binh Hoa</creatorcontrib><creatorcontrib>Dumontet, Charles</creatorcontrib><creatorcontrib>Di Pietro, Attilio</creatorcontrib><creatorcontrib>Dijoux-Franca, Marie-Geneviève</creatorcontrib><creatorcontrib>Guilet, David</creatorcontrib><title>Selective modulation of P-glycoprotein activity by steroidal saponines from Paris polyphylla</title><title>Fitoterapia</title><description>Bio-guided fractionation of the roots of
Paris polyphylla (Trilliaceae), based on inhibition of P-glycoprotein-mediated daunorubicin efflux in K562/R7 cell line, led to isolation and identification of the three saponins 3-
O-Rha(1
→
2)[Ara(1
→
4)]Glc-pennogenine, gracillin and polyphyllin D, and the two ecdysteroids 20-hydroxyecdysone and pinnatasterone. These compounds were tested for multidrug reversion on P-glycoprotein (ABCB1) with both drug-selected and transfected cell lines, and also on Breast Cancer Resistance Protein (BCRP/ABCG2). By contrast to a weak efficiency on BCRP, the three saponins displayed significant effects as inhibitors of P-glycoprotein-mediated drug efflux.</description><subject>ABCB1</subject><subject>Analytical chemistry</subject><subject>BCRP (ABCG2)</subject><subject>Biological and medical sciences</subject><subject>Breast Cancer Resistance Protein</subject><subject>Chemical Sciences</subject><subject>Ecdysteroids</subject><subject>General pharmacology</subject><subject>Life Sciences</subject><subject>MDR</subject><subject>Medical sciences</subject><subject>Multidrug resistance</subject><subject>P-glycoprotein</subject><subject>Paris polyphylla</subject><subject>Pharmaceutical sciences</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. 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Paris polyphylla (Trilliaceae), based on inhibition of P-glycoprotein-mediated daunorubicin efflux in K562/R7 cell line, led to isolation and identification of the three saponins 3-
O-Rha(1
→
2)[Ara(1
→
4)]Glc-pennogenine, gracillin and polyphyllin D, and the two ecdysteroids 20-hydroxyecdysone and pinnatasterone. These compounds were tested for multidrug reversion on P-glycoprotein (ABCB1) with both drug-selected and transfected cell lines, and also on Breast Cancer Resistance Protein (BCRP/ABCG2). By contrast to a weak efficiency on BCRP, the three saponins displayed significant effects as inhibitors of P-glycoprotein-mediated drug efflux.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18940238</pmid><doi>10.1016/j.fitote.2008.09.010</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-8035-214X</orcidid></addata></record> |
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subjects | ABCB1 Analytical chemistry BCRP (ABCG2) Biological and medical sciences Breast Cancer Resistance Protein Chemical Sciences Ecdysteroids General pharmacology Life Sciences MDR Medical sciences Multidrug resistance P-glycoprotein Paris polyphylla Pharmaceutical sciences Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Saponins |
title | Selective modulation of P-glycoprotein activity by steroidal saponines from Paris polyphylla |
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