Protection and reversal of hepatic fibrosis by red wine polyphenols in hyperhomocysteinemic mice
Hyperhomocysteinemia leads to several clinical manifestations and, particularly, liver disease. Lowering homocysteine through nutrition or other means might offer preventive or therapeutic benefits. Polyphenols are natural compounds known for their antioxidant and healing properties for vessels. In...
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Veröffentlicht in: | The Journal of nutritional biochemistry 2011-09, Vol.22 (9), p.856-864 |
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creator | Noll, Christophe Raaf, Lamia Planque, Chris Benard, Ludovic Secardin, Lise Petit, Emile Dairou, Julien Paul, Jean-Louis Samuel, Jane-Lise Delcayre, Claude Rodrigues-Lima, Fernando Janel, Nathalie |
description | Hyperhomocysteinemia leads to several clinical manifestations and, particularly, liver disease. Lowering homocysteine through nutrition or other means might offer preventive or therapeutic benefits. Polyphenols are natural compounds known for their antioxidant and healing properties for vessels. In a previous study we have shown a beneficial effect of a red wine polyphenolic extract (PE) administration on plasma homocysteine level in cystathionine beta synthase deficient mice, a murine model of hyperhomocysteinemia. These mice also develop hepatic fibrosis. As increased matrix metalloproteinase (MMP) 2 has been shown to be involved in the development of hepatic fibrosis, we then focused on the effect of PE administration on expression and activity of MMP-2 in liver of hyperhomocysteinemic mice and its impact on hepatic fibrosis development. PE was added for four weeks to the drinking water of heterozygous cystathionine beta synthase-deficient mice fed a high-methionine diet. Effects of PE administration were examined by histological analysis with Sirius red staining, zymography, immunobloting, real-time quantitative reverse transcriptase polymerase chain reaction, peroxynitrite level, catalase activity and nicotinamide adenine dinucleotide phosphate oxidase activity. We show that administration of PE had a beneficial effect (i) on MMP-2 expression via modulation of nitrotyrosine-modified total protein level and (ii) on MMP-2 activity via modulation of its activator/inhibitor balance. We also demonstrated a reversal effect of PE supplementation on hepatic fibrosis development. Our results demonstrate a preventive action of PE administration on biomarkers of hepatic dysfunction due to hyperhomocysteinemia. |
doi_str_mv | 10.1016/j.jnutbio.2010.07.010 |
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Lowering homocysteine through nutrition or other means might offer preventive or therapeutic benefits. Polyphenols are natural compounds known for their antioxidant and healing properties for vessels. In a previous study we have shown a beneficial effect of a red wine polyphenolic extract (PE) administration on plasma homocysteine level in cystathionine beta synthase deficient mice, a murine model of hyperhomocysteinemia. These mice also develop hepatic fibrosis. As increased matrix metalloproteinase (MMP) 2 has been shown to be involved in the development of hepatic fibrosis, we then focused on the effect of PE administration on expression and activity of MMP-2 in liver of hyperhomocysteinemic mice and its impact on hepatic fibrosis development. PE was added for four weeks to the drinking water of heterozygous cystathionine beta synthase-deficient mice fed a high-methionine diet. Effects of PE administration were examined by histological analysis with Sirius red staining, zymography, immunobloting, real-time quantitative reverse transcriptase polymerase chain reaction, peroxynitrite level, catalase activity and nicotinamide adenine dinucleotide phosphate oxidase activity. We show that administration of PE had a beneficial effect (i) on MMP-2 expression via modulation of nitrotyrosine-modified total protein level and (ii) on MMP-2 activity via modulation of its activator/inhibitor balance. We also demonstrated a reversal effect of PE supplementation on hepatic fibrosis development. Our results demonstrate a preventive action of PE administration on biomarkers of hepatic dysfunction due to hyperhomocysteinemia.</description><identifier>ISSN: 0955-2863</identifier><identifier>EISSN: 1873-4847</identifier><identifier>DOI: 10.1016/j.jnutbio.2010.07.010</identifier><identifier>PMID: 21185709</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Catalase ; Cystathionine beta-Synthase - genetics ; e-NOS ; Feeding. Feeding behavior ; Fibrosis ; Fundamental and applied biological sciences. Psychology ; Homocysteine ; Hyperhomocysteinemia - complications ; Hyperhomocysteinemia - metabolism ; Life Sciences ; Liver Cirrhosis - etiology ; Liver Cirrhosis - metabolism ; Liver Cirrhosis - prevention & control ; Matrix Metalloproteinase 2 - metabolism ; Matrix metalloproteinase-2 ; Methionine - administration & dosage ; Methionine - pharmacology ; Mice ; Mice, Transgenic ; Polyphenols ; Polyphenols - pharmacology ; Polyphenols - therapeutic use ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Wine ; Zymography</subject><ispartof>The Journal of nutritional biochemistry, 2011-09, Vol.22 (9), p.856-864</ispartof><rights>2011 Elsevier Inc.</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c494t-8c9c37fa1724cf7b4b2fee051f07df5389660f40a3e932a3cc2e5c666272c94a3</citedby><cites>FETCH-LOGICAL-c494t-8c9c37fa1724cf7b4b2fee051f07df5389660f40a3e932a3cc2e5c666272c94a3</cites><orcidid>0000-0002-5776-7531</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0955286310001890$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24465901$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21185709$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.inrae.fr/hal-02644414$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Noll, Christophe</creatorcontrib><creatorcontrib>Raaf, Lamia</creatorcontrib><creatorcontrib>Planque, Chris</creatorcontrib><creatorcontrib>Benard, Ludovic</creatorcontrib><creatorcontrib>Secardin, Lise</creatorcontrib><creatorcontrib>Petit, Emile</creatorcontrib><creatorcontrib>Dairou, Julien</creatorcontrib><creatorcontrib>Paul, Jean-Louis</creatorcontrib><creatorcontrib>Samuel, Jane-Lise</creatorcontrib><creatorcontrib>Delcayre, Claude</creatorcontrib><creatorcontrib>Rodrigues-Lima, Fernando</creatorcontrib><creatorcontrib>Janel, Nathalie</creatorcontrib><title>Protection and reversal of hepatic fibrosis by red wine polyphenols in hyperhomocysteinemic mice</title><title>The Journal of nutritional biochemistry</title><addtitle>J Nutr Biochem</addtitle><description>Hyperhomocysteinemia leads to several clinical manifestations and, particularly, liver disease. Lowering homocysteine through nutrition or other means might offer preventive or therapeutic benefits. Polyphenols are natural compounds known for their antioxidant and healing properties for vessels. In a previous study we have shown a beneficial effect of a red wine polyphenolic extract (PE) administration on plasma homocysteine level in cystathionine beta synthase deficient mice, a murine model of hyperhomocysteinemia. These mice also develop hepatic fibrosis. As increased matrix metalloproteinase (MMP) 2 has been shown to be involved in the development of hepatic fibrosis, we then focused on the effect of PE administration on expression and activity of MMP-2 in liver of hyperhomocysteinemic mice and its impact on hepatic fibrosis development. PE was added for four weeks to the drinking water of heterozygous cystathionine beta synthase-deficient mice fed a high-methionine diet. Effects of PE administration were examined by histological analysis with Sirius red staining, zymography, immunobloting, real-time quantitative reverse transcriptase polymerase chain reaction, peroxynitrite level, catalase activity and nicotinamide adenine dinucleotide phosphate oxidase activity. We show that administration of PE had a beneficial effect (i) on MMP-2 expression via modulation of nitrotyrosine-modified total protein level and (ii) on MMP-2 activity via modulation of its activator/inhibitor balance. We also demonstrated a reversal effect of PE supplementation on hepatic fibrosis development. Our results demonstrate a preventive action of PE administration on biomarkers of hepatic dysfunction due to hyperhomocysteinemia.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Catalase</subject><subject>Cystathionine beta-Synthase - genetics</subject><subject>e-NOS</subject><subject>Feeding. Feeding behavior</subject><subject>Fibrosis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Homocysteine</subject><subject>Hyperhomocysteinemia - complications</subject><subject>Hyperhomocysteinemia - metabolism</subject><subject>Life Sciences</subject><subject>Liver Cirrhosis - etiology</subject><subject>Liver Cirrhosis - metabolism</subject><subject>Liver Cirrhosis - prevention & control</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix metalloproteinase-2</subject><subject>Methionine - administration & dosage</subject><subject>Methionine - pharmacology</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Polyphenols</subject><subject>Polyphenols - pharmacology</subject><subject>Polyphenols - therapeutic use</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Wine</subject><subject>Zymography</subject><issn>0955-2863</issn><issn>1873-4847</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2L1DAYxoMo7uzqn6DkIuKhY5LmqydZFt0VBvSg55imb2iGtqlJZ5b-92aYcT16CA-8-b0fPA9CbyjZUkLlx_12Px2WNsQtI6VG1LbIM7ShWtUV11w9RxvSCFExLesrdJ3znhDCuJAv0RWjVAtFmg369T3FBdwS4oTt1OEER0jZDjh63MNsl-CwD22KOWTcruW_w49hAjzHYZ17mOKQcZhwv86Q-jhGt-YFCjCWxvLgFXrh7ZDh9UVv0M8vn3_cPVS7b_df7253leMNXyrtGlcrb6li3HnV8pZ5ACKoJ6rzotaNlMRzYmtoamZr5xgIJ6VkirmG2_oGfTjP7e1g5hRGm1YTbTAPtztzqhEmOeeUH2lh35_ZOcXfB8iLGUN2MAx2gnjIRuta80YrUkhxJl1xICfwT6MpMacczN5ccjCnHAxRpkjpe3vZcGhH6J66_hpfgHcXwGZnB5_s5EL-x3EuRUNOp346c1C8OwZIJrsAk4MupBKb6WL4zyl_AB1Kqag</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Noll, Christophe</creator><creator>Raaf, Lamia</creator><creator>Planque, Chris</creator><creator>Benard, Ludovic</creator><creator>Secardin, Lise</creator><creator>Petit, Emile</creator><creator>Dairou, Julien</creator><creator>Paul, Jean-Louis</creator><creator>Samuel, Jane-Lise</creator><creator>Delcayre, Claude</creator><creator>Rodrigues-Lima, Fernando</creator><creator>Janel, Nathalie</creator><general>Elsevier Inc</general><general>Elsevier</general><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><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-5776-7531</orcidid></search><sort><creationdate>20110901</creationdate><title>Protection and reversal of hepatic fibrosis by red wine polyphenols in hyperhomocysteinemic mice</title><author>Noll, Christophe ; Raaf, Lamia ; Planque, Chris ; Benard, Ludovic ; Secardin, Lise ; Petit, Emile ; Dairou, Julien ; Paul, Jean-Louis ; Samuel, Jane-Lise ; Delcayre, Claude ; Rodrigues-Lima, Fernando ; Janel, Nathalie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-8c9c37fa1724cf7b4b2fee051f07df5389660f40a3e932a3cc2e5c666272c94a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Catalase</topic><topic>Cystathionine beta-Synthase - genetics</topic><topic>e-NOS</topic><topic>Feeding. Feeding behavior</topic><topic>Fibrosis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Homocysteine</topic><topic>Hyperhomocysteinemia - complications</topic><topic>Hyperhomocysteinemia - metabolism</topic><topic>Life Sciences</topic><topic>Liver Cirrhosis - etiology</topic><topic>Liver Cirrhosis - metabolism</topic><topic>Liver Cirrhosis - prevention & control</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix metalloproteinase-2</topic><topic>Methionine - administration & dosage</topic><topic>Methionine - pharmacology</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Polyphenols</topic><topic>Polyphenols - pharmacology</topic><topic>Polyphenols - therapeutic use</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Wine</topic><topic>Zymography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noll, Christophe</creatorcontrib><creatorcontrib>Raaf, Lamia</creatorcontrib><creatorcontrib>Planque, Chris</creatorcontrib><creatorcontrib>Benard, Ludovic</creatorcontrib><creatorcontrib>Secardin, Lise</creatorcontrib><creatorcontrib>Petit, Emile</creatorcontrib><creatorcontrib>Dairou, Julien</creatorcontrib><creatorcontrib>Paul, Jean-Louis</creatorcontrib><creatorcontrib>Samuel, Jane-Lise</creatorcontrib><creatorcontrib>Delcayre, Claude</creatorcontrib><creatorcontrib>Rodrigues-Lima, Fernando</creatorcontrib><creatorcontrib>Janel, Nathalie</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>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The Journal of nutritional biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Noll, Christophe</au><au>Raaf, Lamia</au><au>Planque, Chris</au><au>Benard, Ludovic</au><au>Secardin, Lise</au><au>Petit, Emile</au><au>Dairou, Julien</au><au>Paul, Jean-Louis</au><au>Samuel, Jane-Lise</au><au>Delcayre, Claude</au><au>Rodrigues-Lima, Fernando</au><au>Janel, Nathalie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protection and reversal of hepatic fibrosis by red wine polyphenols in hyperhomocysteinemic mice</atitle><jtitle>The Journal of nutritional biochemistry</jtitle><addtitle>J Nutr Biochem</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>22</volume><issue>9</issue><spage>856</spage><epage>864</epage><pages>856-864</pages><issn>0955-2863</issn><eissn>1873-4847</eissn><abstract>Hyperhomocysteinemia leads to several clinical manifestations and, particularly, liver disease. Lowering homocysteine through nutrition or other means might offer preventive or therapeutic benefits. Polyphenols are natural compounds known for their antioxidant and healing properties for vessels. In a previous study we have shown a beneficial effect of a red wine polyphenolic extract (PE) administration on plasma homocysteine level in cystathionine beta synthase deficient mice, a murine model of hyperhomocysteinemia. These mice also develop hepatic fibrosis. As increased matrix metalloproteinase (MMP) 2 has been shown to be involved in the development of hepatic fibrosis, we then focused on the effect of PE administration on expression and activity of MMP-2 in liver of hyperhomocysteinemic mice and its impact on hepatic fibrosis development. PE was added for four weeks to the drinking water of heterozygous cystathionine beta synthase-deficient mice fed a high-methionine diet. Effects of PE administration were examined by histological analysis with Sirius red staining, zymography, immunobloting, real-time quantitative reverse transcriptase polymerase chain reaction, peroxynitrite level, catalase activity and nicotinamide adenine dinucleotide phosphate oxidase activity. We show that administration of PE had a beneficial effect (i) on MMP-2 expression via modulation of nitrotyrosine-modified total protein level and (ii) on MMP-2 activity via modulation of its activator/inhibitor balance. We also demonstrated a reversal effect of PE supplementation on hepatic fibrosis development. Our results demonstrate a preventive action of PE administration on biomarkers of hepatic dysfunction due to hyperhomocysteinemia.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>21185709</pmid><doi>10.1016/j.jnutbio.2010.07.010</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5776-7531</orcidid></addata></record> |
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subjects | Animals Biological and medical sciences Catalase Cystathionine beta-Synthase - genetics e-NOS Feeding. Feeding behavior Fibrosis Fundamental and applied biological sciences. Psychology Homocysteine Hyperhomocysteinemia - complications Hyperhomocysteinemia - metabolism Life Sciences Liver Cirrhosis - etiology Liver Cirrhosis - metabolism Liver Cirrhosis - prevention & control Matrix Metalloproteinase 2 - metabolism Matrix metalloproteinase-2 Methionine - administration & dosage Methionine - pharmacology Mice Mice, Transgenic Polyphenols Polyphenols - pharmacology Polyphenols - therapeutic use Vertebrates: anatomy and physiology, studies on body, several organs or systems Wine Zymography |
title | Protection and reversal of hepatic fibrosis by red wine polyphenols in hyperhomocysteinemic mice |
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