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Pine bark extract prevents low-density lipoprotein oxidation and regulates monocytic expression of antioxidant enzymes
Abstract Polyphenols are widely distributed in leaves, seeds, bark, and flowers and considered to have beneficial effects on cardiovascular health. We hypothesized that the potent antioxidant properties of pine bark extract (PBE) are exerted by its ability to scavenge free radicals and induce antiox...
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Published in: | Nutrition research (New York, N.Y.) N.Y.), 2015, Vol.35 (1), p.56-64 |
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description | Abstract Polyphenols are widely distributed in leaves, seeds, bark, and flowers and considered to have beneficial effects on cardiovascular health. We hypothesized that the potent antioxidant properties of pine bark extract (PBE) are exerted by its ability to scavenge free radicals and induce antioxidant enzymes. Therefore, we investigated the effects of PBE on low-density lipoprotein (LDL) oxidation and the antioxidant defense system in monocytes. Oxidative susceptibility of LDL was determined by lag time assay in vitro and by using a human umbilical vein endothelial cell–mediated oxidation model. THP-1 monocytic cells were treated with PBE, and the expression of antioxidant enzymes was measured by real-time polymerase chain reaction and Western blot. Pine bark extract showed radical scavenging ability and significantly inhibited free radical-induced and endothelial cell-mediated LDL oxidation in vitro. Pine bark extract treatment resulted in increases in the expressions of antioxidant enzymes, glutathione peroxidase-1, catalase, and heme oxygenase-1 in THP-1 cells. In addition, PBE induced nuclear factor-erythroid-2–related factor 2 activation, which was accompanied by the activation of extracellular signal-regulated kinase and Akt despite a down-regulation of reactive oxygen species. After the monocyte investigations, we further examined the antioxidant effect after the intake of PBE by 10 healthy male volunteers. Pine bark extract significantly prolonged the lag time of LDL oxidation. Based on our findings, it appears that PBE enhances the antioxidant defense capacity of LDL and monocytes and may play a preventive role in atherosclerosis progression. |
doi_str_mv | 10.1016/j.nutres.2014.10.010 |
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We hypothesized that the potent antioxidant properties of pine bark extract (PBE) are exerted by its ability to scavenge free radicals and induce antioxidant enzymes. Therefore, we investigated the effects of PBE on low-density lipoprotein (LDL) oxidation and the antioxidant defense system in monocytes. Oxidative susceptibility of LDL was determined by lag time assay in vitro and by using a human umbilical vein endothelial cell–mediated oxidation model. THP-1 monocytic cells were treated with PBE, and the expression of antioxidant enzymes was measured by real-time polymerase chain reaction and Western blot. Pine bark extract showed radical scavenging ability and significantly inhibited free radical-induced and endothelial cell-mediated LDL oxidation in vitro. Pine bark extract treatment resulted in increases in the expressions of antioxidant enzymes, glutathione peroxidase-1, catalase, and heme oxygenase-1 in THP-1 cells. In addition, PBE induced nuclear factor-erythroid-2–related factor 2 activation, which was accompanied by the activation of extracellular signal-regulated kinase and Akt despite a down-regulation of reactive oxygen species. After the monocyte investigations, we further examined the antioxidant effect after the intake of PBE by 10 healthy male volunteers. Pine bark extract significantly prolonged the lag time of LDL oxidation. Based on our findings, it appears that PBE enhances the antioxidant defense capacity of LDL and monocytes and may play a preventive role in atherosclerosis progression.</description><identifier>ISSN: 0271-5317</identifier><identifier>EISSN: 1879-0739</identifier><identifier>DOI: 10.1016/j.nutres.2014.10.010</identifier><identifier>PMID: 25458248</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Antioxidant ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Atherosclerosis - prevention & control ; Catalase - genetics ; Cell Line ; Down-Regulation ; Extracellular Signal-Regulated MAP Kinases - genetics ; Extracellular Signal-Regulated MAP Kinases - metabolism ; Gastroenterology and Hepatology ; Glutathione Peroxidase - genetics ; Glutathione Peroxidase - metabolism ; Healthy Volunteers ; Heme Oxygenase-1 - genetics ; Heme Oxygenase-1 - metabolism ; Human Umbilical Vein Endothelial Cells - drug effects ; Human Umbilical Vein Endothelial Cells - metabolism ; Humans ; Lipid peroxidation ; Lipoproteins, LDL - metabolism ; Male ; Middle Aged ; Monocytes ; Monocytes - drug effects ; Monocytes - metabolism ; NF-E2-Related Factor 2 - genetics ; NF-E2-Related Factor 2 - metabolism ; NF-E2–related factor 2 ; Pine bark extract ; Pinus - chemistry ; Plant Bark - chemistry ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Polyphenol ; Reactive Oxygen Species - metabolism ; Real-Time Polymerase Chain Reaction</subject><ispartof>Nutrition research (New York, N.Y.), 2015, Vol.35 (1), p.56-64</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c516t-432c036a12ad6eefe80d9fa6a0f44e5128ad2d995f6cb68bcc0456caae7f753a3</citedby><cites>FETCH-LOGICAL-c516t-432c036a12ad6eefe80d9fa6a0f44e5128ad2d995f6cb68bcc0456caae7f753a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25458248$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nakayama, Shiori</creatorcontrib><creatorcontrib>Kishimoto, Yoshimi</creatorcontrib><creatorcontrib>Saita, Emi</creatorcontrib><creatorcontrib>Sugihara, Norie</creatorcontrib><creatorcontrib>Toyozaki, Miku</creatorcontrib><creatorcontrib>Taguchi, Chie</creatorcontrib><creatorcontrib>Tani, Mariko</creatorcontrib><creatorcontrib>Kamiya, Tomoyasu</creatorcontrib><creatorcontrib>Kondo, Kazuo</creatorcontrib><title>Pine bark extract prevents low-density lipoprotein oxidation and regulates monocytic expression of antioxidant enzymes</title><title>Nutrition research (New York, N.Y.)</title><addtitle>Nutr Res</addtitle><description>Abstract Polyphenols are widely distributed in leaves, seeds, bark, and flowers and considered to have beneficial effects on cardiovascular health. We hypothesized that the potent antioxidant properties of pine bark extract (PBE) are exerted by its ability to scavenge free radicals and induce antioxidant enzymes. Therefore, we investigated the effects of PBE on low-density lipoprotein (LDL) oxidation and the antioxidant defense system in monocytes. Oxidative susceptibility of LDL was determined by lag time assay in vitro and by using a human umbilical vein endothelial cell–mediated oxidation model. THP-1 monocytic cells were treated with PBE, and the expression of antioxidant enzymes was measured by real-time polymerase chain reaction and Western blot. Pine bark extract showed radical scavenging ability and significantly inhibited free radical-induced and endothelial cell-mediated LDL oxidation in vitro. Pine bark extract treatment resulted in increases in the expressions of antioxidant enzymes, glutathione peroxidase-1, catalase, and heme oxygenase-1 in THP-1 cells. In addition, PBE induced nuclear factor-erythroid-2–related factor 2 activation, which was accompanied by the activation of extracellular signal-regulated kinase and Akt despite a down-regulation of reactive oxygen species. After the monocyte investigations, we further examined the antioxidant effect after the intake of PBE by 10 healthy male volunteers. Pine bark extract significantly prolonged the lag time of LDL oxidation. Based on our findings, it appears that PBE enhances the antioxidant defense capacity of LDL and monocytes and may play a preventive role in atherosclerosis progression.</description><subject>Adult</subject><subject>Antioxidant</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Atherosclerosis - prevention & control</subject><subject>Catalase - genetics</subject><subject>Cell Line</subject><subject>Down-Regulation</subject><subject>Extracellular Signal-Regulated MAP Kinases - genetics</subject><subject>Extracellular Signal-Regulated MAP Kinases - metabolism</subject><subject>Gastroenterology and Hepatology</subject><subject>Glutathione Peroxidase - genetics</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Healthy Volunteers</subject><subject>Heme Oxygenase-1 - genetics</subject><subject>Heme Oxygenase-1 - metabolism</subject><subject>Human Umbilical Vein Endothelial Cells - drug effects</subject><subject>Human Umbilical Vein Endothelial Cells - metabolism</subject><subject>Humans</subject><subject>Lipid peroxidation</subject><subject>Lipoproteins, LDL - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Monocytes</subject><subject>Monocytes - drug effects</subject><subject>Monocytes - metabolism</subject><subject>NF-E2-Related Factor 2 - genetics</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>NF-E2–related factor 2</subject><subject>Pine bark extract</subject><subject>Pinus - chemistry</subject><subject>Plant Bark - chemistry</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Polyphenol</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Real-Time Polymerase Chain Reaction</subject><issn>0271-5317</issn><issn>1879-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNkk-LFDEQxYMo7rj6DURy9NJjKkmnuy-CLOsfWFBQzyGTVEtme5IxSY_bfnrTzOrBi54Cxe-9Cu8VIc-BbYGBerXfhrkkzFvOQNbRlgF7QDbQd0PDOjE8JBvGO2haAd0FeZLznjHoQIjH5IK3su257Dfk9MkHpDuTbinelWRsoceEJwwl0yn-aByG7MtCJ3-MxxQL-kDjnXem-BioCY4m_DZPpmCmhxiiXYq31aqa5LwicaxUhVdNKBTDz-WA-Sl5NJop47P795J8fXv95ep9c_Px3YerNzeNbUGVRgpumVAGuHEKccSeuWE0yrBRSmyB98ZxNwztqOxO9TtrmWyVNQa7sWuFEZfk5dm3_v37jLnog88Wp8kEjHPWoBSTAnox_AcquWI1NVVReUZtijknHPUx-YNJiwam13L0Xp_L0Ws567SWU2Uv7jfMuwO6P6LfbVTg9RnAGsnJY9LZegwWnU9oi3bR_2vD3wZ28sFbM93ignkf5xRq3Bp05prpz-uBrPcBkjEOfS9-AUHBut8</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Nakayama, Shiori</creator><creator>Kishimoto, Yoshimi</creator><creator>Saita, Emi</creator><creator>Sugihara, Norie</creator><creator>Toyozaki, Miku</creator><creator>Taguchi, Chie</creator><creator>Tani, Mariko</creator><creator>Kamiya, Tomoyasu</creator><creator>Kondo, Kazuo</creator><general>Elsevier Inc</general><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>7T5</scope><scope>H94</scope></search><sort><creationdate>2015</creationdate><title>Pine bark extract prevents low-density lipoprotein oxidation and regulates monocytic expression of antioxidant enzymes</title><author>Nakayama, Shiori ; Kishimoto, Yoshimi ; Saita, Emi ; Sugihara, Norie ; Toyozaki, Miku ; Taguchi, Chie ; Tani, Mariko ; Kamiya, Tomoyasu ; Kondo, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c516t-432c036a12ad6eefe80d9fa6a0f44e5128ad2d995f6cb68bcc0456caae7f753a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Antioxidant</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>Atherosclerosis - prevention & control</topic><topic>Catalase - genetics</topic><topic>Cell Line</topic><topic>Down-Regulation</topic><topic>Extracellular Signal-Regulated MAP Kinases - genetics</topic><topic>Extracellular Signal-Regulated MAP Kinases - metabolism</topic><topic>Gastroenterology and Hepatology</topic><topic>Glutathione Peroxidase - genetics</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Healthy Volunteers</topic><topic>Heme Oxygenase-1 - genetics</topic><topic>Heme Oxygenase-1 - metabolism</topic><topic>Human Umbilical Vein Endothelial Cells - drug effects</topic><topic>Human Umbilical Vein Endothelial Cells - metabolism</topic><topic>Humans</topic><topic>Lipid peroxidation</topic><topic>Lipoproteins, LDL - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Monocytes</topic><topic>Monocytes - drug effects</topic><topic>Monocytes - metabolism</topic><topic>NF-E2-Related Factor 2 - genetics</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>NF-E2–related factor 2</topic><topic>Pine bark extract</topic><topic>Pinus - chemistry</topic><topic>Plant Bark - chemistry</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Polyphenol</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Real-Time Polymerase Chain Reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nakayama, Shiori</creatorcontrib><creatorcontrib>Kishimoto, Yoshimi</creatorcontrib><creatorcontrib>Saita, Emi</creatorcontrib><creatorcontrib>Sugihara, Norie</creatorcontrib><creatorcontrib>Toyozaki, Miku</creatorcontrib><creatorcontrib>Taguchi, Chie</creatorcontrib><creatorcontrib>Tani, Mariko</creatorcontrib><creatorcontrib>Kamiya, Tomoyasu</creatorcontrib><creatorcontrib>Kondo, Kazuo</creatorcontrib><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>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Nutrition research (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nakayama, Shiori</au><au>Kishimoto, Yoshimi</au><au>Saita, Emi</au><au>Sugihara, Norie</au><au>Toyozaki, Miku</au><au>Taguchi, Chie</au><au>Tani, Mariko</au><au>Kamiya, Tomoyasu</au><au>Kondo, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pine bark extract prevents low-density lipoprotein oxidation and regulates monocytic expression of antioxidant enzymes</atitle><jtitle>Nutrition research (New York, N.Y.)</jtitle><addtitle>Nutr Res</addtitle><date>2015</date><risdate>2015</risdate><volume>35</volume><issue>1</issue><spage>56</spage><epage>64</epage><pages>56-64</pages><issn>0271-5317</issn><eissn>1879-0739</eissn><abstract>Abstract Polyphenols are widely distributed in leaves, seeds, bark, and flowers and considered to have beneficial effects on cardiovascular health. We hypothesized that the potent antioxidant properties of pine bark extract (PBE) are exerted by its ability to scavenge free radicals and induce antioxidant enzymes. Therefore, we investigated the effects of PBE on low-density lipoprotein (LDL) oxidation and the antioxidant defense system in monocytes. Oxidative susceptibility of LDL was determined by lag time assay in vitro and by using a human umbilical vein endothelial cell–mediated oxidation model. THP-1 monocytic cells were treated with PBE, and the expression of antioxidant enzymes was measured by real-time polymerase chain reaction and Western blot. Pine bark extract showed radical scavenging ability and significantly inhibited free radical-induced and endothelial cell-mediated LDL oxidation in vitro. Pine bark extract treatment resulted in increases in the expressions of antioxidant enzymes, glutathione peroxidase-1, catalase, and heme oxygenase-1 in THP-1 cells. In addition, PBE induced nuclear factor-erythroid-2–related factor 2 activation, which was accompanied by the activation of extracellular signal-regulated kinase and Akt despite a down-regulation of reactive oxygen species. After the monocyte investigations, we further examined the antioxidant effect after the intake of PBE by 10 healthy male volunteers. Pine bark extract significantly prolonged the lag time of LDL oxidation. Based on our findings, it appears that PBE enhances the antioxidant defense capacity of LDL and monocytes and may play a preventive role in atherosclerosis progression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25458248</pmid><doi>10.1016/j.nutres.2014.10.010</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Antioxidant Antioxidants - chemistry Antioxidants - pharmacology Atherosclerosis - prevention & control Catalase - genetics Cell Line Down-Regulation Extracellular Signal-Regulated MAP Kinases - genetics Extracellular Signal-Regulated MAP Kinases - metabolism Gastroenterology and Hepatology Glutathione Peroxidase - genetics Glutathione Peroxidase - metabolism Healthy Volunteers Heme Oxygenase-1 - genetics Heme Oxygenase-1 - metabolism Human Umbilical Vein Endothelial Cells - drug effects Human Umbilical Vein Endothelial Cells - metabolism Humans Lipid peroxidation Lipoproteins, LDL - metabolism Male Middle Aged Monocytes Monocytes - drug effects Monocytes - metabolism NF-E2-Related Factor 2 - genetics NF-E2-Related Factor 2 - metabolism NF-E2–related factor 2 Pine bark extract Pinus - chemistry Plant Bark - chemistry Plant Extracts - chemistry Plant Extracts - pharmacology Polyphenol Reactive Oxygen Species - metabolism Real-Time Polymerase Chain Reaction |
title | Pine bark extract prevents low-density lipoprotein oxidation and regulates monocytic expression of antioxidant enzymes |
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