Aqueous extract of unripe Rubus coreanus fruit attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II gene expression

The fruit of Rubus coreanus has been used as a traditional herbal medicine for alleviation of inflammatory and vascular diseases in Asian countries. The anti-atherogenic effect of unripe Rubus coreanus fruit extract (URFE) and its underlying mechanism were analyzed in mice fed a high-fat diet (HFD)...

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Veröffentlicht in:Journal of ethnopharmacology 2013-03, Vol.146 (2), p.515-524
Hauptverfasser: Kim, Sookon, Kim, Chun-Ki, Lee, Kwang-Soon, Kim, Ji-Hee, Hwang, Haejun, Jeoung, Dooil, Choe, Jongseon, Won, Moo-Ho, Lee, Hansoo, Ha, Kwon-Soo, Kwon, Young-Geun, Kim, Young-Myeong
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container_issue 2
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container_title Journal of ethnopharmacology
container_volume 146
creator Kim, Sookon
Kim, Chun-Ki
Lee, Kwang-Soon
Kim, Ji-Hee
Hwang, Haejun
Jeoung, Dooil
Choe, Jongseon
Won, Moo-Ho
Lee, Hansoo
Ha, Kwon-Soo
Kwon, Young-Geun
Kim, Young-Myeong
description The fruit of Rubus coreanus has been used as a traditional herbal medicine for alleviation of inflammatory and vascular diseases in Asian countries. The anti-atherogenic effect of unripe Rubus coreanus fruit extract (URFE) and its underlying mechanism were analyzed in mice fed a high-fat diet (HFD) and in cell culture system. Mouse was freely given HFD alone or supplemented with URFE for 14 weeks, followed by analysis of atherosclerotic lesions and serum lipid levels. For in vitro assay, macrophages were pretreated with URFE, followed by stimulation with lipopolysaccharide (LPS). Expression levels of inflammatory genes (TNF-α, IL-1β, and iNOS) and phase II genes (heme oxygenase-1, glutamate cysteine lygase, and peroxiredoxine-1) as well as intracellular reactive oxygen species (ROS) level and NF-κB activation pathway were analyzed in cultured macrophages as well as mouse sera and aortic tissues. URFE supplementation reduced HFD-induced atherosclerotic lesion formation which was correlated with decreased levels of lipids, lipid peroxides, and inflammatory mediators (TNF-α, IL-1β, and nitric oxide) in sera as well as suppression of inflammatory gene in aortic tissues. In addition, pre-treatment of macrophages with URFE also suppressed LPS-induced NF-κB activation, ROS production, and inflammatory and phase II gene expressions. Inhibition of phase II enzyme and protein activities attenuated the suppressive effects URFE on ROS production, NF-κB activation, and inflammatory gene expression. These results suggest that URFE attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II antioxidant gene expression. [Display omitted]
doi_str_mv 10.1016/j.jep.2013.01.016
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The anti-atherogenic effect of unripe Rubus coreanus fruit extract (URFE) and its underlying mechanism were analyzed in mice fed a high-fat diet (HFD) and in cell culture system. Mouse was freely given HFD alone or supplemented with URFE for 14 weeks, followed by analysis of atherosclerotic lesions and serum lipid levels. For in vitro assay, macrophages were pretreated with URFE, followed by stimulation with lipopolysaccharide (LPS). Expression levels of inflammatory genes (TNF-α, IL-1β, and iNOS) and phase II genes (heme oxygenase-1, glutamate cysteine lygase, and peroxiredoxine-1) as well as intracellular reactive oxygen species (ROS) level and NF-κB activation pathway were analyzed in cultured macrophages as well as mouse sera and aortic tissues. URFE supplementation reduced HFD-induced atherosclerotic lesion formation which was correlated with decreased levels of lipids, lipid peroxides, and inflammatory mediators (TNF-α, IL-1β, and nitric oxide) in sera as well as suppression of inflammatory gene in aortic tissues. In addition, pre-treatment of macrophages with URFE also suppressed LPS-induced NF-κB activation, ROS production, and inflammatory and phase II gene expressions. Inhibition of phase II enzyme and protein activities attenuated the suppressive effects URFE on ROS production, NF-κB activation, and inflammatory gene expression. These results suggest that URFE attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II antioxidant gene expression. [Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2013.01.016</identifier><identifier>PMID: 23353895</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animals ; Aorta - metabolism ; Atherosclerosis ; Atherosclerosis - drug therapy ; Atherosclerosis - genetics ; Atherosclerosis - metabolism ; Cell Line ; Cholesterol - blood ; Fruit ; Gene Expression Regulation - drug effects ; Glutamate-Cysteine Ligase - genetics ; Heme Oxygenase-1 - genetics ; Homeodomain Proteins - genetics ; Inflammation ; Interleukin-1beta - metabolism ; Lipid profile ; Male ; Membrane Proteins - genetics ; Mice ; Mice, Inbred C57BL ; NF-E2-Related Factor 2 - metabolism ; NF-kappa B - antagonists &amp; inhibitors ; NF-kappa B - metabolism ; Nitric Oxide Synthase Type II - metabolism ; Phase II gene ; Phytotherapy ; Plant Extracts - pharmacology ; Plant Extracts - therapeutic use ; Rosaceae ; Rubus coreanus fruit ; Tumor Necrosis Factor-alpha - metabolism</subject><ispartof>Journal of ethnopharmacology, 2013-03, Vol.146 (2), p.515-524</ispartof><rights>2013 Elsevier Ireland Ltd.</rights><rights>Copyright © 2013 Elsevier Ireland Ltd. 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The anti-atherogenic effect of unripe Rubus coreanus fruit extract (URFE) and its underlying mechanism were analyzed in mice fed a high-fat diet (HFD) and in cell culture system. Mouse was freely given HFD alone or supplemented with URFE for 14 weeks, followed by analysis of atherosclerotic lesions and serum lipid levels. For in vitro assay, macrophages were pretreated with URFE, followed by stimulation with lipopolysaccharide (LPS). Expression levels of inflammatory genes (TNF-α, IL-1β, and iNOS) and phase II genes (heme oxygenase-1, glutamate cysteine lygase, and peroxiredoxine-1) as well as intracellular reactive oxygen species (ROS) level and NF-κB activation pathway were analyzed in cultured macrophages as well as mouse sera and aortic tissues. URFE supplementation reduced HFD-induced atherosclerotic lesion formation which was correlated with decreased levels of lipids, lipid peroxides, and inflammatory mediators (TNF-α, IL-1β, and nitric oxide) in sera as well as suppression of inflammatory gene in aortic tissues. In addition, pre-treatment of macrophages with URFE also suppressed LPS-induced NF-κB activation, ROS production, and inflammatory and phase II gene expressions. Inhibition of phase II enzyme and protein activities attenuated the suppressive effects URFE on ROS production, NF-κB activation, and inflammatory gene expression. These results suggest that URFE attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II antioxidant gene expression. [Display omitted]</description><subject>Animals</subject><subject>Aorta - metabolism</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis - drug therapy</subject><subject>Atherosclerosis - genetics</subject><subject>Atherosclerosis - metabolism</subject><subject>Cell Line</subject><subject>Cholesterol - blood</subject><subject>Fruit</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Glutamate-Cysteine Ligase - genetics</subject><subject>Heme Oxygenase-1 - genetics</subject><subject>Homeodomain Proteins - genetics</subject><subject>Inflammation</subject><subject>Interleukin-1beta - metabolism</subject><subject>Lipid profile</subject><subject>Male</subject><subject>Membrane Proteins - genetics</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>NF-kappa B - antagonists &amp; inhibitors</subject><subject>NF-kappa B - metabolism</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Phase II gene</subject><subject>Phytotherapy</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Extracts - therapeutic use</subject><subject>Rosaceae</subject><subject>Rubus coreanus fruit</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UUtuFDEQtRCIDIEDsEFesunBv_6MWIWIwEgRkSJYW267nKlRj7ux3SNyI86QQ3CmuDWBJVLJLpVfPVe9R8hbztac8ebDfr2HaS0Yl2vGSzTPyIp3rajaupXPyYrJtqu6VvEz8iqlPWOs5Yq9JGdCylp2m3pFfl_8nGGcE4VfORqb6ejpHCJOQG_nvtTtGMGEkvg4Y6YmZwizyZBKuoM4JjssJyba31M8THE8Yrij_TCOjg44oaOl5nEAaoKjGHbYY14g366qPw-faPkUjybjGOgRDZ12JgHdbukdBChTTRFSKo-vyQtvhgRvnu5z8uPq8_fLr9X1zZft5cV1ZctKuaqdsm7TGMU5F_1mY5XohTHK-E5649tOqt4K4VpoammcVazzvah9Z0URzjTynLw_8ZapizQp6wMmC8NgwqKT5pK3iinGZIHyE9QWAVIEr6eIBxPvNWd6MUjvdTFILwZpxkss9O-e6Of-AO5fx19HCuDjCQBlySNC1MkiBAsOI9is3Yj_oX8E_aul9Q</recordid><startdate>20130327</startdate><enddate>20130327</enddate><creator>Kim, Sookon</creator><creator>Kim, Chun-Ki</creator><creator>Lee, Kwang-Soon</creator><creator>Kim, Ji-Hee</creator><creator>Hwang, Haejun</creator><creator>Jeoung, Dooil</creator><creator>Choe, Jongseon</creator><creator>Won, Moo-Ho</creator><creator>Lee, Hansoo</creator><creator>Ha, Kwon-Soo</creator><creator>Kwon, Young-Geun</creator><creator>Kim, Young-Myeong</creator><general>Elsevier Ireland Ltd</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></search><sort><creationdate>20130327</creationdate><title>Aqueous extract of unripe Rubus coreanus fruit attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II gene expression</title><author>Kim, Sookon ; Kim, Chun-Ki ; Lee, Kwang-Soon ; Kim, Ji-Hee ; Hwang, Haejun ; Jeoung, Dooil ; Choe, Jongseon ; Won, Moo-Ho ; Lee, Hansoo ; Ha, Kwon-Soo ; Kwon, Young-Geun ; Kim, Young-Myeong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-5d4cd96a41112b99c42b2aa4af83faf7834bc22d7e653adc408fb25f8c2872a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Aorta - metabolism</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis - drug therapy</topic><topic>Atherosclerosis - genetics</topic><topic>Atherosclerosis - metabolism</topic><topic>Cell Line</topic><topic>Cholesterol - blood</topic><topic>Fruit</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Glutamate-Cysteine Ligase - genetics</topic><topic>Heme Oxygenase-1 - genetics</topic><topic>Homeodomain Proteins - genetics</topic><topic>Inflammation</topic><topic>Interleukin-1beta - metabolism</topic><topic>Lipid profile</topic><topic>Male</topic><topic>Membrane Proteins - genetics</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>NF-kappa B - antagonists &amp; 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The anti-atherogenic effect of unripe Rubus coreanus fruit extract (URFE) and its underlying mechanism were analyzed in mice fed a high-fat diet (HFD) and in cell culture system. Mouse was freely given HFD alone or supplemented with URFE for 14 weeks, followed by analysis of atherosclerotic lesions and serum lipid levels. For in vitro assay, macrophages were pretreated with URFE, followed by stimulation with lipopolysaccharide (LPS). Expression levels of inflammatory genes (TNF-α, IL-1β, and iNOS) and phase II genes (heme oxygenase-1, glutamate cysteine lygase, and peroxiredoxine-1) as well as intracellular reactive oxygen species (ROS) level and NF-κB activation pathway were analyzed in cultured macrophages as well as mouse sera and aortic tissues. URFE supplementation reduced HFD-induced atherosclerotic lesion formation which was correlated with decreased levels of lipids, lipid peroxides, and inflammatory mediators (TNF-α, IL-1β, and nitric oxide) in sera as well as suppression of inflammatory gene in aortic tissues. In addition, pre-treatment of macrophages with URFE also suppressed LPS-induced NF-κB activation, ROS production, and inflammatory and phase II gene expressions. Inhibition of phase II enzyme and protein activities attenuated the suppressive effects URFE on ROS production, NF-κB activation, and inflammatory gene expression. These results suggest that URFE attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II antioxidant gene expression. [Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>23353895</pmid><doi>10.1016/j.jep.2013.01.016</doi><tpages>10</tpages></addata></record>
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subjects Animals
Aorta - metabolism
Atherosclerosis
Atherosclerosis - drug therapy
Atherosclerosis - genetics
Atherosclerosis - metabolism
Cell Line
Cholesterol - blood
Fruit
Gene Expression Regulation - drug effects
Glutamate-Cysteine Ligase - genetics
Heme Oxygenase-1 - genetics
Homeodomain Proteins - genetics
Inflammation
Interleukin-1beta - metabolism
Lipid profile
Male
Membrane Proteins - genetics
Mice
Mice, Inbred C57BL
NF-E2-Related Factor 2 - metabolism
NF-kappa B - antagonists & inhibitors
NF-kappa B - metabolism
Nitric Oxide Synthase Type II - metabolism
Phase II gene
Phytotherapy
Plant Extracts - pharmacology
Plant Extracts - therapeutic use
Rosaceae
Rubus coreanus fruit
Tumor Necrosis Factor-alpha - metabolism
title Aqueous extract of unripe Rubus coreanus fruit attenuates atherosclerosis by improving blood lipid profile and inhibiting NF-κB activation via phase II gene expression
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