Protocatechuic Acid, a Metabolite of Anthocyanins, Inhibits Monocyte Adhesion and Reduces Atherosclerosis in Apolipoprotein E-Deficient Mice

Polyphenols, including anthocyanins, from various plant foods are effective in the prevention of atherosclerosis in animal and human studies. Protocatechuic acid (PCA), a major metabolite of anthocyanins, has been found to possess the anti-carcinogenic effect, whereas the in vivo effect of PCA as an...

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Veröffentlicht in:Journal of agricultural and food chemistry 2010-12, Vol.58 (24), p.12722-12728
Hauptverfasser: Wang, Dongliang, Wei, Xiaoyi, Yan, Xiao, Jin, Tianru, Ling, Wenhua
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container_end_page 12728
container_issue 24
container_start_page 12722
container_title Journal of agricultural and food chemistry
container_volume 58
creator Wang, Dongliang
Wei, Xiaoyi
Yan, Xiao
Jin, Tianru
Ling, Wenhua
description Polyphenols, including anthocyanins, from various plant foods are effective in the prevention of atherosclerosis in animal and human studies. Protocatechuic acid (PCA), a major metabolite of anthocyanins, has been found to possess the anti-carcinogenic effect, whereas the in vivo effect of PCA as an anti-atherosclerotic agent remains unknown. We demonstrated herein that PCA inhibited monocyte adhesion to tumor necrosis factor-α (TNF-α)-activated mouse aortic endothelial cells, associated with the inhibition of vascular cell adhesion molecule 1 (VCAM-1) and intercellular adhesion molecule 1 (ICAM-1) expression. Furthermore, PCA inhibited the nuclear content of p65, a subunit of nuclear factor-κB (NF-κB), along with reduced NF-κB binding activity. Finally, PCA administration in the apolipoprotein E (ApoE)-deficient mouse model reduced aortic VCAM-1 and ICAM-1 expression, NF-κB activity, and plasma-soluble VCAM-1 and ICAM-1 levels, with inhibiting atherosclerosis development. We suggest that PCA possesses the anti-atherogenic effect at least partially via its anti-inflammatory activity.
doi_str_mv 10.1021/jf103427j
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Protocatechuic acid (PCA), a major metabolite of anthocyanins, has been found to possess the anti-carcinogenic effect, whereas the in vivo effect of PCA as an anti-atherosclerotic agent remains unknown. We demonstrated herein that PCA inhibited monocyte adhesion to tumor necrosis factor-α (TNF-α)-activated mouse aortic endothelial cells, associated with the inhibition of vascular cell adhesion molecule 1 (VCAM-1) and intercellular adhesion molecule 1 (ICAM-1) expression. Furthermore, PCA inhibited the nuclear content of p65, a subunit of nuclear factor-κB (NF-κB), along with reduced NF-κB binding activity. Finally, PCA administration in the apolipoprotein E (ApoE)-deficient mouse model reduced aortic VCAM-1 and ICAM-1 expression, NF-κB activity, and plasma-soluble VCAM-1 and ICAM-1 levels, with inhibiting atherosclerosis development. 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Psychology ; human cell lines ; Humans ; Hydroxybenzoates - metabolism ; Hydroxybenzoates - pharmacology ; Intercellular Adhesion Molecule-1 - genetics ; Intercellular Adhesion Molecule-1 - immunology ; Male ; metabolites ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; monocytes ; Monocytes - cytology ; Monocytes - drug effects ; Monocytes - immunology ; plant-based foods ; protocatechuic acid</subject><ispartof>Journal of agricultural and food chemistry, 2010-12, Vol.58 (24), p.12722-12728</ispartof><rights>Copyright © 2010 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a434t-3b9db013cf59fc450c0cd583b498a7e08dfecd89f7e01f7561899b93ea055de23</citedby><cites>FETCH-LOGICAL-a434t-3b9db013cf59fc450c0cd583b498a7e08dfecd89f7e01f7561899b93ea055de23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf103427j$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf103427j$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23693659$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21090717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Dongliang</creatorcontrib><creatorcontrib>Wei, Xiaoyi</creatorcontrib><creatorcontrib>Yan, Xiao</creatorcontrib><creatorcontrib>Jin, Tianru</creatorcontrib><creatorcontrib>Ling, Wenhua</creatorcontrib><title>Protocatechuic Acid, a Metabolite of Anthocyanins, Inhibits Monocyte Adhesion and Reduces Atherosclerosis in Apolipoprotein E-Deficient Mice</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Polyphenols, including anthocyanins, from various plant foods are effective in the prevention of atherosclerosis in animal and human studies. Protocatechuic acid (PCA), a major metabolite of anthocyanins, has been found to possess the anti-carcinogenic effect, whereas the in vivo effect of PCA as an anti-atherosclerotic agent remains unknown. We demonstrated herein that PCA inhibited monocyte adhesion to tumor necrosis factor-α (TNF-α)-activated mouse aortic endothelial cells, associated with the inhibition of vascular cell adhesion molecule 1 (VCAM-1) and intercellular adhesion molecule 1 (ICAM-1) expression. Furthermore, PCA inhibited the nuclear content of p65, a subunit of nuclear factor-κB (NF-κB), along with reduced NF-κB binding activity. Finally, PCA administration in the apolipoprotein E (ApoE)-deficient mouse model reduced aortic VCAM-1 and ICAM-1 expression, NF-κB activity, and plasma-soluble VCAM-1 and ICAM-1 levels, with inhibiting atherosclerosis development. 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Psychology</subject><subject>human cell lines</subject><subject>Humans</subject><subject>Hydroxybenzoates - metabolism</subject><subject>Hydroxybenzoates - pharmacology</subject><subject>Intercellular Adhesion Molecule-1 - genetics</subject><subject>Intercellular Adhesion Molecule-1 - immunology</subject><subject>Male</subject><subject>metabolites</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Knockout</subject><subject>monocytes</subject><subject>Monocytes - cytology</subject><subject>Monocytes - drug effects</subject><subject>Monocytes - immunology</subject><subject>plant-based foods</subject><subject>protocatechuic acid</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkMFu1DAQhi0EokvhwAuALxwqNTCO4018jEqhlboCAT1HznhMvNraUew99B360HW1pb1wGY_tT__88zP2XsBnAbX4snUCZFO32xdsJVQNlRKie8lWUD6rTq3FEXuT0hYAOtXCa3ZUC9DQinbF7n4uMUc0mXDae-Q9envKDd9QNmPc-Uw8Ot6HPEW8NcGHdMovw-RHnxPfxFBeC9LbiZKPgZtg-S-ye6TE-zzREhPuHqpP3Afez0VyjnOZSeV6Xn0l59FTyHzjkd6yV87sEr17PI_Z9bfzP2cX1dWP75dn_VVlGtnkSo7ajiAkOqUdNgoQ0KpOjo3uTEvQWUdoO-1KL1xb9u-0HrUkA0pZquUxOznoYnGWFnLDvPgbs9wOAoaHRIenRAv74cDO-_GG7BP5L8ICfHoETEKzc4sJ6NMzJ9darpUu3McD50wczN-lMNe_67IGCF3XGrpnJYNp2Mb9EkoI_7F0Dy-clSU</recordid><startdate>20101222</startdate><enddate>20101222</enddate><creator>Wang, Dongliang</creator><creator>Wei, Xiaoyi</creator><creator>Yan, Xiao</creator><creator>Jin, Tianru</creator><creator>Ling, Wenhua</creator><general>American Chemical Society</general><scope>FBQ</scope><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></search><sort><creationdate>20101222</creationdate><title>Protocatechuic Acid, a Metabolite of Anthocyanins, Inhibits Monocyte Adhesion and Reduces Atherosclerosis in Apolipoprotein E-Deficient Mice</title><author>Wang, Dongliang ; Wei, Xiaoyi ; Yan, Xiao ; Jin, Tianru ; Ling, Wenhua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a434t-3b9db013cf59fc450c0cd583b498a7e08dfecd89f7e01f7561899b93ea055de23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>animal models</topic><topic>Animals</topic><topic>anthocyanins</topic><topic>Anthocyanins - metabolism</topic><topic>anticarcinogenic activity</topic><topic>apolipoprotein E</topic><topic>apolipoprotein E-deficient mice</topic><topic>Apolipoproteins E - deficiency</topic><topic>Apolipoproteins E - genetics</topic><topic>atherosclerosis</topic><topic>Atherosclerosis - drug therapy</topic><topic>Atherosclerosis - immunology</topic><topic>Atherosclerosis - physiopathology</topic><topic>Atherosclerosis - prevention &amp; control</topic><topic>Bioactive Constituents</topic><topic>Biological and medical sciences</topic><topic>cell adhesion</topic><topic>Cell Adhesion - drug effects</topic><topic>cell culture</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>Disease Models, Animal</topic><topic>Down-Regulation</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>human cell lines</topic><topic>Humans</topic><topic>Hydroxybenzoates - metabolism</topic><topic>Hydroxybenzoates - pharmacology</topic><topic>Intercellular Adhesion Molecule-1 - genetics</topic><topic>Intercellular Adhesion Molecule-1 - immunology</topic><topic>Male</topic><topic>metabolites</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Knockout</topic><topic>monocytes</topic><topic>Monocytes - cytology</topic><topic>Monocytes - drug effects</topic><topic>Monocytes - immunology</topic><topic>plant-based foods</topic><topic>protocatechuic acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Dongliang</creatorcontrib><creatorcontrib>Wei, Xiaoyi</creatorcontrib><creatorcontrib>Yan, Xiao</creatorcontrib><creatorcontrib>Jin, Tianru</creatorcontrib><creatorcontrib>Ling, Wenhua</creatorcontrib><collection>AGRIS</collection><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><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Dongliang</au><au>Wei, Xiaoyi</au><au>Yan, Xiao</au><au>Jin, Tianru</au><au>Ling, Wenhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protocatechuic Acid, a Metabolite of Anthocyanins, Inhibits Monocyte Adhesion and Reduces Atherosclerosis in Apolipoprotein E-Deficient Mice</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2010-12-22</date><risdate>2010</risdate><volume>58</volume><issue>24</issue><spage>12722</spage><epage>12728</epage><pages>12722-12728</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Polyphenols, including anthocyanins, from various plant foods are effective in the prevention of atherosclerosis in animal and human studies. Protocatechuic acid (PCA), a major metabolite of anthocyanins, has been found to possess the anti-carcinogenic effect, whereas the in vivo effect of PCA as an anti-atherosclerotic agent remains unknown. We demonstrated herein that PCA inhibited monocyte adhesion to tumor necrosis factor-α (TNF-α)-activated mouse aortic endothelial cells, associated with the inhibition of vascular cell adhesion molecule 1 (VCAM-1) and intercellular adhesion molecule 1 (ICAM-1) expression. Furthermore, PCA inhibited the nuclear content of p65, a subunit of nuclear factor-κB (NF-κB), along with reduced NF-κB binding activity. Finally, PCA administration in the apolipoprotein E (ApoE)-deficient mouse model reduced aortic VCAM-1 and ICAM-1 expression, NF-κB activity, and plasma-soluble VCAM-1 and ICAM-1 levels, with inhibiting atherosclerosis development. We suggest that PCA possesses the anti-atherogenic effect at least partially via its anti-inflammatory activity.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21090717</pmid><doi>10.1021/jf103427j</doi><tpages>7</tpages></addata></record>
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source ACS Publications; MEDLINE
subjects animal models
Animals
anthocyanins
Anthocyanins - metabolism
anticarcinogenic activity
apolipoprotein E
apolipoprotein E-deficient mice
Apolipoproteins E - deficiency
Apolipoproteins E - genetics
atherosclerosis
Atherosclerosis - drug therapy
Atherosclerosis - immunology
Atherosclerosis - physiopathology
Atherosclerosis - prevention & control
Bioactive Constituents
Biological and medical sciences
cell adhesion
Cell Adhesion - drug effects
cell culture
Cell Line
Cells, Cultured
Disease Models, Animal
Down-Regulation
Food industries
Fundamental and applied biological sciences. Psychology
human cell lines
Humans
Hydroxybenzoates - metabolism
Hydroxybenzoates - pharmacology
Intercellular Adhesion Molecule-1 - genetics
Intercellular Adhesion Molecule-1 - immunology
Male
metabolites
Mice
Mice, Inbred BALB C
Mice, Knockout
monocytes
Monocytes - cytology
Monocytes - drug effects
Monocytes - immunology
plant-based foods
protocatechuic acid
title Protocatechuic Acid, a Metabolite of Anthocyanins, Inhibits Monocyte Adhesion and Reduces Atherosclerosis in Apolipoprotein E-Deficient Mice
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