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Oligonol, a new lychee fruit-derived low-molecular form of polyphenol, enhances lipolysis in primary rat adipocytes through activation of the ERK1/2 pathway
The effect of Oligonol, a phenolic product from lychee fruit polyphenol (LFP) containing catechin-type monomers and lower oligomers of proanthocyanidin, on lipolysis in primary adipocytes was investigated in order to examine the possible mechanism underlying the regulation of in vivo metabolism in f...
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Published in: | Phytotherapy research 2009-11, Vol.23 (11), p.1626-1633 |
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creator | Ogasawara, Junetsu Kitadate, Kentaro Nishioka, Hiroshi Fujii, Hajime Sakurai, Takuya Kizaki, Takako Izawa, Tetsuya Ishida, Hitoshi Ohno, Hideki |
description | The effect of Oligonol, a phenolic product from lychee fruit polyphenol (LFP) containing catechin-type monomers and lower oligomers of proanthocyanidin, on lipolysis in primary adipocytes was investigated in order to examine the possible mechanism underlying the regulation of in vivo metabolism in fat. Oligonol significantly increased lipolysis, which was accompanied by both activation of extracellular signaling-related kinase 1/2 (ERK1/2) and down-regulation of perilipin protein expression, without an increase in intracellular cAMP production. The increase in lipolysis with Oligonol was prevented completely by pretreatment with either PD98059 or U0126, selective ERK1/2 inhibitors, which also prevented the reduction in the expression of perilipin protein. Tumor necrosis factor-α also down-regulated the expression of perilipin protein. However, there was no significant alteration in the expression of Gαi protein with Oligonol. These findings indicate that Oligonol enhances lipolysis in primary adipocytes, independent of cAMP production, but its effect is dependent on activation of the ERK1/2 pathway, leading to down-regulation of perilipin protein expression. Copyright © 2009 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/ptr.2846 |
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Oligonol significantly increased lipolysis, which was accompanied by both activation of extracellular signaling-related kinase 1/2 (ERK1/2) and down-regulation of perilipin protein expression, without an increase in intracellular cAMP production. The increase in lipolysis with Oligonol was prevented completely by pretreatment with either PD98059 or U0126, selective ERK1/2 inhibitors, which also prevented the reduction in the expression of perilipin protein. Tumor necrosis factor-α also down-regulated the expression of perilipin protein. However, there was no significant alteration in the expression of Gαi protein with Oligonol. These findings indicate that Oligonol enhances lipolysis in primary adipocytes, independent of cAMP production, but its effect is dependent on activation of the ERK1/2 pathway, leading to down-regulation of perilipin protein expression. Copyright © 2009 John Wiley & Sons, Ltd.</description><identifier>ISSN: 0951-418X</identifier><identifier>EISSN: 1099-1573</identifier><identifier>DOI: 10.1002/ptr.2846</identifier><identifier>PMID: 19548254</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Adipocytes - drug effects ; Animals ; Biological and medical sciences ; Butadienes - pharmacology ; Carrier Proteins ; Catechin - analogs & derivatives ; Catechin - pharmacology ; Cyclic AMP - metabolism ; Down-Regulation ; ERK1/2 ; Extracellular Signal-Regulated MAP Kinases - metabolism ; Flavonoids - pharmacology ; Fruit - chemistry ; General pharmacology ; lipolysis ; Lipolysis - drug effects ; Litchi - chemistry ; Male ; Medical sciences ; Molecular Structure ; Nitriles - pharmacology ; Oligonol ; perilipin ; Perilipin-1 ; Pharmacognosy. Homeopathy. Health food ; Pharmacology. 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Res</addtitle><description>The effect of Oligonol, a phenolic product from lychee fruit polyphenol (LFP) containing catechin-type monomers and lower oligomers of proanthocyanidin, on lipolysis in primary adipocytes was investigated in order to examine the possible mechanism underlying the regulation of in vivo metabolism in fat. Oligonol significantly increased lipolysis, which was accompanied by both activation of extracellular signaling-related kinase 1/2 (ERK1/2) and down-regulation of perilipin protein expression, without an increase in intracellular cAMP production. The increase in lipolysis with Oligonol was prevented completely by pretreatment with either PD98059 or U0126, selective ERK1/2 inhibitors, which also prevented the reduction in the expression of perilipin protein. Tumor necrosis factor-α also down-regulated the expression of perilipin protein. However, there was no significant alteration in the expression of Gαi protein with Oligonol. These findings indicate that Oligonol enhances lipolysis in primary adipocytes, independent of cAMP production, but its effect is dependent on activation of the ERK1/2 pathway, leading to down-regulation of perilipin protein expression. Copyright © 2009 John Wiley & Sons, Ltd.</description><subject>Adipocytes - drug effects</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Butadienes - pharmacology</subject><subject>Carrier Proteins</subject><subject>Catechin - analogs & derivatives</subject><subject>Catechin - pharmacology</subject><subject>Cyclic AMP - metabolism</subject><subject>Down-Regulation</subject><subject>ERK1/2</subject><subject>Extracellular Signal-Regulated MAP Kinases - metabolism</subject><subject>Flavonoids - pharmacology</subject><subject>Fruit - chemistry</subject><subject>General pharmacology</subject><subject>lipolysis</subject><subject>Lipolysis - drug effects</subject><subject>Litchi - chemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>Nitriles - pharmacology</subject><subject>Oligonol</subject><subject>perilipin</subject><subject>Perilipin-1</subject><subject>Pharmacognosy. Homeopathy. Health food</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenols - pharmacology</subject><subject>Phosphoproteins - metabolism</subject><subject>primary adipocytes</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><issn>0951-418X</issn><issn>1099-1573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp10d9u1SAYAPDGaNxxmvgEyo3RC7sBhdJe6tym2eLMcYvGG_KVQ09RWirQHfsuPqytp5lXXpHAj-9vkjwl-IhgTI_76I9owfJ7yYrgskwJF9n9ZIVLTlJGiq8HyaMQvmOMS4rZw-SAlJwVlLNV8vvKmq3rnH2NAHV6h-yoGq1R7QcT04325lZvkHW7tHVWq8GCR7XzLXI16p0d-0b__ay7BjqlA7Jmvg4mINOh3psW_Ig8RASb6UWNcTKx8W7YNghUNLcQjevmcLHR6HR9QY4p6iE2OxgfJw9qsEE_Wc7D5Obs9PrkfXp5df7h5M1lqpgo8rQmeSFyJTTlqgLM8ooTqokQJc-YwjjTuIKqIBlQ4LTmlG1AiYLWQvAyV1V2mLzcx-29-znoEGVrgtLWQqfdEKTIGCFZQfEkX-2l8i4Er2u5tCgJlvMq5LQKOa9ios-WoEPV6s0_uMx-Ai8WAEGBrf00QBPuHKW4LEpaTC7du52xevxvQvnper0kXrwJUf-68-B_yFxkgssvH8_l-gKfvWPf3srZP9_7GpyErZ9quPlMMckwERjnU-d_AFwrud0</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Ogasawara, Junetsu</creator><creator>Kitadate, Kentaro</creator><creator>Nishioka, Hiroshi</creator><creator>Fujii, Hajime</creator><creator>Sakurai, Takuya</creator><creator>Kizaki, Takako</creator><creator>Izawa, Tetsuya</creator><creator>Ishida, Hitoshi</creator><creator>Ohno, Hideki</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</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><scope>7X8</scope></search><sort><creationdate>200911</creationdate><title>Oligonol, a new lychee fruit-derived low-molecular form of polyphenol, enhances lipolysis in primary rat adipocytes through activation of the ERK1/2 pathway</title><author>Ogasawara, Junetsu ; Kitadate, Kentaro ; Nishioka, Hiroshi ; Fujii, Hajime ; Sakurai, Takuya ; Kizaki, Takako ; Izawa, Tetsuya ; Ishida, Hitoshi ; Ohno, Hideki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4786-f16876c7e25cba046b512e1779534c003e0bab813a2a52f524dac782f77596cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adipocytes - drug effects</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Butadienes - pharmacology</topic><topic>Carrier Proteins</topic><topic>Catechin - analogs & derivatives</topic><topic>Catechin - pharmacology</topic><topic>Cyclic AMP - metabolism</topic><topic>Down-Regulation</topic><topic>ERK1/2</topic><topic>Extracellular Signal-Regulated MAP Kinases - metabolism</topic><topic>Flavonoids - pharmacology</topic><topic>Fruit - chemistry</topic><topic>General pharmacology</topic><topic>lipolysis</topic><topic>Lipolysis - drug effects</topic><topic>Litchi - chemistry</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>Nitriles - pharmacology</topic><topic>Oligonol</topic><topic>perilipin</topic><topic>Perilipin-1</topic><topic>Pharmacognosy. Homeopathy. Health food</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenols - pharmacology</topic><topic>Phosphoproteins - metabolism</topic><topic>primary adipocytes</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ogasawara, Junetsu</creatorcontrib><creatorcontrib>Kitadate, Kentaro</creatorcontrib><creatorcontrib>Nishioka, Hiroshi</creatorcontrib><creatorcontrib>Fujii, Hajime</creatorcontrib><creatorcontrib>Sakurai, Takuya</creatorcontrib><creatorcontrib>Kizaki, Takako</creatorcontrib><creatorcontrib>Izawa, Tetsuya</creatorcontrib><creatorcontrib>Ishida, Hitoshi</creatorcontrib><creatorcontrib>Ohno, Hideki</creatorcontrib><collection>AGRIS</collection><collection>Istex</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><collection>MEDLINE - Academic</collection><jtitle>Phytotherapy research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ogasawara, Junetsu</au><au>Kitadate, Kentaro</au><au>Nishioka, Hiroshi</au><au>Fujii, Hajime</au><au>Sakurai, Takuya</au><au>Kizaki, Takako</au><au>Izawa, Tetsuya</au><au>Ishida, Hitoshi</au><au>Ohno, Hideki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oligonol, a new lychee fruit-derived low-molecular form of polyphenol, enhances lipolysis in primary rat adipocytes through activation of the ERK1/2 pathway</atitle><jtitle>Phytotherapy research</jtitle><addtitle>Phytother. Res</addtitle><date>2009-11</date><risdate>2009</risdate><volume>23</volume><issue>11</issue><spage>1626</spage><epage>1633</epage><pages>1626-1633</pages><issn>0951-418X</issn><eissn>1099-1573</eissn><abstract>The effect of Oligonol, a phenolic product from lychee fruit polyphenol (LFP) containing catechin-type monomers and lower oligomers of proanthocyanidin, on lipolysis in primary adipocytes was investigated in order to examine the possible mechanism underlying the regulation of in vivo metabolism in fat. Oligonol significantly increased lipolysis, which was accompanied by both activation of extracellular signaling-related kinase 1/2 (ERK1/2) and down-regulation of perilipin protein expression, without an increase in intracellular cAMP production. The increase in lipolysis with Oligonol was prevented completely by pretreatment with either PD98059 or U0126, selective ERK1/2 inhibitors, which also prevented the reduction in the expression of perilipin protein. Tumor necrosis factor-α also down-regulated the expression of perilipin protein. However, there was no significant alteration in the expression of Gαi protein with Oligonol. These findings indicate that Oligonol enhances lipolysis in primary adipocytes, independent of cAMP production, but its effect is dependent on activation of the ERK1/2 pathway, leading to down-regulation of perilipin protein expression. Copyright © 2009 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>19548254</pmid><doi>10.1002/ptr.2846</doi><tpages>8</tpages></addata></record> |
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subjects | Adipocytes - drug effects Animals Biological and medical sciences Butadienes - pharmacology Carrier Proteins Catechin - analogs & derivatives Catechin - pharmacology Cyclic AMP - metabolism Down-Regulation ERK1/2 Extracellular Signal-Regulated MAP Kinases - metabolism Flavonoids - pharmacology Fruit - chemistry General pharmacology lipolysis Lipolysis - drug effects Litchi - chemistry Male Medical sciences Molecular Structure Nitriles - pharmacology Oligonol perilipin Perilipin-1 Pharmacognosy. Homeopathy. Health food Pharmacology. Drug treatments Phenols - pharmacology Phosphoproteins - metabolism primary adipocytes Rats Rats, Wistar Tumor Necrosis Factor-alpha - metabolism |
title | Oligonol, a new lychee fruit-derived low-molecular form of polyphenol, enhances lipolysis in primary rat adipocytes through activation of the ERK1/2 pathway |
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