Differential effects of dietary fatty acids on the regulation of CYP2E1 and protein kinase C in human hepatoma HepG2 cells

We investigated the effects of different fatty acids (FAs) or with different degrees of unsaturation on cytochrome P450 2E1 (CYP2E1) induction and protein kinase C (PKC) activity in human hepatoma HepG2 cells. As the degree of unsaturation increased, the cell survival rate decreased for FAs with 18...

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Veröffentlicht in:Journal of medicinal food 2004-06, Vol.7 (2), p.197-203
Hauptverfasser: Sung, M, Kim, I, Park, M, Whang, Y, Lee, M
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Kim, I
Park, M
Whang, Y
Lee, M
description We investigated the effects of different fatty acids (FAs) or with different degrees of unsaturation on cytochrome P450 2E1 (CYP2E1) induction and protein kinase C (PKC) activity in human hepatoma HepG2 cells. As the degree of unsaturation increased, the cell survival rate decreased for FAs with 18 carbons, but linolenic acid (LNA) or docosahexaenoic acid (DHA) groups were similar even through they have different degrees of unsaturation. Treatment with palmitic acid (PA), oleic acid (OA), linoleic acid (LA), LNA, and DHA resulted in respective cellular FA concentrations of C16:0 (43.1%), C18:1 (18.5%), C18:2 (7.4%), LNA (2.85%), and C22:6 (3.13%), which was highest for the FA that was used as the treatment, indicating that their incorporation within the cell is directly proportional to treatment. After 2 hours of cultivation, the lipid peroxide (LPO) in the DHA group increased 600% compared with control, and was much higher than in the groups treated with the other FAs, with LNA > LA > OA > PA. CYP2E1 induction increased with greater effect as the degree of unsaturation of OA, LA, and DHA increased. PA did not affect PKC activity, but DHA treatment increased PKC activity the most. The effects of LNA and LA were similar, but less than that of DHA, and that of OA was lower still, indicating that activity of PKC is proportional to the degree of unsaturation, and not the configuration of the FA. Increased plasma membrane concentrations of n-3 FA, such as DHA, might exert regulatory effects on PKC by increasing membrane fluidity, causing changes in CYP2E1, elevating levels of LPO, or producing oxidative stress.
doi_str_mv 10.1089/1096620041224157
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As the degree of unsaturation increased, the cell survival rate decreased for FAs with 18 carbons, but linolenic acid (LNA) or docosahexaenoic acid (DHA) groups were similar even through they have different degrees of unsaturation. Treatment with palmitic acid (PA), oleic acid (OA), linoleic acid (LA), LNA, and DHA resulted in respective cellular FA concentrations of C16:0 (43.1%), C18:1 (18.5%), C18:2 (7.4%), LNA (2.85%), and C22:6 (3.13%), which was highest for the FA that was used as the treatment, indicating that their incorporation within the cell is directly proportional to treatment. After 2 hours of cultivation, the lipid peroxide (LPO) in the DHA group increased 600% compared with control, and was much higher than in the groups treated with the other FAs, with LNA &gt; LA &gt; OA &gt; PA. CYP2E1 induction increased with greater effect as the degree of unsaturation of OA, LA, and DHA increased. PA did not affect PKC activity, but DHA treatment increased PKC activity the most. The effects of LNA and LA were similar, but less than that of DHA, and that of OA was lower still, indicating that activity of PKC is proportional to the degree of unsaturation, and not the configuration of the FA. Increased plasma membrane concentrations of n-3 FA, such as DHA, might exert regulatory effects on PKC by increasing membrane fluidity, causing changes in CYP2E1, elevating levels of LPO, or producing oxidative stress.</description><identifier>ISSN: 1096-620X</identifier><identifier>EISSN: 1557-7600</identifier><identifier>DOI: 10.1089/1096620041224157</identifier><identifier>PMID: 15298768</identifier><language>eng</language><publisher>United States</publisher><subject><![CDATA[Carcinoma, Hepatocellular ; cell lines ; Cell Membrane - chemistry ; cell membranes ; cytochrome P-450 ; Cytochrome P-450 CYP2E1 - biosynthesis ; dietary fat ; Dietary Fats, Unsaturated - administration & dosage ; docosahexaenoic acid ; Docosahexaenoic Acids - administration & dosage ; Docosahexaenoic Acids - analysis ; enzyme activity ; Enzyme Induction - drug effects ; Fatty Acids, Omega-3 - analysis ; Fatty Acids, Unsaturated - administration & dosage ; hepatoma ; Humans ; linoleic acid ; Linoleic Acid - administration & dosage ; lipid content ; lipid peroxide ; Lipid Peroxides - analysis ; Liver - enzymology ; Liver Neoplasms ; membrane fluidity ; Membrane Fluidity - drug effects ; oleic acid ; Oleic Acid - administration & dosage ; oxidative stress ; palmitic acid ; Palmitic Acid - administration & dosage ; peroxides ; Peroxides - metabolism ; physiological regulation ; protein kinase C ; Protein Kinase C - metabolism ; Tumor Cells, Cultured]]></subject><ispartof>Journal of medicinal food, 2004-06, Vol.7 (2), p.197-203</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-fe18e9c726e65f04ac7612e0bc1db0aabd0b38a0f14e035efb980db8578221e03</citedby><cites>FETCH-LOGICAL-c319t-fe18e9c726e65f04ac7612e0bc1db0aabd0b38a0f14e035efb980db8578221e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3028,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15298768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sung, M</creatorcontrib><creatorcontrib>Kim, I</creatorcontrib><creatorcontrib>Park, M</creatorcontrib><creatorcontrib>Whang, Y</creatorcontrib><creatorcontrib>Lee, M</creatorcontrib><title>Differential effects of dietary fatty acids on the regulation of CYP2E1 and protein kinase C in human hepatoma HepG2 cells</title><title>Journal of medicinal food</title><addtitle>J Med Food</addtitle><description>We investigated the effects of different fatty acids (FAs) or with different degrees of unsaturation on cytochrome P450 2E1 (CYP2E1) induction and protein kinase C (PKC) activity in human hepatoma HepG2 cells. As the degree of unsaturation increased, the cell survival rate decreased for FAs with 18 carbons, but linolenic acid (LNA) or docosahexaenoic acid (DHA) groups were similar even through they have different degrees of unsaturation. Treatment with palmitic acid (PA), oleic acid (OA), linoleic acid (LA), LNA, and DHA resulted in respective cellular FA concentrations of C16:0 (43.1%), C18:1 (18.5%), C18:2 (7.4%), LNA (2.85%), and C22:6 (3.13%), which was highest for the FA that was used as the treatment, indicating that their incorporation within the cell is directly proportional to treatment. After 2 hours of cultivation, the lipid peroxide (LPO) in the DHA group increased 600% compared with control, and was much higher than in the groups treated with the other FAs, with LNA &gt; LA &gt; OA &gt; PA. CYP2E1 induction increased with greater effect as the degree of unsaturation of OA, LA, and DHA increased. PA did not affect PKC activity, but DHA treatment increased PKC activity the most. The effects of LNA and LA were similar, but less than that of DHA, and that of OA was lower still, indicating that activity of PKC is proportional to the degree of unsaturation, and not the configuration of the FA. Increased plasma membrane concentrations of n-3 FA, such as DHA, might exert regulatory effects on PKC by increasing membrane fluidity, causing changes in CYP2E1, elevating levels of LPO, or producing oxidative stress.</description><subject>Carcinoma, Hepatocellular</subject><subject>cell lines</subject><subject>Cell Membrane - chemistry</subject><subject>cell membranes</subject><subject>cytochrome P-450</subject><subject>Cytochrome P-450 CYP2E1 - biosynthesis</subject><subject>dietary fat</subject><subject>Dietary Fats, Unsaturated - administration &amp; dosage</subject><subject>docosahexaenoic acid</subject><subject>Docosahexaenoic Acids - administration &amp; dosage</subject><subject>Docosahexaenoic Acids - analysis</subject><subject>enzyme activity</subject><subject>Enzyme Induction - drug effects</subject><subject>Fatty Acids, Omega-3 - analysis</subject><subject>Fatty Acids, Unsaturated - administration &amp; dosage</subject><subject>hepatoma</subject><subject>Humans</subject><subject>linoleic acid</subject><subject>Linoleic Acid - administration &amp; dosage</subject><subject>lipid content</subject><subject>lipid peroxide</subject><subject>Lipid Peroxides - analysis</subject><subject>Liver - enzymology</subject><subject>Liver Neoplasms</subject><subject>membrane fluidity</subject><subject>Membrane Fluidity - drug effects</subject><subject>oleic acid</subject><subject>Oleic Acid - administration &amp; dosage</subject><subject>oxidative stress</subject><subject>palmitic acid</subject><subject>Palmitic Acid - administration &amp; dosage</subject><subject>peroxides</subject><subject>Peroxides - metabolism</subject><subject>physiological regulation</subject><subject>protein kinase C</subject><subject>Protein Kinase C - metabolism</subject><subject>Tumor Cells, Cultured</subject><issn>1096-620X</issn><issn>1557-7600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkM1r3jAMxs1YWT-2-06dT72lk-zEdo7jbdcWCitshe0UlERu3eXjXewcur9-Lu8Lg16kR9JPQjxCfEQ4R3D1Z4TaGAVQolIlVvaNOMKqsoU1AG-zzuMiz38eiuMYnwBAl9q-E4dYqdpZ447E34vgPS88pUCD5Ky7FOXsZR840fIsPaX0LKkLfW5PMj2yXPhhHSiFXGZw8-tOXaKkqZfbZU4cJvk7TBRZbmTWj-tIOfKW0jySvObtlZIdD0N8Lw48DZE_7POJuP96-WNzXdx-u7rZfLktOo11Kjyj47qzyrCpPJTUWYOKoe2wb4Go7aHVjsBjyaAr9m3toG9dZZ1SmFsn4mx3N7_3Z-WYmjHElw9o4nmNjTHWags6g7ADu2WOcWHfbJcwZhMahObF7-a133nldH97bUfu_y_sDc7Apx3gaW7oYQmxuf-uADVA7Qxirf8BaBqEBw</recordid><startdate>20040601</startdate><enddate>20040601</enddate><creator>Sung, M</creator><creator>Kim, I</creator><creator>Park, M</creator><creator>Whang, Y</creator><creator>Lee, M</creator><scope>FBQ</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>20040601</creationdate><title>Differential effects of dietary fatty acids on the regulation of CYP2E1 and protein kinase C in human hepatoma HepG2 cells</title><author>Sung, M ; Kim, I ; Park, M ; Whang, Y ; Lee, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-fe18e9c726e65f04ac7612e0bc1db0aabd0b38a0f14e035efb980db8578221e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Carcinoma, Hepatocellular</topic><topic>cell lines</topic><topic>Cell Membrane - chemistry</topic><topic>cell membranes</topic><topic>cytochrome P-450</topic><topic>Cytochrome P-450 CYP2E1 - biosynthesis</topic><topic>dietary fat</topic><topic>Dietary Fats, Unsaturated - administration &amp; dosage</topic><topic>docosahexaenoic acid</topic><topic>Docosahexaenoic Acids - administration &amp; dosage</topic><topic>Docosahexaenoic Acids - analysis</topic><topic>enzyme activity</topic><topic>Enzyme Induction - drug effects</topic><topic>Fatty Acids, Omega-3 - analysis</topic><topic>Fatty Acids, Unsaturated - administration &amp; dosage</topic><topic>hepatoma</topic><topic>Humans</topic><topic>linoleic acid</topic><topic>Linoleic Acid - administration &amp; dosage</topic><topic>lipid content</topic><topic>lipid peroxide</topic><topic>Lipid Peroxides - analysis</topic><topic>Liver - enzymology</topic><topic>Liver Neoplasms</topic><topic>membrane fluidity</topic><topic>Membrane Fluidity - drug effects</topic><topic>oleic acid</topic><topic>Oleic Acid - administration &amp; dosage</topic><topic>oxidative stress</topic><topic>palmitic acid</topic><topic>Palmitic Acid - administration &amp; dosage</topic><topic>peroxides</topic><topic>Peroxides - metabolism</topic><topic>physiological regulation</topic><topic>protein kinase C</topic><topic>Protein Kinase C - metabolism</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sung, M</creatorcontrib><creatorcontrib>Kim, I</creatorcontrib><creatorcontrib>Park, M</creatorcontrib><creatorcontrib>Whang, Y</creatorcontrib><creatorcontrib>Lee, M</creatorcontrib><collection>AGRIS</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>Journal of medicinal food</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sung, M</au><au>Kim, I</au><au>Park, M</au><au>Whang, Y</au><au>Lee, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential effects of dietary fatty acids on the regulation of CYP2E1 and protein kinase C in human hepatoma HepG2 cells</atitle><jtitle>Journal of medicinal food</jtitle><addtitle>J Med Food</addtitle><date>2004-06-01</date><risdate>2004</risdate><volume>7</volume><issue>2</issue><spage>197</spage><epage>203</epage><pages>197-203</pages><issn>1096-620X</issn><eissn>1557-7600</eissn><abstract>We investigated the effects of different fatty acids (FAs) or with different degrees of unsaturation on cytochrome P450 2E1 (CYP2E1) induction and protein kinase C (PKC) activity in human hepatoma HepG2 cells. As the degree of unsaturation increased, the cell survival rate decreased for FAs with 18 carbons, but linolenic acid (LNA) or docosahexaenoic acid (DHA) groups were similar even through they have different degrees of unsaturation. Treatment with palmitic acid (PA), oleic acid (OA), linoleic acid (LA), LNA, and DHA resulted in respective cellular FA concentrations of C16:0 (43.1%), C18:1 (18.5%), C18:2 (7.4%), LNA (2.85%), and C22:6 (3.13%), which was highest for the FA that was used as the treatment, indicating that their incorporation within the cell is directly proportional to treatment. After 2 hours of cultivation, the lipid peroxide (LPO) in the DHA group increased 600% compared with control, and was much higher than in the groups treated with the other FAs, with LNA &gt; LA &gt; OA &gt; PA. CYP2E1 induction increased with greater effect as the degree of unsaturation of OA, LA, and DHA increased. PA did not affect PKC activity, but DHA treatment increased PKC activity the most. The effects of LNA and LA were similar, but less than that of DHA, and that of OA was lower still, indicating that activity of PKC is proportional to the degree of unsaturation, and not the configuration of the FA. Increased plasma membrane concentrations of n-3 FA, such as DHA, might exert regulatory effects on PKC by increasing membrane fluidity, causing changes in CYP2E1, elevating levels of LPO, or producing oxidative stress.</abstract><cop>United States</cop><pmid>15298768</pmid><doi>10.1089/1096620041224157</doi><tpages>7</tpages></addata></record>
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subjects Carcinoma, Hepatocellular
cell lines
Cell Membrane - chemistry
cell membranes
cytochrome P-450
Cytochrome P-450 CYP2E1 - biosynthesis
dietary fat
Dietary Fats, Unsaturated - administration & dosage
docosahexaenoic acid
Docosahexaenoic Acids - administration & dosage
Docosahexaenoic Acids - analysis
enzyme activity
Enzyme Induction - drug effects
Fatty Acids, Omega-3 - analysis
Fatty Acids, Unsaturated - administration & dosage
hepatoma
Humans
linoleic acid
Linoleic Acid - administration & dosage
lipid content
lipid peroxide
Lipid Peroxides - analysis
Liver - enzymology
Liver Neoplasms
membrane fluidity
Membrane Fluidity - drug effects
oleic acid
Oleic Acid - administration & dosage
oxidative stress
palmitic acid
Palmitic Acid - administration & dosage
peroxides
Peroxides - metabolism
physiological regulation
protein kinase C
Protein Kinase C - metabolism
Tumor Cells, Cultured
title Differential effects of dietary fatty acids on the regulation of CYP2E1 and protein kinase C in human hepatoma HepG2 cells
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