Loading…
On the Molecular Pharmacology of Resveratrol on Oxidative Burst Inhibition in Professional Phagocytes
Resveratrol—3,5,4′-trihydroxystilbene—possesses antioxidant activities in vitro. It dose-dependently inhibited the generation of peroxyl, hydroxyl, peroxides, and lipid peroxidation products in cell free systems. Oxidative burst of whole human blood stimulated with PMA, fMLP, OpZ, and A23187 was inh...
Saved in:
Published in: | Oxidative medicine and cellular longevity 2014-01, Vol.2014 (2014), p.1-9 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33 |
---|---|
cites | cdi_FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33 |
container_end_page | 9 |
container_issue | 2014 |
container_start_page | 1 |
container_title | Oxidative medicine and cellular longevity |
container_volume | 2014 |
creator | Harmatha, Juraj Šmidrkal, Jan Lojek, Antonin Ciz, Milan Ambrozova, Gabriela Perečko, Tomáš Jancinova, Viera Drabikova, Katarina Nosál’, Radomír Pekarova, Michaela |
description | Resveratrol—3,5,4′-trihydroxystilbene—possesses antioxidant activities in vitro. It dose-dependently inhibited the generation of peroxyl, hydroxyl, peroxides, and lipid peroxidation products in cell free systems. Oxidative burst of whole human blood stimulated with PMA, fMLP, OpZ, and A23187 was inhibited in a concentration-dependent way, indicating suppression of both receptor and nonreceptor activated chemiluminescence by resveratrol. Results from isolated human neutrophils revealed that resveratrol was active extracellularly as well as intracellularly in inhibiting the generation of reactive oxygen species. Liberation of ATP and analysis of apoptosis showed that in the concentration of 100 μM, resveratrol did not change the viability and integrity of isolated neutrophils. Western blot analysis documented that resveratrol in concentrations of 10 and 100 μM significantly decreased PMA-induced phosphorylation of PKC α/βII. Dose-dependent inhibition of nitrite production and iNOS protein expression in RAW 264.7 cells indicated possible interference of resveratrol with reactive nitrogen radical generation in professional phagocytes. The results suggest that resveratrol represents an effective naturally occurring substance with potent pharmacological effect on oxidative burst of human neutrophils and nitric oxide production by macrophages. It should be further investigated for its pharmacological activity against oxidative stress in ischaemia reperfusion, inflammation, and other pathological conditions, particularly neoplasia. |
doi_str_mv | 10.1155/2014/706269 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3942095</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A417105663</galeid><sourcerecordid>A417105663</sourcerecordid><originalsourceid>FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33</originalsourceid><addsrcrecordid>eNqNkV1rFDEUhgex2A-98l4C3lm2PfmcyY3QlqqFyhbR65DJnOxEZiclmV27_94so0u98yoJ78NzDnmr6i2FC0qlvGRAxWUNiin9ojqhWrAFaC1eHu4Ax9Vpzj8BFGeCvqqOmVA1U7w5qXA5kqlH8jUO6DaDTeSht2ltXRziakeiJ98wbzHZKcWBxJEsn0Jnp7BFcr1JeSJ3Yx_aMIUShZE8pOgx5_Kyw960im43YX5dHXk7ZHzz5zyrfny6_X7zZXG__Hx3c3W_cJLzadHQBpwTHWivlfItAy4lA8C2E1Z0ddtwrGvbIEgL1NvWi5KxVqN0giPnZ9XH2fu4adfYORynZAfzmMLapp2JNph_kzH0ZhW3hpefAi2L4P0sWNkBTRh9LJhbh-zMlaA1BanUfsz5TLkUc07oDxMomH0nZt-JmTsp9LvnSx3YvyUU4MMM9GHs7K_wfzYsCHr7DBY1aM5_A63mn0s</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>On the Molecular Pharmacology of Resveratrol on Oxidative Burst Inhibition in Professional Phagocytes</title><source>Publicly Available Content Database</source><source>Wiley-Blackwell Open Access Titles(OpenAccess)</source><creator>Harmatha, Juraj ; Šmidrkal, Jan ; Lojek, Antonin ; Ciz, Milan ; Ambrozova, Gabriela ; Perečko, Tomáš ; Jancinova, Viera ; Drabikova, Katarina ; Nosál’, Radomír ; Pekarova, Michaela</creator><contributor>Angeloni, Cristina</contributor><creatorcontrib>Harmatha, Juraj ; Šmidrkal, Jan ; Lojek, Antonin ; Ciz, Milan ; Ambrozova, Gabriela ; Perečko, Tomáš ; Jancinova, Viera ; Drabikova, Katarina ; Nosál’, Radomír ; Pekarova, Michaela ; Angeloni, Cristina</creatorcontrib><description>Resveratrol—3,5,4′-trihydroxystilbene—possesses antioxidant activities in vitro. It dose-dependently inhibited the generation of peroxyl, hydroxyl, peroxides, and lipid peroxidation products in cell free systems. Oxidative burst of whole human blood stimulated with PMA, fMLP, OpZ, and A23187 was inhibited in a concentration-dependent way, indicating suppression of both receptor and nonreceptor activated chemiluminescence by resveratrol. Results from isolated human neutrophils revealed that resveratrol was active extracellularly as well as intracellularly in inhibiting the generation of reactive oxygen species. Liberation of ATP and analysis of apoptosis showed that in the concentration of 100 μM, resveratrol did not change the viability and integrity of isolated neutrophils. Western blot analysis documented that resveratrol in concentrations of 10 and 100 μM significantly decreased PMA-induced phosphorylation of PKC α/βII. Dose-dependent inhibition of nitrite production and iNOS protein expression in RAW 264.7 cells indicated possible interference of resveratrol with reactive nitrogen radical generation in professional phagocytes. The results suggest that resveratrol represents an effective naturally occurring substance with potent pharmacological effect on oxidative burst of human neutrophils and nitric oxide production by macrophages. It should be further investigated for its pharmacological activity against oxidative stress in ischaemia reperfusion, inflammation, and other pathological conditions, particularly neoplasia.</description><identifier>ISSN: 1942-0900</identifier><identifier>EISSN: 1942-0994</identifier><identifier>DOI: 10.1155/2014/706269</identifier><identifier>PMID: 24672638</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Cell Line ; Cell Separation ; Cell Survival - drug effects ; Free Radical Scavengers - metabolism ; Health aspects ; Humans ; Lipid Peroxidation - drug effects ; Luminescent Measurements ; Luminol - metabolism ; Mice ; Neutrophils - drug effects ; Neutrophils - metabolism ; Nitric Oxide Synthase Type II - metabolism ; Nitrites - metabolism ; Oxidative stress ; Phagocytes ; Phagocytes - drug effects ; Phagocytes - enzymology ; Phagocytes - metabolism ; Properties ; Protein Kinases - metabolism ; Reactive Oxygen Species - metabolism ; Respiratory Burst - drug effects ; Resveratrol ; Stilbenes - pharmacology ; Tetradecanoylphorbol Acetate - pharmacology ; Thiobarbituric Acid Reactive Substances - metabolism</subject><ispartof>Oxidative medicine and cellular longevity, 2014-01, Vol.2014 (2014), p.1-9</ispartof><rights>Copyright © 2014 Radomír Nosáľ et al.</rights><rights>COPYRIGHT 2014 John Wiley & Sons, Inc.</rights><rights>Copyright © 2014 Radomír Nosáľ et al. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33</citedby><cites>FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24672638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Angeloni, Cristina</contributor><creatorcontrib>Harmatha, Juraj</creatorcontrib><creatorcontrib>Šmidrkal, Jan</creatorcontrib><creatorcontrib>Lojek, Antonin</creatorcontrib><creatorcontrib>Ciz, Milan</creatorcontrib><creatorcontrib>Ambrozova, Gabriela</creatorcontrib><creatorcontrib>Perečko, Tomáš</creatorcontrib><creatorcontrib>Jancinova, Viera</creatorcontrib><creatorcontrib>Drabikova, Katarina</creatorcontrib><creatorcontrib>Nosál’, Radomír</creatorcontrib><creatorcontrib>Pekarova, Michaela</creatorcontrib><title>On the Molecular Pharmacology of Resveratrol on Oxidative Burst Inhibition in Professional Phagocytes</title><title>Oxidative medicine and cellular longevity</title><addtitle>Oxid Med Cell Longev</addtitle><description>Resveratrol—3,5,4′-trihydroxystilbene—possesses antioxidant activities in vitro. It dose-dependently inhibited the generation of peroxyl, hydroxyl, peroxides, and lipid peroxidation products in cell free systems. Oxidative burst of whole human blood stimulated with PMA, fMLP, OpZ, and A23187 was inhibited in a concentration-dependent way, indicating suppression of both receptor and nonreceptor activated chemiluminescence by resveratrol. Results from isolated human neutrophils revealed that resveratrol was active extracellularly as well as intracellularly in inhibiting the generation of reactive oxygen species. Liberation of ATP and analysis of apoptosis showed that in the concentration of 100 μM, resveratrol did not change the viability and integrity of isolated neutrophils. Western blot analysis documented that resveratrol in concentrations of 10 and 100 μM significantly decreased PMA-induced phosphorylation of PKC α/βII. Dose-dependent inhibition of nitrite production and iNOS protein expression in RAW 264.7 cells indicated possible interference of resveratrol with reactive nitrogen radical generation in professional phagocytes. The results suggest that resveratrol represents an effective naturally occurring substance with potent pharmacological effect on oxidative burst of human neutrophils and nitric oxide production by macrophages. It should be further investigated for its pharmacological activity against oxidative stress in ischaemia reperfusion, inflammation, and other pathological conditions, particularly neoplasia.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Cell Separation</subject><subject>Cell Survival - drug effects</subject><subject>Free Radical Scavengers - metabolism</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Luminescent Measurements</subject><subject>Luminol - metabolism</subject><subject>Mice</subject><subject>Neutrophils - drug effects</subject><subject>Neutrophils - metabolism</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Nitrites - metabolism</subject><subject>Oxidative stress</subject><subject>Phagocytes</subject><subject>Phagocytes - drug effects</subject><subject>Phagocytes - enzymology</subject><subject>Phagocytes - metabolism</subject><subject>Properties</subject><subject>Protein Kinases - metabolism</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Respiratory Burst - drug effects</subject><subject>Resveratrol</subject><subject>Stilbenes - pharmacology</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>Thiobarbituric Acid Reactive Substances - metabolism</subject><issn>1942-0900</issn><issn>1942-0994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkV1rFDEUhgex2A-98l4C3lm2PfmcyY3QlqqFyhbR65DJnOxEZiclmV27_94so0u98yoJ78NzDnmr6i2FC0qlvGRAxWUNiin9ojqhWrAFaC1eHu4Ax9Vpzj8BFGeCvqqOmVA1U7w5qXA5kqlH8jUO6DaDTeSht2ltXRziakeiJ98wbzHZKcWBxJEsn0Jnp7BFcr1JeSJ3Yx_aMIUShZE8pOgx5_Kyw960im43YX5dHXk7ZHzz5zyrfny6_X7zZXG__Hx3c3W_cJLzadHQBpwTHWivlfItAy4lA8C2E1Z0ddtwrGvbIEgL1NvWi5KxVqN0giPnZ9XH2fu4adfYORynZAfzmMLapp2JNph_kzH0ZhW3hpefAi2L4P0sWNkBTRh9LJhbh-zMlaA1BanUfsz5TLkUc07oDxMomH0nZt-JmTsp9LvnSx3YvyUU4MMM9GHs7K_wfzYsCHr7DBY1aM5_A63mn0s</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Harmatha, Juraj</creator><creator>Šmidrkal, Jan</creator><creator>Lojek, Antonin</creator><creator>Ciz, Milan</creator><creator>Ambrozova, Gabriela</creator><creator>Perečko, Tomáš</creator><creator>Jancinova, Viera</creator><creator>Drabikova, Katarina</creator><creator>Nosál’, Radomír</creator><creator>Pekarova, Michaela</creator><general>Hindawi Publishing Corporation</general><general>John Wiley & Sons, Inc</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>5PM</scope></search><sort><creationdate>20140101</creationdate><title>On the Molecular Pharmacology of Resveratrol on Oxidative Burst Inhibition in Professional Phagocytes</title><author>Harmatha, Juraj ; Šmidrkal, Jan ; Lojek, Antonin ; Ciz, Milan ; Ambrozova, Gabriela ; Perečko, Tomáš ; Jancinova, Viera ; Drabikova, Katarina ; Nosál’, Radomír ; Pekarova, Michaela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Cell Separation</topic><topic>Cell Survival - drug effects</topic><topic>Free Radical Scavengers - metabolism</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Luminescent Measurements</topic><topic>Luminol - metabolism</topic><topic>Mice</topic><topic>Neutrophils - drug effects</topic><topic>Neutrophils - metabolism</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Nitrites - metabolism</topic><topic>Oxidative stress</topic><topic>Phagocytes</topic><topic>Phagocytes - drug effects</topic><topic>Phagocytes - enzymology</topic><topic>Phagocytes - metabolism</topic><topic>Properties</topic><topic>Protein Kinases - metabolism</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Respiratory Burst - drug effects</topic><topic>Resveratrol</topic><topic>Stilbenes - pharmacology</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>Thiobarbituric Acid Reactive Substances - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Harmatha, Juraj</creatorcontrib><creatorcontrib>Šmidrkal, Jan</creatorcontrib><creatorcontrib>Lojek, Antonin</creatorcontrib><creatorcontrib>Ciz, Milan</creatorcontrib><creatorcontrib>Ambrozova, Gabriela</creatorcontrib><creatorcontrib>Perečko, Tomáš</creatorcontrib><creatorcontrib>Jancinova, Viera</creatorcontrib><creatorcontrib>Drabikova, Katarina</creatorcontrib><creatorcontrib>Nosál’, Radomír</creatorcontrib><creatorcontrib>Pekarova, Michaela</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Oxidative medicine and cellular longevity</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Harmatha, Juraj</au><au>Šmidrkal, Jan</au><au>Lojek, Antonin</au><au>Ciz, Milan</au><au>Ambrozova, Gabriela</au><au>Perečko, Tomáš</au><au>Jancinova, Viera</au><au>Drabikova, Katarina</au><au>Nosál’, Radomír</au><au>Pekarova, Michaela</au><au>Angeloni, Cristina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>On the Molecular Pharmacology of Resveratrol on Oxidative Burst Inhibition in Professional Phagocytes</atitle><jtitle>Oxidative medicine and cellular longevity</jtitle><addtitle>Oxid Med Cell Longev</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>2014</volume><issue>2014</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>1942-0900</issn><eissn>1942-0994</eissn><abstract>Resveratrol—3,5,4′-trihydroxystilbene—possesses antioxidant activities in vitro. It dose-dependently inhibited the generation of peroxyl, hydroxyl, peroxides, and lipid peroxidation products in cell free systems. Oxidative burst of whole human blood stimulated with PMA, fMLP, OpZ, and A23187 was inhibited in a concentration-dependent way, indicating suppression of both receptor and nonreceptor activated chemiluminescence by resveratrol. Results from isolated human neutrophils revealed that resveratrol was active extracellularly as well as intracellularly in inhibiting the generation of reactive oxygen species. Liberation of ATP and analysis of apoptosis showed that in the concentration of 100 μM, resveratrol did not change the viability and integrity of isolated neutrophils. Western blot analysis documented that resveratrol in concentrations of 10 and 100 μM significantly decreased PMA-induced phosphorylation of PKC α/βII. Dose-dependent inhibition of nitrite production and iNOS protein expression in RAW 264.7 cells indicated possible interference of resveratrol with reactive nitrogen radical generation in professional phagocytes. The results suggest that resveratrol represents an effective naturally occurring substance with potent pharmacological effect on oxidative burst of human neutrophils and nitric oxide production by macrophages. It should be further investigated for its pharmacological activity against oxidative stress in ischaemia reperfusion, inflammation, and other pathological conditions, particularly neoplasia.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>24672638</pmid><doi>10.1155/2014/706269</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1942-0900 |
ispartof | Oxidative medicine and cellular longevity, 2014-01, Vol.2014 (2014), p.1-9 |
issn | 1942-0900 1942-0994 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3942095 |
source | Publicly Available Content Database; Wiley-Blackwell Open Access Titles(OpenAccess) |
subjects | Animals Cell Line Cell Separation Cell Survival - drug effects Free Radical Scavengers - metabolism Health aspects Humans Lipid Peroxidation - drug effects Luminescent Measurements Luminol - metabolism Mice Neutrophils - drug effects Neutrophils - metabolism Nitric Oxide Synthase Type II - metabolism Nitrites - metabolism Oxidative stress Phagocytes Phagocytes - drug effects Phagocytes - enzymology Phagocytes - metabolism Properties Protein Kinases - metabolism Reactive Oxygen Species - metabolism Respiratory Burst - drug effects Resveratrol Stilbenes - pharmacology Tetradecanoylphorbol Acetate - pharmacology Thiobarbituric Acid Reactive Substances - metabolism |
title | On the Molecular Pharmacology of Resveratrol on Oxidative Burst Inhibition in Professional Phagocytes |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T09%3A50%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=On%20the%20Molecular%20Pharmacology%20of%20Resveratrol%20on%20Oxidative%20Burst%20Inhibition%20in%20Professional%20Phagocytes&rft.jtitle=Oxidative%20medicine%20and%20cellular%20longevity&rft.au=Harmatha,%20Juraj&rft.date=2014-01-01&rft.volume=2014&rft.issue=2014&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=1942-0900&rft.eissn=1942-0994&rft_id=info:doi/10.1155/2014/706269&rft_dat=%3Cgale_pubme%3EA417105663%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c533t-8180cc4d09f966fb20355200ebd4a4d7b83e77a8e05a01fabf40eb2b9e5c43e33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/24672638&rft_galeid=A417105663&rfr_iscdi=true |