Antioxidative and anti-inflammatory effects of Saururus chinensis methanol extract in RAW 264.7 macrophages

Natural products are known to be sources of bioactive components exerting antioxidative and anti-inflammatory activities. We evaluated the suppressive effects of the methanol extract (0-45 microg/mL) of the aerial parts of Saururus chinensis (Lour.) Baill (Saururaceae) on lipopolysaccharide (LPS)-st...

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Veröffentlicht in:Journal of medicinal food 2005-06, Vol.8 (2), p.190-197
Hauptverfasser: Cho, H.Y, Cho, C.W, Song, Y.S
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Cho, C.W
Song, Y.S
description Natural products are known to be sources of bioactive components exerting antioxidative and anti-inflammatory activities. We evaluated the suppressive effects of the methanol extract (0-45 microg/mL) of the aerial parts of Saururus chinensis (Lour.) Baill (Saururaceae) on lipopolysaccharide (LPS)-stimulated nitric oxide (NO) production and oxidative stress buildup in the RAW 264.7 murine macrophages. Treatment of RAW 264.7 cells with S. chinensis methanol extract (SME) significantly reduced LPS-stimulated NO production in a concentration-dependent manner. Treatment with SME reduced thiobarbituric acid-reactive substances accumulation and enhanced glutathione levels and activities of antioxidative enzymes, including superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase, in LPS-stimulated macrophages compared with LPS-only treated cells. Expression of inducible NO synthase (iNOS) mRNA was also suppressed in SMEtreated cells. The specific DNA binding activities of nuclear factor kappaB (NFkappaB) on nuclear extracts from SME-treated cells were significantly suppressed. These results suggest that SME has antioxidative and anti-inflammatory activities by enhancing antioxidative defense systems and suppressing NO production via the down-regulation of iNOS expression and NFkappaB activity.
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We evaluated the suppressive effects of the methanol extract (0-45 microg/mL) of the aerial parts of Saururus chinensis (Lour.) Baill (Saururaceae) on lipopolysaccharide (LPS)-stimulated nitric oxide (NO) production and oxidative stress buildup in the RAW 264.7 murine macrophages. Treatment of RAW 264.7 cells with S. chinensis methanol extract (SME) significantly reduced LPS-stimulated NO production in a concentration-dependent manner. Treatment with SME reduced thiobarbituric acid-reactive substances accumulation and enhanced glutathione levels and activities of antioxidative enzymes, including superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase, in LPS-stimulated macrophages compared with LPS-only treated cells. Expression of inducible NO synthase (iNOS) mRNA was also suppressed in SMEtreated cells. The specific DNA binding activities of nuclear factor kappaB (NFkappaB) on nuclear extracts from SME-treated cells were significantly suppressed. 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We evaluated the suppressive effects of the methanol extract (0-45 microg/mL) of the aerial parts of Saururus chinensis (Lour.) Baill (Saururaceae) on lipopolysaccharide (LPS)-stimulated nitric oxide (NO) production and oxidative stress buildup in the RAW 264.7 murine macrophages. Treatment of RAW 264.7 cells with S. chinensis methanol extract (SME) significantly reduced LPS-stimulated NO production in a concentration-dependent manner. Treatment with SME reduced thiobarbituric acid-reactive substances accumulation and enhanced glutathione levels and activities of antioxidative enzymes, including superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase, in LPS-stimulated macrophages compared with LPS-only treated cells. Expression of inducible NO synthase (iNOS) mRNA was also suppressed in SMEtreated cells. The specific DNA binding activities of nuclear factor kappaB (NFkappaB) on nuclear extracts from SME-treated cells were significantly suppressed. These results suggest that SME has antioxidative and anti-inflammatory activities by enhancing antioxidative defense systems and suppressing NO production via the down-regulation of iNOS expression and NFkappaB activity.</description><subject>aerial parts</subject><subject>Animals</subject><subject>anti-inflammatory activity</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>antioxidant activity</subject><subject>antioxidants</subject><subject>Antioxidants - pharmacology</subject><subject>Cells, Cultured</subject><subject>cytokines</subject><subject>Dose-Response Relationship, Drug</subject><subject>extraction</subject><subject>free radicals</subject><subject>invasive species</subject><subject>lipid peroxidation</subject><subject>Lipid Peroxidation - drug effects</subject><subject>Lipopolysaccharides</subject><subject>Liver - drug effects</subject><subject>Liver - enzymology</subject><subject>macrophages</subject><subject>Macrophages - drug effects</subject><subject>methanol</subject><subject>Mice</subject><subject>NF-kappa B - metabolism</subject><subject>nitric oxide</subject><subject>Nitric Oxide - biosynthesis</subject><subject>Nitric Oxide Synthase - metabolism</subject><subject>Nitric Oxide Synthase Type II</subject><subject>oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>plant extracts</subject><subject>Plant Extracts - pharmacology</subject><subject>RNA, Messenger - metabolism</subject><subject>Saururaceae - chemistry</subject><subject>Saururus</subject><subject>Thiobarbituric Acid Reactive Substances - analysis</subject><subject>Thiobarbituric Acid Reactive Substances - metabolism</subject><subject>thiobarbituric acid-reactive substances</subject><subject>weeds</subject><issn>1096-620X</issn><issn>1557-7600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1rHDEMhk1JaL567bH1qbeZyh6P7TkuIW0KC4EmIb0ZjcfOOp2Pje0Nyb-vwy4U8SIdHgnxEPKZQc1Ad9-fJl9zgLbWNevgAzllbasqJQGOygydrCSHPyfkLKUnAGhEoz6SEyYZUyWn5O9qzmF5DQPm8OIozkNJDlWY_YjThHmJb9R572xOdPH0FnexVKJ2E2Y3p5Do5PIG52Wk7jVHtJmGmf5ePVAuRa3ohDYu2w0-unRBjj2OyX069HNy_-Pq7vK6Wt_8_HW5Wle20U2upMVedKict3pAofqGo5Oi5byTKLSUHvoBBEPrpXSdkryXylltJdN-4Lw5J9_2d7dxed65lM0UknXjiLNbdslI3XLohChgvQfLiylF5802hgnjm2Fg3vWaote86zXaFL1l4cvh8q6f3PAfP_gswNc94HEx-BhDMve3HFgDDJhqlWr-Aax9gIc</recordid><startdate>20050601</startdate><enddate>20050601</enddate><creator>Cho, H.Y</creator><creator>Cho, C.W</creator><creator>Song, Y.S</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>20050601</creationdate><title>Antioxidative and anti-inflammatory effects of Saururus chinensis methanol extract in RAW 264.7 macrophages</title><author>Cho, H.Y ; Cho, C.W ; Song, Y.S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c383t-6cab49a7efc8da47b32ae6452296a4866f0bd041acf66e9762b67ec8c618fd223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>aerial parts</topic><topic>Animals</topic><topic>anti-inflammatory activity</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>antioxidant activity</topic><topic>antioxidants</topic><topic>Antioxidants - pharmacology</topic><topic>Cells, Cultured</topic><topic>cytokines</topic><topic>Dose-Response Relationship, Drug</topic><topic>extraction</topic><topic>free radicals</topic><topic>invasive species</topic><topic>lipid peroxidation</topic><topic>Lipid Peroxidation - drug effects</topic><topic>Lipopolysaccharides</topic><topic>Liver - drug effects</topic><topic>Liver - enzymology</topic><topic>macrophages</topic><topic>Macrophages - drug effects</topic><topic>methanol</topic><topic>Mice</topic><topic>NF-kappa B - metabolism</topic><topic>nitric oxide</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Nitric Oxide Synthase - metabolism</topic><topic>Nitric Oxide Synthase Type II</topic><topic>oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>plant extracts</topic><topic>Plant Extracts - pharmacology</topic><topic>RNA, Messenger - metabolism</topic><topic>Saururaceae - chemistry</topic><topic>Saururus</topic><topic>Thiobarbituric Acid Reactive Substances - analysis</topic><topic>Thiobarbituric Acid Reactive Substances - metabolism</topic><topic>thiobarbituric acid-reactive substances</topic><topic>weeds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cho, H.Y</creatorcontrib><creatorcontrib>Cho, C.W</creatorcontrib><creatorcontrib>Song, Y.S</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>Cho, H.Y</au><au>Cho, C.W</au><au>Song, Y.S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidative and anti-inflammatory effects of Saururus chinensis methanol extract in RAW 264.7 macrophages</atitle><jtitle>Journal of medicinal food</jtitle><addtitle>J Med Food</addtitle><date>2005-06-01</date><risdate>2005</risdate><volume>8</volume><issue>2</issue><spage>190</spage><epage>197</epage><pages>190-197</pages><issn>1096-620X</issn><eissn>1557-7600</eissn><abstract>Natural products are known to be sources of bioactive components exerting antioxidative and anti-inflammatory activities. We evaluated the suppressive effects of the methanol extract (0-45 microg/mL) of the aerial parts of Saururus chinensis (Lour.) Baill (Saururaceae) on lipopolysaccharide (LPS)-stimulated nitric oxide (NO) production and oxidative stress buildup in the RAW 264.7 murine macrophages. Treatment of RAW 264.7 cells with S. chinensis methanol extract (SME) significantly reduced LPS-stimulated NO production in a concentration-dependent manner. Treatment with SME reduced thiobarbituric acid-reactive substances accumulation and enhanced glutathione levels and activities of antioxidative enzymes, including superoxide dismutase, catalase, glutathione peroxidase, and glutathione reductase, in LPS-stimulated macrophages compared with LPS-only treated cells. Expression of inducible NO synthase (iNOS) mRNA was also suppressed in SMEtreated cells. The specific DNA binding activities of nuclear factor kappaB (NFkappaB) on nuclear extracts from SME-treated cells were significantly suppressed. These results suggest that SME has antioxidative and anti-inflammatory activities by enhancing antioxidative defense systems and suppressing NO production via the down-regulation of iNOS expression and NFkappaB activity.</abstract><cop>United States</cop><pmid>16117611</pmid><doi>10.1089/jmf.2005.8.190</doi><tpages>8</tpages></addata></record>
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subjects aerial parts
Animals
anti-inflammatory activity
Anti-Inflammatory Agents - pharmacology
antioxidant activity
antioxidants
Antioxidants - pharmacology
Cells, Cultured
cytokines
Dose-Response Relationship, Drug
extraction
free radicals
invasive species
lipid peroxidation
Lipid Peroxidation - drug effects
Lipopolysaccharides
Liver - drug effects
Liver - enzymology
macrophages
Macrophages - drug effects
methanol
Mice
NF-kappa B - metabolism
nitric oxide
Nitric Oxide - biosynthesis
Nitric Oxide Synthase - metabolism
Nitric Oxide Synthase Type II
oxidative stress
Oxidative Stress - drug effects
plant extracts
Plant Extracts - pharmacology
RNA, Messenger - metabolism
Saururaceae - chemistry
Saururus
Thiobarbituric Acid Reactive Substances - analysis
Thiobarbituric Acid Reactive Substances - metabolism
thiobarbituric acid-reactive substances
weeds
title Antioxidative and anti-inflammatory effects of Saururus chinensis methanol extract in RAW 264.7 macrophages
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