Inhibitory effect of obovatol on nitric oxide production and activation of NF-kappaB/MAP kinases in lipopolysaccharide-treated RAW 264.7cells
The components of Magnolia obovata are known to have many pharmacological activities. In this study, we investigated the effects of obovatol, a neolignan compound isolated from the leaves of M. obovata, on nitric oxide (NO) production and NF-kappaB activity in lipopolysaccharide (LPS)-activated RAW...
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Veröffentlicht in: | European journal of pharmacology 2007-02, Vol.556 (1-3), p.181-189 |
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creator | Choi, Myoung Suk Lee, Seung Ho Cho, Ho Seong Kim, Youngsoo Yun, Yeo Pyo Jung, Hai Young Jung, Jae Kyoung Lee, Bum Chun Pyo, Hyeong Bae Hong, Jin Tae |
description | The components of Magnolia obovata are known to have many pharmacological activities. In this study, we investigated the effects of obovatol, a neolignan compound isolated from the leaves of M. obovata, on nitric oxide (NO) production and NF-kappaB activity in lipopolysaccharide (LPS)-activated RAW 264.7 cells. The results show that obovatol (1-5 microM) significantly inhibited LPS-induced NO production in a concentration-dependent manner (IC(50): 0.91 microM). Consistent with the inhibitory effect on NO production, obovatol inhibits the expression of inducible nitric oxide synthase and cyclooxygenase-2 expression. Furthermore, obovatol suppressed NF-kappaB (p50 and p65) translocation to the nucleus as well as IkappaB release resulting in the inhibition of the DNA binding activity of the NF-kappaB. Obovatol also inhibited c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) signal, which are the most significantly involved signal in NO production and NF-kappaB activation. When the cells were treated with the combination of obovatol with U0126 (an ERK inhibitor) or SP600125 (a JNK inhibitor) as well as with SC-514 (an IKK2 inhibitor), much more inhibition of NO production was observed than that by obovatol alone. The present results suggest that obovatol has an inhibitory effect on NO production through the inhibition of NF-kappaB/MAPK activity, and thus can be used as an anti-inflammatory agent. |
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In this study, we investigated the effects of obovatol, a neolignan compound isolated from the leaves of M. obovata, on nitric oxide (NO) production and NF-kappaB activity in lipopolysaccharide (LPS)-activated RAW 264.7 cells. The results show that obovatol (1-5 microM) significantly inhibited LPS-induced NO production in a concentration-dependent manner (IC(50): 0.91 microM). Consistent with the inhibitory effect on NO production, obovatol inhibits the expression of inducible nitric oxide synthase and cyclooxygenase-2 expression. Furthermore, obovatol suppressed NF-kappaB (p50 and p65) translocation to the nucleus as well as IkappaB release resulting in the inhibition of the DNA binding activity of the NF-kappaB. Obovatol also inhibited c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) signal, which are the most significantly involved signal in NO production and NF-kappaB activation. When the cells were treated with the combination of obovatol with U0126 (an ERK inhibitor) or SP600125 (a JNK inhibitor) as well as with SC-514 (an IKK2 inhibitor), much more inhibition of NO production was observed than that by obovatol alone. The present results suggest that obovatol has an inhibitory effect on NO production through the inhibition of NF-kappaB/MAPK activity, and thus can be used as an anti-inflammatory agent.</description><identifier>ISSN: 0014-2999</identifier><identifier>PMID: 17134693</identifier><language>eng</language><publisher>Netherlands</publisher><subject><![CDATA[Animals ; Anthracenes - pharmacology ; Anti-Inflammatory Agents, Non-Steroidal - pharmacology ; Biphenyl Compounds - pharmacology ; Butadienes - pharmacology ; Cell Line ; Cyclooxygenase 2 - biosynthesis ; Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors ; Extracellular Signal-Regulated MAP Kinases - metabolism ; Lipopolysaccharides - pharmacology ; Macrophages - drug effects ; Macrophages - metabolism ; Magnolia - chemistry ; MAP Kinase Kinase 4 - antagonists & inhibitors ; MAP Kinase Kinase 4 - metabolism ; Mice ; Mitogen-Activated Protein Kinases - antagonists & inhibitors ; Mitogen-Activated Protein Kinases - metabolism ; NF-kappa B - antagonists & inhibitors ; NF-kappa B - metabolism ; Nitric Oxide - antagonists & inhibitors ; Nitric Oxide - biosynthesis ; Nitric Oxide Synthase Type II - antagonists & inhibitors ; Nitric Oxide Synthase Type II - metabolism ; Nitriles - pharmacology ; Phenyl Ethers - pharmacology]]></subject><ispartof>European journal of pharmacology, 2007-02, Vol.556 (1-3), p.181-189</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17134693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choi, Myoung Suk</creatorcontrib><creatorcontrib>Lee, Seung Ho</creatorcontrib><creatorcontrib>Cho, Ho Seong</creatorcontrib><creatorcontrib>Kim, Youngsoo</creatorcontrib><creatorcontrib>Yun, Yeo Pyo</creatorcontrib><creatorcontrib>Jung, Hai Young</creatorcontrib><creatorcontrib>Jung, Jae Kyoung</creatorcontrib><creatorcontrib>Lee, Bum Chun</creatorcontrib><creatorcontrib>Pyo, Hyeong Bae</creatorcontrib><creatorcontrib>Hong, Jin Tae</creatorcontrib><title>Inhibitory effect of obovatol on nitric oxide production and activation of NF-kappaB/MAP kinases in lipopolysaccharide-treated RAW 264.7cells</title><title>European journal of pharmacology</title><addtitle>Eur J Pharmacol</addtitle><description>The components of Magnolia obovata are known to have many pharmacological activities. In this study, we investigated the effects of obovatol, a neolignan compound isolated from the leaves of M. obovata, on nitric oxide (NO) production and NF-kappaB activity in lipopolysaccharide (LPS)-activated RAW 264.7 cells. The results show that obovatol (1-5 microM) significantly inhibited LPS-induced NO production in a concentration-dependent manner (IC(50): 0.91 microM). Consistent with the inhibitory effect on NO production, obovatol inhibits the expression of inducible nitric oxide synthase and cyclooxygenase-2 expression. Furthermore, obovatol suppressed NF-kappaB (p50 and p65) translocation to the nucleus as well as IkappaB release resulting in the inhibition of the DNA binding activity of the NF-kappaB. Obovatol also inhibited c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) signal, which are the most significantly involved signal in NO production and NF-kappaB activation. When the cells were treated with the combination of obovatol with U0126 (an ERK inhibitor) or SP600125 (a JNK inhibitor) as well as with SC-514 (an IKK2 inhibitor), much more inhibition of NO production was observed than that by obovatol alone. The present results suggest that obovatol has an inhibitory effect on NO production through the inhibition of NF-kappaB/MAPK activity, and thus can be used as an anti-inflammatory agent.</description><subject>Animals</subject><subject>Anthracenes - pharmacology</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</subject><subject>Biphenyl Compounds - pharmacology</subject><subject>Butadienes - pharmacology</subject><subject>Cell Line</subject><subject>Cyclooxygenase 2 - biosynthesis</subject><subject>Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors</subject><subject>Extracellular Signal-Regulated MAP Kinases - metabolism</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Magnolia - chemistry</subject><subject>MAP Kinase Kinase 4 - antagonists & inhibitors</subject><subject>MAP Kinase Kinase 4 - metabolism</subject><subject>Mice</subject><subject>Mitogen-Activated Protein Kinases - antagonists & inhibitors</subject><subject>Mitogen-Activated Protein Kinases - metabolism</subject><subject>NF-kappa B - antagonists & inhibitors</subject><subject>NF-kappa B - metabolism</subject><subject>Nitric Oxide - antagonists & inhibitors</subject><subject>Nitric Oxide - biosynthesis</subject><subject>Nitric Oxide Synthase Type II - antagonists & inhibitors</subject><subject>Nitric Oxide Synthase Type II - metabolism</subject><subject>Nitriles - pharmacology</subject><subject>Phenyl Ethers - pharmacology</subject><issn>0014-2999</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kMtOwzAQRbMA0VL4BeQVu4DjRxIvS0WhUnkIVWIZTRxbNU1jEzuIfAT_jCvKau6MzlzdmZNkinHGUiKEmCTn3n9gjLkg_CyZZEVGWS7oNPlZdVtTm2D7ESmtlQzIamRr-wXBtsh2qDOhNxLZb9Mo5HrbDDKYOIeuQRBlBA9t3HpepjtwDu5un-avaGc68Moj06HWOOtsO3qQcgt9NEpDryCoBr3N3xHJ2U0hVdv6i-RUQ-vV5bHOks3yfrN4TNcvD6vFfJ06zmha0rLhGDPAtAFSEJ4RwQtgTGpdZpISiSmrMWM447kGDJSpOlcqw3WhheR0llz_2cZzPgflQ7U3_hAAOmUHX-WlIDinIoJXR3Co96qpXG_20I_V___oL3aBa-w</recordid><startdate>20070205</startdate><enddate>20070205</enddate><creator>Choi, Myoung Suk</creator><creator>Lee, Seung Ho</creator><creator>Cho, Ho Seong</creator><creator>Kim, Youngsoo</creator><creator>Yun, Yeo Pyo</creator><creator>Jung, Hai Young</creator><creator>Jung, Jae Kyoung</creator><creator>Lee, Bum Chun</creator><creator>Pyo, Hyeong Bae</creator><creator>Hong, Jin Tae</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20070205</creationdate><title>Inhibitory effect of obovatol on nitric oxide production and activation of NF-kappaB/MAP kinases in lipopolysaccharide-treated RAW 264.7cells</title><author>Choi, Myoung Suk ; Lee, Seung Ho ; Cho, Ho Seong ; Kim, Youngsoo ; Yun, Yeo Pyo ; Jung, Hai Young ; Jung, Jae Kyoung ; Lee, Bum Chun ; Pyo, Hyeong Bae ; Hong, Jin Tae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p543-838d5004a03da272512957a44cff81c32c034b0440156fa0a34eb6ee10b7f9c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Anthracenes - pharmacology</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - pharmacology</topic><topic>Biphenyl Compounds - pharmacology</topic><topic>Butadienes - pharmacology</topic><topic>Cell Line</topic><topic>Cyclooxygenase 2 - biosynthesis</topic><topic>Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors</topic><topic>Extracellular Signal-Regulated MAP Kinases - metabolism</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>Magnolia - chemistry</topic><topic>MAP Kinase Kinase 4 - antagonists & inhibitors</topic><topic>MAP Kinase Kinase 4 - metabolism</topic><topic>Mice</topic><topic>Mitogen-Activated Protein Kinases - antagonists & inhibitors</topic><topic>Mitogen-Activated Protein Kinases - metabolism</topic><topic>NF-kappa B - antagonists & inhibitors</topic><topic>NF-kappa B - metabolism</topic><topic>Nitric Oxide - antagonists & inhibitors</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Nitric Oxide Synthase Type II - antagonists & inhibitors</topic><topic>Nitric Oxide Synthase Type II - metabolism</topic><topic>Nitriles - pharmacology</topic><topic>Phenyl Ethers - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Myoung Suk</creatorcontrib><creatorcontrib>Lee, Seung Ho</creatorcontrib><creatorcontrib>Cho, Ho Seong</creatorcontrib><creatorcontrib>Kim, Youngsoo</creatorcontrib><creatorcontrib>Yun, Yeo Pyo</creatorcontrib><creatorcontrib>Jung, Hai Young</creatorcontrib><creatorcontrib>Jung, Jae Kyoung</creatorcontrib><creatorcontrib>Lee, Bum Chun</creatorcontrib><creatorcontrib>Pyo, Hyeong Bae</creatorcontrib><creatorcontrib>Hong, Jin Tae</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Myoung Suk</au><au>Lee, Seung Ho</au><au>Cho, Ho Seong</au><au>Kim, Youngsoo</au><au>Yun, Yeo Pyo</au><au>Jung, Hai Young</au><au>Jung, Jae Kyoung</au><au>Lee, Bum Chun</au><au>Pyo, Hyeong Bae</au><au>Hong, Jin Tae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibitory effect of obovatol on nitric oxide production and activation of NF-kappaB/MAP kinases in lipopolysaccharide-treated RAW 264.7cells</atitle><jtitle>European journal of pharmacology</jtitle><addtitle>Eur J Pharmacol</addtitle><date>2007-02-05</date><risdate>2007</risdate><volume>556</volume><issue>1-3</issue><spage>181</spage><epage>189</epage><pages>181-189</pages><issn>0014-2999</issn><abstract>The components of Magnolia obovata are known to have many pharmacological activities. In this study, we investigated the effects of obovatol, a neolignan compound isolated from the leaves of M. obovata, on nitric oxide (NO) production and NF-kappaB activity in lipopolysaccharide (LPS)-activated RAW 264.7 cells. The results show that obovatol (1-5 microM) significantly inhibited LPS-induced NO production in a concentration-dependent manner (IC(50): 0.91 microM). Consistent with the inhibitory effect on NO production, obovatol inhibits the expression of inducible nitric oxide synthase and cyclooxygenase-2 expression. Furthermore, obovatol suppressed NF-kappaB (p50 and p65) translocation to the nucleus as well as IkappaB release resulting in the inhibition of the DNA binding activity of the NF-kappaB. Obovatol also inhibited c-Jun N-terminal kinase (JNK) and extracellular signal-regulated kinase (ERK) signal, which are the most significantly involved signal in NO production and NF-kappaB activation. When the cells were treated with the combination of obovatol with U0126 (an ERK inhibitor) or SP600125 (a JNK inhibitor) as well as with SC-514 (an IKK2 inhibitor), much more inhibition of NO production was observed than that by obovatol alone. The present results suggest that obovatol has an inhibitory effect on NO production through the inhibition of NF-kappaB/MAPK activity, and thus can be used as an anti-inflammatory agent.</abstract><cop>Netherlands</cop><pmid>17134693</pmid><tpages>9</tpages></addata></record> |
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subjects | Animals Anthracenes - pharmacology Anti-Inflammatory Agents, Non-Steroidal - pharmacology Biphenyl Compounds - pharmacology Butadienes - pharmacology Cell Line Cyclooxygenase 2 - biosynthesis Extracellular Signal-Regulated MAP Kinases - antagonists & inhibitors Extracellular Signal-Regulated MAP Kinases - metabolism Lipopolysaccharides - pharmacology Macrophages - drug effects Macrophages - metabolism Magnolia - chemistry MAP Kinase Kinase 4 - antagonists & inhibitors MAP Kinase Kinase 4 - metabolism Mice Mitogen-Activated Protein Kinases - antagonists & inhibitors Mitogen-Activated Protein Kinases - metabolism NF-kappa B - antagonists & inhibitors NF-kappa B - metabolism Nitric Oxide - antagonists & inhibitors Nitric Oxide - biosynthesis Nitric Oxide Synthase Type II - antagonists & inhibitors Nitric Oxide Synthase Type II - metabolism Nitriles - pharmacology Phenyl Ethers - pharmacology |
title | Inhibitory effect of obovatol on nitric oxide production and activation of NF-kappaB/MAP kinases in lipopolysaccharide-treated RAW 264.7cells |
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