The anti-inflammatory effect of 3-deoxysappanchalcone is mediated by inducing heme oxygenase-1 via activating the AKT/mTOR pathway in murine macrophages
3-Deoxysappanchalcone (3-DSC), isolated from Caesalpinia sappan (Leguminosae), is a chalcone that exerts a variety of pharmacological activities. In the present study, we demonstrated that 3-DSC exerts anti-inflammatory activity in murine macrophages by inducing heme oxygenase-1 (HO-1) expression at...
Gespeichert in:
Veröffentlicht in: | International immunopharmacology 2014-10, Vol.22 (2), p.420-426 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 426 |
---|---|
container_issue | 2 |
container_start_page | 420 |
container_title | International immunopharmacology |
container_volume | 22 |
creator | Kim, Jun-Hyeong Choo, Young-Yeon Tae, Nara Min, Byung-Sun Lee, Jeong-Hyung |
description | 3-Deoxysappanchalcone (3-DSC), isolated from Caesalpinia sappan (Leguminosae), is a chalcone that exerts a variety of pharmacological activities. In the present study, we demonstrated that 3-DSC exerts anti-inflammatory activity in murine macrophages by inducing heme oxygenase-1 (HO-1) expression at the translational level. Treatment of RAW264.7 cells with 3-DSC induced HO-1 protein expression in a dose- and time-dependent manner without affecting HO-1 mRNA expression. Mitogen-activated protein kinase inhibitors or actinomycin D, a transcriptional inhibitor, did not block 3-DSC-mediated HO-1 induction. However, 3-DSC-mediated HO-1 induction was completely blocked by treatment with cycloheximide, a translational inhibitor, or rapamycin, an inhibitor of the mammalian target of rapamycin (mTOR). Strikingly, 3-DSC increased the phosphorylation level of mTOR downstream target molecules such as eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1) and S6 kinase 1 (S6K1), as well as AKT in a dose- and time-dependent manner, suggesting that the 3-DSC induces HO-1 expression by activating the AKT/mTOR pathway. Consistent with the notion that HO-1 has anti-inflammatory properties, 3-DSC inhibited the production of nitric oxide (NO) and interleukin (IL)-6 in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Inhibition of HO-1 activity by treatment with tin protoporphyrin IX, a specific HO-1 inhibitor, abrogated the inhibitory effects of 3-DSC on the production of NO and IL-6 in LPS-stimulated RAW264.7 cells. Taken together, 3-DSC may be an effective HO-1 inducer at the translational level that has anti-inflammatory effects, and a valuable compound for modulating inflammatory conditions.
•The anti-inflammatory mechanism of 3-deoxysappanchalcone is proposed.•3-Deoxysappanchalcone induces HO-1 expression by activating the Akt/mTOR pathway.•The mechanism explains the anti-inflammatory effect of 3-deoxysappanchalcone. |
doi_str_mv | 10.1016/j.intimp.2014.07.025 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1563981855</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1567576914003026</els_id><sourcerecordid>1563981855</sourcerecordid><originalsourceid>FETCH-LOGICAL-c362t-57c61a4376850fc4bf040e52465bb6ac273bc4ecd0c0fc6f0d7513ef793f6333</originalsourceid><addsrcrecordid>eNp9Uctu1DAUjRCIlsIfIOQlm6R2HNuZDVJV8RKVKqHsrRvneuJR7ITYGZg_4XPxaApLVrZ8z8P3nKJ4y2jFKJO3h8qF5PxS1ZQ1FVUVrcWz4pq1qi2ZouJ5vgupSqHk7qp4FeOB0vzesJfFVS3ojsmaXxe_uxEJZKHSBTuB95Dm9UTQWjSJzJbwcsD51ynCskAwI0xmDkhcJB4HBwkH0p-IC8NmXNiTET2SDN9jgIglI0cHBExyR0jnecpud9-6W989ficLpPEnnNnEb6vLsh7MOi8j7DG-Ll5YmCK-eTpviu7Tx-7-S_nw-Pnr_d1DabisU97OSAYNV7IV1Jqmt7ShKOpGir6XYGrFe9OgGajJY2npoATjaNWOW8k5vyneX2SXdf6xYUzau2hwmiDgvEWdI-S7lrVCZGhzgeY_xrii1cvqPKwnzag-V6IP-lKJPleiqdK5kkx79-Sw9Tmzf6S_HWTAhwsA85pHh6uOxmEwOd81l6CH2f3f4Q9CjKF-</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1563981855</pqid></control><display><type>article</type><title>The anti-inflammatory effect of 3-deoxysappanchalcone is mediated by inducing heme oxygenase-1 via activating the AKT/mTOR pathway in murine macrophages</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Kim, Jun-Hyeong ; Choo, Young-Yeon ; Tae, Nara ; Min, Byung-Sun ; Lee, Jeong-Hyung</creator><creatorcontrib>Kim, Jun-Hyeong ; Choo, Young-Yeon ; Tae, Nara ; Min, Byung-Sun ; Lee, Jeong-Hyung</creatorcontrib><description>3-Deoxysappanchalcone (3-DSC), isolated from Caesalpinia sappan (Leguminosae), is a chalcone that exerts a variety of pharmacological activities. In the present study, we demonstrated that 3-DSC exerts anti-inflammatory activity in murine macrophages by inducing heme oxygenase-1 (HO-1) expression at the translational level. Treatment of RAW264.7 cells with 3-DSC induced HO-1 protein expression in a dose- and time-dependent manner without affecting HO-1 mRNA expression. Mitogen-activated protein kinase inhibitors or actinomycin D, a transcriptional inhibitor, did not block 3-DSC-mediated HO-1 induction. However, 3-DSC-mediated HO-1 induction was completely blocked by treatment with cycloheximide, a translational inhibitor, or rapamycin, an inhibitor of the mammalian target of rapamycin (mTOR). Strikingly, 3-DSC increased the phosphorylation level of mTOR downstream target molecules such as eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1) and S6 kinase 1 (S6K1), as well as AKT in a dose- and time-dependent manner, suggesting that the 3-DSC induces HO-1 expression by activating the AKT/mTOR pathway. Consistent with the notion that HO-1 has anti-inflammatory properties, 3-DSC inhibited the production of nitric oxide (NO) and interleukin (IL)-6 in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Inhibition of HO-1 activity by treatment with tin protoporphyrin IX, a specific HO-1 inhibitor, abrogated the inhibitory effects of 3-DSC on the production of NO and IL-6 in LPS-stimulated RAW264.7 cells. Taken together, 3-DSC may be an effective HO-1 inducer at the translational level that has anti-inflammatory effects, and a valuable compound for modulating inflammatory conditions.
•The anti-inflammatory mechanism of 3-deoxysappanchalcone is proposed.•3-Deoxysappanchalcone induces HO-1 expression by activating the Akt/mTOR pathway.•The mechanism explains the anti-inflammatory effect of 3-deoxysappanchalcone.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2014.07.025</identifier><identifier>PMID: 25091623</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>3-Deoxysappanchalcone ; Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-inflammatory effect ; Caesalpinia ; Cell Line ; Cell Survival - drug effects ; Chalcones - pharmacology ; Heme oxygenase-1 ; Heme Oxygenase-1 - genetics ; Heme Oxygenase-1 - metabolism ; Lipopolysaccharides ; Macrophages - drug effects ; Macrophages - metabolism ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mice, Inbred C57BL ; mTOR ; Nitric Oxide - metabolism ; Proto-Oncogene Proteins c-akt - metabolism ; RNA, Messenger - metabolism ; Signal Transduction - drug effects ; TOR Serine-Threonine Kinases - metabolism ; Translation</subject><ispartof>International immunopharmacology, 2014-10, Vol.22 (2), p.420-426</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-57c61a4376850fc4bf040e52465bb6ac273bc4ecd0c0fc6f0d7513ef793f6333</citedby><cites>FETCH-LOGICAL-c362t-57c61a4376850fc4bf040e52465bb6ac273bc4ecd0c0fc6f0d7513ef793f6333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.intimp.2014.07.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3541,27915,27916,45986</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25091623$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Jun-Hyeong</creatorcontrib><creatorcontrib>Choo, Young-Yeon</creatorcontrib><creatorcontrib>Tae, Nara</creatorcontrib><creatorcontrib>Min, Byung-Sun</creatorcontrib><creatorcontrib>Lee, Jeong-Hyung</creatorcontrib><title>The anti-inflammatory effect of 3-deoxysappanchalcone is mediated by inducing heme oxygenase-1 via activating the AKT/mTOR pathway in murine macrophages</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>3-Deoxysappanchalcone (3-DSC), isolated from Caesalpinia sappan (Leguminosae), is a chalcone that exerts a variety of pharmacological activities. In the present study, we demonstrated that 3-DSC exerts anti-inflammatory activity in murine macrophages by inducing heme oxygenase-1 (HO-1) expression at the translational level. Treatment of RAW264.7 cells with 3-DSC induced HO-1 protein expression in a dose- and time-dependent manner without affecting HO-1 mRNA expression. Mitogen-activated protein kinase inhibitors or actinomycin D, a transcriptional inhibitor, did not block 3-DSC-mediated HO-1 induction. However, 3-DSC-mediated HO-1 induction was completely blocked by treatment with cycloheximide, a translational inhibitor, or rapamycin, an inhibitor of the mammalian target of rapamycin (mTOR). Strikingly, 3-DSC increased the phosphorylation level of mTOR downstream target molecules such as eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1) and S6 kinase 1 (S6K1), as well as AKT in a dose- and time-dependent manner, suggesting that the 3-DSC induces HO-1 expression by activating the AKT/mTOR pathway. Consistent with the notion that HO-1 has anti-inflammatory properties, 3-DSC inhibited the production of nitric oxide (NO) and interleukin (IL)-6 in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Inhibition of HO-1 activity by treatment with tin protoporphyrin IX, a specific HO-1 inhibitor, abrogated the inhibitory effects of 3-DSC on the production of NO and IL-6 in LPS-stimulated RAW264.7 cells. Taken together, 3-DSC may be an effective HO-1 inducer at the translational level that has anti-inflammatory effects, and a valuable compound for modulating inflammatory conditions.
•The anti-inflammatory mechanism of 3-deoxysappanchalcone is proposed.•3-Deoxysappanchalcone induces HO-1 expression by activating the Akt/mTOR pathway.•The mechanism explains the anti-inflammatory effect of 3-deoxysappanchalcone.</description><subject>3-Deoxysappanchalcone</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-inflammatory effect</subject><subject>Caesalpinia</subject><subject>Cell Line</subject><subject>Cell Survival - drug effects</subject><subject>Chalcones - pharmacology</subject><subject>Heme oxygenase-1</subject><subject>Heme Oxygenase-1 - genetics</subject><subject>Heme Oxygenase-1 - metabolism</subject><subject>Lipopolysaccharides</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - metabolism</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice, Inbred C57BL</subject><subject>mTOR</subject><subject>Nitric Oxide - metabolism</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction - drug effects</subject><subject>TOR Serine-Threonine Kinases - metabolism</subject><subject>Translation</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uctu1DAUjRCIlsIfIOQlm6R2HNuZDVJV8RKVKqHsrRvneuJR7ITYGZg_4XPxaApLVrZ8z8P3nKJ4y2jFKJO3h8qF5PxS1ZQ1FVUVrcWz4pq1qi2ZouJ5vgupSqHk7qp4FeOB0vzesJfFVS3ojsmaXxe_uxEJZKHSBTuB95Dm9UTQWjSJzJbwcsD51ynCskAwI0xmDkhcJB4HBwkH0p-IC8NmXNiTET2SDN9jgIglI0cHBExyR0jnecpud9-6W989ficLpPEnnNnEb6vLsh7MOi8j7DG-Ll5YmCK-eTpviu7Tx-7-S_nw-Pnr_d1DabisU97OSAYNV7IV1Jqmt7ShKOpGir6XYGrFe9OgGajJY2npoATjaNWOW8k5vyneX2SXdf6xYUzau2hwmiDgvEWdI-S7lrVCZGhzgeY_xrii1cvqPKwnzag-V6IP-lKJPleiqdK5kkx79-Sw9Tmzf6S_HWTAhwsA85pHh6uOxmEwOd81l6CH2f3f4Q9CjKF-</recordid><startdate>20141001</startdate><enddate>20141001</enddate><creator>Kim, Jun-Hyeong</creator><creator>Choo, Young-Yeon</creator><creator>Tae, Nara</creator><creator>Min, Byung-Sun</creator><creator>Lee, Jeong-Hyung</creator><general>Elsevier B.V</general><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>20141001</creationdate><title>The anti-inflammatory effect of 3-deoxysappanchalcone is mediated by inducing heme oxygenase-1 via activating the AKT/mTOR pathway in murine macrophages</title><author>Kim, Jun-Hyeong ; Choo, Young-Yeon ; Tae, Nara ; Min, Byung-Sun ; Lee, Jeong-Hyung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-57c61a4376850fc4bf040e52465bb6ac273bc4ecd0c0fc6f0d7513ef793f6333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>3-Deoxysappanchalcone</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-inflammatory effect</topic><topic>Caesalpinia</topic><topic>Cell Line</topic><topic>Cell Survival - drug effects</topic><topic>Chalcones - pharmacology</topic><topic>Heme oxygenase-1</topic><topic>Heme Oxygenase-1 - genetics</topic><topic>Heme Oxygenase-1 - metabolism</topic><topic>Lipopolysaccharides</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - metabolism</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Mice, Inbred C57BL</topic><topic>mTOR</topic><topic>Nitric Oxide - metabolism</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction - drug effects</topic><topic>TOR Serine-Threonine Kinases - metabolism</topic><topic>Translation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Jun-Hyeong</creatorcontrib><creatorcontrib>Choo, Young-Yeon</creatorcontrib><creatorcontrib>Tae, Nara</creatorcontrib><creatorcontrib>Min, Byung-Sun</creatorcontrib><creatorcontrib>Lee, Jeong-Hyung</creatorcontrib><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>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Jun-Hyeong</au><au>Choo, Young-Yeon</au><au>Tae, Nara</au><au>Min, Byung-Sun</au><au>Lee, Jeong-Hyung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The anti-inflammatory effect of 3-deoxysappanchalcone is mediated by inducing heme oxygenase-1 via activating the AKT/mTOR pathway in murine macrophages</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2014-10-01</date><risdate>2014</risdate><volume>22</volume><issue>2</issue><spage>420</spage><epage>426</epage><pages>420-426</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>3-Deoxysappanchalcone (3-DSC), isolated from Caesalpinia sappan (Leguminosae), is a chalcone that exerts a variety of pharmacological activities. In the present study, we demonstrated that 3-DSC exerts anti-inflammatory activity in murine macrophages by inducing heme oxygenase-1 (HO-1) expression at the translational level. Treatment of RAW264.7 cells with 3-DSC induced HO-1 protein expression in a dose- and time-dependent manner without affecting HO-1 mRNA expression. Mitogen-activated protein kinase inhibitors or actinomycin D, a transcriptional inhibitor, did not block 3-DSC-mediated HO-1 induction. However, 3-DSC-mediated HO-1 induction was completely blocked by treatment with cycloheximide, a translational inhibitor, or rapamycin, an inhibitor of the mammalian target of rapamycin (mTOR). Strikingly, 3-DSC increased the phosphorylation level of mTOR downstream target molecules such as eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1) and S6 kinase 1 (S6K1), as well as AKT in a dose- and time-dependent manner, suggesting that the 3-DSC induces HO-1 expression by activating the AKT/mTOR pathway. Consistent with the notion that HO-1 has anti-inflammatory properties, 3-DSC inhibited the production of nitric oxide (NO) and interleukin (IL)-6 in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Inhibition of HO-1 activity by treatment with tin protoporphyrin IX, a specific HO-1 inhibitor, abrogated the inhibitory effects of 3-DSC on the production of NO and IL-6 in LPS-stimulated RAW264.7 cells. Taken together, 3-DSC may be an effective HO-1 inducer at the translational level that has anti-inflammatory effects, and a valuable compound for modulating inflammatory conditions.
•The anti-inflammatory mechanism of 3-deoxysappanchalcone is proposed.•3-Deoxysappanchalcone induces HO-1 expression by activating the Akt/mTOR pathway.•The mechanism explains the anti-inflammatory effect of 3-deoxysappanchalcone.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25091623</pmid><doi>10.1016/j.intimp.2014.07.025</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1567-5769 |
ispartof | International immunopharmacology, 2014-10, Vol.22 (2), p.420-426 |
issn | 1567-5769 1878-1705 |
language | eng |
recordid | cdi_proquest_miscellaneous_1563981855 |
source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | 3-Deoxysappanchalcone Animals Anti-Inflammatory Agents - pharmacology Anti-inflammatory effect Caesalpinia Cell Line Cell Survival - drug effects Chalcones - pharmacology Heme oxygenase-1 Heme Oxygenase-1 - genetics Heme Oxygenase-1 - metabolism Lipopolysaccharides Macrophages - drug effects Macrophages - metabolism Membrane Proteins - genetics Membrane Proteins - metabolism Mice, Inbred C57BL mTOR Nitric Oxide - metabolism Proto-Oncogene Proteins c-akt - metabolism RNA, Messenger - metabolism Signal Transduction - drug effects TOR Serine-Threonine Kinases - metabolism Translation |
title | The anti-inflammatory effect of 3-deoxysappanchalcone is mediated by inducing heme oxygenase-1 via activating the AKT/mTOR pathway in murine macrophages |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T04%3A48%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20anti-inflammatory%20effect%20of%203-deoxysappanchalcone%20is%20mediated%20by%20inducing%20heme%20oxygenase-1%20via%20activating%20the%20AKT/mTOR%20pathway%20in%20murine%20macrophages&rft.jtitle=International%20immunopharmacology&rft.au=Kim,%20Jun-Hyeong&rft.date=2014-10-01&rft.volume=22&rft.issue=2&rft.spage=420&rft.epage=426&rft.pages=420-426&rft.issn=1567-5769&rft.eissn=1878-1705&rft_id=info:doi/10.1016/j.intimp.2014.07.025&rft_dat=%3Cproquest_cross%3E1563981855%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1563981855&rft_id=info:pmid/25091623&rft_els_id=S1567576914003026&rfr_iscdi=true |