Suppression of LPS-Induced Inflammation by Chalcone Flavokawain A through Activation of Nrf2/ARE-Mediated Antioxidant Genes and Inhibition of ROS/NFκB Signaling Pathways in Primary Splenocytes
Oxidative stress is an important contributing factor for inflammation. Piper methysticum, also known as Kava-kava, is a shrub whose root extract has been consumed as a drink by the pacific islanders for a long time. Flavokawain A (FKA) is a novel chalcone derived from the kava plant that is known to...
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description | Oxidative stress is an important contributing factor for inflammation. Piper methysticum, also known as Kava-kava, is a shrub whose root extract has been consumed as a drink by the pacific islanders for a long time. Flavokawain A (FKA) is a novel chalcone derived from the kava plant that is known to have medicinal properties. This study was aimed at demonstrating the antioxidant molecular mechanisms mediated by FKA on lipopolysaccharide- (LPS-) induced inflammation in BALB/c mouse-derived primary splenocytes. In vitro data show that the nontoxic concentrations of FKA (2-30 μM) significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) release but induced the secretion of interleukin-10 (IL-10), an anti-inflammatory cytokine. It was also shown that FKA pretreatment significantly downregulated the LPS-induced ROS production and blocked the activation of the NFκB (p65) pathway leading to the significant suppression of iNOS, COX-2, TNF-α, and IL-1β protein expressions. Notably, FKA favored the nuclear translocation of Nrf2 leading to the downstream expression of antioxidant proteins HO-1, NQO-1, and γ-GCLC via the Nrf2/ARE signaling pathway signifying the FKA’s potent antioxidant mechanism in these cells. Supporting the in vitro data, the ex vivo data obtained from primary splenocytes derived from the FKA-preadministered BALB/c mice (orally) show that FKA significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) secretion in control-, LPS-, or Concanavalin A- (Con A-) stimulated cells. A significant decrease in the ratios of pro- and anti-inflammatory cytokines (IL-6/IL-10; TNF-α/IL-10) showed that FKA possesses strong anti-inflammatory properties. Furthermore, BALB/c mice induced with experimental pancreatitis using cholecystokinin- (CCK-) 8 showed decreased serum lipase levels due to FKA pretreatment. We conclude that with its potent antioxidant and anti-inflammatory properties, chalcone flavokawain A could be a novel therapeutic agent in the treatment of inflammation-associated diseases. |
doi_str_mv | 10.1155/2020/3476212 |
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Piper methysticum, also known as Kava-kava, is a shrub whose root extract has been consumed as a drink by the pacific islanders for a long time. Flavokawain A (FKA) is a novel chalcone derived from the kava plant that is known to have medicinal properties. This study was aimed at demonstrating the antioxidant molecular mechanisms mediated by FKA on lipopolysaccharide- (LPS-) induced inflammation in BALB/c mouse-derived primary splenocytes. In vitro data show that the nontoxic concentrations of FKA (2-30 μM) significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) release but induced the secretion of interleukin-10 (IL-10), an anti-inflammatory cytokine. It was also shown that FKA pretreatment significantly downregulated the LPS-induced ROS production and blocked the activation of the NFκB (p65) pathway leading to the significant suppression of iNOS, COX-2, TNF-α, and IL-1β protein expressions. Notably, FKA favored the nuclear translocation of Nrf2 leading to the downstream expression of antioxidant proteins HO-1, NQO-1, and γ-GCLC via the Nrf2/ARE signaling pathway signifying the FKA’s potent antioxidant mechanism in these cells. Supporting the in vitro data, the ex vivo data obtained from primary splenocytes derived from the FKA-preadministered BALB/c mice (orally) show that FKA significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) secretion in control-, LPS-, or Concanavalin A- (Con A-) stimulated cells. A significant decrease in the ratios of pro- and anti-inflammatory cytokines (IL-6/IL-10; TNF-α/IL-10) showed that FKA possesses strong anti-inflammatory properties. Furthermore, BALB/c mice induced with experimental pancreatitis using cholecystokinin- (CCK-) 8 showed decreased serum lipase levels due to FKA pretreatment. We conclude that with its potent antioxidant and anti-inflammatory properties, chalcone flavokawain A could be a novel therapeutic agent in the treatment of inflammation-associated diseases.</description><identifier>ISSN: 1942-0900</identifier><identifier>EISSN: 1942-0994</identifier><identifier>DOI: 10.1155/2020/3476212</identifier><identifier>PMID: 32617135</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Animals ; Antibodies ; Antioxidant Response Elements - genetics ; Antioxidants ; Antioxidants - metabolism ; Cells, Cultured ; Chalcone - analogs & derivatives ; Chalcone - chemistry ; Chalcone - pharmacology ; Chalcone - therapeutic use ; Cytokines ; Cytokines - metabolism ; Enzymes ; Female ; Gene expression ; Gene Expression Regulation - drug effects ; Inflammation ; Inflammation - blood ; Inflammation - drug therapy ; Inflammation - genetics ; Laboratory animals ; Lipase - blood ; Lipopolysaccharides ; Mice ; Mice, Inbred BALB C ; NF-E2-Related Factor 2 - metabolism ; NF-kappa B - metabolism ; Oxidative stress ; Pancreatitis - blood ; Pancreatitis - pathology ; RAW 264.7 Cells ; Reactive Oxygen Species - metabolism ; Signal Transduction ; Spleen - metabolism ; Tumor necrosis factor-TNF</subject><ispartof>Oxidative medicine and cellular longevity, 2020, Vol.2020 (2020), p.1-14</ispartof><rights>Copyright © 2020 Hsin-Ling Yang et al.</rights><rights>Copyright © 2020 Hsin-Ling Yang et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2020 Hsin-Ling Yang et al. 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-50c4ad22af323f0c8670bc06f702a88591ce5949d402166ff558d50ada454f6c3</citedby><cites>FETCH-LOGICAL-c471t-50c4ad22af323f0c8670bc06f702a88591ce5949d402166ff558d50ada454f6c3</cites><orcidid>0000-0001-5307-6162 ; 0000-0002-3561-7372 ; 0000-0002-7543-3842</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306849/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7306849/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,4012,27906,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32617135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Lillig, Christopher Horst</contributor><contributor>Christopher Horst Lillig</contributor><creatorcontrib>Hseu, You Cheng</creatorcontrib><creatorcontrib>Liao, Jiunn-Wang</creatorcontrib><creatorcontrib>Liao, Chun-Huei</creatorcontrib><creatorcontrib>Gowrisankar, Yugandhar Vudhya</creatorcontrib><creatorcontrib>Yang, Ting-Yu</creatorcontrib><creatorcontrib>Yang, Hsin-Ling</creatorcontrib><creatorcontrib>Huang, Pei-Jane</creatorcontrib><title>Suppression of LPS-Induced Inflammation by Chalcone Flavokawain A through Activation of Nrf2/ARE-Mediated Antioxidant Genes and Inhibition of ROS/NFκB Signaling Pathways in Primary Splenocytes</title><title>Oxidative medicine and cellular longevity</title><addtitle>Oxid Med Cell Longev</addtitle><description>Oxidative stress is an important contributing factor for inflammation. Piper methysticum, also known as Kava-kava, is a shrub whose root extract has been consumed as a drink by the pacific islanders for a long time. Flavokawain A (FKA) is a novel chalcone derived from the kava plant that is known to have medicinal properties. This study was aimed at demonstrating the antioxidant molecular mechanisms mediated by FKA on lipopolysaccharide- (LPS-) induced inflammation in BALB/c mouse-derived primary splenocytes. In vitro data show that the nontoxic concentrations of FKA (2-30 μM) significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) release but induced the secretion of interleukin-10 (IL-10), an anti-inflammatory cytokine. It was also shown that FKA pretreatment significantly downregulated the LPS-induced ROS production and blocked the activation of the NFκB (p65) pathway leading to the significant suppression of iNOS, COX-2, TNF-α, and IL-1β protein expressions. Notably, FKA favored the nuclear translocation of Nrf2 leading to the downstream expression of antioxidant proteins HO-1, NQO-1, and γ-GCLC via the Nrf2/ARE signaling pathway signifying the FKA’s potent antioxidant mechanism in these cells. Supporting the in vitro data, the ex vivo data obtained from primary splenocytes derived from the FKA-preadministered BALB/c mice (orally) show that FKA significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) secretion in control-, LPS-, or Concanavalin A- (Con A-) stimulated cells. A significant decrease in the ratios of pro- and anti-inflammatory cytokines (IL-6/IL-10; TNF-α/IL-10) showed that FKA possesses strong anti-inflammatory properties. Furthermore, BALB/c mice induced with experimental pancreatitis using cholecystokinin- (CCK-) 8 showed decreased serum lipase levels due to FKA pretreatment. We conclude that with its potent antioxidant and anti-inflammatory properties, chalcone flavokawain A could be a novel therapeutic agent in the treatment of inflammation-associated diseases.</description><subject>Animals</subject><subject>Antibodies</subject><subject>Antioxidant Response Elements - genetics</subject><subject>Antioxidants</subject><subject>Antioxidants - metabolism</subject><subject>Cells, Cultured</subject><subject>Chalcone - analogs & derivatives</subject><subject>Chalcone - chemistry</subject><subject>Chalcone - pharmacology</subject><subject>Chalcone - therapeutic use</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Enzymes</subject><subject>Female</subject><subject>Gene expression</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Inflammation</subject><subject>Inflammation - blood</subject><subject>Inflammation - drug therapy</subject><subject>Inflammation - genetics</subject><subject>Laboratory animals</subject><subject>Lipase - blood</subject><subject>Lipopolysaccharides</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>NF-E2-Related Factor 2 - metabolism</subject><subject>NF-kappa B - metabolism</subject><subject>Oxidative stress</subject><subject>Pancreatitis - blood</subject><subject>Pancreatitis - pathology</subject><subject>RAW 264.7 Cells</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Signal Transduction</subject><subject>Spleen - metabolism</subject><subject>Tumor necrosis factor-TNF</subject><issn>1942-0900</issn><issn>1942-0994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqNkU9v0zAYhyMEYmNw44wscYRQ27Hz54IUqnVUKlu1wDl669iNR2qHOGnpV9ttX4DPhKt0BW6cbOn3-Hlf6xcErwn-QAjnE4opnkQsiSmhT4JzkjEa4ixjT093jM-CF87dYRxHlJHnwVlEY5KQiJ8HD8XQtp10TluDrEKLZRHOTTUIWaG5UQ1sNtAfstUeTWtohDUSzRrY2u-wA21Qjvq6s8O6Rrno9XaEvei6U3SS316GX2Slofe63Pjsp67A9OhKGukQmMOQWq_046vbm2JyPft1_wkVem2g0WaNltDXO9g75KctO72Bbo-KtpHGin0v3cvgmYLGyVfH8yL4Nrv8Ov0cLm6u5tN8EQqWkD7kWDCoKAUV0UhhkcYJXgkcqwRTSFOeESF5xrKKYUriWCnO04pjqIBxpmIRXQQfR287rDayEtL0HTRlO25UWtDlv4nRdbm22zKJcJyyzAveHgWd_TFI15d3duj8J13pW-GUZAlhnno_UqKzznVSnSYQXB4KLw-Fl8fCPf7m761O8GPDHng3ArU2Fez0f-qkZ6SCPzTFjMYs-g1jy8Aj</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Hseu, You Cheng</creator><creator>Liao, Jiunn-Wang</creator><creator>Liao, Chun-Huei</creator><creator>Gowrisankar, Yugandhar Vudhya</creator><creator>Yang, Ting-Yu</creator><creator>Yang, Hsin-Ling</creator><creator>Huang, Pei-Jane</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>Hindawi Limited</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5307-6162</orcidid><orcidid>https://orcid.org/0000-0002-3561-7372</orcidid><orcidid>https://orcid.org/0000-0002-7543-3842</orcidid></search><sort><creationdate>2020</creationdate><title>Suppression of LPS-Induced Inflammation by Chalcone Flavokawain A through Activation of Nrf2/ARE-Mediated Antioxidant Genes and Inhibition of ROS/NFκB Signaling Pathways in Primary Splenocytes</title><author>Hseu, You Cheng ; Liao, Jiunn-Wang ; Liao, Chun-Huei ; Gowrisankar, Yugandhar Vudhya ; Yang, Ting-Yu ; Yang, Hsin-Ling ; Huang, Pei-Jane</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-50c4ad22af323f0c8670bc06f702a88591ce5949d402166ff558d50ada454f6c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Antibodies</topic><topic>Antioxidant Response Elements - genetics</topic><topic>Antioxidants</topic><topic>Antioxidants - metabolism</topic><topic>Cells, Cultured</topic><topic>Chalcone - analogs & derivatives</topic><topic>Chalcone - chemistry</topic><topic>Chalcone - pharmacology</topic><topic>Chalcone - therapeutic use</topic><topic>Cytokines</topic><topic>Cytokines - metabolism</topic><topic>Enzymes</topic><topic>Female</topic><topic>Gene expression</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Inflammation</topic><topic>Inflammation - blood</topic><topic>Inflammation - drug therapy</topic><topic>Inflammation - genetics</topic><topic>Laboratory animals</topic><topic>Lipase - blood</topic><topic>Lipopolysaccharides</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>NF-E2-Related Factor 2 - metabolism</topic><topic>NF-kappa B - metabolism</topic><topic>Oxidative stress</topic><topic>Pancreatitis - blood</topic><topic>Pancreatitis - pathology</topic><topic>RAW 264.7 Cells</topic><topic>Reactive Oxygen Species - 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Piper methysticum, also known as Kava-kava, is a shrub whose root extract has been consumed as a drink by the pacific islanders for a long time. Flavokawain A (FKA) is a novel chalcone derived from the kava plant that is known to have medicinal properties. This study was aimed at demonstrating the antioxidant molecular mechanisms mediated by FKA on lipopolysaccharide- (LPS-) induced inflammation in BALB/c mouse-derived primary splenocytes. In vitro data show that the nontoxic concentrations of FKA (2-30 μM) significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) release but induced the secretion of interleukin-10 (IL-10), an anti-inflammatory cytokine. It was also shown that FKA pretreatment significantly downregulated the LPS-induced ROS production and blocked the activation of the NFκB (p65) pathway leading to the significant suppression of iNOS, COX-2, TNF-α, and IL-1β protein expressions. Notably, FKA favored the nuclear translocation of Nrf2 leading to the downstream expression of antioxidant proteins HO-1, NQO-1, and γ-GCLC via the Nrf2/ARE signaling pathway signifying the FKA’s potent antioxidant mechanism in these cells. Supporting the in vitro data, the ex vivo data obtained from primary splenocytes derived from the FKA-preadministered BALB/c mice (orally) show that FKA significantly suppressed the proinflammatory cytokine (TNF-α, IL-1β, and IL-6) secretion in control-, LPS-, or Concanavalin A- (Con A-) stimulated cells. A significant decrease in the ratios of pro- and anti-inflammatory cytokines (IL-6/IL-10; TNF-α/IL-10) showed that FKA possesses strong anti-inflammatory properties. Furthermore, BALB/c mice induced with experimental pancreatitis using cholecystokinin- (CCK-) 8 showed decreased serum lipase levels due to FKA pretreatment. We conclude that with its potent antioxidant and anti-inflammatory properties, chalcone flavokawain A could be a novel therapeutic agent in the treatment of inflammation-associated diseases.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>32617135</pmid><doi>10.1155/2020/3476212</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0001-5307-6162</orcidid><orcidid>https://orcid.org/0000-0002-3561-7372</orcidid><orcidid>https://orcid.org/0000-0002-7543-3842</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central Open Access; Wiley-Blackwell Open Access Titles; PubMed Central; Alma/SFX Local Collection |
subjects | Animals Antibodies Antioxidant Response Elements - genetics Antioxidants Antioxidants - metabolism Cells, Cultured Chalcone - analogs & derivatives Chalcone - chemistry Chalcone - pharmacology Chalcone - therapeutic use Cytokines Cytokines - metabolism Enzymes Female Gene expression Gene Expression Regulation - drug effects Inflammation Inflammation - blood Inflammation - drug therapy Inflammation - genetics Laboratory animals Lipase - blood Lipopolysaccharides Mice Mice, Inbred BALB C NF-E2-Related Factor 2 - metabolism NF-kappa B - metabolism Oxidative stress Pancreatitis - blood Pancreatitis - pathology RAW 264.7 Cells Reactive Oxygen Species - metabolism Signal Transduction Spleen - metabolism Tumor necrosis factor-TNF |
title | Suppression of LPS-Induced Inflammation by Chalcone Flavokawain A through Activation of Nrf2/ARE-Mediated Antioxidant Genes and Inhibition of ROS/NFκB Signaling Pathways in Primary Splenocytes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-16T14%3A05%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Suppression%20of%20LPS-Induced%20Inflammation%20by%20Chalcone%20Flavokawain%20A%20through%20Activation%20of%20Nrf2/ARE-Mediated%20Antioxidant%20Genes%20and%20Inhibition%20of%20ROS/NF%CE%BAB%20Signaling%20Pathways%20in%20Primary%20Splenocytes&rft.jtitle=Oxidative%20medicine%20and%20cellular%20longevity&rft.au=Hseu,%20You%20Cheng&rft.date=2020&rft.volume=2020&rft.issue=2020&rft.spage=1&rft.epage=14&rft.pages=1-14&rft.issn=1942-0900&rft.eissn=1942-0994&rft_id=info:doi/10.1155/2020/3476212&rft_dat=%3Cproquest_pubme%3E2415219714%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2415219714&rft_id=info:pmid/32617135&rfr_iscdi=true |