Alpinetin attenuates inflammatory responses by interfering toll-like receptor 4/nuclear factor kappa B signaling pathway in lipopolysaccharide-induced mastitis in mice
Alpinetin, a novel plant flavonoid derived from Alpinia katsumadai Hayata, has been reported to exhibit anti-inflammatory properties. However, the effect of alpinetin on mastitis has not been investigated. The aim of this study was to investigate the protective effect of alpinetin against lipopolysa...
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description | Alpinetin, a novel plant flavonoid derived from Alpinia katsumadai Hayata, has been reported to exhibit anti-inflammatory properties. However, the effect of alpinetin on mastitis has not been investigated. The aim of this study was to investigate the protective effect of alpinetin against lipopolysaccharide (LPS)-induced mastitis and to clarify the possible mechanism. In the present study, primary mouse mammary epithelial cells and an LPS-induced mouse mastitis model were used to investigate the effect of alpinetin on mastitis and the possible mechanism. In vivo, we observed that alpinetin significantly attenuated the infiltration of neutrophilic granulocytes, and the activation of myeloperoxidase; down-regulated the level of pro-inflammatory cytokines, including TNF-α, IL-1β and IL-6; inhibited the phosphorylation of IκB-α, NF-κB p65 and the expression of TLR4, caused by LPS. In vitro, we also observed that alpinetin inhibited the expression of TLR4 and the production of TNF-α, IL-1β and IL-6 in LPS-stimulated primary mouse mammary epithelial cells. However, alpinetin could not inhibit the production of IL-1β and IL-6 in TNF-α-stimulated primary mouse mammary epithelial cells. In conclusion, our results suggest that the anti-inflammatory effects of alpinetin against LPS-induced mastitis may be due to its ability to inhibit TLR4-mediated NF-κB signaling pathways. Alpinetin may be a promising potential therapeutic reagent for mastitis treatment.
•Alpinetin markedly inhibited the LPS-induced TNF-α, IL-6 and IL-1β production.•Alpinetin inhibited the phosphorylation of IκB-α and p65 NF-κB, caused by LPS.•Alpinetin inhibited the expression of TLR4, caused by LPS.•Alpinetin attenuated mammary histopathologic changes in the mouse models. |
doi_str_mv | 10.1016/j.intimp.2013.04.030 |
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•Alpinetin markedly inhibited the LPS-induced TNF-α, IL-6 and IL-1β production.•Alpinetin inhibited the phosphorylation of IκB-α and p65 NF-κB, caused by LPS.•Alpinetin inhibited the expression of TLR4, caused by LPS.•Alpinetin attenuated mammary histopathologic changes in the mouse models.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2013.04.030</identifier><identifier>PMID: 23669335</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alpinetin ; Alpinia ; Animals ; Dose-Response Relationship, Drug ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Female ; Flavanones - administration & dosage ; Flavanones - chemistry ; Flavanones - therapeutic use ; Gene Expression Regulation - drug effects ; Inflammation - drug therapy ; Lipopolysaccharide ; Lipopolysaccharides - toxicity ; Male ; Mammary Glands, Animal - cytology ; Mastitis ; Mastitis - chemically induced ; Mastitis - drug therapy ; Mastitis - metabolism ; Mice ; Mice, Inbred BALB C ; Molecular Structure ; NF-kappa B - genetics ; NF-kappa B - metabolism ; Nuclear factor-kappaB ; Peroxidase - genetics ; Peroxidase - metabolism ; Toll-like receptor ; Toll-Like Receptor 4 - genetics ; Toll-Like Receptor 4 - metabolism</subject><ispartof>International immunopharmacology, 2013-09, Vol.17 (1), p.26-32</ispartof><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-4be0b61688f1ac5deaf4877bbe5a7aaa2e1e65a7cad56d14ceb5e860c9013b303</citedby><cites>FETCH-LOGICAL-c446t-4be0b61688f1ac5deaf4877bbe5a7aaa2e1e65a7cad56d14ceb5e860c9013b303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1567576913001768$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23669335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Haijin</creatorcontrib><creatorcontrib>Mo, Xiaodong</creatorcontrib><creatorcontrib>Yu, Jinlong</creatorcontrib><creatorcontrib>Huang, Zonghai</creatorcontrib><title>Alpinetin attenuates inflammatory responses by interfering toll-like receptor 4/nuclear factor kappa B signaling pathway in lipopolysaccharide-induced mastitis in mice</title><title>International immunopharmacology</title><addtitle>Int Immunopharmacol</addtitle><description>Alpinetin, a novel plant flavonoid derived from Alpinia katsumadai Hayata, has been reported to exhibit anti-inflammatory properties. However, the effect of alpinetin on mastitis has not been investigated. The aim of this study was to investigate the protective effect of alpinetin against lipopolysaccharide (LPS)-induced mastitis and to clarify the possible mechanism. In the present study, primary mouse mammary epithelial cells and an LPS-induced mouse mastitis model were used to investigate the effect of alpinetin on mastitis and the possible mechanism. In vivo, we observed that alpinetin significantly attenuated the infiltration of neutrophilic granulocytes, and the activation of myeloperoxidase; down-regulated the level of pro-inflammatory cytokines, including TNF-α, IL-1β and IL-6; inhibited the phosphorylation of IκB-α, NF-κB p65 and the expression of TLR4, caused by LPS. In vitro, we also observed that alpinetin inhibited the expression of TLR4 and the production of TNF-α, IL-1β and IL-6 in LPS-stimulated primary mouse mammary epithelial cells. However, alpinetin could not inhibit the production of IL-1β and IL-6 in TNF-α-stimulated primary mouse mammary epithelial cells. In conclusion, our results suggest that the anti-inflammatory effects of alpinetin against LPS-induced mastitis may be due to its ability to inhibit TLR4-mediated NF-κB signaling pathways. Alpinetin may be a promising potential therapeutic reagent for mastitis treatment.
•Alpinetin markedly inhibited the LPS-induced TNF-α, IL-6 and IL-1β production.•Alpinetin inhibited the phosphorylation of IκB-α and p65 NF-κB, caused by LPS.•Alpinetin inhibited the expression of TLR4, caused by LPS.•Alpinetin attenuated mammary histopathologic changes in the mouse models.</description><subject>Alpinetin</subject><subject>Alpinia</subject><subject>Animals</subject><subject>Dose-Response Relationship, Drug</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Female</subject><subject>Flavanones - administration & dosage</subject><subject>Flavanones - chemistry</subject><subject>Flavanones - therapeutic use</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Inflammation - drug therapy</subject><subject>Lipopolysaccharide</subject><subject>Lipopolysaccharides - toxicity</subject><subject>Male</subject><subject>Mammary Glands, Animal - cytology</subject><subject>Mastitis</subject><subject>Mastitis - chemically induced</subject><subject>Mastitis - drug therapy</subject><subject>Mastitis - metabolism</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Molecular Structure</subject><subject>NF-kappa B - genetics</subject><subject>NF-kappa B - metabolism</subject><subject>Nuclear factor-kappaB</subject><subject>Peroxidase - genetics</subject><subject>Peroxidase - metabolism</subject><subject>Toll-like receptor</subject><subject>Toll-Like Receptor 4 - genetics</subject><subject>Toll-Like Receptor 4 - metabolism</subject><issn>1567-5769</issn><issn>1878-1705</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctu1TAQhiNERUvhDRDykk1S-8Rxkg1SqcpFqtQNrK2JM2nn1HGM7YDOE_U1cTiFJUiWPJr55qL_L4o3gleCC3Wxr8glmn2146KuuKx4zZ8VZ6Jru1K0vHme40a1ZdOq_rR4GeOe85yX4kVxuquV6uu6OSseL60nh4kcg5TQrZAwMnKThXmGtIQDCxj94mJOD4dcSRgmDOTuWFqsLS09YEYM-gwzeeFWYxECm8BsiQfwHtgHFunOgd26PKT7n7BNYpb84hd7iGDMPQQasSQ3rgZHNkNMlGg7hc1k8FVxMoGN-PrpPy--fbz-evW5vLn99OXq8qY0UqpUygH5oITqukmAaUaESXZtOwzYQAsAOxSocmhgbNQopMGhwU5x02cRh5rX58W741wflu8rxqRnigatBYfLGrVoOG87sVPt_9G677PI-WVUHlETlhgDTtoHmiEctOB6c1Pv9dFNvbmpudT89zFvnzasw4zj36Y_9mXg_RHALMkPwqCjIXRZQMqWJD0u9O8NvwD4prgr</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Chen, Haijin</creator><creator>Mo, Xiaodong</creator><creator>Yu, Jinlong</creator><creator>Huang, Zonghai</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><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20130901</creationdate><title>Alpinetin attenuates inflammatory responses by interfering toll-like receptor 4/nuclear factor kappa B signaling pathway in lipopolysaccharide-induced mastitis in mice</title><author>Chen, Haijin ; Mo, Xiaodong ; Yu, Jinlong ; Huang, Zonghai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-4be0b61688f1ac5deaf4877bbe5a7aaa2e1e65a7cad56d14ceb5e860c9013b303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Alpinetin</topic><topic>Alpinia</topic><topic>Animals</topic><topic>Dose-Response Relationship, Drug</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Female</topic><topic>Flavanones - administration & dosage</topic><topic>Flavanones - chemistry</topic><topic>Flavanones - therapeutic use</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Inflammation - drug therapy</topic><topic>Lipopolysaccharide</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Male</topic><topic>Mammary Glands, Animal - cytology</topic><topic>Mastitis</topic><topic>Mastitis - chemically induced</topic><topic>Mastitis - drug therapy</topic><topic>Mastitis - metabolism</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Molecular Structure</topic><topic>NF-kappa B - genetics</topic><topic>NF-kappa B - metabolism</topic><topic>Nuclear factor-kappaB</topic><topic>Peroxidase - genetics</topic><topic>Peroxidase - metabolism</topic><topic>Toll-like receptor</topic><topic>Toll-Like Receptor 4 - genetics</topic><topic>Toll-Like Receptor 4 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Haijin</creatorcontrib><creatorcontrib>Mo, Xiaodong</creatorcontrib><creatorcontrib>Yu, Jinlong</creatorcontrib><creatorcontrib>Huang, Zonghai</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><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>International immunopharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Haijin</au><au>Mo, Xiaodong</au><au>Yu, Jinlong</au><au>Huang, Zonghai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alpinetin attenuates inflammatory responses by interfering toll-like receptor 4/nuclear factor kappa B signaling pathway in lipopolysaccharide-induced mastitis in mice</atitle><jtitle>International immunopharmacology</jtitle><addtitle>Int Immunopharmacol</addtitle><date>2013-09-01</date><risdate>2013</risdate><volume>17</volume><issue>1</issue><spage>26</spage><epage>32</epage><pages>26-32</pages><issn>1567-5769</issn><eissn>1878-1705</eissn><abstract>Alpinetin, a novel plant flavonoid derived from Alpinia katsumadai Hayata, has been reported to exhibit anti-inflammatory properties. However, the effect of alpinetin on mastitis has not been investigated. The aim of this study was to investigate the protective effect of alpinetin against lipopolysaccharide (LPS)-induced mastitis and to clarify the possible mechanism. In the present study, primary mouse mammary epithelial cells and an LPS-induced mouse mastitis model were used to investigate the effect of alpinetin on mastitis and the possible mechanism. In vivo, we observed that alpinetin significantly attenuated the infiltration of neutrophilic granulocytes, and the activation of myeloperoxidase; down-regulated the level of pro-inflammatory cytokines, including TNF-α, IL-1β and IL-6; inhibited the phosphorylation of IκB-α, NF-κB p65 and the expression of TLR4, caused by LPS. In vitro, we also observed that alpinetin inhibited the expression of TLR4 and the production of TNF-α, IL-1β and IL-6 in LPS-stimulated primary mouse mammary epithelial cells. However, alpinetin could not inhibit the production of IL-1β and IL-6 in TNF-α-stimulated primary mouse mammary epithelial cells. In conclusion, our results suggest that the anti-inflammatory effects of alpinetin against LPS-induced mastitis may be due to its ability to inhibit TLR4-mediated NF-κB signaling pathways. Alpinetin may be a promising potential therapeutic reagent for mastitis treatment.
•Alpinetin markedly inhibited the LPS-induced TNF-α, IL-6 and IL-1β production.•Alpinetin inhibited the phosphorylation of IκB-α and p65 NF-κB, caused by LPS.•Alpinetin inhibited the expression of TLR4, caused by LPS.•Alpinetin attenuated mammary histopathologic changes in the mouse models.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>23669335</pmid><doi>10.1016/j.intimp.2013.04.030</doi><tpages>7</tpages></addata></record> |
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subjects | Alpinetin Alpinia Animals Dose-Response Relationship, Drug Epithelial Cells - drug effects Epithelial Cells - metabolism Female Flavanones - administration & dosage Flavanones - chemistry Flavanones - therapeutic use Gene Expression Regulation - drug effects Inflammation - drug therapy Lipopolysaccharide Lipopolysaccharides - toxicity Male Mammary Glands, Animal - cytology Mastitis Mastitis - chemically induced Mastitis - drug therapy Mastitis - metabolism Mice Mice, Inbred BALB C Molecular Structure NF-kappa B - genetics NF-kappa B - metabolism Nuclear factor-kappaB Peroxidase - genetics Peroxidase - metabolism Toll-like receptor Toll-Like Receptor 4 - genetics Toll-Like Receptor 4 - metabolism |
title | Alpinetin attenuates inflammatory responses by interfering toll-like receptor 4/nuclear factor kappa B signaling pathway in lipopolysaccharide-induced mastitis in mice |
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