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Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms
Wogonin (5, 7-dihydroxy-8-methoxyflavone) is a natural di-hydroxyl flavonoid extracted from the root of Scutellaria baicalensis Georgi. This paper was intended to investigate the mechanism of action of wogonin in alleviating the inflammation and apoptosis in acute lung injury (ALI). Lipopolysacchari...
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Published in: | Biomedical engineering online 2021-12, Vol.20 (1), p.125-125, Article 125 |
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description | Wogonin (5, 7-dihydroxy-8-methoxyflavone) is a natural di-hydroxyl flavonoid extracted from the root of Scutellaria baicalensis Georgi. This paper was intended to investigate the mechanism of action of wogonin in alleviating the inflammation and apoptosis in acute lung injury (ALI).
Lipopolysaccharide (LPS) was used to establish the in vitro model of ALI. After wogonin treatment, the cell viability and apoptosis of LPS-induced A549 cells were, respectively, measured by CCK-8, TUNEL assays and acridine orange/ethidium bromide dual staining, while the contents of inflammatory cytokines and oxidative stress markers were estimated by RT-qPCR, ELISA assay, western blot analysis and commercial kits. Western blot was also conducted to assess the expression of proteins involved. Subsequently, the effect of wogonin on the sirtuin 1 (SIRT1)-mediated high-mobility group box 1 protein (HMGB1) deacetylation was investigated. SIRT1 inhibitor EX527 was used to evaluate the regulatory effects of wogonin on SIRT1-mediated HMGB1 deacetylation in A549 cells under LPS stimulation.
LPS induced inflammation, oxidative stress and apoptosis of A549 cells, which was abolished by wogonin. It was also found that wogonin promoted the HMGB1 deacetylation, accompanied by upregulated SIRT1 expression. However, SIRT1 inhibitor EX527 partially reversed the protective effects of wogonin on the inflammation and apoptosis of LPS-induced A549 cells.
Wogonin alleviated the inflammation and apoptosis in LPS-induced A549 cells by SIRT1-mediated HMGB1 deacetylation, which might represent the identification of a novel mechanism by which wogonin exerts protective effects on ALI and provide ideas for the application of wogonin to ALI treatment. |
doi_str_mv | 10.1186/s12938-021-00965-6 |
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Lipopolysaccharide (LPS) was used to establish the in vitro model of ALI. After wogonin treatment, the cell viability and apoptosis of LPS-induced A549 cells were, respectively, measured by CCK-8, TUNEL assays and acridine orange/ethidium bromide dual staining, while the contents of inflammatory cytokines and oxidative stress markers were estimated by RT-qPCR, ELISA assay, western blot analysis and commercial kits. Western blot was also conducted to assess the expression of proteins involved. Subsequently, the effect of wogonin on the sirtuin 1 (SIRT1)-mediated high-mobility group box 1 protein (HMGB1) deacetylation was investigated. SIRT1 inhibitor EX527 was used to evaluate the regulatory effects of wogonin on SIRT1-mediated HMGB1 deacetylation in A549 cells under LPS stimulation.
LPS induced inflammation, oxidative stress and apoptosis of A549 cells, which was abolished by wogonin. It was also found that wogonin promoted the HMGB1 deacetylation, accompanied by upregulated SIRT1 expression. However, SIRT1 inhibitor EX527 partially reversed the protective effects of wogonin on the inflammation and apoptosis of LPS-induced A549 cells.
Wogonin alleviated the inflammation and apoptosis in LPS-induced A549 cells by SIRT1-mediated HMGB1 deacetylation, which might represent the identification of a novel mechanism by which wogonin exerts protective effects on ALI and provide ideas for the application of wogonin to ALI treatment.</description><identifier>ISSN: 1475-925X</identifier><identifier>EISSN: 1475-925X</identifier><identifier>DOI: 10.1186/s12938-021-00965-6</identifier><identifier>PMID: 34906140</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Acridine orange ; Acute lung injury ; Acute respiratory distress syndrome ; Apoptosis ; Bioflavonoids ; Care and treatment ; Cell viability ; Cholecystokinin ; Complications and side effects ; Cytokines ; Deacetylation ; Enzyme-linked immunosorbent assay ; Epithelial Cells ; Epithelium ; Ethidium bromide ; Flavanones ; Flavones ; Flavonoids ; Health aspects ; HMGB1 deacetylation ; HMGB1 protein ; Humans ; Inflammation ; Inflammatory diseases ; Inhibitors ; Kinases ; Lipopolysaccharides ; Lipopolysaccharides - toxicity ; Lung ; Lungs ; Oxidative stress ; Phosphorylation ; Proteins ; Risk factors ; Sepsis ; SIRT1 ; SIRT1 protein ; Wogonin</subject><ispartof>Biomedical engineering online, 2021-12, Vol.20 (1), p.125-125, Article 125</ispartof><rights>2021. The Author(s).</rights><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c597t-8ab8d1224fb12d6b96bbaef46ffd5a0f4b79adbeb4862731308b4d816ba52c713</citedby><cites>FETCH-LOGICAL-c597t-8ab8d1224fb12d6b96bbaef46ffd5a0f4b79adbeb4862731308b4d816ba52c713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670054/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2611245975?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34906140$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ge, Jinlin</creatorcontrib><creatorcontrib>Yang, Huanhuan</creatorcontrib><creatorcontrib>Zeng, Yufeng</creatorcontrib><creatorcontrib>Liu, Yunjie</creatorcontrib><title>Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms</title><title>Biomedical engineering online</title><addtitle>Biomed Eng Online</addtitle><description>Wogonin (5, 7-dihydroxy-8-methoxyflavone) is a natural di-hydroxyl flavonoid extracted from the root of Scutellaria baicalensis Georgi. This paper was intended to investigate the mechanism of action of wogonin in alleviating the inflammation and apoptosis in acute lung injury (ALI).
Lipopolysaccharide (LPS) was used to establish the in vitro model of ALI. After wogonin treatment, the cell viability and apoptosis of LPS-induced A549 cells were, respectively, measured by CCK-8, TUNEL assays and acridine orange/ethidium bromide dual staining, while the contents of inflammatory cytokines and oxidative stress markers were estimated by RT-qPCR, ELISA assay, western blot analysis and commercial kits. Western blot was also conducted to assess the expression of proteins involved. Subsequently, the effect of wogonin on the sirtuin 1 (SIRT1)-mediated high-mobility group box 1 protein (HMGB1) deacetylation was investigated. SIRT1 inhibitor EX527 was used to evaluate the regulatory effects of wogonin on SIRT1-mediated HMGB1 deacetylation in A549 cells under LPS stimulation.
LPS induced inflammation, oxidative stress and apoptosis of A549 cells, which was abolished by wogonin. It was also found that wogonin promoted the HMGB1 deacetylation, accompanied by upregulated SIRT1 expression. However, SIRT1 inhibitor EX527 partially reversed the protective effects of wogonin on the inflammation and apoptosis of LPS-induced A549 cells.
Wogonin alleviated the inflammation and apoptosis in LPS-induced A549 cells by SIRT1-mediated HMGB1 deacetylation, which might represent the identification of a novel mechanism by which wogonin exerts protective effects on ALI and provide ideas for the application of wogonin to ALI treatment.</description><subject>Acridine orange</subject><subject>Acute lung injury</subject><subject>Acute respiratory distress syndrome</subject><subject>Apoptosis</subject><subject>Bioflavonoids</subject><subject>Care and treatment</subject><subject>Cell viability</subject><subject>Cholecystokinin</subject><subject>Complications and side effects</subject><subject>Cytokines</subject><subject>Deacetylation</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Epithelial Cells</subject><subject>Epithelium</subject><subject>Ethidium bromide</subject><subject>Flavanones</subject><subject>Flavones</subject><subject>Flavonoids</subject><subject>Health aspects</subject><subject>HMGB1 deacetylation</subject><subject>HMGB1 protein</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Inflammatory diseases</subject><subject>Inhibitors</subject><subject>Kinases</subject><subject>Lipopolysaccharides</subject><subject>Lipopolysaccharides - toxicity</subject><subject>Lung</subject><subject>Lungs</subject><subject>Oxidative stress</subject><subject>Phosphorylation</subject><subject>Proteins</subject><subject>Risk factors</subject><subject>Sepsis</subject><subject>SIRT1</subject><subject>SIRT1 protein</subject><subject>Wogonin</subject><issn>1475-925X</issn><issn>1475-925X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkstu1DAUhiMEoqXwAixQJDawSPEtjrNBqiouI1UCcZHYWb4cZ1w59hAnhT4DL41nppQOQlnEcr7zWfn9V9VTjE4xFvxVxqSnokEENwj1vG34veoYs65tetJ-u39nfVQ9yvkSIYIQ7x9WR5T1iGOGjqtfH6c0g5n9FdTgXFnlOrn6RxpS9LFOsQ5-kzYpXGdlzFpN3kLjo10M2NpHF9Q4qtkXTkVbq4LOKfudIyxxqGHj5zUEr0JtIIS8w3w5ZJNy9jpAPULRRp_H_Lh64FTI8OTmfVJ9ffvmy_n75uLDu9X52UVj2r6bG6G0sJgQ5jQmluuea63AMe6cbRVyTHe9sho0E5x0FFMkNLMCc61aYjpMT6rV3muTupSbyY9qupZJebnbSNMg1TR7E0BSSkrGJSxqCWOOKKACKYQ0EoYwDsX1eu_aLHoEayDOkwoH0sMv0a_lkK6k4B1CLSuCFzeCKX1fIM9y9HkblYqQliwJx4hhJGhf0Of_oJdpmWKJakthwko87V9qUOUHyhWlcq7ZSuUZ72nbCsa2GZz-hyqPhdGbFMH5sn8w8PJgoDAz_JwHteQsV58_HbJkz5qp3PIE7jYPjOS2unJfXVmqK3fVlbwMPbub5O3In67S38kC6vs</recordid><startdate>20211214</startdate><enddate>20211214</enddate><creator>Ge, Jinlin</creator><creator>Yang, Huanhuan</creator><creator>Zeng, Yufeng</creator><creator>Liu, Yunjie</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20211214</creationdate><title>Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms</title><author>Ge, Jinlin ; Yang, Huanhuan ; Zeng, Yufeng ; Liu, Yunjie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c597t-8ab8d1224fb12d6b96bbaef46ffd5a0f4b79adbeb4862731308b4d816ba52c713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acridine orange</topic><topic>Acute lung injury</topic><topic>Acute respiratory distress syndrome</topic><topic>Apoptosis</topic><topic>Bioflavonoids</topic><topic>Care and treatment</topic><topic>Cell viability</topic><topic>Cholecystokinin</topic><topic>Complications and side effects</topic><topic>Cytokines</topic><topic>Deacetylation</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Epithelial Cells</topic><topic>Epithelium</topic><topic>Ethidium bromide</topic><topic>Flavanones</topic><topic>Flavones</topic><topic>Flavonoids</topic><topic>Health aspects</topic><topic>HMGB1 deacetylation</topic><topic>HMGB1 protein</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Inflammatory diseases</topic><topic>Inhibitors</topic><topic>Kinases</topic><topic>Lipopolysaccharides</topic><topic>Lipopolysaccharides - toxicity</topic><topic>Lung</topic><topic>Lungs</topic><topic>Oxidative stress</topic><topic>Phosphorylation</topic><topic>Proteins</topic><topic>Risk factors</topic><topic>Sepsis</topic><topic>SIRT1</topic><topic>SIRT1 protein</topic><topic>Wogonin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ge, Jinlin</creatorcontrib><creatorcontrib>Yang, Huanhuan</creatorcontrib><creatorcontrib>Zeng, Yufeng</creatorcontrib><creatorcontrib>Liu, Yunjie</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biomedical engineering online</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ge, Jinlin</au><au>Yang, Huanhuan</au><au>Zeng, Yufeng</au><au>Liu, Yunjie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms</atitle><jtitle>Biomedical engineering online</jtitle><addtitle>Biomed Eng Online</addtitle><date>2021-12-14</date><risdate>2021</risdate><volume>20</volume><issue>1</issue><spage>125</spage><epage>125</epage><pages>125-125</pages><artnum>125</artnum><issn>1475-925X</issn><eissn>1475-925X</eissn><abstract>Wogonin (5, 7-dihydroxy-8-methoxyflavone) is a natural di-hydroxyl flavonoid extracted from the root of Scutellaria baicalensis Georgi. This paper was intended to investigate the mechanism of action of wogonin in alleviating the inflammation and apoptosis in acute lung injury (ALI).
Lipopolysaccharide (LPS) was used to establish the in vitro model of ALI. After wogonin treatment, the cell viability and apoptosis of LPS-induced A549 cells were, respectively, measured by CCK-8, TUNEL assays and acridine orange/ethidium bromide dual staining, while the contents of inflammatory cytokines and oxidative stress markers were estimated by RT-qPCR, ELISA assay, western blot analysis and commercial kits. Western blot was also conducted to assess the expression of proteins involved. Subsequently, the effect of wogonin on the sirtuin 1 (SIRT1)-mediated high-mobility group box 1 protein (HMGB1) deacetylation was investigated. SIRT1 inhibitor EX527 was used to evaluate the regulatory effects of wogonin on SIRT1-mediated HMGB1 deacetylation in A549 cells under LPS stimulation.
LPS induced inflammation, oxidative stress and apoptosis of A549 cells, which was abolished by wogonin. It was also found that wogonin promoted the HMGB1 deacetylation, accompanied by upregulated SIRT1 expression. However, SIRT1 inhibitor EX527 partially reversed the protective effects of wogonin on the inflammation and apoptosis of LPS-induced A549 cells.
Wogonin alleviated the inflammation and apoptosis in LPS-induced A549 cells by SIRT1-mediated HMGB1 deacetylation, which might represent the identification of a novel mechanism by which wogonin exerts protective effects on ALI and provide ideas for the application of wogonin to ALI treatment.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>34906140</pmid><doi>10.1186/s12938-021-00965-6</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acridine orange Acute lung injury Acute respiratory distress syndrome Apoptosis Bioflavonoids Care and treatment Cell viability Cholecystokinin Complications and side effects Cytokines Deacetylation Enzyme-linked immunosorbent assay Epithelial Cells Epithelium Ethidium bromide Flavanones Flavones Flavonoids Health aspects HMGB1 deacetylation HMGB1 protein Humans Inflammation Inflammatory diseases Inhibitors Kinases Lipopolysaccharides Lipopolysaccharides - toxicity Lung Lungs Oxidative stress Phosphorylation Proteins Risk factors Sepsis SIRT1 SIRT1 protein Wogonin |
title | Protective effects of wogonin on lipopolysaccharide-induced inflammation and apoptosis of lung epithelial cells and its possible mechanisms |
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