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Corylin Attenuates CCl4-Induced Liver Fibrosis in Mice by Regulating the GAS6/AXL Signaling Pathway in Hepatic Stellate Cells
Liver fibrosis is reversible when treated in its early stages and when liver inflammatory factors are inhibited. Limited studies have investigated the therapeutic effects of corylin, a flavonoid extracted from Psoralea corylifolia L. (Fabaceae), on liver fibrosis. Therefore, we evaluated the anti-in...
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Published in: | International journal of molecular sciences 2023-12, Vol.24 (23), p.16936 |
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description | Liver fibrosis is reversible when treated in its early stages and when liver inflammatory factors are inhibited. Limited studies have investigated the therapeutic effects of corylin, a flavonoid extracted from Psoralea corylifolia L. (Fabaceae), on liver fibrosis. Therefore, we evaluated the anti-inflammatory activity of corylin and investigated its efficacy and mechanism of action in ameliorating liver fibrosis. Corylin significantly inhibited inflammatory responses by inhibiting the activation of mitogen-activated protein kinase signaling pathways and the expression of interleukin (IL)-1β, IL-6, and tumor necrosis factor-alpha in human THP-1 and mouse RAW264.7 macrophages. Furthermore, corylin inhibited the expression of growth arrest-specific gene 6 in human hepatic stellate cells (HSCs) and the activation of the downstream phosphoinositide 3-kinase/protein kinase B pathway. This inhibited the activation of HSCs and the expression of extracellular matrix proteins, including α-smooth muscle actin and type I collagen. Additionally, corylin induced caspase 9 and caspase 3 activation, which promoted apoptosis in HSCs. Moreover, in vivo experiments confirmed the regulatory effects of corylin on these proteins, and corylin alleviated the symptoms of carbon tetrachloride-induced liver fibrosis in mice. These findings revealed that corylin has anti-inflammatory activity and inhibits HSC activation; thus, it presents as a potential adjuvant in the treatment of liver fibrosis. |
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Limited studies have investigated the therapeutic effects of corylin, a flavonoid extracted from Psoralea corylifolia L. (Fabaceae), on liver fibrosis. Therefore, we evaluated the anti-inflammatory activity of corylin and investigated its efficacy and mechanism of action in ameliorating liver fibrosis. Corylin significantly inhibited inflammatory responses by inhibiting the activation of mitogen-activated protein kinase signaling pathways and the expression of interleukin (IL)-1β, IL-6, and tumor necrosis factor-alpha in human THP-1 and mouse RAW264.7 macrophages. Furthermore, corylin inhibited the expression of growth arrest-specific gene 6 in human hepatic stellate cells (HSCs) and the activation of the downstream phosphoinositide 3-kinase/protein kinase B pathway. This inhibited the activation of HSCs and the expression of extracellular matrix proteins, including α-smooth muscle actin and type I collagen. Additionally, corylin induced caspase 9 and caspase 3 activation, which promoted apoptosis in HSCs. Moreover, in vivo experiments confirmed the regulatory effects of corylin on these proteins, and corylin alleviated the symptoms of carbon tetrachloride-induced liver fibrosis in mice. These findings revealed that corylin has anti-inflammatory activity and inhibits HSC activation; thus, it presents as a potential adjuvant in the treatment of liver fibrosis.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms242316936</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>anti-inflammation ; Bacterial infections ; Cancer therapies ; Collagen ; corylin ; Cytokines ; Flavonoids ; growth arrest-specific gene 6/AXL signaling pathway ; hepatic stellate cell ; Hepatitis ; Infections ; Inflammation ; Kinases ; Liver cancer ; Liver cirrhosis ; liver fibrosis ; Natural products ; Physiology ; Proteins ; Tumor necrosis factor-TNF</subject><ispartof>International journal of molecular sciences, 2023-12, Vol.24 (23), p.16936</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-c302f3d110d20079f97e3e84513ed0f2e28dd1cab28a057d575790f816fd4b783</citedby><cites>FETCH-LOGICAL-c403t-c302f3d110d20079f97e3e84513ed0f2e28dd1cab28a057d575790f816fd4b783</cites><orcidid>0000-0001-9248-9031 ; 0000-0002-1649-6798 ; 0000-0003-0893-4185 ; 0000-0003-1759-9120</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2899430798/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2899430798?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590,75126</link.rule.ids></links><search><creatorcontrib>Chen, Chin-Chuan</creatorcontrib><creatorcontrib>Chen, Chi-Yuan</creatorcontrib><creatorcontrib>Yeh, Chau-Ting</creatorcontrib><creatorcontrib>Liu, Yi-Tsen</creatorcontrib><creatorcontrib>Leu, Yann-Lii</creatorcontrib><creatorcontrib>Chuang, Wen-Yu</creatorcontrib><creatorcontrib>Shih, Yin-Hwa</creatorcontrib><creatorcontrib>Chou, Li-Fang</creatorcontrib><creatorcontrib>Shieh, Tzong-Ming</creatorcontrib><creatorcontrib>Wang, Tong-Hong</creatorcontrib><title>Corylin Attenuates CCl4-Induced Liver Fibrosis in Mice by Regulating the GAS6/AXL Signaling Pathway in Hepatic Stellate Cells</title><title>International journal of molecular sciences</title><description>Liver fibrosis is reversible when treated in its early stages and when liver inflammatory factors are inhibited. Limited studies have investigated the therapeutic effects of corylin, a flavonoid extracted from Psoralea corylifolia L. (Fabaceae), on liver fibrosis. Therefore, we evaluated the anti-inflammatory activity of corylin and investigated its efficacy and mechanism of action in ameliorating liver fibrosis. Corylin significantly inhibited inflammatory responses by inhibiting the activation of mitogen-activated protein kinase signaling pathways and the expression of interleukin (IL)-1β, IL-6, and tumor necrosis factor-alpha in human THP-1 and mouse RAW264.7 macrophages. Furthermore, corylin inhibited the expression of growth arrest-specific gene 6 in human hepatic stellate cells (HSCs) and the activation of the downstream phosphoinositide 3-kinase/protein kinase B pathway. This inhibited the activation of HSCs and the expression of extracellular matrix proteins, including α-smooth muscle actin and type I collagen. Additionally, corylin induced caspase 9 and caspase 3 activation, which promoted apoptosis in HSCs. Moreover, in vivo experiments confirmed the regulatory effects of corylin on these proteins, and corylin alleviated the symptoms of carbon tetrachloride-induced liver fibrosis in mice. These findings revealed that corylin has anti-inflammatory activity and inhibits HSC activation; thus, it presents as a potential adjuvant in the treatment of liver fibrosis.</description><subject>anti-inflammation</subject><subject>Bacterial infections</subject><subject>Cancer therapies</subject><subject>Collagen</subject><subject>corylin</subject><subject>Cytokines</subject><subject>Flavonoids</subject><subject>growth arrest-specific gene 6/AXL signaling pathway</subject><subject>hepatic stellate cell</subject><subject>Hepatitis</subject><subject>Infections</subject><subject>Inflammation</subject><subject>Kinases</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>liver fibrosis</subject><subject>Natural products</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Tumor necrosis factor-TNF</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkc1v1DAQxSNEJUrhyN0SFy6h43G-fFxFtF1pEYhtpd4sx55svcomi-2A9sD_jsMiBJzeaPSbp3kzWfaGw3shJFy7_SFggYJXUlTPskteIOYAVf38r_pF9jKEPQAKLOVl9qOd_GlwI1vFSOOsIwXWtkORr0c7G7Js476RZzeu81NwgSXyozPEuhP7Qrt50NGNOxafiN2uttX16nHDtm436mFpf9bx6bs-LUN3dEyoYdtIQxoi1iYNr7KLXg-BXv_Wq-zh5sN9e5dvPt2u29UmNwWImBsB2AvLOVgEqGUvaxLUFCUXZKFHwsZabnSHjYaytmVd1hL6hle9Lbq6EVfZ-uxrJ71XR-8O2p_UpJ361Zj8Tmmf1htIGVNiiaYGqmRBndRcl1ZWkizvEcTi9e7sdfTT15lCVAcXzJJqpGkOCiWgrLCRRULf_ofup9mn4ySqkQlIWRbD_EyZdOLgqf-zIAe1PFb981jxE2MilII</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Chen, Chin-Chuan</creator><creator>Chen, Chi-Yuan</creator><creator>Yeh, Chau-Ting</creator><creator>Liu, Yi-Tsen</creator><creator>Leu, Yann-Lii</creator><creator>Chuang, Wen-Yu</creator><creator>Shih, Yin-Hwa</creator><creator>Chou, Li-Fang</creator><creator>Shieh, Tzong-Ming</creator><creator>Wang, Tong-Hong</creator><general>MDPI AG</general><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>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9248-9031</orcidid><orcidid>https://orcid.org/0000-0002-1649-6798</orcidid><orcidid>https://orcid.org/0000-0003-0893-4185</orcidid><orcidid>https://orcid.org/0000-0003-1759-9120</orcidid></search><sort><creationdate>20231201</creationdate><title>Corylin Attenuates CCl4-Induced Liver Fibrosis in Mice by Regulating the GAS6/AXL Signaling Pathway in Hepatic Stellate Cells</title><author>Chen, Chin-Chuan ; Chen, Chi-Yuan ; Yeh, Chau-Ting ; Liu, Yi-Tsen ; Leu, Yann-Lii ; Chuang, Wen-Yu ; Shih, Yin-Hwa ; Chou, Li-Fang ; Shieh, Tzong-Ming ; Wang, Tong-Hong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-c302f3d110d20079f97e3e84513ed0f2e28dd1cab28a057d575790f816fd4b783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>anti-inflammation</topic><topic>Bacterial infections</topic><topic>Cancer therapies</topic><topic>Collagen</topic><topic>corylin</topic><topic>Cytokines</topic><topic>Flavonoids</topic><topic>growth arrest-specific gene 6/AXL signaling pathway</topic><topic>hepatic stellate cell</topic><topic>Hepatitis</topic><topic>Infections</topic><topic>Inflammation</topic><topic>Kinases</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>liver fibrosis</topic><topic>Natural products</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Chin-Chuan</creatorcontrib><creatorcontrib>Chen, Chi-Yuan</creatorcontrib><creatorcontrib>Yeh, Chau-Ting</creatorcontrib><creatorcontrib>Liu, Yi-Tsen</creatorcontrib><creatorcontrib>Leu, Yann-Lii</creatorcontrib><creatorcontrib>Chuang, Wen-Yu</creatorcontrib><creatorcontrib>Shih, Yin-Hwa</creatorcontrib><creatorcontrib>Chou, Li-Fang</creatorcontrib><creatorcontrib>Shieh, Tzong-Ming</creatorcontrib><creatorcontrib>Wang, Tong-Hong</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Chin-Chuan</au><au>Chen, Chi-Yuan</au><au>Yeh, Chau-Ting</au><au>Liu, Yi-Tsen</au><au>Leu, Yann-Lii</au><au>Chuang, Wen-Yu</au><au>Shih, Yin-Hwa</au><au>Chou, Li-Fang</au><au>Shieh, Tzong-Ming</au><au>Wang, Tong-Hong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Corylin Attenuates CCl4-Induced Liver Fibrosis in Mice by Regulating the GAS6/AXL Signaling Pathway in Hepatic Stellate Cells</atitle><jtitle>International journal of molecular sciences</jtitle><date>2023-12-01</date><risdate>2023</risdate><volume>24</volume><issue>23</issue><spage>16936</spage><pages>16936-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Liver fibrosis is reversible when treated in its early stages and when liver inflammatory factors are inhibited. Limited studies have investigated the therapeutic effects of corylin, a flavonoid extracted from Psoralea corylifolia L. (Fabaceae), on liver fibrosis. Therefore, we evaluated the anti-inflammatory activity of corylin and investigated its efficacy and mechanism of action in ameliorating liver fibrosis. Corylin significantly inhibited inflammatory responses by inhibiting the activation of mitogen-activated protein kinase signaling pathways and the expression of interleukin (IL)-1β, IL-6, and tumor necrosis factor-alpha in human THP-1 and mouse RAW264.7 macrophages. Furthermore, corylin inhibited the expression of growth arrest-specific gene 6 in human hepatic stellate cells (HSCs) and the activation of the downstream phosphoinositide 3-kinase/protein kinase B pathway. This inhibited the activation of HSCs and the expression of extracellular matrix proteins, including α-smooth muscle actin and type I collagen. Additionally, corylin induced caspase 9 and caspase 3 activation, which promoted apoptosis in HSCs. Moreover, in vivo experiments confirmed the regulatory effects of corylin on these proteins, and corylin alleviated the symptoms of carbon tetrachloride-induced liver fibrosis in mice. These findings revealed that corylin has anti-inflammatory activity and inhibits HSC activation; thus, it presents as a potential adjuvant in the treatment of liver fibrosis.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/ijms242316936</doi><orcidid>https://orcid.org/0000-0001-9248-9031</orcidid><orcidid>https://orcid.org/0000-0002-1649-6798</orcidid><orcidid>https://orcid.org/0000-0003-0893-4185</orcidid><orcidid>https://orcid.org/0000-0003-1759-9120</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | anti-inflammation Bacterial infections Cancer therapies Collagen corylin Cytokines Flavonoids growth arrest-specific gene 6/AXL signaling pathway hepatic stellate cell Hepatitis Infections Inflammation Kinases Liver cancer Liver cirrhosis liver fibrosis Natural products Physiology Proteins Tumor necrosis factor-TNF |
title | Corylin Attenuates CCl4-Induced Liver Fibrosis in Mice by Regulating the GAS6/AXL Signaling Pathway in Hepatic Stellate Cells |
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