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Ling-Gui-Zhu-Gan decoction inhibits cardiomyocyte pyroptosis via the NLRP3/Caspase-1 signaling pathway
The objective of this study was to investigate the protective mechanism of Ling-Gui-Zhu-Gan decoction (LGZGD) against LPS-ATP-induced pyroptosis in H9c2 cells. LPS and ATP were used to induce pyroptosis in the H9c2 cell, and the cells were divided into the control, model and LGZGD groups. LDH level...
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Published in: | Tissue & cell 2024-12, Vol.91, p.102588, Article 102588 |
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description | The objective of this study was to investigate the protective mechanism of Ling-Gui-Zhu-Gan decoction (LGZGD) against LPS-ATP-induced pyroptosis in H9c2 cells.
LPS and ATP were used to induce pyroptosis in the H9c2 cell, and the cells were divided into the control, model and LGZGD groups. LDH level was detected using a colorimetric assay. ELISA was used to detect the expressions of IL-1β. Flow cytometry was utilized to observe apoptosis, while Hoechst/PI staining was used to detect pyroptosis. Immunofluorescence was employed to observe the expression levels of NLRP3 in cardiomyocytes, and RT-PCR was used to detect NLRP3, Caspase-1, GSDMD, and ASC mRNA expression. The cells were separated into seven groups: control, model, LGZGD, MCC950, LGZGD+MCC950, Nigericin and LGZGD+Nigericin. The mRNA and protein expressions were determined by RT-PCR and Western blot.
LPS (10 μg/mL) for 12 h and ATP (8 mM) for 2 h were used as modeling condition. LGZGD demonstrated a significant reduction in LDH, and IL-1β levels (P |
doi_str_mv | 10.1016/j.tice.2024.102588 |
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LPS and ATP were used to induce pyroptosis in the H9c2 cell, and the cells were divided into the control, model and LGZGD groups. LDH level was detected using a colorimetric assay. ELISA was used to detect the expressions of IL-1β. Flow cytometry was utilized to observe apoptosis, while Hoechst/PI staining was used to detect pyroptosis. Immunofluorescence was employed to observe the expression levels of NLRP3 in cardiomyocytes, and RT-PCR was used to detect NLRP3, Caspase-1, GSDMD, and ASC mRNA expression. The cells were separated into seven groups: control, model, LGZGD, MCC950, LGZGD+MCC950, Nigericin and LGZGD+Nigericin. The mRNA and protein expressions were determined by RT-PCR and Western blot.
LPS (10 μg/mL) for 12 h and ATP (8 mM) for 2 h were used as modeling condition. LGZGD demonstrated a significant reduction in LDH, and IL-1β levels (P<0.05, P<0.01). LGZGD dramatically reduced apoptosis rate, inhibited pyroptosis, decreased the fluorescence expressions of NLRP3, and reduced the mRNA expressions of NLRP3, ASC, Caspase-1, and GSDMD (P<0.01). Further mechanism studies showed that NLRP3, ASC, Caspase-1, and GSDMD decreased significantly when combined with NLRP3 inhibitor MCC950. Furthermore, LGZGD was able to effectively reverse the upregulation of protein and gene expression of Nigericin group (P<0.01).
LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell via the NLRP3/Caspase-1 signaling pathway.
•Myocardial pyroptosis is related to activation of NLRP3/Caspase-1 signaling pathway.•LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell.•LGZGD inhibits myocardial pyroptosis via the NLRP3/Caspase-1 signaling pathway.</description><identifier>ISSN: 0040-8166</identifier><identifier>ISSN: 1532-3072</identifier><identifier>EISSN: 1532-3072</identifier><identifier>DOI: 10.1016/j.tice.2024.102588</identifier><identifier>PMID: 39442311</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Adenosine Triphosphate - metabolism ; Animals ; Caspase 1 - metabolism ; Cell Line ; Drugs, Chinese Herbal - pharmacology ; Interleukin-1beta - metabolism ; Ling-Gui-Zhu-Gan decoction ; Lipopolysaccharides - pharmacology ; Myocardial protection ; Myocytes, Cardiac - drug effects ; Myocytes, Cardiac - metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism ; NLRP3/Caspase-1 pathway ; Pyroptosis - drug effects ; Rats ; Signal Transduction - drug effects</subject><ispartof>Tissue & cell, 2024-12, Vol.91, p.102588, Article 102588</ispartof><rights>2024</rights><rights>Copyright © 2024. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c237t-ba612d48f137fbe666c407c04028488bdf11ce6eab48482c07963b09c921a2ef3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39442311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Xiao-ni</creatorcontrib><creatorcontrib>Ding, Hui-min</creatorcontrib><creatorcontrib>Ma, Yao-yao</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Zhou, Peng</creatorcontrib><title>Ling-Gui-Zhu-Gan decoction inhibits cardiomyocyte pyroptosis via the NLRP3/Caspase-1 signaling pathway</title><title>Tissue & cell</title><addtitle>Tissue Cell</addtitle><description>The objective of this study was to investigate the protective mechanism of Ling-Gui-Zhu-Gan decoction (LGZGD) against LPS-ATP-induced pyroptosis in H9c2 cells.
LPS and ATP were used to induce pyroptosis in the H9c2 cell, and the cells were divided into the control, model and LGZGD groups. LDH level was detected using a colorimetric assay. ELISA was used to detect the expressions of IL-1β. Flow cytometry was utilized to observe apoptosis, while Hoechst/PI staining was used to detect pyroptosis. Immunofluorescence was employed to observe the expression levels of NLRP3 in cardiomyocytes, and RT-PCR was used to detect NLRP3, Caspase-1, GSDMD, and ASC mRNA expression. The cells were separated into seven groups: control, model, LGZGD, MCC950, LGZGD+MCC950, Nigericin and LGZGD+Nigericin. The mRNA and protein expressions were determined by RT-PCR and Western blot.
LPS (10 μg/mL) for 12 h and ATP (8 mM) for 2 h were used as modeling condition. LGZGD demonstrated a significant reduction in LDH, and IL-1β levels (P<0.05, P<0.01). LGZGD dramatically reduced apoptosis rate, inhibited pyroptosis, decreased the fluorescence expressions of NLRP3, and reduced the mRNA expressions of NLRP3, ASC, Caspase-1, and GSDMD (P<0.01). Further mechanism studies showed that NLRP3, ASC, Caspase-1, and GSDMD decreased significantly when combined with NLRP3 inhibitor MCC950. Furthermore, LGZGD was able to effectively reverse the upregulation of protein and gene expression of Nigericin group (P<0.01).
LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell via the NLRP3/Caspase-1 signaling pathway.
•Myocardial pyroptosis is related to activation of NLRP3/Caspase-1 signaling pathway.•LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell.•LGZGD inhibits myocardial pyroptosis via the NLRP3/Caspase-1 signaling pathway.</description><subject>Adenosine Triphosphate - metabolism</subject><subject>Animals</subject><subject>Caspase 1 - metabolism</subject><subject>Cell Line</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Interleukin-1beta - metabolism</subject><subject>Ling-Gui-Zhu-Gan decoction</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Myocardial protection</subject><subject>Myocytes, Cardiac - drug effects</subject><subject>Myocytes, Cardiac - metabolism</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</subject><subject>NLRP3/Caspase-1 pathway</subject><subject>Pyroptosis - drug effects</subject><subject>Rats</subject><subject>Signal Transduction - drug effects</subject><issn>0040-8166</issn><issn>1532-3072</issn><issn>1532-3072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kE1rGzEQhkVJaZy0f6CHomMucvRl7Rp6CSZ1AqYtpb30IrTa2XiMvdpI2pT995FxkmNPwwzPvPA-hHwWfC64MNe7eUYPc8mlLge5qOt3ZCYWSjLFK3lGZpxrzmphzDm5SGnHOa-0qD6Qc7XUWiohZqTbYP_A1iOyv9uRrV1PW_DBZww9xX6LDeZEvYsthsMU_JSBDlMMQw4JE31CR_MW6PfNr5_qeuXS4BIwQRM-9G5fkung8vafmz6S953bJ_j0Mi_Jn2-3v1d3bPNjfb-62TAvVZVZ44yQra47oaquAWOM17zypYasdV03bSeEBwOu0WWXnldLoxq-9EspnIROXZKrU-4Qw-MIKdsDJg_7veshjMkqITlfmFK_oPKE-hhSitDZIeLBxckKbo9-7c4e_dqjX3vyW56-vOSPzQHat5dXoQX4egKgtHxCiDZ5hN5DixF8tm3A_-U_Ayvoi78</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Zhao, Xiao-ni</creator><creator>Ding, Hui-min</creator><creator>Ma, Yao-yao</creator><creator>Wang, Liang</creator><creator>Zhou, Peng</creator><general>Elsevier Ltd</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>20241201</creationdate><title>Ling-Gui-Zhu-Gan decoction inhibits cardiomyocyte pyroptosis via the NLRP3/Caspase-1 signaling pathway</title><author>Zhao, Xiao-ni ; Ding, Hui-min ; Ma, Yao-yao ; Wang, Liang ; Zhou, Peng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c237t-ba612d48f137fbe666c407c04028488bdf11ce6eab48482c07963b09c921a2ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adenosine Triphosphate - metabolism</topic><topic>Animals</topic><topic>Caspase 1 - metabolism</topic><topic>Cell Line</topic><topic>Drugs, Chinese Herbal - pharmacology</topic><topic>Interleukin-1beta - metabolism</topic><topic>Ling-Gui-Zhu-Gan decoction</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Myocardial protection</topic><topic>Myocytes, Cardiac - drug effects</topic><topic>Myocytes, Cardiac - metabolism</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - metabolism</topic><topic>NLRP3/Caspase-1 pathway</topic><topic>Pyroptosis - drug effects</topic><topic>Rats</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Xiao-ni</creatorcontrib><creatorcontrib>Ding, Hui-min</creatorcontrib><creatorcontrib>Ma, Yao-yao</creatorcontrib><creatorcontrib>Wang, Liang</creatorcontrib><creatorcontrib>Zhou, Peng</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>Tissue & cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Xiao-ni</au><au>Ding, Hui-min</au><au>Ma, Yao-yao</au><au>Wang, Liang</au><au>Zhou, Peng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ling-Gui-Zhu-Gan decoction inhibits cardiomyocyte pyroptosis via the NLRP3/Caspase-1 signaling pathway</atitle><jtitle>Tissue & cell</jtitle><addtitle>Tissue Cell</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>91</volume><spage>102588</spage><pages>102588-</pages><artnum>102588</artnum><issn>0040-8166</issn><issn>1532-3072</issn><eissn>1532-3072</eissn><abstract>The objective of this study was to investigate the protective mechanism of Ling-Gui-Zhu-Gan decoction (LGZGD) against LPS-ATP-induced pyroptosis in H9c2 cells.
LPS and ATP were used to induce pyroptosis in the H9c2 cell, and the cells were divided into the control, model and LGZGD groups. LDH level was detected using a colorimetric assay. ELISA was used to detect the expressions of IL-1β. Flow cytometry was utilized to observe apoptosis, while Hoechst/PI staining was used to detect pyroptosis. Immunofluorescence was employed to observe the expression levels of NLRP3 in cardiomyocytes, and RT-PCR was used to detect NLRP3, Caspase-1, GSDMD, and ASC mRNA expression. The cells were separated into seven groups: control, model, LGZGD, MCC950, LGZGD+MCC950, Nigericin and LGZGD+Nigericin. The mRNA and protein expressions were determined by RT-PCR and Western blot.
LPS (10 μg/mL) for 12 h and ATP (8 mM) for 2 h were used as modeling condition. LGZGD demonstrated a significant reduction in LDH, and IL-1β levels (P<0.05, P<0.01). LGZGD dramatically reduced apoptosis rate, inhibited pyroptosis, decreased the fluorescence expressions of NLRP3, and reduced the mRNA expressions of NLRP3, ASC, Caspase-1, and GSDMD (P<0.01). Further mechanism studies showed that NLRP3, ASC, Caspase-1, and GSDMD decreased significantly when combined with NLRP3 inhibitor MCC950. Furthermore, LGZGD was able to effectively reverse the upregulation of protein and gene expression of Nigericin group (P<0.01).
LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell via the NLRP3/Caspase-1 signaling pathway.
•Myocardial pyroptosis is related to activation of NLRP3/Caspase-1 signaling pathway.•LGZGD inhibits LPS-ATP-induced pyroptosis in H9c2 cell.•LGZGD inhibits myocardial pyroptosis via the NLRP3/Caspase-1 signaling pathway.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>39442311</pmid><doi>10.1016/j.tice.2024.102588</doi></addata></record> |
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subjects | Adenosine Triphosphate - metabolism Animals Caspase 1 - metabolism Cell Line Drugs, Chinese Herbal - pharmacology Interleukin-1beta - metabolism Ling-Gui-Zhu-Gan decoction Lipopolysaccharides - pharmacology Myocardial protection Myocytes, Cardiac - drug effects Myocytes, Cardiac - metabolism NLR Family, Pyrin Domain-Containing 3 Protein - metabolism NLRP3/Caspase-1 pathway Pyroptosis - drug effects Rats Signal Transduction - drug effects |
title | Ling-Gui-Zhu-Gan decoction inhibits cardiomyocyte pyroptosis via the NLRP3/Caspase-1 signaling pathway |
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