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Gut microbiota aggravate cardiac ischemia-reperfusion injury via regulating the formation of neutrophils extracellular traps
Myocardial infarction (MI) is a leading cause of death worldwide for which there is no cure. Percutaneous coronary intervention (PCI) can restore blood supply in a timely manner, which greatly reduces the mortality of patients, but ischemia/reperfusion (I/R) injury is inevitable. A number of clinica...
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Published in: | Life sciences (1973) 2022-08, Vol.303, p.120670-120670, Article 120670 |
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container_title | Life sciences (1973) |
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creator | Chen, Chunxia Zhang, Hao Xie, Ran Wang, Yaohui Ma, Yuanfang |
description | Myocardial infarction (MI) is a leading cause of death worldwide for which there is no cure. Percutaneous coronary intervention (PCI) can restore blood supply in a timely manner, which greatly reduces the mortality of patients, but ischemia/reperfusion (I/R) injury is inevitable. A number of clinical studies have shown that gut microbiota play an essential role in cardiovascular diseases. This study aims to explore the mechanism of gut microbiota to limit I/R injury.
This study adopted the myocardial I/R model using gut microbiota clearance mice, neutrophil clearance mice and double-scavenging mice, and explored the relationship between gut microbiota and NETs during I/R injury. Neutrophils were isolated in vitro to explore the effect of NETs on myocardial cell injury and its molecular mechanism.
Gut microbiota aggravate cardiac I/R injury via regulating the formation of NETs. The migration of gut microbiota to blood stimulated the formation of NETs after cardiac I/R. NETs, which can directly lead to apoptosis of myocardial cells and myocardial microvascular endothelial cells. The time point of NETs formation in tissue and blood after I/R were determined by experiments.
It was confirmed that gut microbiota participates in cardiac I/R injury by regulating the formation of NETs, which reveals a new mechanism of I/R injury and provides a new potential target for the treatment of I/R injury. |
doi_str_mv | 10.1016/j.lfs.2022.120670 |
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This study adopted the myocardial I/R model using gut microbiota clearance mice, neutrophil clearance mice and double-scavenging mice, and explored the relationship between gut microbiota and NETs during I/R injury. Neutrophils were isolated in vitro to explore the effect of NETs on myocardial cell injury and its molecular mechanism.
Gut microbiota aggravate cardiac I/R injury via regulating the formation of NETs. The migration of gut microbiota to blood stimulated the formation of NETs after cardiac I/R. NETs, which can directly lead to apoptosis of myocardial cells and myocardial microvascular endothelial cells. The time point of NETs formation in tissue and blood after I/R were determined by experiments.
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This study adopted the myocardial I/R model using gut microbiota clearance mice, neutrophil clearance mice and double-scavenging mice, and explored the relationship between gut microbiota and NETs during I/R injury. Neutrophils were isolated in vitro to explore the effect of NETs on myocardial cell injury and its molecular mechanism.
Gut microbiota aggravate cardiac I/R injury via regulating the formation of NETs. The migration of gut microbiota to blood stimulated the formation of NETs after cardiac I/R. NETs, which can directly lead to apoptosis of myocardial cells and myocardial microvascular endothelial cells. The time point of NETs formation in tissue and blood after I/R were determined by experiments.
It was confirmed that gut microbiota participates in cardiac I/R injury by regulating the formation of NETs, which reveals a new mechanism of I/R injury and provides a new potential target for the treatment of I/R injury.</description><subject>Gut microbiota</subject><subject>I/R injury</subject><subject>NETs</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE2LFDEQhoMo7rj6A7xIjl56zMd00osnWdZVWPCi51Cdrsxk6O60lfTggj_eDLN6lBwqKZ56ST2MvZViK4U0H47bMeStEkptpRLGimdsIzt70wij5XO2EULtGq1Ee8Ve5XwUQrSt1S_ZlW7NTlhrN-z3_Vr4FD2lPqYCHPZ7ghMU5B5oiOB5zP6AU4SGcEEKa45p5nE-rvTITxE44X4docR5z8sBeUg01VdlUuAzroXScohj5virEHgcx0oTr_clv2YvAowZ3zzVa_bj89332y_Nw7f7r7efHhqvW10aI3u48Vr7znRW7gBaG1AF6ASA7YWRSmMvbWjb2pE4hC54NLu-wzD0AFJfs_eX3IXSzxVzcVPdqn4FZkxrdspYpesxZ1Re0GokZ8LgFooT0KOTwp2lu6Or0t1ZurtIrzPvnuLXfsLh38RfyxX4eAGwLnmKSC77iLPHIRL64oYU_xP_B7Fklk0</recordid><startdate>20220815</startdate><enddate>20220815</enddate><creator>Chen, Chunxia</creator><creator>Zhang, Hao</creator><creator>Xie, Ran</creator><creator>Wang, Yaohui</creator><creator>Ma, Yuanfang</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20220815</creationdate><title>Gut microbiota aggravate cardiac ischemia-reperfusion injury via regulating the formation of neutrophils extracellular traps</title><author>Chen, Chunxia ; Zhang, Hao ; Xie, Ran ; Wang, Yaohui ; Ma, Yuanfang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-61ba9c33c868714aa57fe2fa80aa7b06123eb17f5580a1edf8fce64b8efdbaa13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Gut microbiota</topic><topic>I/R injury</topic><topic>NETs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Chunxia</creatorcontrib><creatorcontrib>Zhang, Hao</creatorcontrib><creatorcontrib>Xie, Ran</creatorcontrib><creatorcontrib>Wang, Yaohui</creatorcontrib><creatorcontrib>Ma, Yuanfang</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Chunxia</au><au>Zhang, Hao</au><au>Xie, Ran</au><au>Wang, Yaohui</au><au>Ma, Yuanfang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gut microbiota aggravate cardiac ischemia-reperfusion injury via regulating the formation of neutrophils extracellular traps</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>2022-08-15</date><risdate>2022</risdate><volume>303</volume><spage>120670</spage><epage>120670</epage><pages>120670-120670</pages><artnum>120670</artnum><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Myocardial infarction (MI) is a leading cause of death worldwide for which there is no cure. Percutaneous coronary intervention (PCI) can restore blood supply in a timely manner, which greatly reduces the mortality of patients, but ischemia/reperfusion (I/R) injury is inevitable. A number of clinical studies have shown that gut microbiota play an essential role in cardiovascular diseases. This study aims to explore the mechanism of gut microbiota to limit I/R injury.
This study adopted the myocardial I/R model using gut microbiota clearance mice, neutrophil clearance mice and double-scavenging mice, and explored the relationship between gut microbiota and NETs during I/R injury. Neutrophils were isolated in vitro to explore the effect of NETs on myocardial cell injury and its molecular mechanism.
Gut microbiota aggravate cardiac I/R injury via regulating the formation of NETs. The migration of gut microbiota to blood stimulated the formation of NETs after cardiac I/R. NETs, which can directly lead to apoptosis of myocardial cells and myocardial microvascular endothelial cells. The time point of NETs formation in tissue and blood after I/R were determined by experiments.
It was confirmed that gut microbiota participates in cardiac I/R injury by regulating the formation of NETs, which reveals a new mechanism of I/R injury and provides a new potential target for the treatment of I/R injury.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>35640777</pmid><doi>10.1016/j.lfs.2022.120670</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Gut microbiota I/R injury NETs |
title | Gut microbiota aggravate cardiac ischemia-reperfusion injury via regulating the formation of neutrophils extracellular traps |
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