梓醇调节MiR-126/TWEAK-FN14通路抗心肌再灌注损伤机制的体外及计算机模拟研究

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-05-09 eCollection Date: 2025-05-20 DOI:10.1021/acsomega.4c11357
Ting Wang, Chongyu Shao, Huiyan An, Guanfeng Xu, Haitong Wan, Jiehong Yang
{"title":"梓醇调节MiR-126/TWEAK-FN14通路抗心肌再灌注损伤机制的体外及计算机模拟研究","authors":"Ting Wang, Chongyu Shao, Huiyan An, Guanfeng Xu, Haitong Wan, Jiehong Yang","doi":"10.1021/acsomega.4c11357","DOIUrl":null,"url":null,"abstract":"<p><p>The objective of this study was to investigate the mechanism through which catalpol (CAT) exerts its protective effects in the context of myocardial ischemia-reperfusion injury. Preliminary results showed that Cat significantly attenuated oxygen-glucose deprivation/reoxygenation (OGD/R) damage to H9C2 cells, inhibited intracellular reactive oxygen species levels, and downregulated the protein expression of TWEAK and Fn14 post-OGD/R. The intracellular level of miR-126 was downregulated after OGD/R, and this effect was reversed by CAT administration. To further elucidate its mechanisms, a miR-126 inhibitor was used in the H9C2 cells, and the inhibitory effect was validated using real-time fluorescence quantitative polymerase chain reaction (RT-PCR). Following CAT treatment, lactate dehydrogenase (LDH) levels within the cells were assessed. The results revealed that CAT not only decreased LDH levels but also modulated the miR-126/TWEAK-FN14 signaling axis and the expression of inflammatory-related mediators, as evidenced through RT-PCR and Western blot. Additionally, molecular docking (MD) studies suggested that CAT exhibited a strong binding affinity to both the signaling pathway and inflammatory-related components. Furthermore, molecular dynamics simulations (MDS) demonstrated that the CAT-protein complex exhibited high stability, flexibility, and low binding free energy under physiological conditions. Additionally, CAT showed favorable absorption, distribution, metabolism, excretion, and toxicity characteristics. In summary, this study, through in vitro experimentation, confirmed that CAT regulates the miR-126 and inflammatory proteins within the signaling pathway, with these results being further supported by MD and MDS analyses.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"10 19","pages":"19538-19551"},"PeriodicalIF":4.3000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12096214/pdf/","citationCount":"0","resultStr":"{\"title\":\"Catalpol Research on the Mechanism of Antimyocardial Reperfusion Injury by Regulating the MiR-126/TWEAK-FN14 Pathway: In Vitro and Computer Simulation Studies.\",\"authors\":\"Ting Wang, Chongyu Shao, Huiyan An, Guanfeng Xu, Haitong Wan, Jiehong Yang\",\"doi\":\"10.1021/acsomega.4c11357\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The objective of this study was to investigate the mechanism through which catalpol (CAT) exerts its protective effects in the context of myocardial ischemia-reperfusion injury. Preliminary results showed that Cat significantly attenuated oxygen-glucose deprivation/reoxygenation (OGD/R) damage to H9C2 cells, inhibited intracellular reactive oxygen species levels, and downregulated the protein expression of TWEAK and Fn14 post-OGD/R. The intracellular level of miR-126 was downregulated after OGD/R, and this effect was reversed by CAT administration. To further elucidate its mechanisms, a miR-126 inhibitor was used in the H9C2 cells, and the inhibitory effect was validated using real-time fluorescence quantitative polymerase chain reaction (RT-PCR). Following CAT treatment, lactate dehydrogenase (LDH) levels within the cells were assessed. The results revealed that CAT not only decreased LDH levels but also modulated the miR-126/TWEAK-FN14 signaling axis and the expression of inflammatory-related mediators, as evidenced through RT-PCR and Western blot. Additionally, molecular docking (MD) studies suggested that CAT exhibited a strong binding affinity to both the signaling pathway and inflammatory-related components. Furthermore, molecular dynamics simulations (MDS) demonstrated that the CAT-protein complex exhibited high stability, flexibility, and low binding free energy under physiological conditions. Additionally, CAT showed favorable absorption, distribution, metabolism, excretion, and toxicity characteristics. In summary, this study, through in vitro experimentation, confirmed that CAT regulates the miR-126 and inflammatory proteins within the signaling pathway, with these results being further supported by MD and MDS analyses.</p>\",\"PeriodicalId\":22,\"journal\":{\"name\":\"ACS Omega\",\"volume\":\"10 19\",\"pages\":\"19538-19551\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-05-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12096214/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Omega\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acsomega.4c11357\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/5/20 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsomega.4c11357","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/20 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

本研究旨在探讨梓醇(CAT)在心肌缺血再灌注损伤中发挥保护作用的机制。初步结果显示,Cat可显著减轻氧葡萄糖剥夺/再氧化(OGD/R)对H9C2细胞的损伤,抑制细胞内活性氧水平,下调OGD/R后TWEAK和Fn14蛋白表达。细胞内miR-126水平在OGD/R后下调,这种作用被CAT逆转。为了进一步阐明其机制,我们在H9C2细胞中使用miR-126抑制剂,并通过实时荧光定量聚合酶链反应(RT-PCR)验证其抑制作用。CAT处理后,评估细胞内乳酸脱氢酶(LDH)水平。RT-PCR和Western blot结果显示,CAT不仅降低了LDH水平,还调节了miR-126/ twist - fn14信号轴和炎症相关介质的表达。此外,分子对接(MD)研究表明,CAT对信号通路和炎症相关成分都具有很强的结合亲和力。此外,分子动力学模拟(MDS)表明,CAT-protein复合物在生理条件下具有高稳定性、柔韧性和低结合自由能。此外,CAT具有良好的吸收、分布、代谢、排泄和毒性特性。综上所述,本研究通过体外实验证实了CAT在信号通路中调控miR-126和炎症蛋白,MD和MDS分析进一步支持了这些结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catalpol Research on the Mechanism of Antimyocardial Reperfusion Injury by Regulating the MiR-126/TWEAK-FN14 Pathway: In Vitro and Computer Simulation Studies.

The objective of this study was to investigate the mechanism through which catalpol (CAT) exerts its protective effects in the context of myocardial ischemia-reperfusion injury. Preliminary results showed that Cat significantly attenuated oxygen-glucose deprivation/reoxygenation (OGD/R) damage to H9C2 cells, inhibited intracellular reactive oxygen species levels, and downregulated the protein expression of TWEAK and Fn14 post-OGD/R. The intracellular level of miR-126 was downregulated after OGD/R, and this effect was reversed by CAT administration. To further elucidate its mechanisms, a miR-126 inhibitor was used in the H9C2 cells, and the inhibitory effect was validated using real-time fluorescence quantitative polymerase chain reaction (RT-PCR). Following CAT treatment, lactate dehydrogenase (LDH) levels within the cells were assessed. The results revealed that CAT not only decreased LDH levels but also modulated the miR-126/TWEAK-FN14 signaling axis and the expression of inflammatory-related mediators, as evidenced through RT-PCR and Western blot. Additionally, molecular docking (MD) studies suggested that CAT exhibited a strong binding affinity to both the signaling pathway and inflammatory-related components. Furthermore, molecular dynamics simulations (MDS) demonstrated that the CAT-protein complex exhibited high stability, flexibility, and low binding free energy under physiological conditions. Additionally, CAT showed favorable absorption, distribution, metabolism, excretion, and toxicity characteristics. In summary, this study, through in vitro experimentation, confirmed that CAT regulates the miR-126 and inflammatory proteins within the signaling pathway, with these results being further supported by MD and MDS analyses.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信