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Apoptotic Cell Death in Cardiomyocytes Induced by Hypoxia from Cobalt Chloride Is Hastened by SGLT-1 Inhibition 抑制SGLT-1可加速氯化钴缺氧诱导心肌细胞凋亡
Q2 Health Professions Pub Date : 2023-09-01 DOI: 10.1089/aivt.2023.0006
Abhinav Kanwal, Lu Liu, Puneet Kumar Bansal, Hemant Kumar, Shailendra Pratap Singh
Introduction: Myocardial ischemia is responsible for the deaths of millions of people every year. Cardiac hypoxia reduces the efficiency with which the heart muscle pumps blood. When one or more of the coronary arteries abruptly and severely narrows or closes off, this is known as an acute coronary syndrome (ACS). Ischemia of the heart muscle can also cause potentially fatal arrhythmias. More information about this topic is required. Methods: The effects of SGLT-1 inhibition were studied using a different disease model, the cobalt chloride (CoCl2) hypoxia paradigm. The MTT assay was used to examine the effects of CoCl2 with and without Phlorizin (PZ) on glucose uptake, caspase activity, and metabolic/cytotoxic activities in SGLT-1 overexpressed H9C2 cells. Both SGLT-1 siRNA silencing and PZ treatment of SGLT-1 overexpressed neonatal rat cardiomyocytes were studied. Results and Discussion: Using flow cytometry, we were able to distinguish between metabolically active (PI-stained) and inactive (annexin-stained) live cells, as well as apoptotic (annexin-stained) and necrotic (PI-stained) cells. Caspase 3, 9, bcl-2, HIF-1a, and SGLT-1 expression, as well as oxidative stress, were examined using Western blotting. H9C2 cells showed increased caspase 3 and 9 activity in the CoCl2 group compared to the control, and these increases were further amplified by PZ cotreatment. PZ did not counteract CoCl2's effects of decreased glucose absorption and MTT activity. Conclusion: PZ increased cardiomyocyte apoptosis and decreased metabolic quiescent cells. PZ had no effect on the oxidative stress and necrosis that CoCl2 caused. CoCl2-induced SGLT-1 reduction leads to rapid apoptotic cell death.
导读:心肌缺血每年导致数百万人死亡。心源性缺氧降低了心肌泵血的效率。当一个或多个冠状动脉突然严重狭窄或关闭时,这被称为急性冠状动脉综合征(ACS)。心肌缺血也可能导致潜在的致命性心律失常。需要了解有关此主题的更多信息。方法:采用不同的疾病模型——氯化钴(CoCl2)缺氧模式,研究SGLT-1抑制的效果。MTT试验用于检测CoCl2加和不加Phlorizin (PZ)对SGLT-1过表达的H9C2细胞中葡萄糖摄取、半胱天冬酶活性和代谢/细胞毒性活性的影响。研究了SGLT-1 siRNA沉默和PZ对SGLT-1过表达新生大鼠心肌细胞的影响。结果和讨论:使用流式细胞术,我们能够区分代谢活性(pi染色)和无活性(膜联蛋白染色)活细胞,以及凋亡(膜联蛋白染色)和坏死(pi染色)细胞。采用Western blotting检测Caspase 3、9、bcl-2、HIF-1a和SGLT-1的表达以及氧化应激。与对照组相比,CoCl2组H9C2细胞显示caspase 3和caspase 9活性增加,PZ共处理进一步放大了这些增加。PZ不抵消CoCl2降低葡萄糖吸收和MTT活性的影响。结论:PZ增加心肌细胞凋亡,减少代谢静止细胞。PZ对CoCl2引起的氧化应激和坏死无明显影响。cocl2诱导的SGLT-1减少导致细胞快速凋亡。
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引用次数: 0
Kombucha Mushroom Extract: Anticancer, Antioxidant, and Antimicrobial Properties 康普茶蘑菇提取物:抗癌,抗氧化和抗菌特性
Q2 Health Professions Pub Date : 2023-07-19 DOI: 10.1089/aivt.2023.0005
F. Motafeghi, P. Mortazavi, Romina Shahsavari, Maryam Shaker, Hamideh Mohammadi-Berenjestanaki, M. Shokrzadeh
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引用次数: 0
PeakAUC: An R Shiny Application for Area Under the Peak Calculations and Nitric Oxide Analysis 峰下面积计算和一氧化氮分析的R闪亮应用
Q2 Health Professions Pub Date : 2023-06-01 DOI: 10.1089/aivt.2023.0002
Gregory Pappas, Andrew Gow
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引用次数: 0
Assessment of the Predictivity of DIO1-SK Assay to Investigate DIO1 Inhibition in Human Liver Microsomes DIO1-SK测定对人肝微粒体中DIO1抑制作用的预测性评估
Q2 Health Professions Pub Date : 2023-06-01 DOI: 10.1089/aivt.2022.0016
A. Weber, B. Birk, Varun Giri, S. Hoffmann, K. Renko, S. Coecke, S. Schneider, D. Funk-Weyer, R. Landsiedel
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引用次数: 0
Expression Analysis of Exosomal MicroRNAs in Chlorpromazine Treated Human Hepatic Spheroids: A Promising Tool for Novel Drug-Induced Liver Injury Biomarker Discovery 氯丙嗪治疗的人肝球体中外泌体MicroRNAs的表达分析:发现新型药物性肝损伤生物标志物的一个有希望的工具
Q2 Health Professions Pub Date : 2023-05-25 DOI: 10.1089/aivt.2023.0004
A. Borgström, B. Filippi, P. Hewitt, A. Wolf, M. Gebauer
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引用次数: 0
Influence of Uric Acid on Erythrocytes Subjected to H2O2-Induced Oxidative Stress 尿酸对h2o2诱导的红细胞氧化应激的影响
Q2 Health Professions Pub Date : 2023-04-12 DOI: 10.1089/aivt.2023.0001
M. Pallavi, G. S. S. Nithindran, R.V. Ranjithvishal, N. S. Laavanyaa, C. Bhat, Prerana Banerjee, Aastha Choudhary, Vani Rajashekaraiah
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引用次数: 2
Estrogenic Activity of Perfluoro Carboxylic and Sulfonic Acids in Rainbow Trout Estrogen Receptor Binding and Liver Slice Vtg mRNA Expression Assays. 全氟羧酸和磺酸对虹鳟雌激素受体结合和肝切片Vtg mRNA表达的影响
Q2 Health Professions Pub Date : 2023-03-17 DOI: 10.1089/aivt.2022.0013
Mark A Tapper, Jeffrey S Denny, Barbara R Sheedy, Ben Johnson, Richard C Kolanczyk

Perfluoroalkylated substances (PFAS) such as carboxylic acids, and sulfonic acids were manufactured in high quantities and are ubiquitous environmental contaminants. These chemicals persist in the environment and tend to bioaccumulate. In the current study, the estrogenic potential of a series of perfluoro carboxylic acids and select perfluoro sulfonic acids were assessed in an in vitro rainbow trout estrogen receptor (rtER) binding assay and an ex vivo rtER dependent vitellogenin (Vtg) expression rainbow trout liver slice assay. Perfluoro carboxylic acids with perfluoroalkyl chain lengths of four to six did not significantly bind to the rtER or induce Vtg expression in liver slices. Perfluoro carboxylic acids with chain lengths of seven to ten, and sulfonic acids with seven and eight carbon chains bound to the rtER, but with low relative binding affinities. While affinity for the rtER increased with increasing chain length the highest affinity measured was only 0.0025% relative to the endogenous hormone 17ß-estradiol at 100%. Both the eight-carbon carboxylic acid and eight-carbon sulfonic acid induced Vtg expression in ex vivo liver slices. However, toxicity did not allow expression to achieve maximum efficacy relative to estradiol.

羧酸和磺酸等全氟烷基化物质 (PFAS) 被大量生产,是无处不在的环境污染物。这些化学物质会在环境中持续存在,并有生物累积的趋势。本研究通过体外虹鳟鱼雌激素受体(rtER)结合试验和体内外依赖于 rtER 的卵黄素(Vtg)表达虹鳟鱼肝切片试验,评估了一系列全氟羧酸和部分全氟磺酸的雌激素潜力。全氟烷基链长度为 4 至 6 的全氟羧酸与 rtER 结合不明显,也不能诱导肝切片中 Vtg 的表达。链长为 7 至 10 的全氟羧酸以及碳链为 7 和 8 的磺酸与 rtER 结合,但相对结合亲和力较低。虽然与 rtER 的亲和力随着链长的增加而增加,但相对于 100%的内源性激素 17ß-estradiol 而言,测得的最高亲和力仅为 0.0025%。八碳羧酸和八碳磺酸都能诱导体内外肝脏切片中 Vtg 的表达。然而,与雌二醇相比,毒性并不能使表达达到最大效果。
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引用次数: 0
Using Rabbit Induced Pluripotent Stem Cell-Derived Cardiomyocytes to Investigate Drug-Induced Fetal Heart Malformations 利用兔诱导的多能干细胞来源的心肌细胞研究药物诱导的胎儿心脏畸形
Q2 Health Professions Pub Date : 2023-03-06 DOI: 10.1089/aivt.2022.0017
John T. Szilagyi, K. Kolaja
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引用次数: 0
Acknowledgment of Reviewers 2022 审稿人致谢
Q2 Health Professions Pub Date : 2023-03-01 DOI: 10.1089/aivt.2022.29032.ack
Applied In Vitro ToxicologyVol. 9, No. 1 AcknowledgmentFree AccessAcknowledgment of Reviewers 2022Published Online:17 Mar 2023https://doi.org/10.1089/aivt.2022.29032.ackAboutSectionsPDF/EPUB Permissions & CitationsPermissionsDownload CitationsTrack CitationsAdd to favorites Back To Publication ShareShare onFacebookTwitterLinked InRedditEmail Critical evaluations of articles by expert reviewers make a vital contribution to ensuring the high quality of a journal's content. The editorial leadership of Applied In Vitro Toxicology is very grateful for the support of the highly qualified peer reviewers who have dedicated their time and effort to reviewing our articles. We would like to show our appreciation by thanking the following individuals for their assistance with the review of articles for the journal in 2022.**Data through November 30, 2022.Raha AminiMarcelo ArboAnita BoelenChad DeisenrothEdvande dos Santos FilhoChantra EskesStephen FergusonLeonardo FranchiAnne GourmelonJosé GranjeiroRhiannon HardwickJulia HerbertHelena HogbergJian JiangAnne KahruHajime KojimaVirkas KumarGhislaine LacroixK. LeeDavid LehmannBrett LidburyLarissa Matuda MacedoShadab MdMartha MooreFiona MurphyClive RoperTimothy ShaferMaqsood A. SiddiquiDavid ThorneErwin van VlietRoman WieczorekFiguresReferencesRelatedDetails Volume 9Issue 1Mar 2023 InformationCopyright 2023, Mary Ann Liebert, Inc., publishersTo cite this article:Acknowledgment of Reviewers 2022.Applied In Vitro Toxicology.Mar 2023.35-35.http://doi.org/10.1089/aivt.2022.29032.ackPublished in Volume: 9 Issue 1: March 17, 2023PDF download
应用体外毒理学卷。9、第1位致谢免费访问审稿人致谢2022出版在线:2023年3月17日https://doi.org/10.1089/aivt.2022.29032.ackAboutSectionsPDF/EPUB许可和引文missionsdownload CitationsTrack引文添加到收藏返回出版共享分享上facebook推特链接InRedditEmail专家审稿人对文章的关键评估对确保期刊内容的高质量做出了重要贡献。《应用体外毒理学》的编辑领导非常感谢高素质的同行审稿人的支持,他们花了大量的时间和精力来审查我们的文章。我们想通过感谢以下个人对2022年期刊文章审稿的帮助来表达我们的谢意。**截至2022年11月30日的数据。Raha AminiMarcelo ArboAnita BoelenChad DeisenrothEdvande dos Santos FilhoChantra EskesStephen FergusonLeonardo FranchiAnne gourmelonjos GranjeiroRhiannon HardwickJulia HerbertHelena HogbergJian JiangAnne KahruHajime KojimaVirkas KumarGhislaine LacroixK。LeeDavid LehmannBrett LidburyLarissa Matuda MacedoShadab MdMartha MooreFiona MurphyClive rove timothy shafermaqood A. SiddiquiDavid ThorneErwin van VlietRoman wieczorek数据参考资料相关细节第9卷第1期2023年3月信息版权所有2023,Mary Ann Liebert, Inc,出版商引用本文:感谢审稿人2022。应用体外毒理学。2023.35-35.http://doi.org/10.1089/aivt.2022.29032.ackPublished卷:9第1期:2023年3月17日pdf下载
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引用次数: 0
Validation is the Key to Furthering In Vitro Toxicology 验证是推进体外毒理学的关键
Q2 Health Professions Pub Date : 2023-03-01 DOI: 10.1089/aivt.2023.29033.editorial
Andrew Gow
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引用次数: 0
期刊
Applied In Vitro Toxicology
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