{"title":"\"MicroRNA Profiling of Plasma Exosomes in Type 2 Diabetes Following Exercises\"","authors":"Xinwen Cui","doi":"10.26717/bjstr.2023.53.008336","DOIUrl":null,"url":null,"abstract":"A total of 12 male participants, including 7 patients and 5 healthy individuals, were recruited. T2D patients underwent a randomized three-period crossover 1-hour postprandial intervention: high-intensity interval exercise (T2D-HIIE), moderate-intensity continuous exercise (T2D-MICE) with cycling and sedentary control (T2D-CON) for 30 min, while healthy participants served as controls (HP-CON) without exercise intervention. Exosomes were extracted from plasma using differential ultracentrifugation at 1.5 hours postprandial, which equates to immediate post-exercise for T2D patients. Exosomal miRNA sequencing was conducted. KEGG analysis was performed to identify pathways linked with altered expression of miRNAs.","PeriodicalId":9187,"journal":{"name":"Biomedical Journal of Scientific and Technical Research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedical Journal of Scientific and Technical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26717/bjstr.2023.53.008336","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
A total of 12 male participants, including 7 patients and 5 healthy individuals, were recruited. T2D patients underwent a randomized three-period crossover 1-hour postprandial intervention: high-intensity interval exercise (T2D-HIIE), moderate-intensity continuous exercise (T2D-MICE) with cycling and sedentary control (T2D-CON) for 30 min, while healthy participants served as controls (HP-CON) without exercise intervention. Exosomes were extracted from plasma using differential ultracentrifugation at 1.5 hours postprandial, which equates to immediate post-exercise for T2D patients. Exosomal miRNA sequencing was conducted. KEGG analysis was performed to identify pathways linked with altered expression of miRNAs.