Laboratory of Physiologic Studies, National Institute on Alcohol Abuse and Alcoholism, National Institute of Health, Bethesda, Maryland, United States of America.
PLoS One. 2010 Dec 23;5(12):e15705. doi: 10.1371/journal.pone.0015705.
Resveratrol, a constituent of red wine, is important for cardioprotection. MicroRNAs are known regulators for genes involved in resveratrol-mediated cardiac remodeling and the regulatory pathway involving microRNA has not been studied so far.
We explored the cardioprotection by resveratrol in ischemia/reperfusion model of rat and determined cardiac functions. miRNA profile was determined from isolated RNA using quantitative Real-time PCR based array. Systemic analyses of miRNA array and theirs targets were determined using a number of computational approaches.
Cardioprotection by resveratrol and its derivative in ischemia/reperfusion [I/R] rat model was examined with miRNA expression profile. Unique expression pattern were found for each sample, particularly with resveratrol [pure compound] and longevinex [commercial resveratrol formulation] pretreated hearts. Longevinex and resveratrol pretreatment modulates the expression pattern of miRNAs close to the control level based on PCA analyses. Differential expression was observed in over 25 miRNAs, some of them, such as miR-21 were previously implicated in cardiac remodeling. The target genes for the differentially expressed miRNA include genes of various molecular function such as metal ion binding, sodium-potassium ion, transcription factors, which may play key role in reducing I/R injury.
Rats pretreated with resveratrol for 3 weeks leads to significant cardioprotection against ischemia/reperfusion injury. A unique signature of miRNA profile is observed in control heart pretreated with resveratrol or longevinex. We have determined specific group of miRNA in heart that have altered during IR injuries. Most of those altered microRNA expressions modulated close to their basal level in resveratrol or longevinex treated I/R mice.
白藜芦醇是红酒的一种成分,对心脏保护很重要。microRNA 是已知的调节参与白藜芦醇介导的心脏重构的基因的调节剂,到目前为止,还没有研究涉及 microRNA 的调节途径。
我们在大鼠缺血/再灌注模型中探索了白藜芦醇的心脏保护作用,并测定了心脏功能。使用基于定量实时 PCR 的阵列从分离的 RNA 中测定 miRNA 谱。使用多种计算方法对 miRNA 阵列及其靶标进行了系统分析。
使用 miRNA 表达谱研究了白藜芦醇及其衍生物在缺血/再灌注(I/R)大鼠模型中的心脏保护作用。每个样本都发现了独特的表达模式,特别是在用白藜芦醇(纯化合物)和 Longevinex(商业白藜芦醇配方)预处理的心脏中。基于 PCA 分析,Longevinex 和白藜芦醇预处理使 miRNA 的表达模式接近对照水平。在超过 25 个 miRNA 中观察到差异表达,其中一些,如 miR-21,先前被认为与心脏重构有关。差异表达的 miRNA 的靶基因包括各种分子功能的基因,如金属离子结合、钠离子-钾离子、转录因子,它们可能在减少 I/R 损伤中发挥关键作用。
用白藜芦醇预处理 3 周的大鼠可显著对抗缺血/再灌注损伤。在用白藜芦醇或 Longevinex 预处理的对照心脏中观察到 miRNA 谱的独特特征。我们已经确定了在 IR 损伤期间心脏中改变的特定 miRNA 组。在白藜芦醇或 Longevinex 处理的 I/R 小鼠中,大多数改变的 microRNA 表达接近其基础水平。