Feng Hong, Li Haiying, Zhang Derong, Zhao Yungang, Jiang Ning, Zhao Xiaoling, Zhang Y U, Tan Junzhen, Fang Wen, Zhang Yong, Liu Wei
Tianjin Key Laboratory of Exercise Physiology and Sports Medicine, Tianjin University of Sport, Tianjin 300381, P.R. China.
Institute of Health and Environmental Medicine, Tianjin 300050, P.R. China.
Biomed Rep. 2015 Sep;3(5):681-686. doi: 10.3892/br.2015.488. Epub 2015 Jul 10.
Decreased arterial compliance is one of the earliest detectable manifestations of adverse structural and functional changes within the vessel wall in hypertension. The proteomic approach is a powerful technique to analyze a complex mixture of proteins in various settings. Physical activity level was negatively associated with blood pressure. Sixteen 4-week-old male spontaneously hypertensive rats (SHR) and 16 Wistar-Kyoto (WKY) rats were randomly divided into four groups: i) SHR exercise group, ii) SHR rest group, iii) WKY exercise group and iv) WKY rest group. In the SHR and WKY exercise groups, rats were treated with a 6-week load-free swimming protocol (1 h/day, 5 days/week). The blood pressure of the rats was tested by the CODA single non-invasive blood pressure measurement appliance. After the 6-week swimming protocol, the total aorta excluding abdominal aorta was extracted. The proteins were separated by two-dimensional gel electrophoresis and identified via LC-mass spectrometry (MS)/MS. After 6-week load-free swimming, blood pressure decreased in the SHRs. Compared with sedentary SHRs, 11 spots on the 2D-gel showed a significant difference in exercised SHRs. Nine of these were chosen for further identification. There were 5 upregulated proteins (long-chain specific acyl-CoA dehydrogenase, heat shock protein β-1, isocitrate dehydrogenase subunit α, actin, α cardiac muscle 1 preprotein and calmodulin isoform 2) and 4 downregulated proteins (adipocyte-type fatty acid-binding protein, tubulin β-2C chain, 78 kDa glucose-regulated protein precursor and mimecan). Proteomics is an effective method to identify the target proteins of exercise intervention for hypertension.
动脉顺应性降低是高血压患者血管壁不良结构和功能变化最早可检测到的表现之一。蛋白质组学方法是一种在各种情况下分析复杂蛋白质混合物的强大技术。身体活动水平与血压呈负相关。将16只4周龄雄性自发性高血压大鼠(SHR)和16只Wistar-Kyoto(WKY)大鼠随机分为四组:i)SHR运动组,ii)SHR休息组,iii)WKY运动组和iv)WKY休息组。在SHR和WKY运动组中,大鼠接受为期6周的无负荷游泳方案(每天1小时,每周5天)。用CODA单通道无创血压测量仪测量大鼠血压。经过6周的游泳方案后,取出除腹主动脉外的整个主动脉。通过二维凝胶电泳分离蛋白质,并通过液相色谱-质谱联用(LC-MS)/MS进行鉴定。经过6周的无负荷游泳后,SHR的血压下降。与久坐的SHR相比,运动的SHR在二维凝胶上有11个斑点显示出显著差异。其中9个被选作进一步鉴定。有5种上调蛋白(长链特异性酰基辅酶A脱氢酶、热休克蛋白β-1、异柠檬酸脱氢酶亚基α、肌动蛋白、α心肌1前体蛋白和钙调蛋白异构体2)和4种下调蛋白(脂肪细胞型脂肪酸结合蛋白、微管蛋白β-2C链、78 kDa葡萄糖调节蛋白前体和mimecan)。蛋白质组学是鉴定运动干预高血压靶蛋白的有效方法。