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Dynamic changes of the renin-angiotensin and associated systems in the rat after pharmacological and dietary interventions in vivo

机译:体内药理和饮食干预后大鼠肾素-血管紧张素及相关系统的动态变化

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To address the multiplicity of the renin-angiotensin system (RAS) with particular interest in its local, synergistic regulation, we investigate dynamic changes of the RAS and associated systems in response to external stimuli in the rat. We tested influences of the RAS blockade (candesartan and enalapril), diuretics (hydrochlorothiazide), high lipid diet, and salt loading on tissue mRNA level of 12 principal genes. Under the hemodynamic conditions appropriately predetermined, we quantitatively evaluated mRNA level changes with and without each intervention in five organs–the brain, heart, kidney, liver, and adipose tissues–of male rats (n = 5 each). A total of 250 tissues were examined by real-time PCR. Significant changes in mRNA level (P < 0.05) were found in a drug-, diet- and tissue-specific manner. For instance, 29% of genes (14 out of 48 tissues showing detectable mRNA levels) were differentially regulated by candesartan and enalapril, although both drugs reduced blood pressure to similar extents. When the overall interactions among 12 genes were compared between interventions, the RAS and associated systems appeared to change in the opposite direction between candesartan and high lipid diet in the adipose tissue and between candesartan and salt loading in the heart. Enalapril, however, induced unique patterns of perturbation in the local RAS under the corresponding conditions. Thus, this study provides a fundamental picture of gene expression profile in vivo in the RAS and associated systems. In particular, our data highlight differential regulation between candesartan and enalapril, which may reflect the individual pharmacological properties regarding clinical implications.
机译:为了解决对肾素-血管紧张素系统(RAS)的多样性,特别是对其局部协同调节感兴趣的问题,我们研究了RAS和相关系统对大鼠外部刺激的动态变化。我们测试了RAS阻滞剂(坎地沙坦和依那普利),利尿剂(氢氯噻嗪),高脂饮食和盐负荷对12种主要基因的组织mRNA水平的影响。在适当预定的血液动力学条件下,我们定量评估了雄性大鼠的大脑,心脏,肾脏,肝脏和脂肪组织的五个器官(每组n = 5)中有无干预的mRNA水平变化。通过实时PCR检查总共250个组织。以药物,饮食和组织特异的方式发现了mRNA水平的显着变化(P <0.05)。例如,尽管两种药物都能将血压降低至相似程度,但29%的基因(48个组织中的14个显示出可检测的mRNA水平)受到坎地沙坦和依那普利的差异调节。当比较干预之间的12个基因之间的整体相互作用时,RAS和相关系统似乎在坎地沙坦和脂肪组织中高脂饮食之间以及坎地沙坦和心脏中的盐负荷之间以相反的方向变化。然而,依那普利在相应条件下在局部RAS中引起了独特的摄动模式。因此,该研究提供了RAS和相关系统中体内基因表达谱的基本图片。特别是,我们的数据强调了坎地沙坦和依那普利之间的差异调节,这可能反映了有关临床意义的个体药理学特性。

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