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超声靶向微泡破坏对心脏基因表达的影响。

Effects of ultrasound-targeted microbubble destruction on cardiac gene expression.

作者信息

Bekeredjian Raffi, Chen Shuyuan, Pan Wentong, Grayburn Paul A, Shohet Ralph V

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.

出版信息

Ultrasound Med Biol. 2004 Apr;30(4):539-43. doi: 10.1016/j.ultrasmedbio.2003.12.006.

Abstract

Ultrasound (US) contrast agents are increasingly used in diagnostic echocardiography. Recent studies have suggested unanticipated effects of microbubble destruction. This study was designed to evaluate gene regulation caused by US-mediated destruction of microbubbles in the heart. During IV infusion of Optison trade mark, triggered US was applied to rat hearts to destroy microbubbles. A control group received only saline and US. RNA was isolated from hearts 24 and 72 h after treatment. Analysis with a deeply representative murine cardiac-specific microarray was used to identify regulated genes. Real-time polymerase chain reaction (PCR) was then applied to verify regulated genes. Microarray analysis revealed only 5 regulated genes in the 24-h group and 4 in the 72-h group. Of these genes, only carbonic anhydrase was significantly upregulated in the 24-h Optison trade mark group (4.3 fold; p = 0.0005) when examined in individual animals by real-time PCR. By this very sensitive technique, the bioeffects of microbubble destruction are negligible.

摘要

超声(US)造影剂在诊断性超声心动图中的应用越来越广泛。最近的研究表明微泡破坏存在意想不到的影响。本研究旨在评估超声介导的心脏微泡破坏所引起的基因调控。在静脉输注Optison商标制剂期间,对大鼠心脏施加触发超声以破坏微泡。对照组仅接受生理盐水和超声。在治疗后24小时和72小时从心脏分离RNA。使用具有高度代表性的小鼠心脏特异性微阵列进行分析以鉴定受调控的基因。然后应用实时聚合酶链反应(PCR)来验证受调控的基因。微阵列分析显示,24小时组中有5个受调控基因,72小时组中有4个。在通过实时PCR对个体动物进行检测时,在24小时Optison商标制剂组中,这些基因中只有碳酸酐酶显著上调(4.3倍;p = 0.0005)。通过这种非常灵敏的技术,微泡破坏的生物效应可以忽略不计。

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