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通过体内转染针对大鼠血管紧张素原的反义寡脱氧核苷酸使高血压短暂降低。

Transient decrease in high blood pressure by in vivo transfer of antisense oligodeoxynucleotides against rat angiotensinogen.

作者信息

Tomita N, Morishita R, Higaki J, Aoki M, Nakamura Y, Mikami H, Fukamizu A, Murakami K, Kaneda Y, Ogihara T

机构信息

Department of Geriatric Medicine, Osaka (Japan) University Medical School.

出版信息

Hypertension. 1995 Jul;26(1):131-6. doi: 10.1161/01.hyp.26.1.131.

DOI:10.1161/01.hyp.26.1.131
PMID:7541778
Abstract

The renin-angiotensin system plays an important role in blood pressure regulation. Angiotensinogen, which is mainly produced in the liver, is a unique component of the renin-angiotensin system, because angiotensinogen is only known as a substrate for angiotensin I generation. It is unclear whether circulating angiotensinogen is a rate-limiting step in blood pressure regulation. Recent findings of genetic studies and analyses suggest that the angiotensinogen gene may be a candidate as a determinant of hypertension. To test the hypothesis that angiotensinogen may modulate blood pressure, we transfected antisense oligonucleotides against rat angiotensinogen into the rat liver via the portal vein using liposomes that contain viral agglutinins to promote fusion with target cells, a technique that has been reported to be highly efficient. Transfection of antisense oligonucleotides resulted in a transient decrease in plasma angiotensinogen levels in spontaneously hypertensive rats from day 1 to day 7 after the injection, consistent with the reduction of hepatic angiotensinogen mRNA. Plasma angiotensin II concentration was also decreased in rats transfected with antisense oligonucleotides. Moreover, a transient decrease in blood pressure from day 1 to day 4 was observed, whereas transfection of sense and scrambled oligonucleotides did not result in any changes in plasma angiotensinogen level, blood pressure, or angiotensinogen mRNA level. Overall, our results demonstrate that transfection of antisense oligonucleotides against rat angiotensinogen resulted in a transient decrease in the high blood pressure of spontaneously hypertensive rats, accompanied by a decrease in angiotensinogen and angiotensin II levels.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

肾素-血管紧张素系统在血压调节中起重要作用。血管紧张素原主要在肝脏产生,是肾素-血管紧张素系统的一个独特组成部分,因为血管紧张素原仅被认为是生成血管紧张素I的底物。目前尚不清楚循环中的血管紧张素原是否是血压调节中的限速步骤。近期基因研究和分析的结果表明,血管紧张素原基因可能是高血压的一个决定因素。为了验证血管紧张素原可能调节血压这一假说,我们使用含有病毒凝集素以促进与靶细胞融合的脂质体,通过门静脉将针对大鼠血管紧张素原的反义寡核苷酸转染到大鼠肝脏中,据报道该技术效率很高。注射后第1天至第7天,反义寡核苷酸转染导致自发性高血压大鼠血浆血管紧张素原水平短暂下降,这与肝脏血管紧张素原mRNA的减少一致。反义寡核苷酸转染的大鼠血浆血管紧张素II浓度也降低。此外,在第1天至第4天观察到血压短暂下降,而正义寡核苷酸和乱序寡核苷酸转染并未导致血浆血管紧张素原水平、血压或血管紧张素原mRNA水平发生任何变化。总体而言,我们的结果表明,针对大鼠血管紧张素原的反义寡核苷酸转染导致自发性高血压大鼠的高血压短暂下降,同时伴有血管紧张素原和血管紧张素II水平降低。(摘要截短至250字)

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