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血管紧张素II和氯沙坦对大鼠血管紧张素转换酶的组织特异性调节

Tissue-specific regulation of angiotensin-converting enzyme by angiotensin II and losartan in the rat.

作者信息

Metsärinne K P, Helin K H, Saijonmaa O, Stewen P, Sirviö M L, Fyhrquist F Y

机构信息

Minerva Foundation Institute for Medical Research, Helsinki, Finland.

出版信息

Blood Press. 1996 Nov;5(6):363-70. doi: 10.3109/08037059609078076.

Abstract

Angiotensin II (Ang II) may regulate the release of components of the renin-angiotensin system in a tissue-specific manner. In order to study: (1) the effect of Ang II on gene expression and tissue levels of angiotensin-converting enzyme (ACE), and (2) the mechanism of the possible Ang II effect, we treated normal rats with Ang II and Losartan, an angiotensin AT1-receptor antagonist. Forty normal rats received Ang II (n = 20) at a rate of 200 ng kg-1 min-1 or 0.9% NaCl (n = 20) subcutaneously for 3 days using osmotic Alzet minipumps. Ten rats in both groups received Losartan (15 mg kg-1 day-1) in their drinking water, while the rest received tap water. ACE activity and mRNA levels were measured from pulmonary, cardiac, and renal tissue. Ang II treatment resulted in significant increases in blood pressure and heart weight as well as an increase in plasma Ang II concentration and a decrease in plasma renin activity. Simultaneous treatment with Losartan reduced the Ang II-induced effects on blood pressure and heart weight, and attenuated the Ang II-induced decrease in plasma renin activity. Pulmonary ACE activity and mRNA levels decreased during Ang II treatment, and these effects were not modified by simultaneous treatment with Losartan. Cardiac and kidney ACE activities and mRNA levels did not change significantly during Ang II treatment, but Losartan increased cardiac ACE activity (and decreased pulmonary ACE activity). The data indicate that Ang II regulates gene expression and activity of ACE in a tissue-specific manner in the rat, an effect probably involving angiotensin receptor subtype(s) different from the AT1-receptor.

摘要

血管紧张素II(Ang II)可能以组织特异性方式调节肾素-血管紧张素系统各成分的释放。为了研究:(1)Ang II对血管紧张素转换酶(ACE)基因表达和组织水平的影响,以及(2)Ang II可能作用的机制,我们用Ang II和血管紧张素AT1受体拮抗剂氯沙坦处理正常大鼠。40只正常大鼠使用渗透式Alzet微型泵以200 ng kg-1 min-1的速率皮下注射Ang II(n = 20)或0.9%氯化钠(n = 20),持续3天。两组中的10只大鼠在饮水中给予氯沙坦(15 mg kg-1天-1),其余大鼠给予自来水。从肺、心脏和肾脏组织中测量ACE活性和mRNA水平。Ang II处理导致血压和心脏重量显著增加,同时血浆Ang II浓度升高,血浆肾素活性降低。氯沙坦同时处理可减轻Ang II对血压和心脏重量的影响,并减弱Ang II引起的血浆肾素活性降低。Ang II处理期间肺ACE活性和mRNA水平降低,氯沙坦同时处理并未改变这些效应。Ang II处理期间心脏和肾脏ACE活性及mRNA水平无显著变化,但氯沙坦增加了心脏ACE活性(并降低了肺ACE活性)。数据表明,Ang II在大鼠中以组织特异性方式调节ACE的基因表达和活性,这种作用可能涉及不同于AT1受体的血管紧张素受体亚型。

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