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血管紧张素II对微血管生长和动脉血压的相反作用。

Opposing actions of angiotensin II on microvascular growth and arterial blood pressure.

作者信息

Munzenmaier D H, Greene A S

机构信息

Department of Physiology, Medical College of Wisconsin, Milwaukee 53226, USA.

出版信息

Hypertension. 1996 Mar;27(3 Pt 2):760-5. doi: 10.1161/01.hyp.27.3.760.

Abstract

We performed studies to further elucidate the mechanisms of angiotensin II (Ang II)-induced angiogenesis of the microvasculature. Rats were placed on a high salt diet (4% NaCl), and Ang II was infused at a subpressor rate (5 ng/kg per minute) for 3 days. Blood pressure was measured daily for 2 control and 3 infusion days. Microvessel density in the cremaster muscle was measured at the end of the infusion. Vessel density in rats that received subpressor Ang II infusion increased by 12.6% compared with rats that received vehicle infusion. When the angiotensin type 2 (AT2) receptor antagonist PD 123319 was coinfused with Ang II, blood pressure was elevated and vessel density increased above that observed with Ang II infusion alone (23% increase). When the AT1 receptor antagonist losartan was coinfused with Ang II, blood pressure was lower than control and vessel density was reduced compared with the Ang II group but was still greater than control (7.8% increase). In this study, Ang II stimulated angiogenesis in the rat cremaster muscle; this effect was enhanced by AT2 antagonism and inhibited by AT1 antagonism. Ang II infusion at a subpressor dose resulted in a pressor response with AT2 antagonism and a depressor response with AT1 antagonism. This suggests that in the microvasculature, the AT1 receptor mediates angiogenesis and vasoconstriction, and the AT2 receptor mediates an inhibition of angiogenesis and vasodilation.

摘要

我们进行了多项研究,以进一步阐明血管紧张素II(Ang II)诱导的微脉管系统血管生成机制。将大鼠置于高盐饮食(4%氯化钠)环境中,并以亚升压速率(每分钟5纳克/千克)输注Ang II,持续3天。在2天对照期和3天输注期内每天测量血压。在输注结束时测量提睾肌中的微血管密度。与接受载体输注的大鼠相比,接受亚升压剂量Ang II输注的大鼠的血管密度增加了12.6%。当血管紧张素2型(AT2)受体拮抗剂PD 123319与Ang II共同输注时,血压升高,血管密度增加幅度高于单独输注Ang II时(增加23%)。当AT1受体拮抗剂氯沙坦与Ang II共同输注时,血压低于对照组,与Ang II组相比血管密度降低,但仍高于对照组(增加7.8%)。在本研究中,Ang II刺激大鼠提睾肌中的血管生成;这种作用通过AT2拮抗作用增强,通过AT1拮抗作用抑制。以亚升压剂量输注Ang II时,与AT2拮抗作用一起产生升压反应,与AT1拮抗作用一起产生降压反应。这表明在微脉管系统中,AT1受体介导血管生成和血管收缩,而AT2受体介导血管生成抑制和血管舒张。

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