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Ang (1–7) is a modulator of the vasoconstrictor actions of Ang I and Ang II

机译:Ang(1-7)是Ang I和Ang II血管收缩作用的调节剂

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Introduction: The role of angiotensin (Ang) (1–7) on the vasoconstrictor effect induced by angiotensins could be different in the presence of an ACE inhibitor or an ARB because Ang II is formed through several pathways. Therefore, the role of Ang (1–7) in Ang I and Ang II contraction was evaluated in aortas from Wistar rats after 48-hour coronary occlusion treated with captopril or losartan. Methods: Concentration-response curves to Ang I or Ang II were conducted in the absence or presence of Ang (1–7) and A779: a) sham group; b) 48-hour coronary occlusion; c) treated with captopril or d) losartan (3.1 mg/kg, i.m.). Results: Captopril caused a significant increase in the contractile effect of Ang I and Ang II, while losartan reduced it. The presence of Ang (1–7) in the captopril group showed a reduction of the contraction compared to the sham group, while the treatment with losartan did not show a significant difference. Ang (1–7) presents effects different from Ang I or Ang II. Conclusion: Ang (1–7) showed a modulatory role, suggesting Ang I did as well after treatment with an ACE inhibitor but not with an AT1 receptor antagonist.
机译:简介:在存在ACE抑制剂或ARB的情况下,血管紧张素(Ang)(1–7)在血管紧张素诱导的血管收缩作用中的作用可能有所不同,因为Ang II是通过多种途径形成的。因此,在用卡托普利或氯沙坦治疗冠状动脉闭塞48小时后,在Wistar大鼠的主动脉中评估了Ang(1–7)在Ang I和Ang II收缩中的作用。方法:在不存在或存在Ang(1-7)和A779的情况下对Ang I或Ang II进行浓度-反应曲线:a)假手术组; b)48小时冠状动脉闭塞; c)用卡托普利治疗或d)氯沙坦(3.1 mg / kg,i.m.)。结果:卡托普利引起Ang I和Ang II的收缩作用显着增加,而氯沙坦降低了它的收缩作用。与假手术组相比,卡托普利组中Ang(1–7)的存在显示收缩减少,而氯沙坦治疗则无显着差异。 Ang(1–7)呈现出与Ang I或Ang II不同的效果。结论:Ang(1–7)具有调节作用,表明Ang I在用ACE抑制剂治疗后也表现良好,但不使用AT1受体拮抗剂治疗。

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