首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Angiotensin-(1-7) potentiates the coronary vasodilatatory effect of bradykinin in the isolated rat heart
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Angiotensin-(1-7) potentiates the coronary vasodilatatory effect of bradykinin in the isolated rat heart

机译:血管紧张素-(1-7)增强缓激肽在离体大鼠心脏中的冠状血管舒张作用

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摘要

It has been shown that angiotensin-(1-7) (Ang-(1-7)) infusion potentiates the bradykinin (BK)-induced hypotensive response in conscious rats. The present study was conducted to identify Ang-(1-7)-BK interactions in the isolated rat heart perfused according to the Langendorff technique. Hearts were excised and perfused through the aortic stump under a constant flow with Krebs-Ringer solution and the changes in perfusion pressure and heart contractile force were recorded. Bolus injections of BK (2.5, 5, 10 and 20 ng) produced a dose-dependent hypotensive effect. Ang-(1-7) added to the perfusion solution (2 ng/ml) did not change the perfusion pressure or the contractile force but doubled the hypotensive effect of the lower doses of BK. The BK-potentiating Ang-(1-7) activity was blocked by pretreatment with indomethacin (5 mg/kg, ip) or L-NAME (30 mg/kg, ip). The Ang-(1-7) antagonist A-779 (50 ng/ml in Krebs-Ringer) completely blocked the effect of Ang-(1-7) on BK-induced vasodilation. These data suggest that the potentiation of the BK-induced vasodilation by Ang-(1-7) can be attributed to the release of nitric oxide and vasodilator prostaglandins through an Ang-(1-7) receptor-mediated mechanism.
机译:已经显示,血管紧张素-(1-7)(Ang-(1-7))输注增强了缓激肽(BK)引起的清醒大鼠降压反应。根据Langendorff技术,本研究旨在确定灌注的离体大鼠心脏中的Ang-(1-7)-BK相互作用。用克雷布斯-林格(Krebs-Ringer)溶液在恒定流量下切除心脏并通过主动脉桩进行灌注,并记录灌注压力和心脏收缩力的变化。注射BK(2.5、5、10和20 ng)产生剂量依赖性的降压作用。添加到灌注溶液(2 ng / ml)中的Ang-(1-7)不会改变灌注压力或收缩力,但使低剂量BK的降压作用加倍。通过用吲哚美辛(5 mg / kg,ip)或L-NAME(30 mg / kg,ip)预处理可阻断BK增强Ang-(1-7)的活性。 Ang-(1-7)拮抗剂A-779(在Krebs-Ringer中为50 ng / ml)完全阻断了Ang-(1-7)对BK诱导的血管舒张的作用。这些数据表明,Ang-(1-7)对BK诱导的血管舒张的增强作用可归因于通过Ang-(1-7)受体介导的机制释放的一氧化氮和血管舒张素。

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