首页> 外文期刊>Vascular pharmacology >Effects of antagonists for endothelin ET(A) and ET(B) receptors on coronary endothelial and myocardial function after ischemia-reperfusion in anesthetized goats.
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Effects of antagonists for endothelin ET(A) and ET(B) receptors on coronary endothelial and myocardial function after ischemia-reperfusion in anesthetized goats.

机译:内皮素ET(A)和ET(B)受体拮抗剂对麻醉山羊缺血再灌注后冠状动脉内皮和心肌功能的影响。

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摘要

To compare the effects of antagonists for endothelin ET(A) and ET(B) receptors on the action of ischemia-reperfusion on endothelial and myocardial function, 30 min of partial or total occlusion followed by 60 min of reperfusion of the left circumflex coronary artery was induced in anesthetized goats treated with intracoronary administration of saline (vehicle), BQ-123 (endothelin ET(A) receptors antagonist) or BQ-788 (endothelin ET(B) receptors antagonist). During reperfusion after partial occlusion, coronary vascular conductance and left ventricle dP/dt were decreased after saline or BQ-788, and they normalized after BQ-123. In these three groups of animals, the coronary effects of acetylcholine (3-100 ng) and sodium nitroprusside (1-10 microg) during reperfusion were as under control. During reperfusion after total occlusion, coronary vascular conductance and left ventricle dP/dt were decreased after saline, and they normalized after BQ-123 or BQ-788. In these three groups of animals, the coronary effects of acetylcholine but not those of sodium nitroprusside during reperfusion were decreased after saline, and they reversed after BQ-123 or BQ-788. Therefore, selective antagonists of endothelin ET(B) and ET(A) receptors may produce similar protection of coronary vasculature and myocardium against reperfusion after severe ischemia. Selective antagonists of endothelin ET(B) receptors, contrarily to those of endothelin ET(A) receptors, may be ineffective to protect coronary vasculature and myocardium against reperfusion after mild ischemia.
机译:为了比较内皮素ET(A)和ET(B)受体拮抗剂对局部缺血/再灌注对内皮和心肌功能的作用,先进行30分钟部分或全部闭塞,然后再进行60分钟左旋支冠状动脉再灌注在冠状动脉内注射生理盐水(媒介物),BQ-123(内皮素ET(A)受体拮抗剂)或BQ-788(内皮素ET(B)受体拮抗剂)处理的麻醉山羊中诱导了TNF-α的诱导。在部分闭塞后的再灌注过程中,盐水或BQ-788后冠状血管电导和左心室dP / dt降低,而BQ-123后则恢复正常。在这三组动物中,在再灌注过程中,乙酰胆碱(3-100 ng)和硝普钠(1-10 microg)的冠状动脉作用已得到控制。完全闭塞后再灌注期间,盐水后冠状血管电导和左心室dP / dt降低,在BQ-123或BQ-788后恢复正常。在这三组动物中,盐水后,乙酰胆碱的冠状动脉作用而不是硝普钠的冠状动脉作用减弱,而在BQ-123或BQ-788之后,它们的作用相反。因此,内皮素ET(B)和ET(A)受体的选择性拮抗剂可能对严重缺血后的再灌注产生类似的保护作用,保护冠状血管和心肌。与内皮素ET(A)受体的拮抗剂相反,内皮素ET(B)受体的选择性拮抗剂可能无法有效保护轻度缺血后的冠脉血管和心肌免受再灌注。

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