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腺苷与搏动性灌注协同增强犬冠状动脉血流的特异性

Specificity of synergistic coronary flow enhancement by adenosine and pulsatile perfusion in the dog.

作者信息

Pagliaro P, Senzaki H, Paolocci N, Isoda T, Sunagawa G, Recchia F A, Kass D A

机构信息

The Division of Cardiology, Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, MD 21287, USA.

出版信息

J Physiol. 1999 Oct 1;520 Pt 1(Pt 1):271-80. doi: 10.1111/j.1469-7793.1999.00271.x.

Abstract
  1. Coronary flow elevation from enhanced perfusion pulsatility is synergistically amplified by adenosine. This study determined the specificity of this interaction and its potential mechanisms. 2. Mean and phasic coronary flow responses to increasing pulsatile perfusion were assessed in anaesthetized dogs, with the anterior descending coronary artery servoperfused to regulate real-time physiological flow pulsatility at constant mean pressure. Pulsatility was varied between 40 and 100 mmHg. Hearts ejected into the native aorta whilst maintaining stable loading. 3. Increasing pulsatility elevated mean coronary flow +11.5 +/- 1.7 % under basal conditions. Co-infusion of adenosine sufficient to raise baseline flow 66 % markedly amplified this pulsatile perfusion response (+82. 6 +/- 14.3 % increase in mean flow above adenosine baseline), due to a leftward shift of the adenosine-coronary flow response curve at higher pulsatility. Flow augmentation with pulsatility was not linked to higher regional oxygen consumption, supporting direct rather than metabolically driven mechanisms. 4. Neither bradykinin, acetylcholine nor verapamil reproduced the synergistic amplification of mean flow by adenosine and higher pulsatility, despite being administered at doses matching basal flow change with adenosine. 5. ATP-sensitive potassium (KATP) activation (pinacidil) amplified the pulse-flow response 3-fold, although this remained significantly less than with adenosine. Co-administration of the phospholipase A2 inhibitor quinacrine virtually eliminated adenosine-induced vasodilatation, yet synergistic interaction between adenosine and pulse perfusion persisted, albeit at a reduced level. 6. Thus, adenosine and perfusion pulsatility specifically interact to enhance coronary flow. This synergy is partially explained by KATP agonist action and additional non-flow-dependent mechanisms, and may be important for modulating flow reserve during exercise or other high output states where increased flow demand and higher perfusion pulsatility typically co-exist.
摘要
  1. 增强的灌注搏动性所引起的冠状动脉血流增加会被腺苷协同放大。本研究确定了这种相互作用的特异性及其潜在机制。2. 在麻醉犬中评估了对递增搏动性灌注的平均和相位冠状动脉血流反应,通过对冠状动脉前降支进行伺服灌注以在恒定平均压力下调节实时生理血流搏动性。搏动性在40至100 mmHg之间变化。心脏向天然主动脉射血,同时维持稳定的负荷。3. 在基础条件下,增加搏动性使平均冠状动脉血流升高11.5±1.7%。共输注足以使基线血流增加66%的腺苷显著放大了这种搏动性灌注反应(平均血流比腺苷基线增加82.6±14.3%),这是由于腺苷 - 冠状动脉血流反应曲线在较高搏动性时向左移位。搏动性引起的血流增加与较高的局部氧消耗无关,支持直接而非代谢驱动的机制。4. 尽管缓激肽、乙酰胆碱和维拉帕米的给药剂量与腺苷引起的基础血流变化相匹配,但它们均未重现腺苷和较高搏动性对平均血流的协同放大作用。5. ATP敏感性钾通道(KATP)激活剂(吡那地尔)使脉搏血流反应放大了3倍,尽管这仍显著低于腺苷的作用。磷脂酶A2抑制剂喹那克林的共同给药几乎消除了腺苷诱导的血管舒张,但腺苷与脉搏灌注之间的协同相互作用仍然存在,尽管程度有所降低。6. 因此,腺苷与灌注搏动性特异性相互作用以增强冠状动脉血流。这种协同作用部分由KATP激动剂作用和其他非血流依赖性机制解释,并且对于在运动或其他高输出状态下调节血流储备可能很重要,在这些状态下,增加的血流需求和较高的灌注搏动性通常同时存在。

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