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Effects of Dobutamine on Left Ventricular Performance Coronary Dynamics and Distribution of Cardiac Output in Conscious Dogs

机译:多巴酚丁胺对清醒犬左心室性能冠状动脉动力学和心输出量分布的影响

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摘要

The effects of dobutamine ([±]-4-[2-[[3-(p-hydroxyphenyl)-1-methyl propyl] amino] ethyl] pyrocatechol hydrochloride), a new synthetic cardioactive sympathomimetic amine, were examined on direct and continuous measurements of left ventricular (LV) diameter (D), pressures (P), velocity of shortening (V), dP/dt, dP/dt/P, arterial pressure, cardiac output, and regional blood flows in the left circumflex coronary, mesenteric, renal, and iliac beds in healthy, conscious dogs. At the highest dose of dobutamine examined, 40 μg/kg/min, the drug increased dP/dt/P from 65±3 to 128±4 s-1 and isolength velocity from 72±4 to 120±7 mm/s without affecting LV end diastolic D significantly. Mean arterial P rose from 92±2 to 104±3 mm Hg and heart rate from 78±3 to 111±7 beats/min, while LV end systolic D fell from 24.1±1.4 to 19.9±1.8 mm, reflecting a rise in stroke volume from 30±4 to 42±3 ml. Cardiac output rose from 2.41±0.23 to 4.35±0.28 liter/min, while calculated total peripheral resistance declined from 0.042±0.005 to 0.028±0.003 mm Hg/ml/min. The greatest increases in flow and decreases in calculated resistance occurred in the iliac and coronary beds, and the least occurred in the renal bed. Propranolol blocked the inotropic and beta2 dilator responses while vasoconstricting effects mediated by alpha adrenergic stimulation remained in each of the beds studied. When dobutamine was infused after a combination of practolol and phentolamine, dilatation occurred in each of the beds studied. These observations indicate that dobutamine is a potent positive inotropic agent with relatively slight effects on preload, afterload, or heart rate, and thus may be a potentially useful clinical agent. The one property of this drug which is not ideal is its tendency to cause a redistribution of cardiac output favoring the muscular beds at the expense of the kidney and visceral beds.
机译:研究了一种新的合成心脏活性拟交感神经胺多巴酚丁胺([±] -4- [2-[[3-(对-羟基苯基--1-甲基丙基]氨基]乙基]邻苯二酚盐酸盐)的作用。测量左旋支冠状动脉的左心室(LV)直径(D),压力(P),缩短速度(V),dP / dt,dP / dt / P,动脉压,心输出量和局部血流,健康,意识清醒的狗的肠系膜,肾和床。在多巴酚丁胺的最高剂量40μg/ kg / min下,药物的dP / dt / P从65±3增加到128±4 s -1 ,等长速度从72±4增加到120 ±7 mm / s,而不会显着影响左室舒张末期D。平均动脉P从92±2毫米汞柱升至104±3毫米汞柱,心率从78±3搏动/分钟增至111±7搏动/分钟,而左室收缩末期D从24.1±1.4毫米降至19.9±1.8毫米,反映了中风的增加体积从30±4到42±3 ml。心输出量从2.41±0.23升至4.35±0.28升/分钟,而计算的总外周阻力从0.042±0.005降至0.028±0.003 mm Hg / ml / min。在flow床和冠状动脉床中流量增加最大,而计算出的阻力降低,在肾床中发生最少。普萘洛尔阻断正性肌力和β2扩张剂的反应,而α-肾上腺素刺激介导的血管收缩作用仍保留在每个研究床中。当联合使用倍他洛尔和酚妥拉明输注多巴酚丁胺后,在每个所研究的病床上均发生了扩张。这些观察结果表明多巴酚丁胺是一种强力的正性肌力药,对前负荷,后负荷或心率影响相对较小,因此可能是潜在有用的临床药物。这种药物的一个不理想的特性是它倾向于导致心输出量的重新分配,从而有利于肌肉床,却损害了肾脏床和内脏床。

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