DeWitt Elizabeth S, Black Katherine J, Thiagarajan Ravi R, DiNardo James A, Colan Steven D, McGowan Francis X, Kheir John N
Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts;
Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children's Hospital, Boston, Massachusetts; and.
J Appl Physiol (1985). 2016 Jul 1;121(1):7-14. doi: 10.1152/japplphysiol.00058.2016. Epub 2016 May 5.
Inotropic medications are routinely used to increase cardiac output and arterial blood pressure during critical illness. However, few comparative data exist between these medications, particularly independent of their effects on venous capacitance and systemic vascular resistance. We hypothesized that an isolated working heart model that maintained constant left atrial pressure and aortic blood pressure could identify load-independent differences between inotropic medications. In an isolated heart preparation, the aorta and left atrium of Sprague Dawley rats were cannulated and placed in working mode with fixed left atrial and aortic pressure. Hearts were then exposed to common doses of a catecholamine (dopamine, epinephrine, norepinephrine, or dobutamine), milrinone, or triiodothyronine (n = 10 per dose per combination). Cardiac output, contractility (dP/dtmax), diastolic performance (dP/dtmin and tau), stroke work, heart rate, and myocardial oxygen consumption were compared during each 10-min infusion to an immediately preceding baseline. Of the catecholamines, dobutamine increased cardiac output, contractility, and diastolic performance more than clinically equivalent doses of norepinephrine (second most potent), dopamine, or epinephrine (P < 0.001). The use of triiodothyronine and milrinone was not associated with significant changes in cardiac output, contractility or diastolic function, either alone or added to a baseline catecholamine infusion. Myocardial oxygen consumption was closely related to dP/dtmax (r(2) = 0.72), dP/dtmin (r(2) = 0.70), and stroke work (r(2) = 0.53). In uninjured, isolated working rodent hearts under constant ventricular loading conditions, dobutamine increased contractility and cardiac output more than clinically equivalent doses of norepinephrine, dopamine, and epinephrine; milrinone and triiodothyronine did not have significant effects on contractility.
在危重病期间,强心药物通常用于增加心输出量和动脉血压。然而,这些药物之间的比较数据很少,尤其是独立于它们对静脉容量和全身血管阻力的影响。我们假设,一个维持左心房压力和主动脉血压恒定的离体工作心脏模型可以识别强心药物之间与负荷无关的差异。在一个离体心脏制备实验中,将Sprague Dawley大鼠的主动脉和左心房插管,并置于工作模式,保持左心房和主动脉压力固定。然后让心脏接受常见剂量的儿茶酚胺(多巴胺、肾上腺素、去甲肾上腺素或多巴酚丁胺)、米力农或三碘甲状腺原氨酸(每种组合每剂量n = 10)。在每次10分钟输注期间,将心输出量、收缩性(dP/dtmax)、舒张性能(dP/dtmin和tau)、每搏功、心率和心肌耗氧量与紧接在前的基线进行比较。在儿茶酚胺中,多巴酚丁胺比临床等效剂量的去甲肾上腺素(第二有效)、多巴胺或肾上腺素更能增加心输出量、收缩性和舒张性能(P < 0.001)。单独使用三碘甲状腺原氨酸和米力农,或在基线儿茶酚胺输注基础上加用,均未导致心输出量、收缩性或舒张功能发生显著变化。心肌耗氧量与dP/dtmax(r(2) = 0.72)、dP/dtmin(r(2) = 0.70)和每搏功(r(2) = 0.53)密切相关。在心室负荷恒定的未损伤离体工作啮齿动物心脏中,多巴酚丁胺比临床等效剂量的去甲肾上腺素、多巴胺和肾上腺素更能增加收缩性和心输出量;米力农和三碘甲状腺原氨酸对收缩性没有显著影响。