Newman W H, Webb J G
Cardiovasc Res. 1980 Sep;14(9):530-6. doi: 10.1093/cvr/14.9.530.
We have previously shown that volume overload heart failure is associated with a depressed inotropic response to isoprenaline, noradrenaline, glucagon, and calcium. In these present experiments, the inotropic response of the failing heart to ouabain was examined because ouabain has a mechanism of action that is different from these other agents. The studies were conducted in dogs with heart failure resulting from an aortocaval fistula. The principal finding was that during heart failure the inotropic response to isoprenaline was markedly depressed while the inotropic response to ouabain was unaltered. These findings, coupled with our previous observations, suggest that heart failure is not associated with some common defect in the excitation-contraction coupling mechanism that reduces the response to inotropic agents. Additionally, we made the first measurements of plasma noradrenaline levels in this model of heart failure and found them to be elevated four-fold.
我们之前已经表明,容量超负荷性心力衰竭与对异丙肾上腺素、去甲肾上腺素、胰高血糖素和钙的变力反应降低有关。在目前这些实验中,研究了衰竭心脏对哇巴因的变力反应,因为哇巴因的作用机制与其他这些药物不同。研究在因主动脉腔静脉瘘导致心力衰竭的犬身上进行。主要发现是,在心力衰竭期间,对异丙肾上腺素的变力反应明显降低,而对哇巴因的变力反应未改变。这些发现,再加上我们之前的观察结果,表明心力衰竭与兴奋 - 收缩偶联机制中某种降低对变力药物反应的常见缺陷无关。此外,我们首次在这个心力衰竭模型中测量了血浆去甲肾上腺素水平,发现其升高了四倍。