Durand L G, Langlois Y E, Lanthier T, Chiarella R, Coppens P, Carioto S, Bertrand-Bradley S
Laboratory of Biomedical Engineering, Clinical Research Institute of Montreal, University of Montreal, Quebec, Canada.
Med Biol Eng Comput. 1990 Sep;28(5):439-45. doi: 10.1007/BF02441967.
A surgical protocol was designed to implant in dogs a programmable atrioventricular pacemaker and to destroy the bundle of His with one to four 0.1 ml formaldehyde injections. The heart rate and P-R interval were paced at 100 beats min-1 and 75 ms, respectively. Cardiac inotropy was then varied in five animals by using injections or infusions of cardiotonic drugs (Dobutamine, Betalol and Quinidine). Their effect on the spectra and acoustic transmission of the mitral M1 and aortic A2 closure sound components produced within the left heart and transmitted up to the body surface was studied. Results indicate that changes in cardiac inotropy strongly modify the intensity of M1 and A2 but do not markedly affect their spectral distribution. They also affect the transfer function of the heart/thorax acoustic system, but this influence is small compared with that of a 12 min reference interval. In addition, it was shown that the intensity of M1 is more sensitive to the cardiotonic agents than the intensity of A2.
设计了一种手术方案,用于在犬类体内植入可编程房室起搏器,并通过注射一到四次0.1毫升甲醛来破坏希氏束。心率和P-R间期分别设定为每分钟100次心跳和75毫秒。然后,通过注射或输注强心药物(多巴酚丁胺、倍他洛尔和奎尼丁)来改变五只动物的心肌收缩力。研究了它们对左心内产生并传输至体表的二尖瓣M1和主动脉A2关闭音成分的频谱和声传输的影响。结果表明,心肌收缩力的变化强烈改变M1和A2的强度,但对其频谱分布没有明显影响。它们还影响心脏/胸部声学系统的传递函数,但与12分钟的参考间隔相比,这种影响较小。此外,研究表明M1的强度比A2的强度对强心剂更敏感。