Joho Shuji, Asanoi Hidetsugu, Ishizaka Shinji, Kameyama Tomoki, Inoue Hiroshi
Second Department of Internal Medicine, Toyama Medical and Pharmaceutical University, Toyama, Japan.
J Card Fail. 2002 Dec;8(6):423-30. doi: 10.1054/jcaf.2002.129658.
This study was designed to examine how a calcium sensitizer, pimobendan, affected a force-frequency response (FFR) as compared to the beta-adrenergic agonist dobutamine.
Left ventricular (LV) contractility and relaxation were evaluated by the slope (Ees) of the LV end-systolic pressure-volume relation and the time constant (Tau) of LV pressure decay. Using 6 conscious dogs with tachycardia-induced heart failure, the FFR was examined before and after administration of dobutamine (6 microg/kg/min) or pimobendan (0.5 mg/kg). Despite the similar inotropic and lusitropic action at the baseline heart rate, pimobendan and dobutamine showed different FFR and relaxation-frequency responses. Before administration of these drugs, there was no significant increase in LV contractility and relaxation by increasing heart rate. However, dobutamine amplified FFR (Ees: +3.1 +/- 1.4, P <.05) as compared with Ees for a comparable increase in heart rate before administration of the drug. On the other hand, pimobendan showed relatively mild amplification of FFR compared with dobutamine (Ees: +1.9 +/- 1.1, P <.05). The relaxation-frequency response tended to increase with dobutamine but not with pimobendan.
Mild amplification of FFR observed in pimobendan suggests that this agent could be used more safely than beta-adrenergic agent when heart rate is increased, as seen with exercise.
本研究旨在探究钙增敏剂匹莫苯丹与β肾上腺素能激动剂多巴酚丁胺相比,对力-频率反应(FFR)有何影响。
通过左心室(LV)收缩末期压力-容积关系的斜率(Ees)和LV压力衰减的时间常数(Tau)来评估左心室的收缩性和舒张性。使用6只因心动过速诱发心力衰竭的清醒犬,在给予多巴酚丁胺(6微克/千克/分钟)或匹莫苯丹(0.5毫克/千克)之前和之后检测FFR。尽管在基础心率时两者具有相似的正性肌力和变时性作用,但匹莫苯丹和多巴酚丁胺表现出不同的FFR和舒张频率反应。在给予这些药物之前,通过增加心率,左心室收缩性和舒张性没有显著增加。然而,与给药前心率可比增加时的Ees相比,多巴酚丁胺增强了FFR(Ees:+3.1±1.4,P<.05)。另一方面,与多巴酚丁胺相比,匹莫苯丹对FFR的增强作用相对较弱(Ees:+1.9±1.1,P<.05)。舒张频率反应在多巴酚丁胺作用下有增加趋势,而在匹莫苯丹作用下无增加。
匹莫苯丹中观察到的FFR轻度增强表明,在心率增加(如运动时)的情况下,该药物使用起来可能比β肾上腺素能药物更安全。