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与阿利尼定和UL-FS 49相比,捷利康ZD7288对豚鼠窦房结和心室动作电位的影响。

Effects of Zeneca ZD7288 in comparison with alinidine and UL-FS 49 on guinea pig sinoatrial node and ventricular action potentials.

作者信息

Briggs I, BoSmith R E, Heapy C G

机构信息

Cardiovascular Research Department, ZENECA Pharmaceuticals, Macclesfield, Cheshire, England.

出版信息

J Cardiovasc Pharmacol. 1994 Sep;24(3):380-7. doi: 10.1097/00005344-199409000-00005.

Abstract

ZENECA ZD7288 (4-(N-ethyl-N-phenyl-amino)-1,2-dimethyl-6-(methylamino) pyrimidium chloride) is a novel compound which we compared with alinidine and UL-FS 49 (zatebradine) in guinea pig sinoatrial node (SAN) and papillary muscle preparations, using conventional microelectrode techniques. At low concentrations (1 x 10(-8)-1 x 10(-6) M), ZD7288 caused slowing of the diastolic depolarisation rate of SAN pacemaker cells, thus prolonging the diastolic interval and slowing the beating rate. Alinidine and UL-FS 49 also had qualitatively similar effects on diastolic depolarisation rate, but ZD7288 caused least prolongation of the action potential duration (APD) of SAN cells at the concentrations that had "selective bradycardic actions." ZD7288 affected the APs of ventricular cells in guinea pig papillary muscle only at relatively high concentrations (3 x 10(-6)M-1 x 10(-4) M), which reduced plateau potential duration, although total APD was less affected. Reduced force of contraction (FOC) was also observed at these high concentrations; significant effects on AP Vmax were noted only at concentrations > or = 3 x 10(-5)M. Alinidine also had negative inotropic effects on papillary muscle, but its effects were noted at concentrations similar to those with bradycardic actions; in contrast, UL-FS 49 had marked positive inotropic actions and also increased ventricular APD within the bradycardic concentration range. These data provide a basis for the selective actions of ZD7288 on heart rate (HR).

摘要

泽尼卡ZD7288(4-(N-乙基-N-苯基氨基)-1,2-二甲基-6-(甲氨基)氯化嘧啶)是一种新型化合物,我们使用传统微电极技术,在豚鼠窦房结(SAN)和乳头肌标本中,将其与阿利尼定和UL-FS 49(扎替丁)进行了比较。在低浓度(1×10⁻⁸ - 1×10⁻⁶ M)下,ZD7288导致SAN起搏细胞舒张期去极化速率减慢,从而延长舒张间期并减慢心率。阿利尼定和UL-FS 49对舒张期去极化速率也有定性相似的作用,但在具有“选择性心动过缓作用”的浓度下,ZD7288对SAN细胞动作电位持续时间(APD)的延长作用最小。ZD7288仅在相对高浓度(3×10⁻⁶ M - 1×10⁻⁴ M)下影响豚鼠乳头肌心室细胞的动作电位,这会缩短平台期电位持续时间,尽管总APD受影响较小。在这些高浓度下也观察到收缩力(FOC)降低;仅在浓度≥3×10⁻⁵ M时才注意到对动作电位最大上升速率(Vmax)有显著影响。阿利尼定对乳头肌也有负性肌力作用,但其作用在与心动过缓作用相似的浓度下即可观察到;相比之下,UL-FS 49在心动过缓浓度范围内具有明显的正性肌力作用,并且还增加了心室APD。这些数据为ZD7288对心率(HR)的选择性作用提供了依据。

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