Cao Xin, Nakamura Yuji, Wada Takeshi, Izumi-Nakaseko Hiroko, Ando Kentaro, Zhu Bingmei, Xu Bin, Takahara Akira, Saitoh Masaki, Sugiyama Atsushi
Department of Pharmacology, Faculty of Medicine, Toho University, 5-21-16 Omori-nishi, Ota-ku, Tokyo, 143-8540, Japan.
Key Laboratory of Acupuncture and Medicine Research of Ministry Education, Nanjing University of Chinese Medicine, 138 Xianlin Ave, Qixia, Nanjing, Jiangsu, China.
Heart Vessels. 2016 Dec;31(12):2045-2052. doi: 10.1007/s00380-016-0848-4. Epub 2016 May 18.
We assessed the anti-anginal effects of cilnidipine in comparison with those of nicardipine and nifedipine (1 and 10 µg/kg, n = 6 for each drug) or vehicle (n = 6) by using the vasopressin-induced angina model of rats. The administration of vasopressin (0.5 IU/kg, i.v.) to the rats depressed the S-wave level of the electrocardiogram reflecting the presence of subendocardial ischemia, whereas it significantly increased the mean blood pressure, resulting in the decrease of the heart rate and the prolongation of the PR interval possibly through a reflex-mediated increase in vagal tone. Cilnidipine suppressed the vasopressin-induced depression of the S-wave level in a dose-related manner, which was not observed by nicardipine or nifedipine. In addition, the low dose of cilnidipine hardly affected the vasopressin-induced pressor response, but it attenuated the negative dromotropic effect, suggesting N-type Ca channel inhibition by cilnidipine might have suppressed the parasympathetic nerve activity in vivo like those reported in the sympathetic nerve. Thus, cilnidipine may become a useful strategy for inhibiting coronary vasospasm-induced anginal attack.
我们通过使用大鼠血管加压素诱导的心绞痛模型,比较了西尼地平与尼卡地平及硝苯地平(1和10μg/kg,每种药物n = 6)或赋形剂(n = 6)的抗心绞痛作用。给大鼠静脉注射血管加压素(0.5IU/kg)会降低反映心内膜下缺血存在的心电图S波水平,而它会显著升高平均血压,可能通过反射介导的迷走神经张力增加导致心率降低和PR间期延长。西尼地平以剂量相关的方式抑制血管加压素诱导的S波水平降低,尼卡地平或硝苯地平则未观察到这种情况。此外,低剂量的西尼地平几乎不影响血管加压素诱导的升压反应,但它减弱了负性变传导效应,提示西尼地平对N型钙通道的抑制可能像在交感神经中报道的那样,在体内抑制了副交感神经活动。因此,西尼地平可能成为抑制冠状动脉痉挛诱发心绞痛发作的一种有用策略。