Kido H, Nishikawa M, Hayashi K, Kubo Y, Ohtaki Y, Fujino Y, Egi Y, Ebisu H, Inoue S, Yamanaga K, Uchida T, Nakamura N
Central Research Laboratories, Green Cross Corporation, Osaka, Japan.
Nihon Yakurigaku Zasshi. 1997 Jun;109(6):279-89. doi: 10.1254/fpj.109.279.
The antihypertensive effects of oral or intravenous administration of AE0047, a novel 1,4-dihydropyridine-type calcium antagonist, were investigated in spontaneously hypertensive rats (SHR/crj), one kidney-one clip renal hypertensive rats (RHR), deoxycorticosterone acetate (DOCA)-salt hypertensive rats (DHR) and two kidney-one clip renal hypertensive dogs (RHD). AE0047 (1, 3, 10 mg/kg, p.o.) caused a dose-related reduction of systolic blood pressure (SBP) with low reflex tachycardia in SHR/crj and RHR. The effect reached its maximum at 2-4 hr after administration and was sustained for a long time. In DHR, AE0047 (0.3, 1, 3 mg/kg, p.o.) similarly showed the antihypertensive effects at 2-7 hr with no significant changes in heart rates (HR). The doses (ED30) of AE0047 required to decrease SBP by 30% were 2.6, 3.4 and 0.68 mg/kg in SHR/crj, RHR and DHR, respectively. In RHD, and AE0047 capsule (GJ-0956: 4, 8, 16, 32 mg/body, p.o.) produced dose-dependent and long lasting effects with a transient and slight increase in HR. Furthermore, the intravenous administration of AE0047 (10, 30, 100 micrograms/kg) produced the antihypertensive action slowly, reached a plateau 10 min later and then maintained for many hours. In contrast, nitrendipine (3-100 mg/kg, p.o., 3-30 micrograms/kg, i.v.) and nicardipine (1-30 mg/kg, p.o., 3-30 micrograms/kg, i.v.) exhibited a similar potency to AE0047, but these maximal effects were produced at 1-2 hr and 0.5-1 min in the case of oral and intravenous administration, respectively, with a rapid recovery in the above hypertensive rats. These results indicate that AE0047 exhibits an antihypertensive effect with a slow onset and long-lasting profile.
在自发性高血压大鼠(SHR/crj)、单肾单夹肾性高血压大鼠(RHR)、醋酸脱氧皮质酮(DOCA)-盐性高血压大鼠(DHR)和双肾单夹肾性高血压犬(RHD)中,研究了新型1,4-二氢吡啶类钙拮抗剂AE0047口服或静脉给药的降压作用。AE0047(1、3、10mg/kg,口服)可使SHR/crj和RHR的收缩压(SBP)呈剂量依赖性降低,伴有轻度反射性心动过速。给药后2-4小时作用达到最大,并持续很长时间。在DHR中,AE0047(0.3、1、3mg/kg,口服)在2-7小时同样显示出降压作用,心率(HR)无明显变化。在SHR/crj、RHR和DHR中,使SBP降低30%所需的AE0047剂量(ED30)分别为2.6、3.4和0.68mg/kg。在RHD中,AE0047胶囊(GJ-0956:4、8、16、32mg/只,口服)产生剂量依赖性和持久作用,HR有短暂轻微升高。此外,静脉注射AE0047(10、30、100μg/kg)降压作用起效缓慢,10分钟后达到平台期,然后维持数小时。相比之下,尼群地平(3-100mg/kg,口服,3-30μg/kg,静脉注射)和尼卡地平(1-30mg/kg,口服,3-30μg/kg,静脉注射)与AE0047表现出相似的效力,但口服和静脉给药时,这些最大效应分别在1-2小时和0.5-1分钟产生,上述高血压大鼠血压迅速恢复。这些结果表明,AE0047具有起效缓慢和作用持久的降压作用。