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新型钙拮抗剂MPC-1304对实验性高血压大鼠和犬的降压作用

Antihypertensive effects of MPC-1304, a novel calcium antagonist, in experimental hypertensive rats and dogs.

作者信息

Kanda A, Haruno A, Miyake H, Nagasaka M

机构信息

Biological Research Laboratory, Taiho Pharmaceutical Company, Tokushima, Japan.

出版信息

J Cardiovasc Pharmacol. 1992;20(5):723-30.

PMID:1280733
Abstract

Antihypertensive effects of a novel calcium antagonist, MPC-1304, (+-)-methyl 2-oxopropyl 1,4-dihydro-2,6-dimethyl-4-(2-nitrophenyl)-3,5- pyridine-dicarboxylate and its active metabolites were investigated in experimental hypertensive rats and dogs and compared with those of other dihydropyridine derivatives (nifedipine, nisoldipine, nicardipine, and nitrendipine). MPC-1304 had a dose-related antihypertensive effect with a slight increase in heart rate (HR) in rats. The antihypertensive effects of MPC-1304 were more potent than those of other dihydropyridines, and its active metabolites had antihypertensive effects comparable to those of other dihydropyridines. The hypotensive effects of MPC-1304 were stronger in hypertensive rats than in normotensive rats. During repeated oral administration of MPC-1304 to spontaneously hypertensive rats (SHR, once daily for 4 weeks, 0.3-3 mg/kg), dose-response curves of the antihypertensive effect did not change and body weight gain was equal to that of the vehicle-treated group. When given orally to conscious renal hypertensive dogs, MPC-1304 0.1-0.3 mg/kg had a potency and duration of antihypertensive action comparable to that of nitrendipine (1-3 mg/kg). MPC-1304 increased coronary blood flow (CBF) and aortic blood flow (ABF) in conscious normotensive dogs. In conclusion, MPC-1304 and its active metabolites have potent antihypertensive effects and cause slight tachycardia, and they may be useful in treating hypertension.

摘要

研究了新型钙拮抗剂MPC - 1304(±)-甲基2 - 氧代丙基1,4 - 二氢 - 2,6 - 二甲基 - 4 -(2 - 硝基苯基)- 3,5 - 吡啶二羧酸酯及其活性代谢产物在实验性高血压大鼠和犬中的降压作用,并与其他二氢吡啶衍生物(硝苯地平、尼索地平、尼卡地平和尼群地平)进行了比较。MPC - 1304在大鼠中具有剂量相关的降压作用,心率(HR)略有增加。MPC - 1304的降压作用比其他二氢吡啶类更强,其活性代谢产物的降压作用与其他二氢吡啶类相当。MPC - 1304在高血压大鼠中的降压作用比正常血压大鼠更强。在对自发性高血压大鼠(SHR)重复口服MPC - 1304(每天一次,持续4周,0.3 - 3 mg/kg)期间,降压作用的剂量 - 反应曲线未改变,体重增加与赋形剂处理组相当。当口服给予清醒的肾性高血压犬时,0.1 - 0.3 mg/kg的MPC - 1304的降压效力和持续时间与1 - 3 mg/kg的尼群地平相当。MPC - 1304增加了清醒正常血压犬的冠状动脉血流量(CBF)和主动脉血流量(ABF)。总之,MPC - 1304及其活性代谢产物具有强效降压作用并引起轻微心动过速,它们可能对治疗高血压有用。

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