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一种新型二氢吡啶类钙通道阻滞剂对清醒高血压大鼠和正常血压大鼠的降压作用。

Antihypertensive effect of a new dihydropyridine calcium entry blocker in conscious hypertensive and normotensive rats.

作者信息

Nomura M, Kimura Y, Yoshida M, Satoh S

机构信息

Department of Pharmacology, Tohoku University, Sendai, Japan.

出版信息

Arzneimittelforschung. 1989 Dec;39(12):1542-5.

PMID:2624602
Abstract

The antihypertensive effects of orally administered CD-349, (2-nitratopropyl-3-nitratopropyl-2,6-dimethyl-4-(3-nitrophen yl)- 1,4-dihydropyridine-3,5-dicarboxylate), a new dihydropyridine calcium-entry blocker, were evaluated in comparison with nifedipine in spontaneously hypertensive rats (SHR), renal hypertensive rats (RHR) and normotensive rats (NTR) all in a conscious state. CD-349 (0.3, 1.0 and 3.0 mg/kg) and nifedipine (1.0 mg/kg) produced a long-lasting decrease in mean arterial blood pressure (BP) and an increase in heart rate (HR) in all the rat groups; the effects of CD-349 were dose-dependent and greater in hypertensive rats than in NTR. As compared with nifedipine at the same dose of 1 mg/kg, the hypotensive effect of CD-349 was relatively slower in onset and longer-lasting, thereby suggesting that gastrointestinal absorption of CD-349 was slower than that of nifedipine. The increase in HR associated with the hypotension induced by CD-349 at 1 mg/kg was relatively transient in comparison with that induced by nifedipine at the same dose in both types of hypertensive rat. From these results, it is expected that CD-349 could be a useful antihypertensive drug.

摘要

口服新型二氢吡啶类钙通道阻滞剂CD-349(2-硝丙基-3-硝丙基-2,6-二甲基-4-(3-硝基苯基)-1,4-二氢吡啶-3,5-二羧酸酯)的降压作用,在清醒状态下的自发性高血压大鼠(SHR)、肾性高血压大鼠(RHR)和正常血压大鼠(NTR)中与硝苯地平进行了比较评估。CD-349(0.3、1.0和3.0mg/kg)和硝苯地平(1.0mg/kg)在所有大鼠组中均使平均动脉血压(BP)产生持久下降,并使心率(HR)增加;CD-349的作用呈剂量依赖性,且在高血压大鼠中比在NTR中更明显。与相同剂量1mg/kg的硝苯地平相比,CD-349的降压作用起效相对较慢且持续时间更长,这表明CD-349的胃肠道吸收比硝苯地平慢。在两种高血压大鼠中,与1mg/kg CD-349诱导的低血压相关的HR增加与相同剂量硝苯地平诱导的相比相对短暂。从这些结果来看,预计CD-349可能是一种有用的降压药物。

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