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新一代钙拮抗剂3-吡啶羧酸5-[(环丙基氨基)-羰基]-1,4-二氢-2,6-二甲基-4-(2-硝基苯基)辛酯对清醒自发性高血压大鼠和肾性高血压大鼠的急性降压作用。

Acute antihypertensive effects of the new generation calcium antagonist 3-pyridine carboxylic acid 5-[(cyclopropylamino)-carbonyl]-1,4-dihydro-2,6-dimethyl-4-(2-nitrophen yl) octyl ester on conscious spontaneously hypertensive rats and renal hypertensive rats.

作者信息

Hojo M, Tanaka Y, Katayama O, Teramoto N

机构信息

Pharmacological Department, Nippon Shoji Kaisha Ltd., Osaka, Japan.

出版信息

Arzneimittelforschung. 1993 Aug;43(8):847-51.

PMID:8216440
Abstract

The acute antihypertensive effects of 3-pyridine carboxylic acid 5-[(cyclo-propylamino)carbonyl]-1,4-dihydro-2,6-dimethyl-4-(2-nitroph eny l) octyl ester (NP-252, CAS 132031-81-3) administered orally to conscious spontaneously hypertensive rats (SHRs) and renal hypertensive rats (RHRs) were evaluated using the impedance plethysmographical technique as a modified tail cuff method, and compared with those of nifedipine (NF). In the fitness test of this indirect method, the average value of blood pressure (BP) measured in 7 conscious SHRs was 201 +/- 6.9 mmHg. This value showed good correlation with that (201 +/- 8.8 mmHg) of systolic BP measured by the direct method in the same animals. In the comparative study of antihypertensive activities of the compounds on both models of hypertension using this method, NP-252 and NF dose-dependently lowered BP having a different peak time and restoration after dosing. Therefore, the antihypertensive activities were compared using a 20% effective dose (ED20) for producing hypotension, and the ED20 values of NP-252 and NF were 2.55 and 2.00 mg/kg in SHRs, and 1.25 and 0.67 mg/kg in RHRs, respectively. Moreover, the duration of actions of the compounds were evaluated by the simulated duration time (SDT) which was calculated from the peak time of BP-fall and the pharmacological half life time for the maximum BP-fall and the SDT values of NP-252 and NF were 1.85-4.70 and 0.90-0.75 h in SHRs, and 3.30-12.80 and 0.57-6.90 h in RHRs, respectively. Also, the BP-falls by the compounds were accompanied by an increase in heart rate.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

采用改良尾袖带法,即阻抗体积描记技术,评估了3 - 吡啶羧酸5 - [(环丙基氨基)羰基]-1,4 - 二氢 - 2,6 - 二甲基 - 4 - (2 - 硝基苯基)辛酯(NP - 252,CAS 132031 - 81 - 3)对清醒自发性高血压大鼠(SHRs)和肾性高血压大鼠(RHRs)口服给药后的急性降压作用,并与硝苯地平(NF)进行比较。在这种间接方法的适用性测试中,7只清醒SHRs的平均血压(BP)测量值为201±6.9 mmHg。该值与同一动物直接测量的收缩压(201±8.8 mmHg)显示出良好的相关性。在使用该方法对两种高血压模型进行化合物降压活性的比较研究中,NP - 252和NF均剂量依赖性地降低血压,给药后峰值时间和恢复情况不同。因此,使用产生低血压的20%有效剂量(ED20)比较降压活性,NP - 252和NF在SHRs中的ED20值分别为2.55和2.00 mg/kg,在RHRs中分别为1.25和0.67 mg/kg。此外,通过模拟持续时间(SDT)评估化合物的作用持续时间,SDT由血压下降的峰值时间和最大血压下降的药理学半衰期计算得出,NP - 252和NF在SHRs中的SDT值分别为1.85 - 4.70和0.90 - 0.75小时,在RHRs中分别为3.30 - 12.80和0.57 - 6.90小时。此外,化合物引起的血压下降伴随着心率增加。(摘要截断于250字)

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