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新型钙拮抗剂盐酸贝尼地平对大鼠的降压作用

Antihypertensive effects of the new calcium antagonist benidipine hydrochloride in rats.

作者信息

Karasawa A, Kubo K, Shuto K, Oka T, Nakamizo N

机构信息

Pharmaceutical Research Laboratories, Kyowa Hakko Kogyo, Co., Ltd., Shizuoka, Japan.

出版信息

Arzneimittelforschung. 1988 Nov;38(11A):1684-90.

PMID:3064752
Abstract

Using spontaneously hypertensive rats (SHR), DOCA-NaCl hypertensive rats (DHR) and normotensive rats (NTR), the antihypertensive action of (+/-)-(R*)-2,6-dimethyl-4-(m-nitrophenyl)-1,4-dihydropyridine-3,5-dic arb oxylic acid (R*)-1-benzyl-3-piperidinyl ester, methyl ester hydrochloride (benidipine hydrochloride, KW-3049) was comparatively evaluated with those of nicardipine and hydralazine. Administration of KW-3049 at 0.5, 1 and 3 mg/kg (p.o.) showed dose-dependent antihypertensive action. This action appeared gradually and it lasted longer than those of nicardipine and hydralazine. The administration of KW-3049 at 0.5 mg/kg (p.o.) did not show any effect on the blood pressure of NTR, but a long-lasting blood pressure lowering action was observed by the administration at 1 and 3 mg/kg (p.o.). This antihypertensive action specific to the hypertensive animals was similar to that of nicardipine, however, it was different from that of hydralazine, with which the blood pressure in SHR, DHR and NTR was lowered in similar degrees. Also, administration of KW-3049 caused tachycardia concomitant with the fall of blood pressure, however, it was mild as compared with those of nicardipine and hydralazine. When KW-3049 at doses of 3 and 10 mg/kg (p.o.) once a day was continuously administered to SHR for 31 days and changes of the antihypertensive action were observed, no tolerance developed and rebound hypertension following the discontinuation of medication did not occur. When the effect on the urinary volume and electrolyte excretion was evaluated in rats loaded with physiological saline solution, a natriuretic effect was observed by the administration of KW-3049 at 0.5, 1 and 3 mg/kg (p.o.).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用自发性高血压大鼠(SHR)、去氧皮质酮-氯化钠高血压大鼠(DHR)和正常血压大鼠(NTR),将(±)-(R*)-2,6-二甲基-4-(间硝基苯基)-1,4-二氢吡啶-3,5-二羧酸(R*)-1-苄基-3-哌啶酯盐酸甲酯(盐酸贝尼地平,KW-3049)的降压作用与尼卡地平和肼屈嗪进行了比较评估。以0.5、1和3mg/kg(口服)给予KW-3049显示出剂量依赖性降压作用。这种作用逐渐出现,且持续时间比尼卡地平和肼屈嗪更长。以0.5mg/kg(口服)给予KW-3049对NTR的血压没有任何影响,但以1和3mg/kg(口服)给予时观察到持久的血压降低作用。这种对高血压动物特有的降压作用与尼卡地平相似,然而,与肼屈嗪不同,后者使SHR、DHR和NTR的血压以相似程度降低。此外,给予KW-3049会导致心动过速并伴有血压下降,然而,与尼卡地平和肼屈嗪相比,这种情况较为轻微。当以3和10mg/kg(口服)的剂量每天一次连续给予SHR 31天并观察降压作用的变化时,未产生耐受性,停药后也未发生反跳性高血压。当在给予生理盐水的大鼠中评估对尿量和电解质排泄的影响时,以0.5、1和3mg/kg(口服)给予KW-3049可观察到利钠作用。(摘要截断于250字)

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