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新型α1肾上腺素能受体拮抗剂萘哌地尔(KT-611)对自由活动的实验性高血压大鼠和犬的降压作用

[Antihypertensive effect of naftopidil (KT-611), a novel alpha 1-adrenoceptor antagonist, in freely moving experimental hypertensive rats and dogs].

作者信息

Kawasaki H, Nakamura S, Takasaki K, Iwamoto T, Ohjimi H, Kushiku K, Furukawa T

机构信息

Department of Pharmacology, Miyazaki Medical College, Japan.

出版信息

Nihon Yakurigaku Zasshi. 1990 Sep;96(3):129-39. doi: 10.1254/fpj.96.3_129.

DOI:10.1254/fpj.96.3_129
PMID:1980256
Abstract

The antihypertensive effect of naftopidil (KT-611) following single oral administration was investigated in normotensive Wistar Kyoto rats (WKY), spontaneously hypertensive rats (SHR), DOCA-Salt hypertensive rats (DHR), 2-kidney 1-clip renal hypertensive rats (RHR) and Grollman type renal hypertensive dogs with 1-kidney (RHD); and it was compared with that of the selective alpha 1-adrenoceptor antagonist prazosin. The blood pressure and heart rate were measured under the unanesthetized, unrestrained state through an arterial catheter that was chronically implanted into the abdominal aorta. In SHR and WKY, both KT-611 (10 and 30 mg/kg, p.o.) and prazosin (1 and 3 mg/kg, p.o.) markedly inhibited the pressor response to the alpha 1-adrenoceptor agonist phenylephrine (3 micrograms/kg, i.v.). KT-611 (10 to 100 mg/kg, p.o.) showed a dose-dependent hypotensive effect in SHR, DHR and RHR but not in WKY. The hypotensive effect of KT-611 reached maximum at 0.5-1 hr, lasted for 4-6 hr and was more potent in DHR and RHR than in SHR. The potency of KT-611 was 1/10-1/30 weaker than that of prazosin. In RHD, single oral administration of KT-611 (1 to 10 mg/kg) caused a dose-dependent and long-lasting hypotensive effect. These results suggest that KT-611 has a long-lasting hypotensive effect in experimental hypertensive animal models.

摘要

在正常血压的Wistar Kyoto大鼠(WKY)、自发性高血压大鼠(SHR)、DOCA-盐高血压大鼠(DHR)、二肾一夹肾性高血压大鼠(RHR)和单肾Grollman型肾性高血压犬(RHD)中研究了萘哌地尔(KT-611)单次口服给药后的降压作用;并将其与选择性α1-肾上腺素受体拮抗剂哌唑嗪的降压作用进行了比较。通过长期植入腹主动脉的动脉导管,在未麻醉、不受约束的状态下测量血压和心率。在SHR和WKY中,KT-611(10和30mg/kg,口服)和哌唑嗪(1和3mg/kg,口服)均显著抑制对α1-肾上腺素受体激动剂去氧肾上腺素(3μg/kg,静脉注射)的升压反应。KT-611(10至100mg/kg,口服)在SHR、DHR和RHR中呈现剂量依赖性降压作用,但在WKY中无此作用。KT-611的降压作用在0.5 - 1小时达到峰值,持续4 - 6小时,在DHR和RHR中比在SHR中更强效。KT-611的效力比哌唑嗪弱1/10 - 1/30。在RHD中,单次口服KT-611(1至10mg/kg)产生剂量依赖性和持久的降压作用。这些结果表明,KT-611在实验性高血压动物模型中具有持久的降压作用。

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