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塞利洛尔的药理学研究:I.β受体阻滞作用、内在拟交感活性、血管舒张及降压作用

[Pharmacological studies of celiprolol: I. Beta-blocking effect, intrinsic sympathomimetic activity, vasodilating and hypotensive effects].

作者信息

Miura A, Kimura Y, Inoue K, Matsuzaki T, Ochi S, Hamada K, Hayashi S, Tamura M, Kano S, Kimura K

机构信息

Research Laboratories, Nippon Shinyaku Co., Ltd., Japan.

出版信息

Nihon Yakurigaku Zasshi. 1990 Apr;95(4):191-200. doi: 10.1254/fpj.95.4_191.

Abstract

The beta-blocking effect, intrinsic sympathomimetic activity (ISA), and vasodilating and hypotensive effects of celiprolol were tested. 1. Celiprolol competitively antagonized the isoproterenol-induced positive chronotropic and inotropic effects in guinea pig right atrial and papillary muscles and isoproterenol-induced guinea pig tracheal relaxation with pA2 values of 8.03, 7.98 and 6.43, respectively. 2. In dogs, isoproterenol-induced increases in cardiac contractility and heart rate were markedly inhibited by celiprolol (83.1 and 84.8%, respectively), while isoproterenol-induced hypotension was suppressed only by 16.8%. 3. Celiprolol increased the beating rate of the right atrium and relaxed the trachea isolated from normal and reserpinized guinea pigs. Celiprolol also potentiated the contractility of the left atrium isolated from reserpinized animals. These effects of celiprolol were antagonized by propranolol. 4. Celiprolol concentration-dependently relaxed rat femoral arteries contracted by methoxamine. The concentration-relaxation curve was shifted to the right by pretreatment with propranolol. 5. Orally administered celiprolol produced long lasting hypotension in conscious SHR without any heart rate change. 6. These results indicate that celiprolol is a highly cardioselective beta-blocker with a significant ISA, which contributes to its vasodilatory and hypotensive effects.

摘要

对塞利洛尔的β受体阻滞作用、内在拟交感活性(ISA)以及血管舒张和降压作用进行了测试。1. 塞利洛尔竞争性拮抗异丙肾上腺素在豚鼠右心房和乳头肌中诱导的正性变时和变力作用以及异丙肾上腺素诱导的豚鼠气管舒张,其pA2值分别为8.03、7.98和6.43。2. 在犬中,塞利洛尔显著抑制异丙肾上腺素诱导的心脏收缩力增加和心率加快(分别为83.1%和84.8%),而异丙肾上腺素诱导的低血压仅被抑制16.8%。3. 塞利洛尔增加正常和利血平化豚鼠分离的右心房的搏动频率并舒张气管。塞利洛尔还增强利血平化动物分离的左心房的收缩力。塞利洛尔的这些作用被普萘洛尔拮抗。4. 塞利洛尔浓度依赖性地舒张甲氧明收缩的大鼠股动脉。用普萘洛尔预处理后,浓度-舒张曲线右移。5. 口服塞利洛尔可使清醒的自发性高血压大鼠产生持久的低血压,且心率无任何变化。6. 这些结果表明,塞利洛尔是一种具有显著内在拟交感活性的高度心脏选择性β受体阻滞剂,这有助于其血管舒张和降压作用。

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