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ICI 147,798对家兔的β受体产生不可克服的阻断作用。

Insurmountable beta receptor blockade by ICI 147,798 in rabbits.

作者信息

Murthy V S, Hwang T F, Wurm R, Zagar M E, Keith R A, Kau S T, Salama A I, Giles R E

机构信息

Department of Medicine, University of Wisconsin Medical School, Sinai Samaritan Medical Center, Milwaukee.

出版信息

J Pharmacol Exp Ther. 1989 Jan;248(1):249-55.

PMID:2563289
Abstract

In rabbits, the characteristics of cardiac beta-1 receptor blockade produced by ICI 147,798, a novel beta receptor blocking agent with diuretic properties, were evaluated and compared with those of propranolol. In conscious rabbits, i.v. injections of 0.31, 1.0 and 3.1 mg/kg of ICI 147,798 and 1.0 mg/kg of propranolol caused significant bradycardia. ICI 147,798 produced a dose-dependent shift to the right of the dose-response (chronotropic) curve of isoproterenol with suppression of the maximal tachycardia, an effect characteristic of insurmountable beta receptor blockade. Propranolol also produced a shift to the right of the dose-response curve of isoproterenol without affecting the maximal tachycardia. ICI 147,798-induced antagonism was specific for beta adrenoceptors as it failed to modify the effects of acetylcholine, angiotensin II, phenylephrine, adenosine, histamine and prostaglandin E2 on mean arterial pressure and heart rate. In rabbits with prior autonomic blockade, ICI 147,798, like propranolol, failed to inhibit the positive chronotropic effects of theophylline which are mediated by postreceptor mechanisms. In reserpinized rabbits, ICI 147,798 was found to have no intrinsic sympathomimetic activity. Unlike the effects of propranolol, which were attenuated by first-pass through the hepatic vascular bed, the effects of ICI 147,798 were unaffected suggesting an absence of first-pass metabolism. The effects of propranolol (1.0 mg/kg i.v.) were not detectable at 24 hr after injection, whereas significant beta receptor blocking activity was still present at 24 hr after ICI 147,798 (1.0 mg/kg i.v.). The results suggest that ICI 147,798 is a specific, long-acting, insurmountable beta-1 receptor blocking agent without intrinsic sympathomimetic activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在兔体内,对新型具有利尿特性的β受体阻滞剂ICI 147,798所产生的心脏β-1受体阻滞特征进行了评估,并与普萘洛尔的特征进行了比较。在清醒兔中,静脉注射0.31、1.0和3.1mg/kg的ICI 147,798以及1.0mg/kg的普萘洛尔均引起显著心动过缓。ICI 147,798使异丙肾上腺素的剂量-反应(变时性)曲线剂量依赖性右移,同时最大心动过速受到抑制,这是不可克服的β受体阻滞的特征性效应。普萘洛尔也使异丙肾上腺素的剂量-反应曲线右移,但不影响最大心动过速。ICI 147,798诱导的拮抗作用具有β肾上腺素受体特异性,因为它未能改变乙酰胆碱、血管紧张素II、去氧肾上腺素、腺苷、组胺和前列腺素E2对平均动脉压和心率的影响。在预先进行自主神经阻滞的兔中,ICI 147,798与普萘洛尔一样,未能抑制由受体后机制介导的茶碱的正性变时作用。在利血平化的兔中,发现ICI 147,798没有内在拟交感活性。与普萘洛尔经肝血管床首过代谢后作用减弱不同,ICI 147,798的作用未受影响,提示不存在首过代谢。注射后24小时,普萘洛尔(1.0mg/kg静脉注射)的作用无法检测到,而ICI 147,798(1.0mg/kg静脉注射)在24小时后仍存在显著的β受体阻滞活性。结果表明,ICI 147,798是一种特异性、长效、不可克服的β-1受体阻滞剂,无内在拟交感活性。(摘要截短于250字)

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