普瑞特罗的基本药理学特性。 - Suppr

Suppr

超能文献

Basic pharmacological properties of prenalterol.

作者信息

Mattsson H, Hedberg A, Carlsson E

出版信息

Acta Med Scand Suppl. 1982;659:9-37. doi: 10.1111/j.0954-6820.1982.tb00833.x.

DOI:10.1111/j.0954-6820.1982.tb00833.x

PMID:6127902

Abstract

摘要

相似文献

Basic pharmacological properties of prenalterol.普瑞特罗的基本药理学特性。

Acta Med Scand Suppl. 1982;659:9-37. doi: 10.1111/j.0954-6820.1982.tb00833.x.

Prenalterol as an antidote to massive doses of metoprolol--a cardiovascular study in the dog.普瑞纳洛尔作为大剂量美托洛尔的解毒剂——一项在犬类中的心血管研究。

Acta Med Scand Suppl. 1982;659:71-88. doi: 10.1111/j.0954-6820.1982.tb00837.x.

Actions of prenalterol, a new cardioselective beta1-agonist, terbutaline and isoprenaline on electrophysiological and mechanical parameters of guinea pig atrial and papillary muscles.

Acta Pharmacol Toxicol (Copenh). 1982 Jul;51(1):12-9. doi: 10.1111/j.1600-0773.1982.tb01056.x.

Characterization of the beta-adrenergic inhibition of motility in cat colon strips.猫结肠条中β-肾上腺素能对运动的抑制作用的表征

Eur J Pharmacol. 1982 Jan 8;77(1):25-31. doi: 10.1016/0014-2999(82)90530-1.

The measurement of the relative efficacy of agonists by selective potentiation of tissue responses: studies with isoprenaline and prenalterol in cardiac tissue.通过组织反应的选择性增强来测量激动剂的相对效力：在心脏组织中使用异丙肾上腺素和普瑞特罗的研究

J Auton Pharmacol. 1984 Sep;4(3):153-9. doi: 10.1111/j.1474-8673.1984.tb00092.x.

In vitro studies on the cardiac activity of prenalterol with reference to use in congestive heart failure.关于普瑞特罗用于充血性心力衰竭的心脏活性的体外研究。

J Pharmacol Exp Ther. 1982 Jan;220(1):77-85.

beta 1-and beta 2-adrenoceptor stimulatory effects of prenalterol.普瑞特罗对β1和β2肾上腺素能受体的刺激作用。

Naunyn Schmiedebergs Arch Pharmacol. 1982 Dec;321(4):302-8. doi: 10.1007/BF00498518.

Intrinsic sympathomimetic activity of the partial agonist prenalterol in relation to beta adrenoceptor interaction in various tissues, in vitro.部分激动剂普瑞特罗的内在拟交感活性与体外各种组织中β肾上腺素能受体相互作用的关系。

J Pharmacol Exp Ther. 1983 Mar;224(3):654-61.

The lack of a pronounced preference of prenalterol for the beta-l-adrenoceptor subtype.普瑞特罗对β₁-肾上腺素能受体亚型缺乏明显的偏好。

Naunyn Schmiedebergs Arch Pharmacol. 1980;315(1):85-8. doi: 10.1007/BF00504235.

Studies of catecholamine effect on cyclic AMP in human cultured thyroid cells: their interaction with thyrotrophin receptor.

Acta Endocrinol (Copenh). 1983 Jan;102(1):62-7. doi: 10.1530/acta.0.1020062.

引用本文的文献

Effect of norepinephrine, prenalterol and metoprolol on the histochemical localization of adenylate cyclase activity in the brown adipose tissue of newborn rat.去甲肾上腺素、普瑞特罗和美托洛尔对新生大鼠棕色脂肪组织中腺苷酸环化酶活性组织化学定位的影响。

Histochemistry. 1982;76(4):489-95. doi: 10.1007/BF00489904.

Arrhythmogenic dose of acetylstrophanthidin unchanged by beta-sympathomimetics in conscious dogs.在清醒犬中，拟交感神经药不改变乙酰毒毛旋花子苷元的致心律失常剂量。

Basic Res Cardiol. 1984 Nov-Dec;79(6):679-89. doi: 10.1007/BF01908385.

Influence of long-term beta receptor stimulation with prenalterol on intrinsic heart rate in rats.普瑞特罗长期刺激β受体对大鼠固有心率的影响。

Eur J Appl Physiol Occup Physiol. 1984;53(1):48-52. doi: 10.1007/BF00964689.

Acute haemodynamic effects of oral prenalterol in severe heart failure.口服普瑞特罗对重症心力衰竭的急性血流动力学效应

Br Heart J. 1984 Jul;52(1):49-52. doi: 10.1136/hrt.52.1.49.

Effect of prenalterol in asthmatic patients.普瑞特罗对哮喘患者的影响。

Eur J Clin Pharmacol. 1982 Oct;23(4):297-302. doi: 10.1007/BF00613609.

Studies of the agonist and antagonist activity of cicloprolol in man.环丙洛尔在人体中的激动剂和拮抗剂活性研究。

Eur J Clin Pharmacol. 1988;34(6):569-75. doi: 10.1007/BF00615219.

An assessment of the partial agonist activity of Ro 31-1118, flusoxolol and pindolol in man.罗 31-1118、氟索洛尔和吲哚洛尔在人体中的部分激动剂活性评估。

Br J Clin Pharmacol. 1987 Nov;24(5):571-80. doi: 10.1111/j.1365-2125.1987.tb03215.x.

Are the clinical benefits of oral prenalterol in ischaemic heart failure due to beta blockade? A six month randomised double blind comparison with placebo.口服普瑞特罗对β受体阻滞剂所致缺血性心力衰竭的临床益处如何？与安慰剂进行的为期6个月的随机双盲对照研究。

Br Heart J. 1985 Feb;53(2):208-15. doi: 10.1136/hrt.53.2.208.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验