Suppr超能文献

莫索尼定与可乐定对正常血压受试者血流动力学及行为影响的比较。

A comparison of the haemodynamic and behavioural effects of moxonidine and clonidine in normotensive subjects.

作者信息

Macphee G J, Howie C A, Elliott H L, Reid J L

机构信息

Department of Medicine and Therapeutics, Stobhill General Hospital, Glasgow.

出版信息

Br J Clin Pharmacol. 1992 Mar;33(3):261-7. doi: 10.1111/j.1365-2125.1992.tb04033.x.

Abstract
  1. This randomised double-blind placebo controlled crossover study in healthy normotensive males compared the haemodynamic and behavioural responses following single oral doses of moxonidine (200 micrograms), clonidine (200 micrograms) and placebo. 2. Both active drugs significantly reduced blood pressure as compared with placebo: on average (over the study day) by -5.6/-0.8 with moxonidine and by -13.3/-5.3 mm Hg with clonidine. The hypotensive effect of clonidine was significantly greater (95% CI 3.2-12.2). Heart rate was unchanged by either drug. 3. Psychomotor testing, salivary flow and side effect reporting showed a consistent treatment rank order similar to that of the hypotensive response: clonidine greater than moxonidine greater than placebo. 4. Although moxonidine produced less adverse effects than clonidine, an equivalent hypotensive response was not demonstrated in normal subjects. Further study at comparable antihypertensive doses is required to clarify the relative side effect profile of these agents.
摘要
  1. 这项针对健康血压正常男性的随机双盲安慰剂对照交叉研究,比较了单次口服莫索尼定(200微克)、可乐定(200微克)和安慰剂后血液动力学及行为学反应。2. 与安慰剂相比,两种活性药物均显著降低了血压:平均而言(在研究日期间),莫索尼定使血压降低-5.6/-0.8,可乐定使血压降低-13.3/-5.3毫米汞柱。可乐定的降压效果显著更强(95%置信区间为3.2 - 12.2)。两种药物均未使心率发生改变。3. 精神运动测试、唾液分泌量及副作用报告显示出与降压反应相似的一致治疗排序:可乐定大于莫索尼定大于安慰剂。4. 尽管莫索尼定产生的不良反应比可乐定少,但在正常受试者中未显示出等效的降压反应。需要在相当的抗高血压剂量下进行进一步研究,以阐明这些药物相对的副作用情况。

相似文献

1
A comparison of the haemodynamic and behavioural effects of moxonidine and clonidine in normotensive subjects.
Br J Clin Pharmacol. 1992 Mar;33(3):261-7. doi: 10.1111/j.1365-2125.1992.tb04033.x.
8
Effect of moxonidine on blood pressure and sympathetic tone in conscious spontaneously hypertensive rats.
Eur J Pharmacol. 1998 Nov 27;362(1):61-7. doi: 10.1016/s0014-2999(98)00726-2.

引用本文的文献

1
Pharmacological profiles of alpha 2 adrenergic receptor agonists identified using genetically altered mice and isobolographic analysis.
Pharmacol Ther. 2009 Aug;123(2):224-38. doi: 10.1016/j.pharmthera.2009.04.001. Epub 2009 Apr 23.
5
The I1-imidazoline receptor: from binding site to therapeutic target in cardiovascular disease.
J Hypertens Suppl. 1997 Jan;15(1):S9-23. doi: 10.1097/00004872-199715011-00002.
6
Clinical experience with moxonidine.
Cardiovasc Drugs Ther. 1994 Mar;8 Suppl 1:49-58. doi: 10.1007/BF00877084.
7
Moxonidine. A review of its pharmacology, and therapeutic use in essential hypertension.
Drugs. 1992 Dec;44(6):993-1012. doi: 10.2165/00003495-199244060-00008.

本文引用的文献

2
Sedative and cardiovascular effects of clonidine and nitrazepam.
Clin Pharmacol Ther. 1980 Aug;28(2):167-76. doi: 10.1038/clpt.1980.146.
4
Psychomotor function and psychoactive drugs.
Br J Clin Pharmacol. 1980 Sep;10(3):189-209. doi: 10.1111/j.1365-2125.1980.tb01745.x.
6
Crossover comparison of moxonidine and clonidine in mild to moderate hypertension.
Eur J Clin Pharmacol. 1984;27(2):147-52. doi: 10.1007/BF00544037.
7
Investigations into the mechanism of the hypotensive effect of 2-(2,6-dichlorphenylamino)-2-imidazoline-HCl.
Eur J Pharmacol. 1967 Dec;2(3):155-62. doi: 10.1016/0014-2999(67)90080-5.
8
Intraindividual comparison of moxonidine and prazosin in hypertensive patients.
Eur J Clin Pharmacol. 1986;29(6):645-50. doi: 10.1007/BF00615953.
9
Pharmacokinetics of moxonidine after single and repeated daily doses in healthy volunteers.
J Clin Pharmacol. 1987 Dec;27(12):988-93. doi: 10.1002/j.1552-4604.1987.tb05602.x.
10
Comparison of moxonidine and clonidine HCl in treating patients with hypertension.
J Clin Pharmacol. 1987 Jan;27(1):46-51. doi: 10.1177/009127008702700107.

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