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本文引用的文献

1
Digitalis glycosides: mechanisms and manifestations of toxicity. Part III.洋地黄苷:毒性机制与表现。第三部分。
Prog Cardiovasc Dis. 1984 Jul-Aug;27(1):21-56. doi: 10.1016/0033-0620(84)90018-5.
2
Cardiovascular alpha 2-receptors.心血管α2受体
J Mol Cell Cardiol. 1983 Nov;15(11):717-33. doi: 10.1016/0022-2828(83)90332-2.
3
Alpha-adrenergic drugs. Pharmacological tools for the study of the central vasomotor control.α-肾上腺素能药物。用于研究中枢血管舒缩控制的药理学工具。
Biochem Pharmacol. 1983 May 1;32(9):1459-65. doi: 10.1016/0006-2952(83)90466-5.
4
Effect of different beta-blocking agents on an in vitro model of ventricular automaticity.不同β受体阻滞剂对心室自律性体外模型的影响。
Methods Find Exp Clin Pharmacol. 1982;4(5):307-11.
5
Interactions between the autonomic nervous system and the cardiovascular effects of ouabain in guinea-pigs.豚鼠自主神经系统与哇巴因心血管效应之间的相互作用。
Eur J Pharmacol. 1982 Feb 19;78(1):21-32. doi: 10.1016/0014-2999(82)90368-5.
6
A comparison of the cardiovascular and sedative actions of the alpha-adrenoceptor agonists, FLA-136 and clonidine, in the rat.大鼠体内α-肾上腺素能受体激动剂FLA - 136与可乐定的心血管及镇静作用比较
Br J Pharmacol. 1982 Jan;75(1):13-21. doi: 10.1111/j.1476-5381.1982.tb08753.x.
7
The capacity of different digitalis materials to induce ventricular rhythm disturbances in the reserpine-pretreated cat.不同洋地黄制剂在利血平预处理猫中诱发心室节律紊乱的能力。
J Pharmacol Exp Ther. 1967 Apr;156(1):159-65.
8
[Pharmacological effects of 2-(2,6-dichlorophenylamino)-2-imidazoline hydrochloride, a new, antihypertensive substance].新型抗高血压物质2-(2,6-二氯苯基氨基)-2-咪唑啉盐酸盐的药理作用
Arzneimittelforschung. 1966 Aug;16(8):1038-50.
9
Effect of 6-hydroxydopamine on cardiotoxicity of ouabain in guinea pigs.6-羟基多巴胺对哇巴因致豚鼠心脏毒性的影响。
Jpn J Pharmacol. 1974 Dec;24(6):923-5. doi: 10.1254/jjp.24.923.
10
Autonomic nervous system and control of cardiac rhythm.自主神经系统与心律控制
Nature. 1967 May 27;214(5091):912-3. doi: 10.1038/214912a0.

可乐定对哇巴因致豚鼠心律失常及致死作用的保护作用。

Protective action of clonidine against the arrhythmogenic and lethal effects of ouabain in guinea-pigs.

作者信息

Thomas G P, Stephen P M

机构信息

Department of Pharmacology, Christian Medical College, Vellore, India.

出版信息

Br J Pharmacol. 1991 Dec;104(4):995-9. doi: 10.1111/j.1476-5381.1991.tb12539.x.

DOI:10.1111/j.1476-5381.1991.tb12539.x
PMID:1687372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1908856/
Abstract
  1. Clonidine (1.25, 2.5 and 5.0 micrograms kg-1) was studied for its effect on the cardiac arrhythmias and lethality induced by slow intravenous infusion of ouabain in guinea-pigs. 2. Clonidine produced significant delays in the onset of the arrhythmic stages and lethality. However, clonidine did not offer any such protection in reserpinised guinea-pigs, whereas its effects were unaltered in atropinized guinea-pigs. 3. Idazoxan (100 micrograms kg-1, i.v.) abolished the antiarrhythmic effect of clonidine whereas corynanthine (1 mg kg-1, i.v.) had no such effect. 4. Clonidine inhibited the rate of the ouabain-induced rise in blood pressure and the peak pressor response. 5. In isolated paced left atria of the guinea-pig, clonidine (3.75 x 10(-4) M) did not offer any protection against rapid and/or irregular extrasystolic contractions induced by ouabain. 6. It is concluded that the antiarrhythmic effect of clonidine is due to its effects on the indirect neural components of digitalis toxicity mediated by the stimulation of alpha 2-adrenoceptors, without any direct antiarrhythmic effect on the myocardium.
摘要
  1. 研究了可乐定(1.25、2.5和5.0微克/千克)对豚鼠缓慢静脉注射哇巴因所致心律失常和致死率的影响。2. 可乐定显著延迟了心律失常阶段和致死率的出现。然而,可乐定对利血平化豚鼠没有提供任何此类保护作用,而其在阿托品化豚鼠中的作用未改变。3. 咪唑克生(100微克/千克,静脉注射)消除了可乐定的抗心律失常作用,而育亨宾(1毫克/千克,静脉注射)没有这种作用。4. 可乐定抑制了哇巴因引起的血压升高速率和升压反应峰值。5. 在豚鼠离体起搏左心房中,可乐定(3.75×10⁻⁴M)对哇巴因诱导的快速和/或不规则期外收缩没有提供任何保护作用。6. 得出结论,可乐定的抗心律失常作用是由于其对由α₂肾上腺素能受体刺激介导的洋地黄毒性间接神经成分的作用,而对心肌没有任何直接抗心律失常作用。